Sorafenib for patients with advanced angiosarcoma: a phase II Trial from the French Sarcoma Group (GSF/GETO)

Isabelle Ray-Coquard1, Antoine Italiano, Emmanuelle Bompas

  • 1Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

The Oncologist
|January 31, 2012
PubMed
Abstract

Insights

Sorafenib demonstrated limited antitumor activity in advanced angiosarcoma patients, showing brief tumor control primarily in those previously treated with chemotherapy. The drug was ineffective in chemotherapy-naïve individuals.

Area of Science:

  • Oncology
  • Medical Oncology
  • Sarcoma Research

Background:

  • Angiosarcomas are rare, aggressive soft tissue sarcomas with poor prognosis in advanced stages.
  • Current treatments offer limited progression-free survival (PFS) and overall survival (OS).

Purpose of the Study:

  • To evaluate the antitumor activity of sorafenib in patients with metastatic or advanced angiosarcoma.
  • To assess the efficacy of sorafenib in superficial (stratum A) and visceral (stratum B) angiosarcomas.

Main Methods:

  • A stratified phase II clinical trial (NCT00874874) using an optimal Simon design.
  • Patients received sorafenib 400 mg twice daily for 9 months.
  • Primary endpoint was the 9-month progression-free rate (PFR); central pathological and radiological reviews were performed.

Main Results:

  • The 9-month PFR was 3.8% for superficial and 0.0% for visceral angiosarcoma.
  • Median PFS was 1.8 months (stratum A) and 3.8 months (stratum B). Median OS was 12.0 months (stratum A) and 9.0 months (stratum B).
  • Sorafenib showed activity only in pretreated patients (40% tumor control, 23% response rate), not in chemotherapy-naïve patients. No KDR gene mutations were detected.

Conclusions:

  • Sorafenib exhibited limited antitumor activity in advanced angiosarcoma, mainly in pretreated patients.
  • Tumor control was transient, highlighting the need for more effective therapies.
  • The drug showed minimal benefit in superficial or visceral angiosarcoma subtypes.

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