Targeting angiosarcomas of the soft tissues: A challenging effort in a heterogeneous and rare disease

Crit Rev Oncol Hematol. 2019 Jun:138:120-131. doi: 10.1016/j.critrevonc.2019.04.010. Epub 2019 Apr 15.

Abstract

Angiosarcomas are rare malignant tumors with a heterogeneous clinical presentation and generally poor prognosis. It has been difficult to establish consistent molecular characteristics and driver events in angiosarcoma development. Oncogenic and angiogenesis-related pathways have been investigated pre-clinically and clinically with varying results. A few promising responses to checkpoint inhibitors have been described, but immunological features require further elucidation. With this review we present an overview of the critical biological pathways and processes affected in angiosarcoma, and their potential role in novel, non-cytotoxic, systemic treatments.

Keywords: Angiogenesis; Angiosarcoma; Immunotherapy; Oncogenic pathways; Translational research.

Publication types

  • Review

MeSH terms

  • Female
  • Hemangiosarcoma / pathology*
  • Hemangiosarcoma / therapy*
  • Humans
  • Male
  • Rare Diseases
  • Soft Tissue Neoplasms / pathology*
  • Soft Tissue Neoplasms / therapy*