Renal Cell Carcinoma
- Renal Cell Carcinoma
What every physician needs to know.
- Are you sure your patient has renal cell carcinoma? What should you expect to find?
Beware of other conditions that can mimic renal cell carcinoma:
- Which individuals are most at risk for developing renal cell carcinoma:
- What laboratory and imaging studies should you order to characterize this patient's tumor (i.e., stage, grade, CT/MRI vs PET/CT, cellular and molecular markers, immunophenotyping, etc.) How should you interpret the results and use them to establish prognosis and plan initial therapy?
- What therapies should you initiate immediately i.e., emergently?
- What should the initial definitive therapy for the cancer be?
What other therapies are helpful for reducing complications?
What should you tell the patient and the family about prognosis?
What if scenarios.
- Follow-up surveillance and therapy/management of recurrences.
What other clinical manifestations may help me to diagnose renal cell carcinoma?
What other additional laboratory studies may be ordered?
What's the evidence?
Renal Cell Carcinoma
What every physician needs to know.
Renal cell carcinoma (RCC) accounts for 3% of malignant tumors and is the seventh leading cause of cancer deaths in the USA. An estimated 63,000 new renal tumors were diagnosed in 2013 with over 13,000 deaths. It is most common in the seventh decade of life, and there is consistent male to female predominance (2:1).
There has been significant progress in the understanding and management of this RCC within the past 10 years, and emerging surgical and systemic therapy strategies have revolutionized the management of this disease.
In localized disease, partial nephrectomy for small tumors and radical nephrectomy for larger tumors are now the gold standard. Currently, there is an emphasis on less invasive approaches with preservation of renal function.
Cytoreductive nephrectomy in patients with synchronous metastatic disease remains a standard before patients receive systemic treatment. The current approaches for management of patients with metastatic RCC (mRCC) utilize knowledge of histology, molecular abnormalities, clinical prognostic factors and the efficacy/toxicity of available agents.
The role of immunotherapy with cytokines remains controversial, and mainly limited to good prognosis patients. Development of immune checkpoint inhibitors represents a major advance in the application of immunotherapy, and multiple agents inhibiting cytotoxic T-lymphocyte antigen 4 (CTLA4), programmed death 1 (PD1), and PD ligand 1 (PDL1) are now in clinical trials. Development of therapies which target relevant biologic pathway elements also represent a principal treatment advance. Agents blocking angiogenic pathways - such as sunitinib, pazopanib, sorafenib, and bevacizumab - as well as the mammalian target of rapamycin (mTOR) inhibitors, everolimus and temsirolimus, have demonstrated efficacy and offer new strategic options for patients with metastatic RCC.
Are you sure your patient has renal cell carcinoma? What should you expect to find?
Patients with RCC can present with either local or systemic symptoms; however, the most frequent presentation currently is incidental. This is secondary to the widespread use of abdominal imaging and the incidental discovery of a small renal mass.
Local signs and symptoms:
palpable abdominal mass
When present, these clinical features may carry negative prognostic implications. Systemic symptoms can be due to metastases or paraneoplastic phenomena such as:
The diversity of paraneoplastic syndromes associated with RCC is remarkable, and historically RCC was often termed “The Internist's Tumor.” Since ultrasonography and computed tomography (CT) imaging are associated with incidental detection of many asymptomatic renal tumors, RCC is also often referred to as “The Radiologist's Tumor.”
Renal cell carcinoma subtypes
A major advance in understanding RCC is the realization that this disease is not a single entity but rather a collection of different tumor types, each derived from the various parts of the nephron and possessing distinct genetic characteristics, histologic features and - to some extent - clinical phenotype.
Clear cell renal cell carcinoma
The most common epithelial renal tumor is clear cell RCC (80 to 85%). The name reflects the tumor cell's high cytoplasmic lipid content, which dissolves during histologic preparation to leave a clear area in the cytoplasm.
The Fuhrman grading system based on nuclear morphology is a significant prognostic factor in clear cell RCC.
Papillary renal cell carcinoma
Papillary RCC represents a smaller fraction of renal tumors (10 to 15%), and is further divided into type 1 and a more aggressive type 2 variety.
Chromophobe, collecting duct, unclassified and medullary - the latter occurring almost exclusively in patients with sickle cell trait - are more rare subtypes.
Sarcomatoid differentiation is a not a histologic subtype, but refers to a growth pattern which can be found in any subtype. Sarcomatoid tumors contain spindle cells, increased cellularity and atypical cell that indicate a potentially aggressive disease course.
Beware of other conditions that can mimic renal cell carcinoma:
The differential diagnosis of a renal mass lesion depends upon the lesion size and its radiographic characteristics. The majority of renal masses are currently detected as incidental findings (>50% of patients), and not all are malignant tumors.
In view of their characteristic radiographic appearance and ease of removal, small renal masses are not routinely biopsied. In the past, it was assumed these lesions were malignant, and they were managed accordingly. Presently, the management of such small lesions is under study. Active surveillance is considered reasonable in patients with small lesions. Larger tumors (>3cm) and those with aggressive appearance, such as an infiltrative growth pattern, are more likely malignant, and should be approached accordingly.
In patients with large renal masses where removal is planned, biopsy likewise offers no advantages. In the setting of metastatic disease or locally advanced, inoperable lesions, biopsy of the renal mass is a viable diagnostic option.
Renal tumors, such as angiomyolipomas, can be differentiated from RCC utilizing radiographic means.
Which individuals are most at risk for developing renal cell carcinoma:
RCC is a male-predominant (2:1) cancer.
RCC typically presents in the sixth or seventh decade of life. The median age at presentation is approximately 60 years.
The majority of RCC tumors are sporadic, and only 2-3% of RCC cases are familial. In patients with bilateral renal tumors or who are young (<40 years old), a search for genetic causes of RCC should be considered. There are several autosomal dominant syndromes described, each with a distinct genetic basis and phenotype.
Von Hippel Lindau (VHL) syndrome is the most common genetic syndrome associated with RCC. These patients are at risk for the development of tumors in a variety of organs, including the kidney. In RCC patients with a family history of retinal angioma, cerebellar or spinal hemangioblastoma, pancreatic neuroendocrine tumors, or pheochromocytomas, the presence of this syndrome should be suspected. In these cases, testing for germline mutations of the VHL gene should be considered.
A hereditary syndrome in which the VHL gene does not contain a mutation, but is associated with an increased risk of developing clear cell RCC, has also been described. This familial syndrome should be considered if more than one family member has been diagnosed with clear cell carcinoma, and germline mutations of the VHL gene are absent.
When patients are found to have multifocal papillary RCC tumors, hereditary papillary cancer syndromes should be considered. In patients with multifocal papillary type 1 cancers, hereditary papillary renal carcinoma HPRC) should be suspected. HPRC is caused by germline mutation of the MET gene.
Hereditary leiomyomatosis renal cell carcinoma (HLRCC) is another hereditary renal cancer syndrome.
These patients can develop bilateral kidney tumors and cysts, as well as cutaneous and uterine leiomyomas. HLRCC is characterized by a germline mutation of the Krebs cycle enzyme, fumarate hydratase. The renal tumors in HLRCC have pathologic features of type 2 papillary cancers, and demonstrate aggressive behavior. Lymph node metastases are common, and even when the primary tumor is small (<1 cm) metastatic disease may be found.
When multifocal chromophobe and oncocytic tumors are present, the Birt-Hogg-Dube (BHD) syndrome should be suspected. These patients also demonstrate benign cutaneous tumors, fibrofolliculomas, pulmonary cysts, and recurrent pneumothoraces. BHD is characterized by germline mutations of the BHD gene. In patients at risk, germline mutation testing for the BHD gene is recommended.
In patients with multiple oncytomas of the kidneys, familial renal oncocytoma (FRO) should be suspected. These patients do not develop chromophobe tumors, do not have a mutation of the BHD gene, and do not develop the extra-renal manifestations of the BHD syndrome.
Patients with tuberous sclerosis (TSC) are at risk to develop bilateral renal tumors. These individuals may also have cutaneous lesions, central nervous system (CNS) hamartomas, and pulmonary cysts. Renal tumors in these patients are generally benign, and are most commonly angiomyolipomas. Reports of TSC patients with either clear cell, chromophobe, or papillary renal tumors have appeared.
The major environmental risk factor associated with RCC development is either active or passive cigarette smoking, with a relative risk of approximately 2-3 fold. Other potential environmental etiologies such as acetaminophen/analgesic use, asbestos or trichloroethylene exposure have not been convincingly linked to RCC.
Obesity (specifically body mass index [BMI]) is also a recognized risk factor. It has also been suggested hypertension is an RCC risk factor. Data suggests anti-hypertensive therapy such as diuretics is not independently associated with RCC development.
Finally, RCC is more common in patients with end-stage renal disease (ESRD), acquired renal cystic disease, and tuberous sclerosis. Autosomal Dominant Polycystic Kidney Disease (ADPKD) is not currently considered to be a risk factor for RCC; however, recent data suggests that the incidence of RCC in patients with ADPKD is higher than the rate for RCC in the general population, as well as that in patients with ESRD.
Most patients do not have an identifiable risk factor, and the pathogenic mechanisms underlying the established risk factors remain obscure.
What laboratory and imaging studies should you order to characterize this patient's tumor (i.e., stage, grade, CT/MRI vs PET/CT, cellular and molecular markers, immunophenotyping, etc.) How should you interpret the results and use them to establish prognosis and plan initial therapy?
Tumor staging is an important component of current risk assessment techniques. Advanced tumor stages have been clearly correlated with poor prognosis, regardless of therapy. Using TNM staging guidelines, 5-year survival rates are as follows:
stage I: 95%
stage II: 88%
stage III: 59%
Stage IV: <20%
Several nomograms have been developed that utilize characteristics such as tumor size, stage, grade, pathologic findings and patient symptoms to predict disease-free and overall survival in patients with localized tumors.
The Fuhrman nuclear grade of a renal tumor is another well established prognostic indicator. This scheme is based on nuclear size and shape, along with the prominence of nucleoli. 5-year survival rates are as follows:
grade I: 94%
grade II: 86%
grade III: 59%
grade IV: 51%
Patients with localized disease and non-clear cell histology have an improved prognosis compared to those having clear cell RCC. However, once metastases develop, non-clear cell histology is associated with a much poorer prognosis. Tumor size may also be a useful predictor for both local and locally advanced RCC.
A significant association between disease-free survival and tumor size has been reported. Additionally, patients with larger tumors are more likely to develop metastatic disease.
Survival is also associated with clinical presentation, especially if the patient is symptomatic at diagnosis. The median 5-year disease-free survival rates for initially symptomatic and asymptomatic patients are 57% and 83%, respectively.
Approach to staging
In patients with localized renal tumors, staging is accomplished primarily utilizing an abdominal/pelvic CT which will assess local invasiveness, lymph node involvement, and the presence of other metastases. Additional studies utilized for clinical staging include a chest CT, laboratory studies including complete blood counts, biochemical profiles (liver, renal, metabolic, LDH), and in selected patients CNS imaging and bone scans.
In patients with known or suspected metastatic RCC, staging plays a very important role in assessment of disease extent and prognosis. In contrast to individuals with localized renal tumors, end organ targets of metastatic disease are thoroughly investigated.
Based on analyses from Memorial Sloan Kettering Cancer Center (MSKCC) and the Cleveland Clinic, the following factors have been associated with poor prognosis in stage IV disease:
Low Karnofsky performance status (<80%).
Low serum hemoglobin (<lower limit of normal).
High corrected calcium (>10 mg/dl).
Elevated LDH (>1.5 x upper limit of normal).
Short disease-free interval (<1 year from diagnosis to start of systemic therapy).
Prognostic groups were defined as:
Favorable (no factors): median overall survival 28 months.
Intermediate (1-2 factors): median overall survival 13.6 months.
>=3 factors): median overall survival 4.6 months.
These risk criteria were then utilized in a series of phase II and III clinical trials for purposes of patient stratification. They can also be utilized to assist in guiding initial choice of therapy for patients with mRCC. Even though these criteria were developed in the cytokine era, they remain valuable prognostic tools in the current era of targeted therapy.
The MSKCC scheme was developed to assess untreated patients. In refractory patients, this scheme has been modified. In patients with prior therapy, three factors have been identified as associated with poor risk:
Low performance status
High corrected serum calcium
Median overall survival according the number of risk factors:
0: 22 months
1: 11.9 months
>2: 5.4 months
This scheme has been utilized in several recent clinical trials for stratifying patients upon study entry. It is unclear if this approach is of value clinically, since analysis of data from the recent RECORD 1 trial did not demonstrate different efficacy patterns for the three prognostic categories.
An alternate classification has been recently developed utilizing patients receiving anti-vascular endothelial growth factor (VEGF) therapy. Four of the five adverse MSKCC prognostic factors were independent predictors of short survival including:
Hemoglobin less than the lower limit of normal.
Corrected calcium greater than the upper limit of normal.
Karnofsky performance status less than 80%.
Time from diagnosis to treatment of less than 1 year.
In addition, neutrophils greater than normal and thrombocytosis were independent adverse prognostic factors.
Patients were again segregated into three categories:
Favorable (no adverse factors): median OS not reached; 2-year OS 75%.
Intermediate (1-2 factors): median OS 27 months.
Poor risk (
>3 factors): median OS 8.8 months.
This model validated components of the MSKCC model, with the addition of platelet and neutrophil counts. It is under evaluation for patients receiving VEGF-targeted agents.
What therapies should you initiate immediately i.e., emergently?
Immediate therapy may be required if a medical emergency related to metastatic RCC has developed. These are uncommon at the time of initial diagnosis, but the following list summarizes the potential varieties that may be encountered:
Spinal cord compression
Impending fracture and pain
Gross hematuria secondary to primary tumor
Hemoptysis secondary to intra-bronchial lesion
IVC thrombus with Budd-Chiari Syndrome
Left atrial thrombus
Multiple pulmonary emboli
The majority of these require some form of emergent therapy. Treatment should be initiated rapidly, while a tissue diagnosis and staging studies are conducted. The type of therapy required is determined by the nature of the complication. Nephrectomy for locally advanced RCC may play a prominent role in patients presenting with IVC or left atrial thrombi. CNS metastases and spinal cord compression may require radiation therapy and/or surgery for optimal palliation.
The metabolic complication of hypercalcemia may be seen in RCC patients with extensive osseous metastases, but has become less common with the widespread use of bisphosphonates to decrease the skeletal complication rate in RCC patients.
What should the initial definitive therapy for the cancer be?
The treatment of patients with RCC can be considered from the perspective of the roles of surgery and systemic therapy. RCC is still predominantly a surgical disease for which radical surgery is justified and strongly indicated in specific situations. The role of systemic therapy has evolved within the past five years, and is increasingly important in patient management.
The application of these two modalities depends upon stage, histology, prognostic factors, and the patient's co-morbid disease.
Localized renal cell carcinoma
Patients with small renal masses are being seen with increased frequency. Treatment options have recently expanded, and have produced some controversies. Traditionally, these patients are treated aggressively, with radical nephrectomy. It is now clear that this approach may predispose patients to development of chronic kidney disease with attendant cardiovascular risks.
Nephron-sparing approaches such as partial nephrectomy, thermal ablation, and active surveillance have emerged as viable options. Nephron-sparing approaches are considered in patients with small renal masses, if tumor control is possible. Partial nephrectomy remains the reference standard for the management of small renal masses.
Radical nephrectomy remains a viable option when dictated by tumor size, location or radiographic appearance.
Active surveillance or observation is a reasonable approach for management of small localized renal tumors. It is a primary consideration for patients who have a decreased life expectancy and/or significant comorbidities making them high risk for surgery.
The thermal ablative procedures (cryoablation, radiofrequency ablation) are also options for high-risk patients who desire active therapy rather than observation. A tumor biopsy should be obtained prior to treatment to define histology. Post-treatment biopsy should also be considered.
Patients should be informed of the increased risk of local recurrence, the potential need for repeat ablation, or the possibility of difficult salvage surgery if tumor progression develops. Larger tumors, and those with an infiltrative appearance may be associated with an increased risk of recurrence compared to surgery.
A tumor over 7.0 cm has an increased potential of malignancy and invasiveness. In approximately 5 to 10% of renal tumors, tumor thrombus may extend into the venous system, often involving the ascending inferior vena cava, up to and including the right atrium. Generally, these tumors are managed by radical surgery.
The goal is total surgical excision, presuming the patient is a surgical candidate and vital structures are not compromised by surgery. Locally advanced renal tumors are managed with radical nephrectomy. Occasionally, en bloc resection of adjacent structures, isolation and temporary occlusion of vessels with thrombectomy, and cardiopulmonary bypass may be required. Despite the locally advanced nature of their tumors, over 40% of patients can be cured with such aggressive approaches.
The role of postoperative adjuvant systemic therapy is currently unknown, and of no proven value. Therapy in this setting with a variety of tyrosine kinase inhibitors is currently being studied in a series of clinical trials.
Metastatic renal cell carcinoma
In the past, it was estimated that 25 to 30% of RCC patients presented with metastatic disease and their primary tumor in place. Recently, this presentation has become less common, perhaps related to the increased frequency of incidentally discovered renal masses.
Nephrectomy in patients with metastatic RCC (debulking or cytoreductive nephrectomy) is often part of an integrated management strategy. In the 1990s, two studies were conducted in which patients were randomized to either nephrectomy or no surgery, both followed by interferon alfa (IFN-a). In the combined analysis of these trials, the median survival was 13.6 months for the group treated with debulking nephrectomy followed by IFN-a compared to 7.8 months for IFN-a alone.
The mechanisms responsible for this beneficial effect are unknown. The cytoreductive paradigm remains the recommended approach in these patients, even though it has not yet been tested prospectively in patients who receive targeted therapy.
Presumably, the major effect seen is in patients with clear cell carcinoma. Cytoreductive nephrectomy in patients presenting with synchronous metastatic non-clear cell carcinoma has not been formally investigated. The type of systemic therapy recommended following cytoreductive nephrectomy is similar to that utilized in patients discussed in the subsequent paragraphs.
Patients with limited metastatic disease should be considered for metastasectomy. These individuals represent a minority (2-3%) of cases, but long-term disease control occurs in selected patients. Favorable prognostic factors include a long disease-free interval between diagnosis and metastasis development. This reflects an indolent course and the possibility that a metastasis may be solitary.
Patients with favorable features and isolated pulmonary metastases may have a 30% five-year survival with metastasectomy. Surgical resection of solitary metastases should be an option in selected patients.
Current therapeutic approaches for management of metastatic RCC utilize knowledge of histology, molecular abnormalities, clinical prognostic factors, knowledge of the natural history of RCC, and the efficacy and toxicity of the available agents.
Since December 2005, seven new agents have been approved in the US for the treatment of advanced RCC:
Four are multi-targeted tyrosine kinase inhibitors (TKIs) including sunitinib, sorafenib, pazopanib, and recently axitinib.
Two (temsirolimus and everolimus) target the mammalian target of rapamycin (mTOR)
One is a humanized monoclonal antibody (bevacizumab, administered in combination with INFa) which targets vascular endothelial growth factor (VEGF).
Previously, interferon-a (INF-a) and interleukin-2 (IL-2) were the mainstays of therapy.
Currently, therapy recommendations depend upon histology (clear versus non-clear cell), prognostic group (favorable, intermediate, poor), and prior treatment status (naïve versus refractory). These individual groups provide a framework for consideration of current treatment. Patients with co-morbid conditions such as a recent cardiovascular event, impaired renal or hepatic function, and CNS metastases are considered separately.
Additionally, several unique categories such as sarcomatoid differentiation and rare histologic subtypes are included. The preferred treatment recommendations have been reviewed by numerous groups including the National Comprehensive Cancer Network (NCCN), European Society of Medical Oncology (ESMO), European Urological Association (EUA), and during recent American Society of Clinical Oncology (ASCO) meetings. The data from the recent RCC clinical trials performed have been utilized to help define therapy in the treatment naïve and refractory groups, in other settings, the information is from individual reviews, retrospective analyses, and clinical anecdotes.
Metastatic clear cell carcinoma
The histologic diagnosis of clear cell carcinoma is important to assist in determining therapy. If there is uncertainty, the likelihood exists the underlying histologic pattern represents clear cell carcinoma, and therapy can be administered for this presumed diagnosis.
These individuals have not received previous systemic therapy. Most individuals will fall into this category.
Treatment naïve, favorable risk metastatic clear cell carcinoma
Patients in this category should have no poor risk factors (10 to 20% of patients). They generally have low volume metastatic disease, predominantly pulmonary metastases, are asymptomatic, and may have long disease-free intervals.
The therapy recommended in this group would include:
a TKI such as sunitinib or pazopanib,
or the combination of bevacizumab plus IFN-a.
All of these options are associated with clinical toxicity; therefore, risk-benefit assessment may be helpful when estimating the potential utility of starting treatment. There are patients in this category where therapy can be delayed, the rate of disease progression observed, and therapy initiated at a later time. Recently, the COMPARZ (phase 3) and PISCES (phase 2) trials have compared pazopanib and sunitinib as first line therapeutic options. Pazopanib was found to be non-inferior to sunitinib, but importantly patient tolerance and preference favoured pazapanib.
No published criteria are available that define this group; however, it probably includes the patient with low-volume disease, small but stable lung metastases, and a long disease-free interval. Not all patients with newly diagnosed metastatic RCC should receive immediate systemic therapy. Active surveillance, as in the case of small renal masses is a viable option.
An alternate therapeutic option in this category is cytokine therapy with high dose IL-2. This approach requires hospitalization, is associated with toxicity from the capillary leak syndrome, and a low rate of treatment associated mortality. It is generally utilized only in centers with significant expertise in administering high dose IL-2, and in patients who can tolerate this type of aggressive treatment.
Treatment naïve, intermediate risk metastatic clear cell carcinoma
This group contains the largest number of patients (60 to 70%). They are minimally symptomatic, most have had a prior nephrectomy, and have few, if any, laboratory abnormalities.
Therapy for this group should consist of:
A TKI, or
Combined bevacizumab and IFN-a.
Selection of the specific agent or regimen will depend on the presumed risk benefit of each approach in patients; however, all of the options are acceptable. No comparative trials have been published that define differences or similarities between these treatments.
Occasionally, patients in this group will have disease compromising vital organ function, e.g. mediastinal lymph nodes producing respiratory compromise, hematuria secondary to a primary tumor. In this setting, rapid tumor response is desirable. The agent with the highest likelihood of response may be the best alternative.
As with the favorable group, high dose IL-2 therapy is an option to be discussed with these patients dependent upon their age and cardiovascular status. The issues discussed in the favorable group are applicable in these patients.
Treatment naïve, poor risk metastatic clear cell carcinoma
This group of patients has the largest tumor burden, are symptomatic, may have their primary tumors in place (10 to 15% of patients).
Treatment generally consists of:
The mTOR inhibitor temsirolimus.
This is the only treatment that has been examined in a phase 3 trial in these patients. This agent was well tolerated by poor-risk patients, without excessive toxicity noted. In view of these level 1 data, therapy with weekly intravenous temsirolimus is recommended for poor-risk patients. Use of sunitinib in this group is poorly defined; however, a phase 3 trial comparing sunitinib to IFN-a suggested selected poor risk patients may benefit. The role of other first-line treatment options such as pazopanib or bevacizumab plus IFN-a remains poorly defined.
The majority of patients receiving a targeted agent will have partial responses or stable disease, and will ultimately progress. The mechanisms responsible for the development of resistance are unclear, and therapeutic decisions require knowledge of previous therapy, as well as response or clinical benefit related to front-line treatment. Therapy for refractory patients is best defined by considering the type of initial treatment, and whether the resistance is acquired or intrinsic.
Use of cytokines as initial therapy is currently limited, but some of the earlier clinical trials have defined treatment of this patient population. The TKIs sorafenib, sunitinib, pazopanib, or axitinib can be utilized. The data for sorafenib and axitinib are from randomized trials. Axitinib proved superior in prolonging progression-free survival (PFS), and is generally considered as the first choice for these patients. Sunitinib and pazopanib represent alternatives. Response rates to sunitinib or pazopanib are 30 to 40%, and PFS between 7 and 8 months. The recent data for axitinib suggest a similar response rate and PFS.
The available data in cytokine refractory patients suggest initial therapy with the TKI axitinib should be considered based on the trial size and design. Alternatively, either sorafenib, sunitinib, or pazopanib can be utilized based on available data.
Although targeted therapies have become the new cornerstone of systemic RCC therapy, eventual treatment-emergent resistance has become a major impediment to long-term success with these new agents.
To address this issue the mTOR inhibitor everolimus was tested in patients progressing after sorafenib and/or sunitinib. Patients receiving everolimus compared to placebo showed prolongation of PFS with acceptable side effects. These data support the use of this agent as second-line therapy in patients failing initial treatment with a TKI. One rationale for this sequence is the use of an agent with an alternate mechanism of action.
Another approach in these refractory patients is re-challenge with the same agent, or another TKI. The concept of sequential utilization of several TKI's has been proposed. Evidence demonstrating efficacy comes from phase 2 trials and a recent phase 3 trial comparing axitinib to sorafenib. In the setting of sunitinib failure, second responses to the same drug have been described.
More commonly, patients with progressive disease following either sunitinib or sorafenib therapy have received with an alternate TKI. Recent data suggests either pazopanib or axitinib are also effective in these patients.
The standard of care in TKI refractory patients based on level 1 evidence is everolimus or axitinib. Comparative studies in which an mTOR inhibitor is compared to a TKI such as axitinib, or the best TKI sequence defined, are needed to determine the best option for second-line therapy.
The group of patients who fail first-line therapy with an agent such as temsirolimus generally represent poor-risk patients who had initially responded or had disease stability. The numbers of patients in this group represent approximately 35% of those treated in first-line. Data to assist treatment decisions in this group is lacking currently; however, a second line TKI is a reasonable alternative. For dosing, schedule, and toxicity of targeted agents, see
Recent cardiovascular event
Cardiovascular toxicity in the form of hypertension appears to represent a class effect of the VEGF/VEGF receptor (VEGFR) inhibitors. Treatment-induced hypertension also appears to correlate with clinical outcomes in RCC. This has been shown retrospectively for therapy utilizing sunitinib, axitinib, or bevacizumab.
These analyses have utilized several definitions of hypertension such as grade of toxicity or specific systolic and/or diastolic blood pressure levels. Correlations with objective response, PFS, and overall survival have been consistently found in patients who develop treatment-induced hypertension. This finding is being investigated prospectively, and the mechanisms underlying this phenomenon are unclear. Pre-existing hypertension should not therefore be considered a contraindication to the use of TKI's or bevacizumab.
Cardiac dysfunction in the form of left ventricular dysfunction has been reported with the TKI's sunitinib and sorefenib (>10%). A history of congestive heart failure or a decreased LVEF is a relative contraindication to the use of these agents. Studies with pazopanib suggest cardiac dysfunction is not seen with this TKI. In view of this, pazopanib appears to represent an alternative for this patient group, as well as individuals with a recent (<6 months) acute cardiovascular episode such as a myocardial infarction.
Impaired renal function
Abnormal renal function is frequently noted in patients with advanced RCC. The safety and efficacy of VEGF-targeted agents in patients with renal insufficiency is therefore relevant. Pharmacokinetic studies of various TKIs have demonstrated renal elimination is a minor component of drug metabolism. Hepatic metabolism is the major pathway. Therefore, it was assumed that the TKIs can be safely given to patients with renal insufficiency.
Retrospective reviews have shown that sunitinib and sorafenib can be administered to patients with impaired renal function. Monitoring of renal function is recommended, since TKI administration may produce serum creatinine elevations. Patients with worsening renal function may require dose modifications. Recent data from the CALGB has suggested that sorafenib dose can be maintained with a creatinine clearance above 40 mL/min, but below this level, dose reductions are required.
Patients with metastatic RCC on hemodialysis represent a distinct population. Information is largely anecdotal in this group, and two recent retrospective reports suggest administration of sunitinib is possible with acceptable toxicity. Dose levels have varied, with patients receiving either 50, 37.5 or 25 mg PO daily utilizing the 4 weeks on/2 weeks off schedule.
Impaired hepatic function
Hepatotoxicity is a recognized class toxicity of the TKIs, irrespective of the targets inhibited. Metabolism of these agents is primarily by the liver, and administration to patients with impaired liver function has not been studied adequately. However, some information is available in this patient group.
Preliminary data from a dose escalation study with pazopanib demonstrated that drug clearance is decreased by 50% in patients with moderate hepatic impairment when compared to individuals with normal hepatic function. The maximum tolerated dose in patients with moderate impairment of hepatic function is 200 mg PO daily. No data is available for patients with severe hepatic impairment, and pazopanib is not recommended in this setting.
Hepatic toxicity with sunitinib has also been reported. Comparison of data from the phase 3 pivotal trials suggests grade 3 toxicity may be more common with pazopanib. The safety of sunitinib in patients with hepatic enzyme elevation over 2.5 times normal or, if due to liver metastases, above 5.0 times normal, has not been established, and it is not recommended in these individuals
The use of sorafenib in patients with hepatic impairment has been more adequately characterized. Pharmacokinetic studies of sorafenib have been conducted in patients with hepatocellular carcinoma. Hepatic impairment may reduce plasma concentrations of sorafenib, and comparison suggests sorafenib levels may be lower in these patients than in non-hepatocellular patients (without hepatic impairment).
The area under the time-concentration curve (AUC) of sorafenib is similar in patients with mild (Child-Pugh A) and moderate (Child-Pugh B) hepatic impairment who have hepatomas. No dose adjustment is necessary in patients with Child-Pugh A and B hepatic impairment. Sorafenib has not been studied in patients with severe (Child-Pugh C) hepatic impairment.
The mTOR inhibitors everolimus and temsirolimus require dose modification in patients with hepatic impairment. For temsirolimus, the recommended starting dose in patients with mild hepatic impairment (bilirubin > 1.0 to 1.5 x normal, or AST > normal with normal bilirubin) is 15 mg IV weekly. Similarly, a dose reduction of everolimus to 5mg daily is recommended in patients with Child-Pugh class B. These agents have not been adequately studied in patients with severe hepatic impairment.
Finally, bevacizumab can be utilized in RCC patients with impaired hepatic function. Although no formal evaluation in this patient population is available, hepatic toxicity is not a prominent feature of this agent.
Because of the limited information available for RCC patients with hepatic impairment, liver function tests (ALT, AST, bilirubin) should be monitored before initiation of treatment, during each treatment cycle, and as clinically indicated.
Unique patient categories, clear cell carcinoma
Sarcomatoid differentiation in RCC occurs when the malignant cells acquire a higher grade, have a spindle cell appearance, and evidence of epithelial and mesenchymal differentiation. The reported incidence of RCC sarcomatoid differentiation is estimated between 1% and 23% of cases.
Patients whose pathology report notes “sarcomatoid change” appear to have a worse prognosis with a median survival less than one year. There is no uniform definition of sarcomatoid RCC such as the percentage of sarcomatoid differentiation required for the diagnosis. Chemotherapy with doxorubicin-containing combinations has been evaluated in these patients, and occasional tumor shrinkage is seen.
Targeted agents have also been evaluated in this patient group. In these reports, tumor shrinkage has been reported, but the data are retrospective for the most part. Several important points are noted:
The prognosis of patients with sarcomatoid tumors is poor.
Pathologic criteria for a diagnosis are variable.
The underlying histologic pattern may be crucial for determining therapy.
Currently, the data does not support one particular option, however, responses to sunitinib in clear cell carcinoma with sarcomatoid elements have been reported.
Chemotherapy with agents such as fluorouracil and/or cisplatin has also been reported to produce tumor regressions in selected patients, but the overall results with this group of agents is poorly characterized.
Patients with brain metastases are generally not eligible for clinical trials, and therefore prospective data are limited. Therapy for patients with newly diagnosed CNS metastases will generally require radiation (whole brain and/or stereotactic) or surgical removal, dependent upon the location, size and number of lesions.
Previously, patients with CNS metastases secondary to RCC received only supportive therapy, but aggressive approaches in selected patients will often permit additional systemic therapy to be considered. The effects of systemic therapy in this patient population are not entirely clear. A retrospective subgroup analysis of patients receiving sorafenib suggested a decreased incidence of CNS metastases in patients treated with sorafenib compared to placebo (3% vs. 12%, P<0.05). This data has not been confirmed.
In the sunitinib expanded access study, 7% of patients (n=321) had treated brain metastases and received open label sunitinib. The median PFS of this group was 5.6 months, and median survival was 9.2 months. No differences in toxicity were seen when patients with CNS metastases and the overall population were compared.
The overall incidence of treatment-related adverse events was 92%, regardless whether CNS metastases were present or not. These results suggest that it is possible to utilize agents such as sunitinib in RCC patients with treated CNS metastases. Toxicity is acceptable, and control of systemic disease may be seen. The best systemic therapy for patients with CNS metastases remains unclear, but if considered, a TKI is a reasonable option.
Bone is a common site of metastasis in RCC patients, with a frequency of solitary or multiple osseous metastases ranging from 24% to 51%. Complications associated with bone metastases include decreased performance status, pain, pathologic fracture, spinal cord compression and hypercalcemia. Management of this patient group depends upon patient status, presence of co-morbid factors, and whether the osseous metastases are solitary or multiple sites are involved.
Supportive measures include:
surgical removal and/or fixation
bisphosphonates or denosumab
Patients should receive supportive measures as previously described, the indicated systemic therapy for their disease, and treatment with a bisphosphonate such as zoledronic acid based on the results of a randomized placebo controlled trial (zoledronic acid versus placebo) in solid tumor patients with bone metastases.
RCC patients receiving zoledronic acid have reduced numbers of skeletal related events (SREs), delayed the time to the first SRE, and interestingly prolonged time to disease progression versus a placebo. Of interest are several reports suggesting a rapid improvement in metastatic bone lesions and patient symptoms after receiving zoledronic acid in combination with sunitinib.
Although there are no trials of bisphosphonates specifically in an RCC population, the available data suggests therapy with zoledronic acid and a TKI such as sunitinib has acceptable toxicity, and use of bisphosphonates delays the complications of bone metastases.
Recently, denosumab, a monoclonal antibody that binds and neutralizes receptor activator of nuclear factor kappa-B ligand (RANKL) was investigated in patients with solid tumors. A phase 3 trial comparing the effects of denosumab to zoledronic acid was conducted. Patients with RCC and osseous metastases were eligible; however, the report does not provide subset data on this population of patients. The results demonstrated the non-inferiority of denosumab in delaying skeletal complications. It is likely this agent has effects in RCC patients with bone metastases equivalent to zoledronic acid, but data are not yet available to confirm this.
It has been suggested that older individuals may not benefit from treatment with the currently available targeted agents, and will develop an increased frequency of adverse events. Despite these concerns, age has not emerged as a poor-risk factor in recent analyses of prognostic factors. These issues have been examined in several of the recently reported trials with sunitinib, sorafenib, and bevacizumab + IFN.
Overall, data from these clinical trials and meta-analyses demonstrate elderly patients aged greater than 65 or 70 years can be treated in a fashion similar to their younger counterparts. They appear to have similar degrees of benefit, and tolerate TKI or bevacizumab plus IFN-a therapy in a manner similar to younger patients.
Metastatic non-clear cell carcinoma
RCC is a heterogeneous disease, comprised of several different histological types with distinct genetic alterations, varying clinical course, and variable responsiveness to systemic therapy.
The main histopathological RCC subtypes based on tumor morphology, immunohistochemistry, cytogenetics and molecular studies include:
clear cell carcinoma (60-70%)
collecting duct carcinoma (0.3%)
Xp11 translocation carcinomas (<1%)
renal cell carcinoma unclassifiable (4-5%).
In earlier studies, RCC was considered a single disease classification. Currently these subtypes are categorized as either clear cell or collectively non-clear cell. Clinical studies have suggested chromophobe and papillary RCC have a better prognosis following nephrectomy for localized disease compared to clear cell RCC. The reverse appears true for patients with metastatic disease.
A recent retrospective analysis demonstrated metastatic non-clear cell RCC is resistant to systemic therapy and is associated with poor survival. It also was noted that patients with chromophobe RCC may have longer survival than those with papillary RCC. The treatment of patients with metastatic non-clear cell carcinoma remains an area that is poorly defined. Clinical trials for these tumors have been limited, and the available data is largely retrospective and/or analysis of patient subsets.
Temsirolimus, an mTOR inhibitor, was evaluated in an international prospectively randomized phase 3 trial which included 626 patients with metastatic RCC. The entry criteria only specified metastatic renal cell carcinoma. Therefore, approximately 20% (n=124) of patients entered had non-clear cell histology. In a retrospective subgroup analysis, the histologic subtypes included as non-clear cell carcinoma were: papillary carcinoma (n=55), chromophobe carcinoma (n=12), collecting duct, other, and indeterminate (n=57).
The subset analysis noted an overall survival improvement for patients treated with temsirolimus versus IFN-a (11.6 vs 4.3 months). Based on this exploratory analysis, temsirolimus appears to be efficacious in patients regardless of the underlying tumor histology, and importantly may be a useful drug for the treatment of patients with non-clear cell histology.
Retrospective analyses of patients with non-clear cell RCC receiving TKI's suggest sunitinib may have a low level of activity, but its overall efficacy remains unclear.
Unlike clear cell carcinoma, minimal information is available on the therapy of patients failing initial therapy. Presumably, an agent such as temsirolimus may be utilized as front-line treatment. At disease progression, it is likely a TKI may be utilized. There is no standard of care for this patient group. Patient functional status, co-morbid factors, and type of initial treatment will influence the choice for second-line therapy.
As in the patient with metastatic clear cell carcinoma, the various co-morbid conditions may influence therapy. The reader is referred to that section for a discussion of cardiovascular, renal, and hepatic factors that may modify or influence treatment.
Unique categories, non-clear cell carcinoma
The influence of sarcomatoid elements in the various non-clear cell histologic groups on treatment outcomes for patients with metastatic disease is poorly defined. The role of chemotherapy versus the targeted agents such as the TKIs has not been adequately defined. Metastatic sarcomatoid RCC is associated with a poor response to systemic therapy. Studies to characterize the underlying tumor biology, to assess outcome to targeted agents, and to develop novel treatment strategies are needed.
Data on frequency of CNS metastases in patients with the various non-clear cell histologies are not available. Therapy for these patients is similar to that described for clear cell carcinoma.
RCC associated with Xp11.2 translocations (TFE3 gene fusions) are rare tumors predominantly in the pediatric age group; however, a small number of adult Xp11.2 translocation RCC cases have been described.
Histologically, this tumor can resemble either the clear cell or papillary carcinoma, and may contain elements of both. Given the degree to which these tumors overlap morphologically with clear cell and/or papillary RCC, many adult Xp11.2 translocation RCC may be misclassified. Optimal therapy is not defined for this patient group, but recognition is important since this type of tumor may not benefit from currently available targeted agents, although prolonged responses to a TKI such as sunitinib have been reported.
Collecting duct carcinoma (CDC) also referred to as “Bellini duct carcinoma,” is an uncommon, aggressive form of renal cell carcinoma, accounting for less than 2% of kidney cancers. CDC arises from the epithelium of the distal collecting system in the renal medullary pyramids. Prospective reports suggest chemotherapy may be useful, and data with TKIs such as sunitinib suggest no benefit. Current recommendations are to treat this histologic variant with chemotherapy utilizing a platinum based regimen.
Renal medullary carcinoma is also a rare tumor that is most common in young black men with sickle cell disease or trait. This entity is often confused with CDC or poorly differentiated transitional cell carcinoma. In the majority of experiences reported, this rare subtype is characterized as a highly aggressive disease. Recent reports suggest chemotherapy has anti-tumor activity in this variant.
Regimens utilized for the treatment of urothelial carcinoma include:
MVAC (methotrexate, vinblastine, doxorubicin, and cisplatin) or
Combination of cisplatin, paclitaxel, and gemcitabine.
Additional studies are needed to define the overall activity of platinum based chemotherapy in medullary RCC, but the anecdotal data available suggest this non-clear variant should be approached as a urothelial neoplasm.
What other therapies are helpful for reducing complications?
Supportive therapies that may be of value in the management of patients with metastatic RCC include those utilized to decrease the complications of osseous metastases:
Bisphosphonates: zoledronic acid
RANK ligand inhibitor: denosumab
What should you tell the patient and the family about prognosis?
Since treatment of metastatic RCC rarely produces complete responses, and cure is unlikely, current therapy is focused on control of disease progression. The median overall survival of these patients was in the range of 14 to 16 months during the cytokine era, and recently, median survivals of 23 to 26 months have been reported with various targeted agents.
The prognosis for patients with advanced metastatic disease can be estimated by utilizing the MSKCC criteria. They can be classified as having favorable, intermediate, or poor-risk disease, with median survivals of 28.0, 13.6 and 4.6 months. This data is from the cytokine era; recent reports indicate that with utilization of the current treatment paradigm, median survivals of 20.7 and 5.3 months in the intermediate and poor-risk groups respectively. In favorable-risk patients, median survival is now approaching 3 years.
The goal of therapy in metastatic RCC patients is to maximize therapeutic benefit, delay the development of a disease burden that becomes life threatening, and maximize a patient's quality of life and convenience. This translates into selection of therapy with the optimal risk/benefit ratio for an individual patient. Unfortunately, only limited clinical criteria are available that predict efficacy, and ultimately multiple sequential treatments with available agents is utilized.
What if scenarios.
Recognition of histologic RCC subtypes is a frequent issue, and as pathologists become more familiar with current classification schemes, this will be less of an issue. Major issues in the field currently relate to the following questions:
1) What is the best therapy or standard of care in treatment naïve mRCC?
This will require comparative trials, several of which are underway.
2) Is the use of the MSKCC scheme mandatory?
In the absence of biomarkers, this classification should be utilized to assist with treatment decisions.
3) What is the definition of refractory?
No pre-specified criteria are available, except as listed when utilizing RECIST criteria. In some patients, RECIST disease progression may be documented, but the patient is asymptomatic or minimally symptomatic. In this setting, continuation of current therapy is justified, until definitive evidence of new sites of disease is found, especially in patients with small volume metastases.
4) How should the adverse events associated with targeted therapy be managed?
This will vary with the agent and the adverse event type. A complete discussion of toxicity management for each agent is beyond the scope of this review, but several more common class effects are relevant to discuss:
a) Dose and schedule:
Lower doses may be employed if there are significant concerns about potential side effects; however, the results reported in the various phase 3 pivotal studies utilized a standard dose and schedule. In the case of sunitinib, a significant relationship between sunitinib exposure and efficacy/toxicity has been identified.
Patients with the highest exposure not only displayed a higher probability of a response and tumor shrinkage, but also longer time to progression and, most importantly, longer overall survival. This emphasizes the importance of maintaining patients at 50 mg dose of sunitinib and striving to avoid any unnecessary dose reductions during treatment.
Continuous dosing versus the intermittent schedule have been compared in a phase 2 randomized trial. No differences in adverse events were found, and the traditional intermittent schedule appeared superior.
Recently, use of sunitinib in alternate schedules has been studied. Two weeks of therapy followed by one week of rest has been suggested to be better tolerated than the traditional "4/2 schedule." The "2/1schedule," however, has not been compared directly to the original sunitinib schedule.
b) How should patient fatigue related to TKI therapy be managed?
Potential alternative causes for fatigue such as underlying dehydration, hypothyroidism, hypercalcemia, anemia or depression should be excluded. All patients should have thyroid function tests prior to and during TKI treatment (every 8 to 12 weeks) and be treated according to standard medical practice.
Thyroid hormone replacement is recommended in mRCC patients with overt hypothyroidism (defined as an elevated serum thyroid-stimulating hormone (TSH) level and a low T4 level) and possible hypothyroidism-related symptoms. Blood transfusions may be used at the discretion of the treating physician to correct anemia.
Depression, a frequent finding in metastatic cancer patients, is known to impact upon the severity of fatigue. Fatigue improves in some patients who have received antidepressants. Finally, patient education about fatigue and its occurrence is very important. On occasion drug holidays may be helpful, and if severe fatigue is a recurrent problem, dose reduction may be appropriate.
Currently, there are no evidence-based interventions to treat fatigue, and therefore when it interferes with quality of life, management by changes in dose would be appropriate.
c) How can the hand-foot syndrome be managed?
The frequency of this cutaneous complication varies dependent upon the TKI utilized. The lowest frequency is seen with pazopanib, and the highest with sorafenib. Hand–foot changes may present as painful symmetrical erythematous areas on the palms and soles. Patients may experience paraesthesias, tingling or numbness.
Desquamation can occur in severe cases. Painful hyperkeratotic areas in pressure regions surrounded by rings of erythema as well as bullous lesions and/or blisters may be noted. These are seen in areas of pressure, and pre-existing hyperkeratotic areas seem predisposed to development of these changes. When functional consequences develop, patients may refuse to continue therapy.
Palliative interventions include:
foot and hand care products (e.g. gel pad inserts, cotton gloves)
medication for pain management
instructing patients to decrease pressure on the areas affected, by staying off their feet if possible and avoiding pressure on their hands.
Treatment for grade 2 hand-foot syndrome usually involves these measures, as well as dose interruptions, and if necessary dose reductions. Dose interruptions for 5 to 7 days are generally sufficient to permit resolution of most severe skin changes. Anecdotal reports suggest steroid creams can be helpful, but well designed prospective studies are lacking. This complication is not an inflammatory response, but steroid creams may prevent secondary inflammatory changes.
When patients with hand-foot changes does not respond to dose interruption or reduction, other diagnoses should be considered such as fungal infection, allergic contact dermatitis, and irritant dermatitis. At this time referral to a dermatologic consultant would be appropriate. Finally, recent analysis of the sunitinib phase 3 trials suggests the development of hand-foot syndrome may correlate with efficacy.
d) How should diarrhea be managed?
Diarrhea occurs frequently, and over 50% of patients may experience this toxicity. Grade 3 and 4 diarrhea is uncommon. Some degree of diarrhea often remains when other common side effects have been controlled with dose/schedule changes.
In contrast to chemotherapy-induced diarrhea, which is usually continuous, TKI-induced diarrhea may be irregular. Dose reductions are rarely necessary for grade 1 and 2 diarrhea, which can be managed by oral anti-diarrheal agents as needed, such as loperamide. Treatment should be interrupted for grade 3 diarrhea until it has decreased to grade 1 or has returned to baseline. Patients should temporarily discontinue use of stool softeners and fiber supplements.
e) How should the hematologic toxicity secondary to the TKIs be managed?
Severe hematologic toxicity is infrequent in patients receiving either pazopanib or sorafenib, and most common in sunitinib-treated patients. Only 5 to 8% of sunitinib-treated patients develop grade 3/4 neutropenia or thrombocytopenia and few cases of neutropenic fever have been reported.
Blood counts usually recover quickly within the 2-week treatment break. Due to the usually rapid recovery of blood counts during the 2-week treatment break, hematologic growth factors are not routinely recommended.
Dose modification for grade 4 neutropenia or grade 3 thrombocytopenia may be required. Severe anemia usually does not require dose modification. Of interest are the macrocytic indices that frequently develop in sunitinib treated patients. These are related to therapy, and do not have an underlying nutritional cause. Due to recent data concerning potential risks and toxicities, the use of erythropoietin-stimulating agents should be utilized only when necessary.
f) How should hypertension induced by TKI therapy be managed?
Hypertension is a class effect of VEGF/VEGFR inhibitors, and can be seen in 30-50% of patients receiving these agents. Hypertension is therefore commonly observed event during treatment, and is generally manageable with use of standard antihypertensive agents. An interesting association between hypertension and clinical efficacy appears to exist with TKI therapy.
In a retrospective analysis the occurrence of hypertension was associated with increased PFS and survival. This data suggests that in patients with mRCC, hypertension may not only be an adverse event, but also a potential prognostic biomarker. Pre-existing hypertension is not a contraindication to therapy, and worsening hypertension (grade 3) generally should be manageable with a change in antihypertensive medications, with dose reductions or interruption reserved for uncontrolled elevations of blood pressure.
g) How should pneumonitis secondary to administration of mTOR inhibitors be managed?
Non-infectious pneumonitis is a potentially serious adverse event associated with rapamycin and rapamycin derivative therapy. Clinically, it can present as a typical radiographic appearance of interstitial pneumonitis with or without signs and symptoms (pleural effusion, hypoxia, cough, dyspnea, malaise). It is defined as the radiographic lung change irrespective of signs or symptoms, in the absence of a non-drug cause.
Administration of both everolimus and temsirolimus has been reported to produce pulmonary toxicity. In the RECORD 1 trial, 8% of patients receiving everolimus developed pneumonitis, and 8 (3%) were grade 3. Of the 8 patients with grade 3 pneumonitis, six discontinued everolimus, four resolved completely, and three improved to grade 2 or less.
Recommendations for management depend upon the severity of the pneumonitis. Patients should be instructed to report any new or changing respiratory symptoms. In asymptomatic patients, with radiographic changes only, everolimus can be continued, and patients observed closely.
In patients with moderate symptoms, therapy should be held, and restarted when symptoms improve with a dose reduction of everolimus to 5mg daily. In patients with severe pneumonitis (grade 3), everolimus should be discontinued. The role of corticosteroids in improving the interstitial pneumonitis is unclear, but they can be utilized in this group.
The development of pneumonitis secondary to temsirolimus was investigated retrospectively in the phase 3 pivotal trial (ARCC) utilizing blinded radiology review. 29% of the evaluable patients receiving temsirolimus developed radiographic evidence of drug-related pneumonitis, compared to 6% of patient receiving IFN-a.
In contrast, the investigators reported the incidence of temsirolimus-related pneumonitis as 2%. 16/52 patients with pneumonitis developed symptoms (31%), which developed during the first 8 weeks of therapy in 60% of patients. Patients with radiographic changes of pneumonitis who are asymptomatic should continue treatment and be monitored closely for respiratory symptoms. Patients who develop symptoms and radiographic changes should have treatment held. Treatment with temsirolimus may be resumed, with or without dose reduction (15mg weekly), depending on the patient's clinical course.
An important concept in the evaluation of the pneumonitis related to mTOR inhibitors involves further assessment with pulmonary function tests and bronchoscopy to exclude other causes, e.g. infection. Empiric therapy with corticosteroids and antibiotics may be initiated if clinically warranted. Continuation of these agents in patients who are benefiting from treatment involves the availability of other treatment options, and the overall risk/benefit assessment.
Follow-up surveillance and therapy/management of recurrences.
Recommendations for follow-up and surveillance will vary depending upon the stage, type of surveillance and whether active therapy is ongoing. These individual situations are discussed in the following paragraphs.
Patient with recent nephrectomy, partial nephrectomy, or thermal ablative procedure and stage 1A, 1B, II, or III renal cell carcinoma
Every 6 months for 2 years, then annually for total of 5 years:
History and physical examination.
Chest and abdominal CT with contrast.
At 4 to 6 months then as indicated:
Complete blood count.
These recommendations are based on the NCCN treatment guidelines for localized RCC. The possibility that more prolonged observation for selected patients should be considered has been suggested.
Patients with small renal mass (<4.0 cm) being considered for active surveillance
In this setting determination of the characteristics of the renal mass and the growth rate are important. No accepted guidelines exist; however, the NCCN guidelines for follow-up of patients following therapy for a localized renal tumor are applicable. These can be individualized depending upon the patient and tumor characteristics.
Patients with metastatic renal cell carcinoma
a) Receiving systemic therapy including TKIs, mTOR inhibitors, and bevacizumab plus IFN-a. Standardized guidelines do not exist, however, the following should be considered during active therapy, until disease progression.
Every 4 to 6 weeks, dependent upon type of therapy and treatment schedule:
Complete blood count.
Fasting blood sugar, triglycerides, cholesterol (for patients receiving an mTOR inhibitor).
Thyroid function studies: TSH, T4 levels (for patients receiving a TKI).
Every 12 weeks:
History and physical examination.
CT scan: chest, abdomen, pelvis.
Chest x-ray (for patients receiving an mTOR inhibitor).
Bone scan – if positive at baseline.
Radionuclide LVEF if at baseline this was abnormal, or the patient has a history of cardiovascular disease.
Annually: CT scan or MRI of brain
These recommendations will vary depending upon the patient, type of tumor, and type of systemic therapy. The guidelines for follow-up of patients with metastatic RCC reflect the type of follow-up obtained during the clinical trials of the approved agents for treating RCC, as well as the natural history of mRCC.
b) Patients with metastatic RCC, under observation and not receiving active therapy. The recommendations reflect the underlying metastatic RCC, no standard accepted guidelines are available.
Every 3 months:
History and physical examination.
CT scans: chest, abdomen, pelvis.
Complete blood count, metabolic profile.
CT or MRI of brain.
The molecular characteristics of RCC have been intensively studied during the past 20 years. Approximately 2 to 3% of RCC tumors are familial. Several autosomal dominant syndromes have now been described, each having a distinct genetic basis and phenotype. The von Hippel-Lindau (VHL) syndrome is the most common.
These patients develop vascular tumors including clear cell RCC, hemangioblastomas, and pheochromocytomas. The VHL tumor suppressor gene is located on chromosome 3 (3p25-26). In patients with the VHL syndrome, a defect on one VHL gene allele is inherited, and a second in the remaining allele is then acquired.
Studies in the 1990s demonstrated most patients (>80%) with sporadic clear cell RCC acquire defects of both VHL gene alleles, producing dysfunction of the VHL protein. This functions as a tumor suppressor, and is responsible for proteasome degradation of hypoxia-inducible factor (HIF), a regulator of the hypoxic response. When VHL protein is absent or non-functioning, HIF-1-alpha accumulates, and activates transcription of hypoxia-inducible genes, such as vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF).
Clear cell cancers are characterized by high vascular content, secondary to enhanced tumor associated angiogenesis. The loss of VHL gene function results in constitutive expression of HIF, over secretion of VEGF, PDGF, and produces the vascular phenotype characteristic of clear cell RCC.
Cytogenetics and gene expression profiling studies have also clarified the molecular characteristics of RCC non-clear cell histologic subtypes. Morphologically, papillary RCC is divided into type 1 and type 2, but genetic patterns in the inherited papillary RCC syndromes may also differentiate the two. Chromophobe carcinomas and oncytomas are uncommon non-clear cell variants. Chromophobe tumors may present as extremely large abdominal masses, are generally locally advanced tumors, and are slow growing. Oncocytomas are generally considered benign tumors, grow very slowly, and may be multifocal.
Collecting duct carcinomas (CDC) and medullary cancers of the kidney are related to transitional cell carcinomas, based on histology and gene expression profiles. They arise in the collecting ducts and medullary systems of the kidney. Collecting duct carcinoma, also referred to as “Bellini duct carcinoma,” is an uncommon, aggressive form of RCC, and accounts for less than 2% of renal tumors. It arises from the epithelium of the distal collecting system in the renal medullary pyramids. CDC is associated with a poor prognosis in patients with advanced disease.
Renal medullary carcinoma (RMC) is also a rare tumor which typically affects younger individuals with sickle cell disease or trait. It is a highly aggressive malignancy and most often produces locally advanced and metastatic disease at diagnosis. Increased levels of topoisomerase II have been recently described along with deregulation of DNA remodellng and repair. As with CDC, this RCC variant resembles more the patterns described in urothelial rather than epithelial cancers.
Translocation carcinomas of the kidney, which were first described in children, were considered as aggressive tumors. These Xp11.2 translocations RCC now constitute a well-recognized entity. In children, these tumors comprise at least one third of RCC tumors reported, but in adults, they remain a rare entity. In view of the fact these tumors overlap morphologically with clear cell and/or papillary RCC, many adult Xp11.2 translocation RCC may be misclassified as clear cell or papillary RCC.
The histologic variant of high-grade RCC referred to as sarcomatoid carcinoma refers to the spindled morphology of a dedifferentiated subset of RCC tumor cells. Approximately 4% of RCC tumors will have a sarcomatoid component. Renal cell carcinoma with sarcomatoid features is a variant of other RCC subtypes, not a separate entity. At present, the diagnosis rests on demonstration of conventional histopathologic features, assessment of the percentage of sarcomatoid dedifferentiation, and immunohistochemical stains confirming epithelial rather than mesenchymal lineage.
Finally, the category of unclassified RCC is utilized for tumors that cannot be placed in one of the previous histologic subtypes. Unclassified RCC represents a category assigned when a tumor does not fit into the other RCC histological subtypes, based on pathological and/or genetic analyses. It is a rare variant and accounts for 3–5% of RCC cases. A recent study indicated that unclassified RCC presents with a higher stage and grade, and has a higher mortality than clear cell carcinoma.
What other clinical manifestations may help me to diagnose renal cell carcinoma?
The majority of renal tumors are now discovered incidentally during an imaging procedure, and patients are asymptomatic. The classic presentation that included the triad of hematuria, flank pain and a palpable mass are seldom seen currently.
Past medical history and smoking history are important, as well as a work and environmental exposure history. Patients with suspected RCC should be examined carefully to document any evidence of metastatic or advanced disease. This includes a careful system review focusing on the skeletal, genitourinary and systemic systems.
In young patients (<40 years) with RCC, a family history is relevant, and any manifestations of the various inherited RCC syndromes should be determined.
What other additional laboratory studies may be ordered?
In patients with advanced or metastatic RCC, routine hematologic and biochemical studies are recommended. Hemoglobin levels, calcium and serum albumin, and serum LDH should be obtained to allow MSKCC classification of the untreated newly diagnosed RCC patient. There are no biomarkers or other specialized laboratory studies that are helpful during the initial evaluation. In the future, SNP analyses and tumor genetic studies may be helpful in this regard.
What's the evidence?
"Surveillance, Epidemiology, and End Results Program National Cancer Institute". 2014.
2014.(Incidence of RCC in the USA discussed.)
Butman, JA, Linehan, WM, Lonser, RR. "Neurologic manifestations of von Hippel-Lindau disease". JAMA. vol. 300. 2008. pp. 1334-1342.(Clinical manifestations of the VHL syndrome discussed.)
Linehan, WM, Srinivasan, R, Schmidt, LS. "The genetic basis of kidney cancer: a metabolic disease". Nat Rev Urol. vol. 7. 2010. pp. 277-285.(Review of genetic basis of RCC and the various inherited syndromes associated with RCC.)
Linehan, WM, Bratslavsky, G, Pinto, PA. "Molecular Diagnosis and Therapy of Kidney Cancer". Annu Rev Med. vol. 61. 2010. pp. 329-343.(Excellent review of genetic basis of RCC, potential targets, and targeted approaches to mRCC.)
Edge, SB, Byrd, DR, Compton, CC. "AJCC Cancer Staging Manual". Springer SBM, LLC. 2009.
Tsivian, M, Moreira, DM, Caso, JR. "Cigarette Smoking Is Associated With Advanced Renal Cell Carcinoma". J Clin Oncol. vol. 29. 2011. pp. 2027-2031.
Lane, W, Lacefield, E, Tran, R. "The Clinical Association of Autosomal Dominant Polycystic Kidney Disease and Renal Cell Carcinoma". Open Journal of Urology. vol. 1. 2011. pp. 11-14.
Young, AC, Craven, RA, Cohen, D. "Analysis of VHL Gene Alterations and their Relationship to Clinical Parameters in Sporadic Conventional Renal Cell Carcinoma". Clin Cancer Res. vol. 15. 2009. pp. 7582-7592.(VHL gene analysis in sporadic RCC.)
George, DJ, Kaelin, WG. "The von Hippel-Lindau protein, vascular endothelial growth factor, and kidney cancer". N Engl J Med. vol. 349. 2003. pp. 419-421.(Biology and functions of the VHL protein and are discussed.)
Latif, F, Tory, K, Gnarra, J. "Identification of the von Hippel–Lindau disease tumor suppressor gene". Science. vol. 260. 1993. pp. 1317-1320.(Original description of the VHL mutation.)
Motzer, RJ, Bacik, J, Murphy, BA. "Interferon-alfa as a comparative treatment for clinical trials of new therapies against advanced renal cell carcinoma". J Clin Oncol. vol. 20. 2002. pp. 289-296.(MSKCC prognostic factor analysis in untreated patients with mRCC.)
Mekhail, TM, Abou-Jawde, RM, BouMerhi, G. "Validation and Extension of the Memorial Sloan-Kettering Prognostic Factors Model for Survival in Patients With Previously Untreated Metastatic Renal Cell Carcinoma". J Clin Oncol. vol. 23. 2005. pp. 832-841.(Independent confirmation of MSKCC prognostic factor system.)
Heng, DY, Xie, W, Regan, M. "Prognostic factors for overall survival in patients with metastatic renal cell carcinoma treated with vascular endothelial growth factor-targeted agents: results from a large, multicenter study". J Clin Oncol. vol. 27. 2009. pp. 5794-5799.(Prognostic factor analysis in patients treated with targeted agents.)
Zisman, A, Pantuck, AL, Wieder, J. "Risk Group Assessment and Clinical Outcome Algorithm to Predict the Natural History of Patients With Surgically Resected Renal Cell Carcinoma". J Clin Oncol. vol. 20. 2004. pp. 4559-4566.(Risk group assessment of localized RCC from UCLA group – UISS system)
Frank, I, Blute, ML, Cheville, JC. "An Outcome Prediction Model for Patients with Clear Cell Renal Cell CarcinomaTreated with Radical Nephrectomy Based on Tumor Stage, Size, Grade, Necrosis: the SSIGN Score". J Urol. vol. 168. 2002. pp. 2395-2400.(Risk group assessment incorporating tumor necrosis – SSIGN score from Mayo Clinic.)
Sorbellini, M, Kattan, MW, Snyder, ME. "A Postoperative Nomogram predicting recurrence for patients with conventionial clear cell renal cell carcinoma". J Urol. vol. 173. 2005. pp. 48-51.
Motzer, RJ, Bukowski, RM, Figlin, RA. "Prognostic Nomogram for Sunitinib Patients with Metastatic Renal Cell Carcinoma". Cancer. vol. 113. 2008. pp. 1552-8.(These two manuscripts develop nomograms to predict DFS for patients with localized RCC [Sorbellini] and PFS in sunitinib treated patients [Motzer].)
Motzer, RJ, Bacik, J, Schwartz, LH. "Prognostic Factors for Survival in Previously treated Patients With Metastatic Renal Cell Carcinoma". J Clin Oncol. vol. 22. 2004. pp. 454-463.(Analysis of prognostic factors in refractory patients with prior therapy.)
Fyfe, G, Fisher, RI, Rosenberg, SA. "Results of treatment of 225 patients with metastatic renal cell carcinoma who received high-dose recombinant interleukin-2 therapy". J Clin Oncol. vol. 13. 1995. pp. 688-696.(High dose IL-2 therapy: description of pivotal phase 2 trial.)
Gore, ME, Griffin, CL, Hancock, B. "Interferon alfa-2a versus combination therapy with nterferon alfa-2a, interleukin-2, and fluorouracil in patients with untreated metastatic renal cell carcinoma (MRC RE04/EORTC GU 30012): an open-label randomised trial". Lancet. vol. 375. 2010. pp. 641-648.(Randomized trial utizing cytokine therapy in mRCC.)
Atkins, MB, Regan, M, McDermott, D. "Update on the Role of Interleukin 2 and Other Cytokines in the Treatment of Patients with Stage IV Renal Carcinoma". Clin Cancer Res. vol. 10. 2004. pp. 6342S-6346S.(Discussion of cytokine therapy in patients with mRCC.)
Coppin, C, Porzsolt, F, Awa, A. "Immunotherapy for advanced renal cell cancer". Cochrane Database of Systematic Reviews Issue. vol. 3. 2008.(Meta-analysis of cytokine efficacy in mRCC.)
Motzer, RJ, Hutson, TE, Tomczak, P. "Sunitinib versus interferon alfa in metastatic renal-cell carcinoma". N Engl J Med. vol. 356. 2007. pp. 115-124.(Phase 3 pivotal trial comparing sunitinib and IFN-a in metastatic clear cell carcinoma.)
Motzer, RJ, Rini, BI, Bukowski, RM. "Sunitinib in Patients With Metastatic Renal Cell Carcinoma". JAMA. vol. 295. 2006. pp. 2516-24.(Summary of phase 2 sunitinib data in cytokine refractory patients.)
Motzer, RJ, Hutson, TE, Tomczak, P. "Overall Survival and Updated Results for Sunitinib Compared With Interferon Alfa in Patients With Metastatic Renal Cell Carcinoma". J Clin Oncol. vol. 27. 2009. pp. 3584-3590.(Final survival analysis of phase 3 sunitinib versus IFN-a trial.)
Houk, BE, Bello, CL, Poland, B. "Relationship between exposure to sunitinib and efficacy and tolerability endpoints in patients with cancer: results of a pharmacokinetic/pharmacodynamic meta-analysis". Cancer Chemother Pharmacol. vol. 66. 2010. pp. 357-371.(Analysis of sunitinib plasma levels and AUC relationship to efficacy in mRCC and GIST patients.)
Park, S, Lee, J, Park, SH. "Treatment of Hemodialyzed Patients with Sunitinib in Renal Cell Carcinoma". Chemotherapy. vol. 56. 2010. pp. 485-491.(Two reports on the efficacy of sunitinib in patients with mRCC on dialysis.)
Rini, BI, Tamaskar, I, Shaheen, P. "Hypothyroidism in Patients With Metastatic Renal Cell Carcinoma Treated With Sunitinib". J Natl Cancer Inst. vol. 99. 2007. pp. 81-83.(Hypothyroidism and sunitinib: review and clinical features.)
Rini, BI, Choueiri, TK, Elson, P. "Sunitinib-induced Macrocytosis in Patients with Metastatic Renal Cell Carcinoma". Cancer. vol. 113. 2008. pp. 1309-14.(Hematologic findings in patients receiving sunitinib.)
Escudier, B, Roigas, J, Gillessen, S. "Phase II Study of Sunitinib administered in a continuous once-daily dosing regimen in patients with cytokine-refractory metastatic renal cell carcinoma".(Phase trial of continuous sunitinib in cytokine refractory mRCC.)
Motzer, RJ, Hutson, TE, Olsen, MR. "Randomized phase II trial of sunitinib on an intermittent versus continuous dosing schedule as first-line therapy for advanced renal cell carcinoma". J Clin Oncol. vol. 30. 2012. pp. 1371-77.(Phase 2 randomized trial comparing intermittent and continuous schedules of sunitinib in patients with mRCC.)
Zama, IN, Hutson, TE, Elson, P. "Sunitinib rechallenge in metastatic renal cell carcinoma patients". Cancer. vol. 116. 2010. pp. 5400-6.(Retrospective analysis of efficacy related to sunitinib retreatment.)
Escudier, B, Eisen, T, Stadler, WM. "Sorafenib in advanced clear-cell renal-cell carcinoma". N Engl J Med. vol. 356. 2007. pp. 125-34.(Phase 3 pivotal trial comparing sorafenib and a placebo in cytokine refractory mRCC.)
Escudier, B, Szczylik, C, Hutson, TE. "Randomized phase II trial of first-line treatment with sorafenib versus interferon Alfa-2a in patients with metastatic renal cell carcinoma". J Clin Oncol. vol. 27. 2009. pp. 1280-1287.(Report of negative phase 2 randomized trial comparing sorafenib and IFN-a.)
Escudier, B, Eisen, T, Stadler, WM. "Sorafenib for Treatment of Renal Cell Carcinoma: Final Efficacy and Safety Results of the Phase III Treatment Approaches in Renal Cancer Global Evaluation Trial". J Clin Oncol. vol. 27. 2009. pp. 3312-3318.(Final survival analysis of phase 3 TARGETs trial investigating sorafenib in cytokine refractory patients.)
Stadler, WM, Figlin, RA, McDermott, D. "Safety and Efficacy Results of the Advance Renal Cell Carcinoma Sorafenib Expanded Access Program in North America". Cancer. vol. 116. 2010. pp. 1272-80.(Report of the North American sorafenib expanded access trial.)
Eisen, T, Oudard, S, Szczylik, C. "Sorafenib for Older Patients With Renal Cell Carcinoma: Subset Analysis from a Randomized Trial". J Natl Cancer Inst. vol. 100. 2008. pp. 1454-1463.(Analysis of efficacy and safety in an elderly mRCC patient group from the TARGET trial.)
Sternberg, CN, Davis, IA, Mardiak, J. "Pazopanib in locally advanced or metastatic renal cell carcinoma: results of a randomized phase III trial". J Clin Oncol. vol. 28. 2010. pp. 1061-1068.(Phase 3 pivotal trial comparing pazopanib and a placebo in treatment naïve and refractory patients.)
Hutson, TE, Davis, ID, Machiels, JH. "Efficacy and Safety of Pazopanib in Patients with Metastatic Renal Cell Carcinoma". J Clin Oncol. vol. 27. 2010. pp. 475-80.(Report of phase 2 randomized discontinuation trial utilizing pazopanib in mRCC.)
Sternberg, CN, Hawkins, RE, Wagstaff, J. "A randomized, double-blind phase III study of pazopanib in patients with advanced and/or metastatic renal cell carcinoma: final overall survival results and safety update". Eur J Cancer. vol. 49. 2013. pp. 1287-96.(Final survival data from phase 3 pivotal pazopanib trial in mRCC.)
Sternberg, CN, Davis, ID, Mardiak, J. "Pazopanib in locally advanced or metastatic renal cell carcinoma: results of a randomized phase III trial". J Clin Oncol. vol. 28. 2010. pp. 1061-8.(Efficacy results and safety data from phase 3 pazopanib trial.)
Reeves, JA, Spigel, DR, Daniel, DB. "Pazopanib in patients with metastatic renal cell carcinoma previously treated with sunitinib or bevacizumab: A Sarah Cannon Research Institute phase II trial". J Clin Oncol. vol. 29. 2011.(Abstract reporting efficacy of pazopanib in TKI refractory mRCC)
Matrana, MR, Atkinson, BJ, Corn, PG. "Metastatic renal cell carcinoma treated with pazopanib after progression on other targeted agents: A single-institution experience". J Clin Oncol. vol. 29. 2011.(Abstract reporting retrospective assessment of pazopanib in refractory mRCC)
Kapadia, S, Hapani, S, Wu, S. "Risk of high-grade liver toxicity with pazopanib in patients with cancer: A meta-analysis". J Clin Oncol. vol. 29. 2011.(Abstract reporting a meta-analysis of pazopanib hepatic toxicity.)
Bukowski, RM, Yasothan, U, Kirkpatrick, P. "Pazopanib: Nature Rev Drug Discovery". vol. 9. 2010. pp. 1-2.(Brief review of pazopanib trials and clinical data.)
Sonpavde, G, Hutson, TE, Sternberg, CN. "Pazopanib, a potent orally administered small-molecule multitargeted tyrosine kinase inhibitor for renal cell carcinoma. Expert Opin. Investig". Drugs. vol. 17. 2008. pp. 253-261.(Excellent review of pazopanib clinical development.)
"FDA Oncologic Drugs Advisory Committee Briefing Document (NDA 22-465): Votrient™ (Pazopanib) Tablets". ODAC Meeting. 2009.(FDA review of pazopanib therapy for RCC.)
Motzer, RJ, Hutson, TE, Cella, D. "Pazopanib versus sunitinib in metastatic renal cell carcinoma". N Engl J Med.. vol. 369. 2013. pp. 722-31.(Phase 3 trial comparing sunitinib and pazopanib.)
Escudier, BJ, Porta, C, Bono, P. "Randomized, controlled, double-blind, cross-over trial assessing treatment preference for pazopanib versus sunitinib in patients with metastatic renal cell carcinoma: PISCES study". J Clin Oncol. vol. 32. 2014. pp. 1412-8.(Phase 2 patient preference trial comparing sunitinib and pazopanib.)
Escudier, B, Pluzanska, A, Koralewski, P. "Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial". Lancet. vol. 370. 2007. pp. 2103-2111.(Phase 3 pivotal trial of IFN-a ± bevacizumab in treatment naïve mRCC patients.)
Escudier, B, Bellmunt, J, Negrier, S. "Phase III Trial of Bevacizumab Plus Interferon Alfa-2a in Patients With Metastatic Renal Cell Carcinoma (AVOREN): Final Analysis of Overall Survival". J Clin Oncol. vol. 28. 2010. pp. 2144-2150.(Final survival analysis of phase 3 AVOREN trial.)
Melichar, B, Koralewski, P, Ravaud, A. "First-line bevacizumab combined with reduced dose interferon-2a is active in patients with metastatic renal cell CA". Ann Oncol. vol. 19. 2008. pp. 1470-76.(Analysis of the AVOREN study and patients who received lower doses of IFN-a indicating efficacy is maintained.)
Rini, BI, Halabi, S, Rosenberg, JE. "Phase III Trial of Bevacizumab Plus Interferon Alfa Versus Interferon Alfa Monotherapy in Patients With Metastatic Renal Cell Carcinoma: Final Results of CALGB 90206". J Clin Oncol. vol. 28. 2010. pp. 2137-2143.(Phase 3 CALGB trial comparing bevacizumab + IFN-a to IFN-a alone.)
Hudes, G, Carducci, M, Tomczak, P. "Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma". N Engl J Med. vol. 356. 2007. pp. 2271-2281.(Phase 3 pivotal trial of temsirolimus ± IFN-a or single agent IFN-a in poor risk mRCC patients.)
Hutson, TE, Escudier, B, Esteban, E. "Randomized phase III trial of temsirolimus versus sorafenib as second-line therapy after sunitinib in patients with metastatic renal cell carcinoma". J Clin Oncol. vol. 32. 2014. pp. 760-7.(Phase 3 trial comparing temsirolimus and sorafenib.)
Dutcher, JP, De, SP, McDermott, D. "Effect of temsirolimus versus interferon-alpha on outcome of patients with advanced renal cell carcinoma of different tumor histologies". Med Oncol. vol. 26. 2009. pp. 202-209.(Subset analysis of temsirolimus pivotal trial with a focus on effects in non-clear cell histology.)
Maroto, JP, Hudes, G, Dutcher, JP. "Drug-Related Pneumonitis in Patients With Advanced Renal Cell Carcinoma Treated With Temsirolimus". J Clin Oncol. vol. 29. 2011. pp. 1750-1756.(Analysis of non-infectious pneumonitis related to temsirolimus administration.)
Motzer, RJ, Escudier, B, Oudard, S. "Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial". Lancet. vol. 372. 2008. pp. 449-456.(Phase 3 pivotal trial of everolimus versus a placebo in TKI refractory mRCC.)
Hiu-yan Chan, Y, Grossman, AB, Bukowski, RM. "Everolimus in the Treatment of Renal Cell Carcinoma and Neuroendocrine Tumors". Adv Ther. vol. 27. 2010. pp. 495-511.(Review of everolimus and activity in mRCC and NET.)
Rini, BI, Escudier, B, Tomczak, P. "Comparative effectiveness of axitinib versus sorafenib in advanced renal cell carcinoma (AXIS): a randomised phase 3 trial". Lancet. vol. 378. 2011. pp. 1931-9.(Results of randomized phase 3 trial comparing axitinib and sorafenib in refractory patients.)
Rini, BI, Schiller, JH, Fruehauf, JP. "Diastolic Blood Pressure as a Biomarker of Axitinib Efficacy in Solid Tumors". Clin Can Res. vol. 17. 2011. pp. 3841-3849.(Analysis of hypertension and the efficacy of the investigational TKI axitinib.)
Votrient, TM. "Full prescribing information". 2009.
"Nexavar™: Full prescribing information". 2011.
"Torisel™: Full prescribing information". 2011.
"Sutent™: Full prescribing information". 2011.
"Avastin™: Full prescribing information". 2009.
"Afinitor™: Full prescribing information". 2012.
Choueiri, TK, Plantade, A, Elson, P. "Efficacy of sunitinib and sorafenib in metastatic papillary and chromophobe renal cell carcinoma". J Clin Oncol. vol. 26. 2008. pp. 127-131.(Retrospective analysis of the efficacy of targeted agents in non-clear cell RCC.)
Escudier, B, Droz, JP, Rolland, F. "Doxorubicin and ifosfamide in patients with metastatic sarcomatoid renal cell carcinoma: a phase II study of the Genitourinary Group of the French Federation of Cancer Centers". J Urol. vol. 168. 2002. pp. 959-961.(Treatment of sarcomatoid RCC with chemotherapy.)
Nanus, DM, Garino, A, Milowsky, MI. "Active chemotherapy for sarcomatoid and rapidly progressing renal cell carcinoma". Cancer. vol. 101. 2004. pp. 1545-51.
Choueiri, TK, Mosquera, JM, Hirsch, MS. "Vascular endothelial growth factor-targeted therapy for the treatment of adult metastatic Xp11.2 translocation renal cell carcinoma". Cancer. vol. 116. 2010. pp. 5219-25.(Informative case report of an adult with Xp11.2 translocation.)
Rini, BI. "New Strategies in Kidney Cancer: Therapeutic Advances through Understanding the Molecular Basis of Response and Resistance". Clin Cancer Res. vol. 16. 2010. pp. 1348-54.(Review of targeted agents including mechanisms of action, and development new strategies.)
Rini, BI, Campbell, SC, Escudier, B. "Renal cell carcinoma". Lancet. vol. 373. 2009. pp. 1119-1132.(Review of renal cell carcinoma including roles of surgery and systemic therapy.)
Henry, DH, Costa, L, Goldwasser, F. "Randomized, Double-Blind Study of Denosumab Versus Zoledronic Acid in the Treatment of Bone Metastases in Patients with Advanced Cancer (Excluding Breast and Prostate Cancer) or Multiple Myeloma". J Clin Oncol. vol. 29. 2011. pp. 1125-1132.(Report of the phase 3 pivotal trial comparing zoledronic acid and denosumab in patients with solid tumors and osseous metastases.)
Rosen, LS, Gordon, D, Tchekmedyian, NS. "Long-term efficacy and safety of zoledronic acid in the treatment of skeletal metastases in patients with nonsmall cell lung carcinoma and other solid tumors: A randomized, Phase III, double-blind, placebo-controlled trial". Cancer. vol. 100. 2004. pp. 2613-2621.(Pivotal trial of zometa in patients with solid tumors, including mRCC, and osseous metastases.)
Lipton, A, Zheng, M, Seaman, J. "Zoledronic acid delays the onset of skeletal-related events and progression of skeletal disease in patients with advanced renal cell carcinoma". Cancer. vol. 98. 2003. pp. 962-969.(Subset analysis of mRCC patients in pivotal trial of zoledronic acid.)
Campbell, SC, Novick, AC, Belldegrun, A. "Guideline for Management of the Clinical T1 Renal Mass". J Urol. vol. 182. 2009. pp. 1271-1279.(Guidelines from the AUA for treating small renal masses [<4.0 cm].)
"NCCN Guidelines™ Version 2". 2011 Updates Kidney Cancer. 2011.(Treatment guidelines from NCCN for localized and metastatic RCC.)
Smith, AD, Lieber, ML, Shah, SN. "Assessing Tumor Response and Detecting Recurrence in Metastatic Renal Cell Carcinomaon Targeted Therapy: Importance of Size and Attenuation on Contrast-Enhanced CT". AJR. vol. 194. 2010. pp. 157-165.(Article focusing on the radiologic evaluation of mRCC.)
Gill, IS, Aron, M, Gervais, DA. "Small Renal Mass". N Engl J Med. vol. 362. 2010. pp. 624-34.(Review article focusing on small renal masses, diagnosis and therapy.)
Chawla, SN, Crispen, PL, Hanlon, AL. "The Natural History of Observed Enhancing Renal Masses: Meta-Analysis and Review of the World Literature". J Urol. vol. 175. 2006. pp. 425-31.(Meta-analysis of the small renal mass literature – excellent overview.)
Margulis, V, Matin, SF, Wood, CG. “Surveillance Strategies following curative therapy for localized renal cell carcinoma” in Clinical Management of Renal Tumors, Eds Bukowski RM. Novick AC; Humana Press Inc. 2008. pp. 265-274.(Discussion of surveillance approaches for localized renal tumors.)
Novakovic, KR, Campbell, SC. "“Rare malignancies of the Kidney: Evaluation and Management” in Bukowski RM, Novick AC (eds): Clinical Management of Renal Tumors". Humana Press Inc.. 2008. pp. 617-636.(Review of uncommon renal tumors and their management.)
Upton, MP, Parker, RA, Youmans, A. "Histologic predictors of renal cell carcinoma response to interleukin-2-based therapy". J Immunother. vol. 28. 2005. pp. 488-495.(Pathologic analysis of IL-2 treated patients.)
Karakiewicz, PI, Hutterer, GC, Trinh, QD. "Unclassified renal cell carcinoma: an analysis of 85 cases". BJU International. vol. 100. 2007. pp. 802-808.(Review of unclassified RCC – discuss pathologic findings and clinical course in a large group of patients)
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