Therapeutic target
Prolonging survival in metastatic renal cell carcinoma (RCC).
Therapy recommendations
- Therapy procedure of first choice is surgery.
- In metastatic clear cell renal cell carcinoma (approximately 75-80% of cases):
- first-line therapy for metastatic renal cell carcinoma (mNCC) should be risk-adapted [S3 guideline]Criteria for this are: 6 International Metastatic RCC Database Consortium (IMDC) criteria: Anemia (anemia), neutrophilia (increase in the number of neutrophil granulocytes in the blood), thrombocytosis (increased number of platelets (thrombocytes) in the blood), hypercalcemia (calcium excess), Karnofsky index 80%, time to relapse after initial diagnosis (12 months).
- Median overall survival:
- Without risk factors: 43 months
- Intermediate risk profile (one or 2 risk factors): 22, 5 months.
- > 2 risk factors: 7, 8 months
- Median overall survival:
- cytokine therapy based on subcutaneous IL-2 and/or IFN alone should not be performed [recommendation grade A]The standard is always a combination therapy of two immunotherapeutics or of one immunotherapeutic and a tyrosine kinase inhibitor (TKI).
- Low- or intermediate-risk patients should use sunitinib, pazopanib, or bevacizumab + INF in first-line therapy
- Second-line therapy is TKI-based therapy.
- Only after failure of at least one VEGF inhibitor should everolimus be used.
- Low- or intermediate-risk patients should use sunitinib, pazopanib, or bevacizumab + INF in first-line therapy
- first-line therapy for metastatic renal cell carcinoma (mNCC) should be risk-adapted [S3 guideline]Criteria for this are: 6 International Metastatic RCC Database Consortium (IMDC) criteria: Anemia (anemia), neutrophilia (increase in the number of neutrophil granulocytes in the blood), thrombocytosis (increased number of platelets (thrombocytes) in the blood), hypercalcemia (calcium excess), Karnofsky index 80%, time to relapse after initial diagnosis (12 months).
- If multiple metastases (daughter tumors) occur metachronously (“occurring at different times”) in only one organ system, local (topical) treatment should be considered.
- See also under “Further therapy”.
Further notes on clear cell renal cell carcinoma.
- Stratification into patients with favorable prognosis on one side and intermediate or unfavorable prognosis on the other side is performed to plan the first line of therapy.
- Patients with favorable prognosis:
- First-line therapy: bevacizumab/IFN; pazonib, sunitinib, tivozanib.
- Second-line therapy: VEGFR failure: cabozantinib, nivolumab, lenvatinib/everolib.
- Third-line therapy: see below.
- Patients with intermediate prognosis:
- First-line therapy: nivolumab + ipilimumab, carbozantinib.
- Second-line therapy: CPI failure: no standard, cabozantinib, lenvatinib/everolism, other TKIs.
- Third-line therapy: see below.
- Patients with unfavorable prognosis:
- First-line therapy: nivolumab + ipilimumab, cabozantinib, temsirolism.
- Second-line therapy: mTor.failure: no standard, cabozantinib, nivolumab, lenvatinib/everolism, other TKIs.
- Third-line therapy: see below.
- Third-line therapy:
- After TKI + TKI: cabozantinib, nivolumab, everolism.
- After TKI + mTort: no standard, cabozantinib, nivolumab.
- After TKI + CPI: no standard, cabozantinib, lenvatinib/everolumab.
- After CPI + TKI: no standard, other TKI, everolism, lenvatinib/everolism.
- Patients with favorable prognosis:
Legend: IFNI: Interferon, TKI: tyrosine kinase inhibitor, CPI: checkpoint inhibition, VEGFR: vascular endothelial growth factor receptor, mTOR: mechanistic target of rapamycin.
Additional notes
- In a study of high-risk hypernephroma patients, patients treated with sunitinib relapsed in 6.8 years. In the placebo group, relapse occurred after 5.4 years.
- Second-line therapy with the PD-1 inhibitor (checkpoint inhibitor) nivolumab as another pillar of immunotherapeutic treatment: this blocks the receptor PD-1 on activated T lymphocytes and thus prevents the interaction with the ligand PD-L1 on other immune and tumor cells. This leads to the originally inhibited T cells being able to attack the tumor again. In a study, a significantly prolonged overall survival was shown compared to therapy with everolimus.
- The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive marketing authorization recommendation for avelumab in combination with axitinib for the first-line treatment of adult patients with advanced renal cell carcinoma (based on positive results from the phase III JAVELIN Renal 101 study: significant prolongation of median
- A combination therapy of VEGF and checkpoint inhibitors as first-line therapy for advanced renal cell carcinoma:
- Avelumab/auxitinib prolonged progression free survival (PFS).
- Pembrolizumab/auxitinib prolonged overall survival (OS).
Both combinations have the potential to become new standards of first-line therapy.
- Bisphosphonates should be used for bone metastases; in addition to local radiatio (radiotherapy).
Agents (main indication)
Active ingredient group | Active ingredients | Special features |
Interferons | Interferon alpha (IFN-alfa) | Immunotherapycombination with interleukin-2 (IL-2)Contraindications in renal and severe hepatic insufficiency. |
Tyrosine kinase inhibitors (TKi)/VEGF (vascular endothelial growth factor). | Axitinib | Second-line therapyIn second-line therapy after sunitinib or cytokines, axitinib can be used |
Bevacizumab | First-line therapy in combination with interferon-alpha (IFN-alfa) | |
Cabozantinib | First-line therapy of adults with advanced renal cell carcinoma (RCC) at intermediate or high risk Second-line therapy after antiangiogenic therapy | |
Pazopanib |
First- and second-line
First-line therapy for low or intermediate riskSecond-line therapy after cytokine therapy. |
|
Sorafenib |
First- and second-line
Second-line therapyIndication for contraindication or failure of immunotherapy. |
|
Sunitinib |
First- and second-line First-line therapy with high response rate |
|
Tivozanib | First- and second-line | |
Multikinase inhibitor | Lenvatinib | Ind : advanced renal cell carcinomin combination with everolimus. |
mTOR inhibitors | Everolimus |
Second-line therapy
Everolimus may be used after failure of at least one VEGF inhibitor. |
Temsirolimus | First-line therapy of advanced renal cell carcinoma in patients with poor prognosisAfter temsirolimus axitinib pazopanib sorafenib sunitinib | |
PD-1 inhibitor | Nivolumab |
Second-line therapy
Ind : advanced renal cell carcinoma after prior therapy. Note: Monitor closely and up to twelve months after end of therapy for immune-mediated side effects (see below)! The combination nivolumab/ipilimumab is approved as first-line therapy for patients with advanced renal cell carcinoma with an intermediate or unfavorable risk profile.Note: Ipilimumab is a fully humanized monoclonal antibody used in the treatment of melanoma that targets the protein CTLA-4. |
Pembrolizumab | After a median observation time of 12.8 months, 89.9% of patients in the pembrolizumab-auxitinib group were still alive versus 78.3% of patients in the sunitinib group |