Treatment Options for Renal Cancer
Surgical resection remains the most effective therapy for clinically localized renal cell carcinoma (RCC), with options including radical nephrectomy and nephron-sparing surgery depending on tumor characteristics and patient factors. 1
Diagnosis and Initial Evaluation
Laboratory evaluation should include:
- Complete blood count
- Comprehensive metabolic panel (including serum calcium, liver function tests, lactate dehydrogenase, serum creatinine)
- Coagulation profile
- Urinalysis 1
Imaging studies essential for diagnosis and staging:
- Contrast-enhanced CT of abdomen and pelvis
- Chest imaging (chest radiograph or CT scan)
- Abdominal MRI if tumor involvement of inferior vena cava is suspected or when contrast cannot be administered 1
- Bone scan only if elevated serum alkaline phosphatase or bone pain 1
- Brain CT/MRI only if clinical signs suggest brain metastases 1
Treatment of Localized Disease
Stage I (T1a, tumor ≤4 cm)
Nephron-sparing surgery (partial nephrectomy) is the preferred treatment 1
- Can be performed via open, laparoscopic, or robotic techniques
- Preserves renal function
- Associated with decreased overall mortality and reduced cardiovascular events compared to radical nephrectomy
- 5-year cancer-specific survival exceeds 94% 2
Alternative options for selected patients:
- Ablative techniques (cryosurgery, radiofrequency ablation) for:
- Small cortical tumors
- Frail patients
- High surgical risk
- Solitary kidney
- Compromised renal function 1
- Active surveillance for:
- Ablative techniques (cryosurgery, radiofrequency ablation) for:
Stage I (T1b, tumor 4-7 cm)
- Partial nephrectomy preferred if technically feasible 1
- Laparoscopic radical nephrectomy if partial nephrectomy not feasible 1
Stage II (T2, tumor >7 cm, confined to kidney)
- Laparoscopic radical nephrectomy is preferred option 1
Stage III-IV (locally advanced)
- Open radical nephrectomy is standard of care 1
- Regional lymph node dissection recommended for patients with adenopathy on preoperative imaging or palpable/visible adenopathy during surgery 1
- Adrenal gland resection may be omitted if uninvolved 1
Treatment of Advanced/Metastatic Disease
Cytoreductive Nephrectomy
- Recommended in patients with good performance status (ECOG PS <2) 1
- Not recommended for intermediate/poor-risk patients with asymptomatic primary tumors when systemic therapy is required 1
- Patients with excellent performance status and small-volume metastases may benefit from cytoreductive nephrectomy followed by systemic therapy 1
Systemic Therapy for Clear Cell RCC
First-line options:
For good and intermediate-risk patients:
For poor-risk patients:
Systemic Therapy for Non-Clear Cell RCC
Everolimus
Lenvatinib + everolimus
Nivolumab
Pazopanib
Sorafenib
Temsirolimus (Category 1 for poor-prognosis patients) 1
For collecting duct or medullary subtypes:
- Platinum-based chemotherapy (carboplatin + gemcitabine, carboplatin + paclitaxel, or cisplatin + gemcitabine) 1
Radiation Therapy
- Not primary treatment for RCC but useful for:
Follow-up Recommendations
For localized disease under active surveillance:
- History and physical exam every 6 months for 2 years, then annually up to 5 years after diagnosis 1
For patients receiving systemic therapy:
- History and physical examination every 6-16 weeks
- Imaging (CT or MRI) before starting treatment and every 6-16 weeks as clinically indicated 1
Important Considerations
- Renal function assessment is crucial as over 25% of surgically managed patients with small renal masses have preexisting renal dysfunction 1
- Biopsy may be considered to establish diagnosis of RCC and guide surveillance or ablative strategies 1
- Multifocal lesions can be difficult to identify with standard imaging; evaluation of unenhanced CT scans together with enhanced corticomedullary and nephrogenic phase may improve detection 5
Treatment Outcomes
- 5-year survival rates: 96% for stage I, 82% for stage II, 64% for stage III, and 23% for stage IV disease 1
- For advanced/metastatic RCC, combinations of immune checkpoint inhibitors or immune checkpoint inhibitors with tyrosine kinase inhibitors are associated with tumor response rates of 42-71% and median overall survival of 46-56 months 2