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Updated: Feb 16, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Utilization and efficacy of second-line targeted therapy in metastatic renal cell carcinoma: data from a national
Radek Lakomy1, Alexandr Poprach1, Zbynek Bortlicek2
1Department of Comprehensive Cancer Care and Faculty of Medicine, Masaryk Memorial Cancer Institute and Masaryk University, Brno, Czech Republic.
Background:
It is well known that patient characteristics and survival outcomes in randomized trials may not necessarily be similar to those in real-life clinical practice. The aim of the present study was to analyse second line treatment strategies in the real-world practice and to estimate the outcomes of patients treated with second-line targeted therapy for metastatic renal cell carcinoma (mRCC).
Methods:
This is a retrospective, registry-based study using data from the national registry of targeted therapies for mRCC. The RENIS registry contains data on 3049 patients who started the therapy with at least one targeted agent before 31 December, 2014. Of these patients, 1029 had a record of at least two different targeted therapies and sufficient data for analysis. Survival analysis was carried out using the Kaplan-Meier method. Statistical significance of differences in survival between subgroups was assessed using the log-rank test.
Results:
The median overall survival from the start of second-line treatment was 17.0 months (95% confidence interval [CI] 14.5-19.5 months), 17.1 months (95% CI 14.5-19.8), and 15.4 months (95% CI 11.0-19.7) for second-line everolimus, sorafenib, and sunitinib, respectively. Patients receiving second-line everolimus were older at the start of second-line treatment, more likely to have metachronous disease, and less likely to be previously treated with cytokines or to continue to third-line treatment than patients treated with second-line sunitinib or sorafenib. Progression-free survival (PFS) correlated with PFS on first-line treatment only for everolimus.
Conclusions:
In this retrospective study, no significant differences in survival were observed between the cohorts treated with different second-line agents including everolimus, sorafenib, and sunitinib.
Insights
Second-line targeted therapies for metastatic renal cell carcinoma (mRCC) showed similar survival outcomes in real-world practice. Everolimus, sorafenib, and sunitinib demonstrated comparable overall survival in mRCC patients receiving second-line treatment.
Area of Science:
- Oncology
- Clinical Pharmacology
- Epidemiology
Background:
- Real-world data on second-line targeted therapy for metastatic renal cell carcinoma (mRCC) is crucial as clinical trial populations may differ from real-world patients.
- Understanding treatment strategies and outcomes in routine clinical practice is essential for optimizing patient care in mRCC.
Purpose of the Study:
- To analyze second-line treatment strategies for metastatic renal cell carcinoma (mRCC) in real-world clinical practice.
- To estimate the survival outcomes of patients treated with second-line targeted therapy for mRCC.
Main Methods:
- Retrospective, registry-based study utilizing data from the RENIS registry.
- Inclusion of 1029 patients with at least two different targeted therapies for mRCC.
- Survival analysis performed using Kaplan-Meier method and log-rank test for statistical significance.
Main Results:
- Median overall survival from second-line treatment initiation was approximately 15.4–17.1 months across everolimus, sorafenib, and sunitinib cohorts.
- Patients receiving second-line everolimus had distinct baseline characteristics compared to those on sunitinib or sorafenib.
- Progression-free survival (PFS) correlation with first-line PFS was observed only for everolimus.
Conclusions:
- No significant differences in overall survival were observed between different second-line targeted agents (everolimus, sorafenib, sunitinib) in this real-world mRCC cohort.
- Real-world data suggests comparable efficacy for commonly used second-line targeted therapies in mRCC.
- Further research may explore specific patient subgroups that could benefit differentially from these agents.
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