drugset / Trial / NCT02066181

Sorafenib Tosylate in Treating Patients With Desmoid Tumors or Aggressive Fibromatosis

NCT02066181 ↗

Phase 3 Completed 87 enrolled National Cancer Institute (NCI)
RandomizedCrossoverDouble-blindTreatment

Summary

This randomized phase III trial compares the effects, good and/or bad, of sorafenib tosylate in treating patients with desmoid tumors or aggressive fibromatosis. Sorafenib tosylate may stop the growth of tumor cells by blocking some of the proteins needed for cell growth. \[Funding Source - FDA OOPD\]

Timeline

Start
2014-03-21
Primary completion
2019-07-03
Completion
2022-12-01

Outcome

Met primary endpoint

paper the 2-year progression-free survival rate was 81% (95% confidence interval [CI], 69 to 96) in the sorafenib group and 36% PMID 30575484 ↗

paper (hazard ratio for progression or death, 0.13; 95% CI, 0.05 to 0.31; P<0.001). PMID 30575484 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Sorafenib Small molecule 400 mg Oral

Indications