Thrombopoietin Receptor Agonists and Other Second-Line Therapies for Immune Thrombocytopenia: A Narrative Review With a Focus on Drug Access in Canada

Clin Invest Med. 2024 Mar 1;47(1):13-22. doi: 10.3138/cim-2024-2569.

Abstract

Introduction: Immune thrombocytopenia (ITP) is an autoimmune disease characterized by low platelet counts and increased risk of bleeding. After corticosteroids with or without intravenous immune globulin (first-line treatment), second-line treatment options include rituximab, splenectomy, thrombopoietin receptor agonists (TPO-RAs), and fostamatinib. In Canada, the choice of second-line therapy is influenced by access to medications. The goals of this narrative review are to 1) summarize the evidence for the use of TPO-RAs and other second-line therapies in ITP and 2) highlight differences in public funding criteria for TPO-RAs across provinces and territories in Canada.

Methods: We conducted a literature review of second-line therapies for ITP. We solicited information on public funding programs for TPO-RAs in Canada from health care providers, pharmacists, and provincial ministries of health.

Results: Head-to-head trials involving TPO-RAs, rituximab, splenectomy, and fostamatinib are lacking. There is substantial evidence of effect for TPO-RAs in improving platelet count levels, health-related quality of life, bleeding, and fatigue from placebo-controlled trials and observational studies; however, access to TPO-RAs through provincial funding programs in Canada is variable. Splenectomy failure is a prerequisite for the funding of TPO-RAs in Ontario, Manitoba, and Saskatchewan, but not in Alberta or Quebec. Other provinces either do not have access to public funding or funding is provided on a case-by-case basis.

Discussion: TPO-RAs are effective second-line therapies for the treatment of ITP; however, access is variable across Canada, which results in health disparities and poor uptake of international treatment guidelines.

Keywords: Immune thrombocytopenia; drug access; health inequities; platelets; thrombopoietin receptor agonists.

Publication types

  • Review

MeSH terms

  • Aminopyridines* / therapeutic use
  • Humans
  • Morpholines* / therapeutic use
  • Purpura, Thrombocytopenic, Idiopathic* / drug therapy
  • Pyrimidines* / therapeutic use
  • Quality of Life
  • Receptors, Thrombopoietin* / agonists
  • Rituximab / therapeutic use

Substances

  • Aminopyridines
  • fostamatinib
  • Morpholines
  • Pyrimidines
  • Receptors, Thrombopoietin
  • Rituximab