Overview of « druggable » alterations by histological subtypes of sarcomas and connective tissue intermediate malignancies

Crit Rev Oncol Hematol. 2020 Jun:150:102960. doi: 10.1016/j.critrevonc.2020.102960. Epub 2020 Apr 14.

Abstract

We summarize herein the literature data about molecular targeted therapies in sarcomas and conjunctive tissue intermediate malignancies. For each clinical setting, the level of evidence, the mechanism of action and the target are described. The two major axes include (i) identification of subgroups of tumors with druggable alteration irrespective of the histological diagnosis (e.g. NTRK), and (ii) druggable target of pathway related to the physiopathology of the tumor: denosumab and bone giant cell tumor, imatinib and soft tissue giant cell tumor, mTOR inhibitor and PECOMA.

Keywords: Druggable alterations; Molecular targeted therapies; Personalized treatment; Sarcomas.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Humans
  • Imatinib Mesylate
  • Molecular Targeted Therapy / methods*
  • Neoplasms, Connective Tissue / drug therapy*
  • Neoplasms, Connective Tissue / metabolism
  • Neoplasms, Connective Tissue / pathology
  • Sarcoma / drug therapy*
  • Sarcoma / metabolism
  • Sarcoma / pathology
  • Soft Tissue Neoplasms / drug therapy*
  • Soft Tissue Neoplasms / metabolism
  • Soft Tissue Neoplasms / pathology

Substances

  • Antineoplastic Agents
  • Imatinib Mesylate