The burden of immune-mediated refractoriness to platelet transfusions in myelodysplastic syndromes

Transfusion. 2020 Oct;60(10):2192-2198. doi: 10.1111/trf.16029. Epub 2020 Sep 9.

Abstract

Up to 65% of patients with myelodysplastic syndromes (MDS) have thrombocytopenia and require platelet (PLT) transfusion. The current standard of practice is to provide random- or single-donor PLT transfusion and manage PLT refractoriness (PLT-R) if and when it develops. This study assessed the prevalence and risk factors for immune-mediated PLT-R in patients in the South Australian (SA) MDS Registry.

Study design and methods: A retrospective analysis of MDS patients enrolled in the SA-MDS registry was performed. HLA data was analyzed from January 2003 to 30 June 2017 to ensure minimum follow-up of 2 years.

Results: During the study period, 341 of 681 (50%) MDS patients required at least one PLT transfusion, with 29 of 341 (9%) of all PLT transfusion patients requiring HLA-matched PLT transfusion for PLT-R. Of these 29 patients, 70% were females treated with disease-modifying therapies suggesting that these patients are at high risk of HLA alloimmunization.

Conclusions: Immune-mediated PLT-R is common in MDS and can be expensive and difficult to manage once it occurs. Therefore, PLT transfusion practices should be optimized, especially for female MDS patients planned for disease-modifying therapies. This can help save time and streamline management, especially in the provision of PLT products for these patients, where the consequences of alloimmunization and PLT-R can be severe.

Keywords: myelodysplastic syndromes; platelet transfusions; thrombocytopenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blood Platelets / metabolism*
  • Female
  • Follow-Up Studies
  • Humans
  • Isoantibodies / blood*
  • Male
  • Myelodysplastic Syndromes / blood
  • Myelodysplastic Syndromes / therapy*
  • Platelet Transfusion*
  • Retrospective Studies
  • Thrombocytopenia / blood
  • Thrombocytopenia / therapy*

Substances

  • Isoantibodies

Grants and funding