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Treatment efficacy for adult persistent immune thrombocytopenia: a systematic review and network meta-analysis

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posted on 2025-05-09, 19:46 authored by Teeraya Puavilai, Kunlawat Thadanipon, Sasivimol Rattanasiri, Atiporn Ingsathit, Mark McEvoyMark McEvoy, John AttiaJohn Attia, Ammarin Thakkinstian
Persistent immune thrombocytopenia (ITP) patients require second-linetreatments, for which information on clinical outcomes are lacking. A sys-tematic review and network meta-analysis (NMA) were conducted. Onlyrandomised controlled trials (RCT) of second-line drugs in adult persistentITP patients with platelet response, platelet count, any bleeding or seriousadverse events (SAE) outcome were eligible. Twelve RCTs (n=1313) wereincluded in NMA. For platelet response outcome, eltrombopag and romi-plostin were the best relative to placebo; the former had a non-significantadvantage [risk ratio (RR)=1 10 (95% confidence interval: 0 46, 2 67)].Both treatments were superior to rituximab and recombinant humanthrombopoietin (rhTPO)+rituximab, with corresponding RRs of 4 56 (1 89,10 96) and 4 18 (1 21, 14 49) for eltrombopag; 4 13 (1 56, 10 94) and 3 79(1 02, 14 09) for romiplostim. For platelet count, romiplostim ranked high-est, followed by eltrombopag, rhTPO+rituximab, and rituximab. For bleed-ing, rituximab had lowest risk, followed by eltrombopag and romiplostim.For SAEs, rhTPO+rituximab had highest risk, followed by rituximab,eltrombopag and romiplostim. From clustered ranking, romiplostim hadthe best balance between short-term efficacy and SAEs, followed by eltrom-bopag. In conclusion, romiplostim and eltrombopag may yield high efficacyand safety. Rituximab may not be beneficial due to lower efficacy andhigher complications compared with the thrombopoietin receptor agonists.RCTs with long-term clinical outcomes are required.

History

Journal title

British Journal of Haematology

Volume

188

Issue

3

Pagination

450-459

Publisher

Wiley-Blackwell

Language

  • en, English

College/Research Centre

Faculty of Health and Medicine

School

School of Medicine and Public Health

Rights statement

© 2019 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.