Clinical trial end points for assessing efficacy of novel therapies for soft-tissue sarcomas. Issue 9 (September 2012)

• Record Type: Journal Article
• Authors: Chmielowski, Bartosz; Federman, Noah; Tap, William D
• Is Part Of: Expert review of anticancer therapy. Volume 12:Issue 9(2012)
• Page Start: 1217
• Page End: 1228
• Publication Date: 2012-09
• Subjects: clinical benefit rate -- clinical trial end point -- mammalian target of rapamycin -- overall survival -- progression-free survival -- soft-tissue sarcoma; Cancer -- Treatment -- Periodicals; 616.99406
• DOI: 10.1586/era.12.100
• Languages: English
• ISSNs: 1473-7140

Abstract

Soft-tissue sarcomas (STS) comprise a heterogeneous group of rare malignancies from mesenchymal tissues. Although outcome varies by histology, adults with disseminated metastatic STS have a poor prognosis despite current treatment options. The authors reviewed commonly used clinical end points for STS and discussed which end points may be appropriate for evaluating the clinical benefit of novel targeted therapies. In sarcoma, surrogates for both overall survival, the gold standard end point, and the objective response rate, measured by Response Evaluation Criteria in Solid Tumors, are commonly used. More appropriate end points for evaluating newly targeted agents include progression-free survival and clinical benefit rate. Results from recently completed Phase III trials of two targeted therapies in advanced STS, the mTOR inhibitor ridaforolimus and the multikinase inhibitor pazopanib, should shed light on whether progression-free survival and clinical benefit rate are appropriate end points in advanced STS.