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A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
First-Line Immune Combination Therapies for Nonclear Cell Versus Clear Cell Metastatic Renal Cell Carcinoma:
Cristina Cano Garcia1, Benedikt Hoeh1, Subhajit Mandal2
1Department of Urology, University Hospital Frankfurt, Goethe University Frankfurt am Main, Frankfurt, Germany.
Outcomes for clear cell metastatic renal cell carcinoma (ccmRCC) and non-ccmRCC (nccmRCC) patients receiving first-line immunotherapy were similar. This study found no significant differences in overall survival or progression-free survival between the two groups.
Area of Science:
- Oncology
- Immunotherapy
- Renal Cell Carcinoma Research
Background:
- Metastatic renal cell carcinoma (mRCC) treatment has evolved with immune combination therapies.
- Clear cell (ccmRCC) and non-clear cell (nccmRCC) subtypes represent distinct disease entities.
- Comparing treatment outcomes between ccmRCC and nccmRCC is crucial for personalized medicine.
Purpose of the Study:
- To compare treatment outcomes (overall survival and progression-free survival) of ccmRCC versus nccmRCC patients.
- To evaluate the efficacy of first-line immune combination therapies in different mRCC subtypes.
- To identify potential differences in response to immunotherapy based on RCC histology.
Main Methods:
- Retrospective analysis of a multi-institutional database (eight tertiary-care centers).
- Inclusion of mRCC patients treated with first-line immune combination therapies (11/2017-12/2022).
- Log-rank analysis and multivariable Cox regression to compare OS and PFS, adjusting for covariates (age, sex, risk groups, ECOG status, sarcomatoid feature).
Main Results:
- The study included 289 mRCC patients; 39 (13%) had nccmRCC.
- Median overall survival (OS) was 37 months for ccmRCC vs. not reached for nccmRCC (P = .6).
- Median progression-free survival (PFS) was 13 months for ccmRCC vs. 15 months for nccmRCC (P = .9).
- Multivariable analysis showed nccmRCC was not an independent predictor of higher mortality (HR: 1.23; P = .6) or progression (HR: 1.0; P = 1.0).
Conclusions:
- First-line immune combination therapy demonstrated similar OS and PFS in both ccmRCC and nccmRCC patients.
- Histological subtype (ccmRCC vs. nccmRCC) did not significantly impact outcomes in this real-world setting.
- Further prospective clinical trials are warranted to specifically investigate treatment strategies for nccmRCC patients.
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