Renal cell carcinoma (RCC) accounts for 90% to 95% of malignant neoplasms arising from the kidney. Recent advances in surgical and systemic therapies have significantly changed the management of RCC. Targeted therapies against the vascular endothelial growth factor (VEGF) pathway have extended the lives of the patients with advanced disease significantly, with median overall survival currently exceeding 2 years.1


RCC accounts for 2% to 3% of all malignant diseases in adults. It is the seventh most common cancer in men and the ninth most common in women. In the United States, there are approximately 65,000 new cases each year and about 13,500 deaths from RCC annually.2 The incidence of RCC in the US has increased over time.3-5 Between 1992 and 2005, the incidence rose by 1.8% and 2.1% among white men and white women, respectively, and by 2.1% and 1.7% among black men and black women, respectively. In an analysis of more than 29,000 cases from the Surveillance, Epidemiology, and End Results (SEER) database, this increased incidence has been associated with a steady decrease in the average size of tumors at presentation (6.7 cm vs 5.9 cm in 1988 and 2002, respectively).3 Despite the earlier detection of smaller kidney tumors, the rate of RCC-related mortality has increased,6,7 suggesting that recurrence and advanced disease are responsible for mortality.

Within the US, Asian Americans and Pacific Islanders have the lowest incidence of renal cancers compared with American Indians/Alaskan natives, Hispanics, Caucasians, and African Americans.2 Globally, the incidence of RCC varies widely from region to region, with the highest rates observed in the Czech Republic and in North America.8

RCC is approximately 50% more common in men than in women.9 It usually occurs between the sixth and eighth decades of life, with a median age of 65.

Table 1: Renal Cell Carcinoma Risk Factors

Tobacco smoking
Occupational exposures
Polycystic kidney disease
Chronic Hepatitis C infection

Risk Factors

Inhaled tobacco smoke is clearly implicated in the etiology of RCC, with a strong dose-dependent increase in risk associated with numbers of cigarettes smoked per day and a substantial reduction in risk for long-term former smokers.10 Higher body mass index (BMI) and elevated blood pressure independently increase the long-term risk of renal cell cancer in men. A reduction in blood pressure has been associated with a reduced risk of RCC.11 These 3 risk factors together are associated with 49% of cases.12

Other modifiable risk factors, although not convincingly associated, include exposure to asbestos, trichloroethylene, or thiazide, and use of acetaminophen or other analgesic drugs. Renal cell carcinoma also seems to be more common in patients with chronic hepatitis C infection,13 end-stage renal failure, acquired renal cystic disease,14 and tuberous sclerosis15 than in the general population (Table 1).

Detection & Diagnosis


Individuals with a family history of RCC have a 2.8-fold greater chance for developing renal cancer during their lifetimes16 and account for about 4% of all RCC cases. Studies of families with inherited RCC have enabled the identification of 6 hereditary RCC syndromes: von Hippel-Lindau (VHL), hereditary papillary renal carcinoma (HPRC), Birt-Hogg-Dubé syndrome (BHD), hereditary leiomyomatosis RCC (HLRCC), succinate dehydrogenase (SDH)-associated familial cancer, and tuberous sclerosis complex (TSC) (Table 2). The predisposing genes associated with these syndromes are VHL, MET, FLCN, FH, SDH, TSC1 and TSC2, respectively.17

Table 2: Hereditary Renal Cell Carcinoma Syndromes

Syndrome Gene (Chromosome) Histology Major clinical manifestations
von Hippel-Lindau VHL tumor suppressor gene (3p25-26) Clear cell Autosomal dominant, retinal angioma, CNS hemangioblastomas, pheochromocytomas, pancreatic islet cell tumors, paragangliomas, cystadenoma of broad ligament or epididymis.
Hereditary papillary renal carcinoma MET proto-oncogene (7q31) Type 1 papillary Autosomal-dominant, multifocal, bilateral renal cell tumors.
Birt-Hogg-Dubé syndrome FLCN tumor suppressor gene (17p11.2) Chromophobe, hybrid oncocytoma Autosomal-dominant, cutaneous fibro-folliculoma, pulmonary cysts and spontaneous pneumothorax.
Hereditary leiomyomatosis and renal cell carcinoma FH tumor suppressor gene (1q42-43) Type 2 papillary Autosomal-dominant, leiomyomas of skin and uterus, unilateral, solitary, and aggressive renal cell tumors.
Succinate dehydrogenase (SDH)-associated familial cancer40 SDH-B subunit (1p35-36)

SDH-D subunit (11q23)
Clear cell, chromophobe, papillary type 2, renal oncocytoma Head and neck para-ganglioma, and adrenal or extra-adrenal pheochromocytomas.
Tuberous sclerosis complex TSC1 (9q34)

TSC2 (16p13)
Clear cell (common) Autosomal-dominant, facial angiofibromas, multifocal renal angiolipomas, neurologic disorders or seizures, lymphangiomyomatosis of the lungs.
Adapted from The Lancet Vol. 373, Rini BI, Campbell SC, Escudier B, Renal Cell Carcinoma, pages 1119-1132, Copyright 2009, with permission from Elsevier.


RCC consists of a heterogeneous group of tumors with distinct genetic and metabolic defects, as well as histopathologic and clinical features (Table 3).17 Medullary carcinomas are rare but aggressive, and are exclusively associated with sickle cell trait.

Table 3: Histologic Classification of Renal Cell Carcinoma

Histology Frequency Cell of Origin Characteristics
Clear cell 60%-70% Proximal tubule Cells with clear cytoplasm with acinar or sarcomatoid growth pattern.
Papillary 5%-15% Proximal tubule Type I: papillae lined with a layer of tumor cells with scant pale cytoplasm and low-grade nuclei.

Type II: abundant eosinophilic cytoplasm and large pseudo stratified nuclei with prominent nucleoli; aggressive subtype.
Chromophobic 5%-10% Cortical collecting duct Cells are large with finely reticulated eosinophilic cytoplasm, and atypical nuclei with perinuclear halo with solid, tubular or sarcomatoid growth pattern; indolent course.
Oncocytic 5%-10% Cortical collecting duct Benign neoplasms.
Collecting duct <1% Medullary collecting duct Papillary or sarcomatoid growth pattern.
Adapted from The Lancet Vol. 373, Rini BI, Campbell SC, Escudier B, Renal Cell Carcinoma, pages 1119-1132, Copyright 2009 with permission from Elsevier.

Signs and Symptoms

Renal cancers have been called “the internist’s tumor” and are among the great mimics in medicine because they present with systemic symptoms unrelated to the kidney cancer, such as hypertension (renin), hypercalcemia (PTHrP), polycythemia (erythropoietin), eosinophilia, leukemoid reactions, Cushing’s syndrome (ACTH), fever or wasting syndromes, and Stauffer’s syndrome (reversible hepatic dysfunction after primary tumor removal). Most cases of RCC are diagnosed incidentally on radiographic investigation done for other reasons. The classic triad of hematuria, abdominal pain, and a palpable mass is present in ≤ 10% of cases.

Signs or symptoms resulting from metastatic disease include bone pain, adenopathy, pulmonary symptoms attributable to lung parenchyma or mediastinal metastases, upper GI bleed, and neurologic deficits.

Figure 1 and 2 Figure 1. CT Scan of a Patient with Renal Cell Carcinoma Before (A) and After (B) Intravenous Contrast.

Reprinted with permission from Saunders Elsevier (Campbell SC, Novick AC, Bukowski RM. Renal tumors. In: Kavoussi LR, Novick AC, Partin AW, et al, eds. Campbell-Walsh Urology. 9th ed. Philadelphia, PA: Saunders Elsevier; 2007:1571). Copyright © 2007 Elsevier.


The initial workup consists of taking a detailed medical history and performing a physical examination. Appropriate laboratory investigations include a complete blood cell count, a comprehensive metabolic panel (including evaluation of serum calcium level, liver function, and lactate dehydrogenase and serum creatinine levels), a coagulation profile, and urinalysis. Imaging studies should include computed tomography (CT) scans of the abdomen and pelvis (with and without contrast) (Figure 1) and chest imaging (either chest radiograph or CT scan).

Abdominal magnetic resonance imaging (MRI) is used to evaluate tumor extension into the inferior vena cava. MRI can be used instead of CT when contrast media cannot be administered due to allergy or renal insufficiency.18,19 A bone scan or brain imaging is not routinely performed unless signs or symptoms suggest involvement of these areas. PET is not used to diagnose or follow up kidney cancer in any circumstance.20 Needle biopsy is not routinely used to establish diagnosis in patients with large renal masses and radiologic characteristics of malignancy. These patients often undergo immediate kidney removal, which is both diagnostic and therapeutic. However, needle biopsy may be valuable in patients with small (< 3 cm) renal masses not requiring nephrectomy.21

A differential diagnosis of urothelial carcinoma should be considered in a patient with a central renal mass and urine cytology. Alternatively, ureteroscopy should be pursued in addition to biopsy, as indicated.

The severity of disease is staged on the basis of imaging studies and the American Joint Committee on Cancer (AJCC) Cancer Staging Manual (Table 4). Approximately 50% of RCC patients present with localized disease, 25% with locally advanced disease, and 25% to 30% with metastatic disease.

Table 4: American Joint Committee on Cancer TNM Staging System for Kidney Cancer

Primary Tumor (T)
Tx Primary tumor can not be assessed
T0 No evidence of primary tumor
T1a Tumor ≤ 4 cm, confined to the kidney
T1b Tumor 4 cm to < 7 cm, confined to the kidney
T2a Tumor ≥ 7 cm to < 10 cm, confined to the kidney
T2b Tumor ≥ 10 cm, confined to the kidney
T3a Tumor extends into the renal vein or its segmental branches or invades adrenal gland or perinephric fat but not beyond Gerota’s fascia
T3b Tumor extends into the vena cava below diaphragm
T3c Tumor extends into the vena cava above the diaphragm or invades the wall of vena cava
T4 Tumor invades beyond Gerota’s fascia
Regional Lymph Nodes (N)
N1 Metastasis in 1 regional lymph node
N2 Metastasis in > 1 regional lymph node
Distant Metastases (M)
M1 Distant metastasis present
Anatomic Stage
Stage I T1 N0 M0
Stage II T2 N0 M0
Stage III T1/T2
Stage IV T4
Any T
Any N
Any N
Reprinted with permission from Springer (American Joint Committee on Cancer. Kidney. In: Edge SB, Byrd DR, Compton CC, et al., eds. AJCC Cancer Staging Manual. 7th ed. New York, NY: Springer; 2010479-89).

Prognostic Criteria

The Memorial Sloan-Kettering Cancer Center prognostic criteria are commonly used in patients with metastatic disease. These criteria correlate the following features with poor outcomes in patients treated with either cytokines or chemotherapy agents in various clinical trials before the era of targeted therapy:

These risk factors categorize patients’ prognoses into favorable (0 risk factors), intermediate (1-2 risk factors), and poor (3-5 risk factors) risk groups, which were associated with a median survival of 30, 14, and 5 months, respectively.22

Cleveland Clinic has developed another prognostic model for patients with metastatic clear-cell RCC treated with vascular endothelial growth factor (VEGF)-targeted therapy. This single-institution, retrospective study found the following to be predictors of poor outcome:

The median progression-free survival (PFS) in patients with 0 or 1 adverse prognostic factors was 20.1 months compared with 13 months in patients with 2 adverse prognostic factors and 3.9 months in those with 3 or more adverse prognostic factors.23

In another study, the outcomes data from the phase III trial in which sunitinib was compared with interferon-alpha were used to derive a prognostic model for those treated with sunitinib alone (n = 375). A prognostic nomogram was created by using 11 factors, including corrected serum calcium, number of metastatic sites, hemoglobin, prior nephrectomy, presence of lung metastases, presence of liver metastases, Eastern Cooperative Oncology Group (ECOG) performance status, thrombocytosis, time from diagnosis to treatment, alkaline phosphatase, and LDH.24

Although various prognostic models exist, robust clinical and biologic features predictive of outcome in patients with metastatic RCC are scarce. Until appropriate predictive patient variables are identified, available effective agents should be offered even to patients with poor prognoses. Targeted therapies against the VEGF pathway have significantly extended the lives of patients with advanced disease. The median overall survival (OS) duration now exceeds 2 years.1 Overall, the estimated average 5-year survival rates for patients with RCC are 96% for those presenting with stage I disease, 82% for those with stage II, 64% for stage III, and 23% for stage IV.

Patient Care

Treatment and Outcomes

Once a cardiac catheterization has been performed, the three most common therapeutic options are medical therapy, percutaneous coronary intervention (PCI), and coronary artery bypass grafting (CABG).

Stage IA. For tumors ≤ 4 cm in diameter, surgical excision by partial nephrectomy (nephron-sparing surgery) (Figure 2) is recommended. The surgical approach can be either open or laparoscopic, depending on surgeon preference, and tumor size and location. The objective of surgery is to spare as many functioning nephrons as possible and to preserve renal function while excising the tumor. Radical nephrectomy is recommended only if the tumor is not amenable to partial nephrectomy.

In patients with decreased life expectancy (or those considered to be at high risk during surgery), options include active surveillance and thermal ablation (cryoablation or radiofrequency ablation). Although distant recurrence-free survival rates are comparable, thermal ablation has been associated with an increased risk of local recurrence compared with conventional surgery.25,26

Figure 2. Partial Nephrectomy Surgical Technique in a Patient with Localized Kidney Cancer.
Figure 2. Partial Nephrectomy Surgical Technique in a Patient with Localized Kidney Cancer.

Reprinted with permission from Elsevier (Rini BI, Campbell SC, Escudier B. Renal cell carcinoma. Lancet. 2009;373[9669]:1119-1132). Copyright © 2009 Elsevier.

Stage IB. For 4- to 7-cm tumors, partial nephrectomy, if feasible, or radical nephrectomy is the standard of care.

Stage II and III. Locally advanced tumors are managed with radical nephrectomy, which can require resection of adjacent organs, and with tumor thrombectomy from the renal vein and possibly the inferior vena cava.6 Between 40% and 60% of patients can be cured with such an aggressive surgical approach.27,28

After surgical excision, up to 30% of patients with localized tumors experience relapse. The lung is the most common site of distant recurrence, seen in 50% to 60% of patients. The median time to relapse after surgery is approximately 2 years, with most relapses occurring within 5 years. Interferon-alpha and high-dose interleukin-2 (IL-2) have been tested as adjuvant treatments following resection of stage I-II kidney cancer. However, no benefit has been seen in randomized trials.29,30 Observation remains standard care after nephrectomy, and eligible patients should be offered enrollment in randomized clinical trials.

The National Comprehensive Cancer Network (NCCN) Kidney Cancer Panel has recommended that patients be seen every 6 months for the first 2 years after surgery and annually thereafter. Each visit should include a history, physical examination, and comprehensive metabolic panel (eg, blood urea nitrogen, serum creatinine, calcium levels, LDH, and liver function tests). Abdominal and chest imaging studies should be done approximately 2 to 6 months after surgery and as clinically indicated thereafter.31

Stage IV. Cytoreductive nephrectomy before systemic therapy is recommended in patients with a surgically resectable primary tumor.32 Metastasectomy should be considered in patients with favorable features such as a solitary metastasis or a long interval between initial diagnosis and the development of metastatic disease. In these patients, the 5-year disease-free survival rate can be as high as 30%.

Systemic therapy is recommended for patients with residual metastatic disease, though patients with low-volume indolent metastases may initially undergo a period of observation. Several systemic agents exist today that are non-curative and therefore require long-term sequential therapy with multiple agents and management of toxicity.


Targeted therapy

Targeted therapy with tyrosine kinase inhibitors has been used widely in first- and second-line treatments. To date, 7 such agents have been approved by the FDA for the treatment of advanced RCC: sunitinib, sorafenib, pazopanib, axitinib, temsirolimus, everolimus, and bevacizumab in combination with interferon.


References & Suggested Readings


Suggested Readings

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