Metastatic chromophobe renal cell carcinoma treated with targeted therapies: A Renal Cross Channel Group study

Emeline Colomba1, Gwénaël Le Teuff2, Tim Eisen3

  • 1Medical Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

European Journal of Cancer (Oxford, England : 1990)
|May 27, 2017
PubMed
Abstract

Insights

This study found that anti-angiogenic (AA) and mammalian target of rapamycin (mTOR) inhibitors showed no significant difference in outcomes for metastatic chromophobe renal cell carcinoma (mChRCC). Further research is needed to optimize targeted therapy (TT) for non-clear cell RCC.

Area of Science:

  • Oncology
  • Medical Research

Background:

  • Treatment for non-clear cell renal cell carcinoma (RCC) lacks established guidelines, often relying on data from clear cell RCC.
  • Targeted therapies (TT), including Vascular Endothelial Growth Factor (VEGF) and Mammalian Target of Rapamycin (mTOR) inhibitors, are frequently used.

Purpose of the Study:

  • To evaluate outcomes for metastatic chromophobe RCC (mChRCC) patients treated with targeted therapies.
  • To compare the efficacy of anti-angiogenic (AA) and mTOR inhibitors in mChRCC.

Main Methods:

  • Retrospective data analysis of 91 mChRCC patients from the Renal Cross Channel Group.
  • Kaplan-Meier method used to estimate overall survival (OS) and time to treatment failure (TTF).
  • Comparison of AA and mTOR inhibitors using stratified log-rank test, controlling for International Metastatic RCC Database Consortium risk group.

Main Results:

  • Median OS for mChRCC patients was 37.9 months.
  • Among 61 patients receiving TT, 50 received AA and 11 received mTOR inhibitors.
  • No significant difference in TTF (p=0.26) or OS (p=0.55) was observed between AA and mTOR inhibitors.

Conclusions:

  • This study represents the largest retrospective cohort of mChRCC patients treated with TT.
  • Anti-angiogenic and mTOR inhibitors demonstrated comparable efficacy in terms of TTF and OS for mChRCC.
  • The findings suggest current targeted therapies may not offer differential benefits for mChRCC, highlighting the need for further investigation.

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