Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 May 9;2(2):e000185.
doi: 10.1136/esmoopen-2017-000185. eCollection 2017.

New treatment options for metastatic renal cell carcinoma

Affiliations
Review

New treatment options for metastatic renal cell carcinoma

Alejo Rodriguez-Vida et al. ESMO Open. .

Abstract

During the last decade, the treatment of advanced or metastatic renal cell carcinoma (RCC) was revolutionised with the advent of antiangiogenic drugs and tyrosine-kinase inhibitors. Several agents targeting the vascular endothelial growth factor (VEGF) pathway (sunitinib, bevacizumab, pazopanib, axitinib) or the mammalian target of rapamycin pathway (temsirolimus, everolimus) were since then progressively approved for first-line or later-line use in the treatment of patients with advanced RCC and became the new standard of care. As a result, the survival of patients with advanced RCC has significantly improved from a median overall survival of approximately 12 months in the cytokines era to more than 26 months with first-line VEGF inhibitors. During the two last years, the treatment of advanced RCC has witnessed a second revolution with the advent of immune checkpoint inhibitors, especially agents targeting the programmed cell death-1 receptor, as well as with the advent of new generation tyrosine-kinase receptor inhibitors. This article will review the new therapeutic options available for the treatment of advanced RCC, as well as the future potential molecular targets that are currently being investigated.

Keywords: Renal cell carcinoma New treatments Tyrosine-kinase inhibitor Immunotherapy Programmed cell death-1.

PubMed Disclaimer

Conflict of interest statement

Competing interests: JB: Consultant and adboard for Eisai and Exelixis (compensated). The other authors (ARV, TEH and MHS) have no competing interests.

Figures

Figure 1
Figure 1
Proposal of different possible sequential approved therapies for advanced renal cell carcinoma. IFN, interferon; OS, overall survival.

References

    1. Escudier B, Pluzanska A, Koralewski P, et al. . Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial. Lancet 2007;370:2103–11.10.1016/S0140-6736(07)61904-7 - DOI - PubMed
    1. Motzer RJ, Hutson TE, Tomczak P, et al. . Sunitinib versus interferon alfa in metastatic renal-cell carcinoma. N Engl J Med 2007;356:115–24.10.1056/NEJMoa065044 - DOI - PubMed
    1. Sternberg CN, Davis ID, Mardiak J, et al. . Pazopanib in locally advanced or metastatic renal cell carcinoma: results of a randomized phase III trial. J Clin Oncol 2010;28:1061–8.10.1200/JCO.2009.23.9764 - DOI - PubMed
    1. Rini BI, Escudier B, Tomczak P, et al. . Comparative effectiveness of axitinib versus sorafenib in advanced renal cell carcinoma (AXIS): a randomised phase 3 trial. Lancet 2011;378:1931–9.10.1016/S0140-6736(11)61613-9 - DOI - PubMed
    1. Hudes G, Carducci M, Tomczak P, et al. . Temsirolimus, interferon alfa, or both for advanced renal-cell carcinoma. N Engl J Med 2007;356:2271–81.10.1056/NEJMoa066838 - DOI - PubMed