Management of chemotherapy-induced thrombocytopenia: guidance from the ISTH Subcommittee on Hemostasis and Malignancy
- PMID: 37827380
- DOI: 10.1016/j.jtha.2023.09.031
Management of chemotherapy-induced thrombocytopenia: guidance from the ISTH Subcommittee on Hemostasis and Malignancy
Abstract
Thrombocytopenia is a common adverse effect of chemotherapy. The development of chemotherapy-induced thrombocytopenia (CIT) is influenced by cancer type and therapy, occurring in approximately one-third of patients with a solid tumor diagnosis and half of all patients with a hematologic malignancy. CIT may complicate the administration of chemotherapy, leading to therapeutic delays or dose reductions. This guidance document, presented by the International Society on Thrombosis and Haemostasis (ISTH) Subcommittee on Hemostasis and Malignancy, provides a comprehensive summary of the evidence and offers direction on the use of thrombopoietin receptor agonists (TPO-RAs) in various settings of CIT, including solid tumors, acute myeloid leukemia, stem cell transplant, and lymphoma. Studies have shown that TPO-RAs can improve platelet counts in CIT, but the clinical benefits of TPO-RA in terms of reducing bleeding, limiting platelet transfusion, avoiding chemotherapy delay, or dose reduction are uncertain. Further research is needed to optimize the selection of appropriate indications and study design to manage thrombocytopenia following chemotherapy.
Keywords: chemotherapy; hemorrhage; romiplostim; thrombocytopenia; thrombopoietin receptor agonists.
Copyright © 2023 International Society on Thrombosis and Haemostasis. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of competing interests G.A.S. has received research funding to institution from Amgen, Johnson and Johnson/Janssen Scientific Affairs, Sobi/Dova Pharmaceuticals, and Anthos Therapeutics. G.A.S. has consulted for Johnson and Johnson/Janssen Scientific Affairs, Sobi/Dova Pharmaceuticals, Luzsana (HengruiUSA) Biotechnology, and Sanofi. H.A.-S. received research funding to institution from Agios, Amgen, Novartis, Sobi, Vaderis and consultancy fees from Agios, Forma, Novartis, Sobi, Pharmacosmos, Moderna, argenx, and Rigel. A.L. received honoraria from Bayer, Leo Pharma, Pfizer, Novartis, and Sanofi. A.M. has received traveling and CPD support from Bayer, Boehringer Ingelheim, Bristol Myers Squibb, and Pfizer. A.M. also received research support from Bayer, Pfizer, and Bristol Myers Squibb. A.M. also served in the advisory boards for Pfizer, Bristol Myers Squibb, Daiichi-Sankyo, Leo Sanofi, and Bayer and received fees for speaker bureau from Leo, Pfizer, BMS, and Bayer. T.F.W. received advisory board honoraria from Servier and Valeo and research funding to the institution from Leo Pharma. J.I.Z. received research funding from Incyte and Quercegen, served in data safety monitoring boards of Sanofi and CSL Behring, and received consultancy fees from Calyx. J.I.Z. participated in the advisory boards of Pfizer/Bristol Myers Squibb (BMS) and Janssen and is supported in part through the NIH/NCI Cancer Center Support Grant (P30 CA008748). All other authors have no competing interests to disclose.
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