Third-line sorafenib after sequential therapy with sunitinib and mTOR inhibitors in metastatic renal cell carcinoma
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Updated: Jun 8, 2026

A Syngeneic Mouse Model of Metastatic Renal Cell Carcinoma for Quantitative and Longitudinal Assessment of Preclinical Therapies
Published on: April 12, 2017
Giuseppe Di Lorenzo1, Carlo Buonerba, Piera Federico
1Dipartimento di Endocrinologia ed Oncologia Clinica e Molecolare, Università Federico II, Napoli, Italy. giuseppedilorenzoncol@hotmail.com
Background:
Sunitinib and everolimus have been approved for first- and second-line treatment, respectively, in metastatic renal cell carcinoma (mRCC). The role of sorafenib, which is approved for second-line treatment after cytokines failure, is presently to be defined.
Objective:
To determine whether third-line sorafenib after sequential use of sunitinib and mammalian target of rapamycin inhibitors (everolimus or temsirolimus) is feasible and effective.
Design, Setting, And Participants:
One hundred fifty medical records of patients with mRCC treated with first-line sunitinib between January 2006 and January 2010 were reviewed at four participating centers. Data regarding patients treated with the sequence sunitinib-everolimus or temsirolimus-sorafenib were extracted. Central analysis of radiographic images was performed using RECIST criteria to determine progression-free survival (PFS) and overall response rate (oRR) to sorafenib treatment.
Measurements:
PFS and oRR to sorafenib were the primary end points. Secondary outcomes were safety and overall survival (OS).
Results And Limitations:
Thirty-four patients were eligible for the study. A median PFS of 4 mo (range: 3-6 mo) and a median OS of 7 mo since sorafenib treatment (range: 6-10 mo) were reported. Of the patients, 23.5% showed response to sorafenib, with an overall disease control rate (complete responses plus partial responses plus stable disease) of 44%. Selection bias, data incompleteness, and absence of study design are inevitable limitations of the study, although central review can strengthen the quality of presented data.
Conclusions:
Third-line sorafenib appears to be active and well tolerated in mRCC after first-line sunitinib and second-line everolimus or temsirolimus, with no patients interrupting sorafenib because of toxicity or lack of compliance. Prospective, placebo-controlled trials are completely lacking and are required in this setting.
Insights
Third-line sorafenib is active and well-tolerated in metastatic renal cell carcinoma (mRCC) patients following sunitinib and everolimus/temsirolimus. Further prospective trials are needed to confirm these findings in mRCC treatment.
Area of Science:
- Oncology
- Medical Research
- Clinical Trials
Background:
- Sunitinib is approved for first-line treatment of metastatic renal cell carcinoma (mRCC).
- Everolimus is approved for second-line mRCC treatment.
- The role of sorafenib in mRCC after cytokine therapy is not well-defined.
Purpose of the Study:
- To evaluate the feasibility and efficacy of third-line sorafenib in mRCC patients.
- To assess sorafenib after sequential treatment with sunitinib and mammalian target of rapamycin (mTOR) inhibitors (everolimus or temsirolimus).
Main Methods:
- Retrospective review of 150 mRCC patient records treated with first-line sunitinib.
- Extraction of data for patients receiving sunitinib-everolimus or sunitinib-temsirolimus followed by sorafenib.
- Central radiographic analysis using RECIST criteria to determine progression-free survival (PFS) and overall response rate (oRR).
Main Results:
- Thirty-four patients were eligible for analysis.
- Median PFS on sorafenib was 4 months; median overall survival (OS) was 7 months.
- Sorafenib showed a 23.5% response rate and a 44% disease control rate in this mRCC cohort.
Conclusions:
- Third-line sorafenib demonstrates activity and tolerability in mRCC patients post-sunitinib and mTOR inhibitor therapy.
- No patients discontinued sorafenib due to toxicity or non-compliance.
- Prospective, placebo-controlled trials are necessary to validate these findings.
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