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Updated: Mar 1, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
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.
Background:
Treatment of non-clear cell renal cell carcinoma (RCC) remains controversial despite several recent prospective studies of targeted therapies (TT). Often Vascular Endothelial growth Factor (VEGF) and Mammalian Target of Rapamycin (mTOR) inhibitors are used, extrapolating the data from use of these agents in clear cell RCC.
Methods:
We performed a retrospective data analysis within the Renal Cross Channel Group to determine metastatic chromophobe RCC (mChRCC) outcomes in the TT era. The end-points were overall response, overall survival (OS) and time to treatment failure (TTF). The two latter were estimated using the Kaplan-Meier method.
Results:
91 mChRCC patients from 26 centres were included. Median follow-up from the date of first metastasis was 6.1 years (range: 0-13.9). Median OS was 37.9 months (95% confidence interval [CI]: 21.4-46.8) from the diagnosis of metastatic disease. Among the 61 patients who received TT, 50 (82%) were treated with anti-angiogenic (AA) and 11 with mTOR inhibitors. Median TTF and OS in patients receiving a first line of AA was 8.7 months (95% CI: 5.2-10.9) and 22.9 months (95% CI: 17.8-49.2) versus 1.9 months (95% CI: 1.0-6.0) and 3.2 months (95% CI: 2.3-not evaluable) with mTOR inhibitors, respectively. A stratified log-rank test was used to compare AA and mTOR inhibitors TT, while controlling the effect of the International Metastatic RCC Database Consortium risk group and no significant difference between AA and mTOR inhibitors was observed for TTF (p = 0.26) or for OS (p = 0.55).
Conclusion:
We report the largest retrospective cohort of patients with mChRCC treated with TT and no significant difference between AA and mTOR inhibitors was observed for TTF and OS.
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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