Emerging data on thrombopoietin receptor agonists for management of chemotherapy-induced thrombocytopenia

Expert Rev Hematol. 2023 May;16(5):365-375. doi: 10.1080/17474086.2023.2201428. Epub 2023 Apr 14.

Abstract

Introduction: Chemotherapy-induced thrombocytopenia (CIT) is a common complication of cancer treatment, frequently leading to reduced relative dose intensity, and is associated with reduced survival. Given the lack of FDA-approved therapies for CIT, thrombopoietin receptor agonists (TPO-RAs) have received significant attention for treatment and prevention of CIT.

Areas covered: This review will summarize the development of prior agents for treatment of CIT, discuss the existing literature investigating the use of TPO-RAs in CIT primarily in patients with solid tumor malignancies, and offer insights on the future direction of TPO-RAs and other therapeutics for CIT.

Expert opinion: In alignment with NCCN guidelines, we recommend that patients with CIT participate in a clinical trial for consideration of TPO-RA treatment or consider off-label use of romiplostim when participation in clinical trials is not possible. The literature to date supports the use of TPO-RAs for treatment of persistent CIT. Further data is needed to describe the long-term efficacy, safety, and prescribing practices of TPO-RAs in a diverse patient population with a variety of tumor types and chemotherapy regimens in addition to exploring the underlying biology of CIT.

Keywords: TPO-RA; Thrombocytopenia; avatrombopag; chemotherapy induced thrombocytopenia; eltrombopag; romiplostim; thrombopoietin; thrombopoietin receptor agonist.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Benzoates / adverse effects
  • Humans
  • Neoplasms* / complications
  • Neoplasms* / drug therapy
  • Purpura, Thrombocytopenic, Idiopathic* / drug therapy
  • Receptors, Fc / therapeutic use
  • Receptors, Thrombopoietin* / agonists
  • Recombinant Fusion Proteins / adverse effects
  • Thrombocytopenia* / chemically induced
  • Thrombocytopenia* / drug therapy

Substances

  • Antineoplastic Agents
  • Benzoates
  • Receptors, Fc
  • Receptors, Thrombopoietin
  • Recombinant Fusion Proteins