Third-line sorafenib after sequential therapy with sunitinib and mTOR inhibitors in metastatic renal cell carcinoma

Giuseppe Di Lorenzo1, Carlo Buonerba, Piera Federico

  • 1Dipartimento di Endocrinologia ed Oncologia Clinica e Molecolare, Università Federico II, Napoli, Italy. giuseppedilorenzoncol@hotmail.com

European Urology
|October 2, 2010
PubMed
Abstract

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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