Pazopanib in advanced vascular sarcomas: an EORTC Soft Tissue and Bone Sarcoma Group (STBSG) retrospective analysis

A Kollár1, R L Jones2, S Stacchiotti3

  • 1a Sarcoma Unit, Department of Medical Oncology , University Hospital of Bern , Bern , Switzerland.

Abstract

Insights

Pazopanib demonstrated comparable activity in advanced angiosarcoma (AS) to other soft tissue sarcoma (STS) subtypes. This study also found pazopanib showed promising efficacy in epithelioid hemangioendothelioma (HE) and intimal sarcoma (IS).

Area of Science:

  • Oncology
  • Medical Oncology
  • Sarcoma Research

Background:

  • Pazopanib is a tyrosine kinase inhibitor approved for advanced soft tissue sarcoma (STS) after chemotherapy.
  • Limited data exist on pazopanib's efficacy in vascular sarcomas.
  • This study aimed to evaluate pazopanib's activity in vascular sarcomas.

Purpose of the Study:

  • To investigate the clinical activity of pazopanib in patients with advanced vascular sarcomas.
  • To assess response rates and survival outcomes in different subtypes of vascular sarcoma treated with pazopanib.

Main Methods:

  • Retrospective analysis of 52 patients with advanced vascular sarcomas (angiosarcoma, epithelioid hemangioendothelioma, intimal sarcoma).
  • Patients received pazopanib in real-world practice or clinical trials.
  • Response evaluated by RECIST 1.1; survival analysis performed.

Main Results:

  • Pazopanib showed a 20% response rate in angiosarcoma (AS), 20% in epithelioid hemangioendothelioma (HE), and 100% in intimal sarcoma (IS).
  • Median progression-free survival (PFS) was 3 months and median overall survival (OS) was 9.9 months for AS.
  • No significant difference in AS response based on location or radiation history.

Conclusions:

  • Pazopanib's activity in AS is comparable to other STS subtypes.
  • Pazopanib demonstrated promising activity in HE and IS, warranting further investigation.
  • Treatment outcomes were consistent across different angiosarcoma classifications.

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