drugset / Trial / NCT01900743

Phase II Study of Regorafenib in Metastatic Soft Tissue Sarcoma

NCT01900743 ↗

Phase 2 Completed 219 enrolled Centre Oscar Lambret Bayer · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is an international (France, Austria and Germany), randomized, double-blind, placebo-controlled, phase II study to evaluate the efficacy and safety of regorafenib in patients with histologically proven metastatic and/or unresectable Soft Tissue Sarcoma (STS) after failure or intolerance to doxorubicin (or other anthracycline). Five cohorts will be defined: Cohort A: Liposarcoma Cohort B: Leiomyosarcoma Cohort C: Synovial sarcoma Cohort D: other sarcomas (see Appendix C) Cohort E: Leiomyosarcoma, Synovial sarcoma and other sarcomas listed in Appendix C previously treated with pazopanib Approximately 226 patients who meet the eligibility criteria will be randomly assigned in a 1:1 ratio to one of the treatment groups.

Timeline

Start
2013-06-05
Primary completion
2020-09-16
Completion
2020-09-16

Outcome

Mixed primary results

paper The primary endpoint was RECIST-based progression-free survival after central radiological review in the intention-to-treat population. PMID 27751846 ↗

paper progression-free survival was 1·1 months (95% CI 0·9-2·3) with regorafenib versus 1·7 months (0·9-1·8) with placebo (HR 0·89 [95% CI 0·48-1·64] p=0·70). PMID 27751846 ↗

paper progression-free survival was 3·7 months (95% CI 2·5-5·0) with regorafenib versus 1·8 (1·0-2·8) months with placebo (HR 0·46 [95% CI 0·46-0·80] p=0·0045). PMID 27751846 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Regorafenib Small molecule 160 mg Oral

Indications