ICUD-EAU International Consultation on Kidney Cancer 2010: Treatment of Metastatic Disease
Authors
Affiliations
Context: Until the development of novel targeted agents directed against angiogenesis and tumour growth, few treatment options have been available for the treatment of metastatic renal-cell carcinoma (mRCC).
Objective: This review discusses current targeted therapies for mRCC and provides consensus statements regarding treatment algorithms.
Evidence Acquisition: Medical literature was retrieved from PubMed up to April 2011. Additional relevant articles and abstract reviews were included from the bibliographies of the retrieved literature.
Evidence Synthesis: Targeted treatment for mRCC can be categorized for the following patient groups: previously untreated patients, those refractory to immunotherapy, and those refractory to vascular endothelial growth factor (VEGF)-targeted therapy. Sunitinib and bevacizumab combined with interferon alpha are generally considered first-line treatment options in patients with favourable or intermediate prognoses. Temsirolimus is considered a first-line treatment option for poor-risk patients. Either sorafenib or sunitinib may be valid second-line treatments for patients who have failed prior cytokine-based therapies. For patients refractory to treatment with VEGF-targeted therapy, everolimus is now recommended. Pazopanib is a new treatment option in the first- and second-line setting (after cytokine failure). Sequential and combination approaches, and the roles of nephrectomy and tumour metastasectomy will also be discussed.
Conclusions: Increasing clinical evidence is clarifying appropriate first- and second-line treatments with targeted agents for patients with mRCC. Based on phase 2 and 3 trials, a sequential approach is most promising, while combination therapy is still investigational. The role of nephrectomy in mRCC is being evaluated in ongoing phase 3 clinical trials.
Ocak B, Sahin A, Erturk I, Korkmaz M, Erdem D, Cakiroglu U Curr Oncol. 2024; 31(9):5195-5205.
PMID: 39330012 PMC: 11431784. DOI: 10.3390/curroncol31090384.
AK7-deficiency reversal inhibits ccRCC progression and boosts anti-PD1 immunotherapy sensitivity.
Jin Y, Chen M, Chen F, Gao Z, Li X, Hu L Aging (Albany NY). 2024; 16(13):11072-11089.
PMID: 38970774 PMC: 11272107. DOI: 10.18632/aging.206006.
Liu Y, Cheng W, Yang Q, Han Y, Jiang Q, Yang Y Updates Surg. 2024; 76(2):657-676.
PMID: 38165526 DOI: 10.1007/s13304-023-01703-4.
Identifying TYMP as an Immune Prognostic Marker in Clear Cell Renal Cell Carcinoma.
Chen S, Zhang J, Wang N, Chen J Technol Cancer Res Treat. 2023; 22:15330338231194555.
PMID: 38043946 PMC: 10695089. DOI: 10.1177/15330338231194555.
Ren Y, Guo W, Qiao B Heliyon. 2023; 9(10):e20175.
PMID: 37767481 PMC: 10520310. DOI: 10.1016/j.heliyon.2023.e20175.