Your new experience awaits. Try the new design now and help us make it even better

ORIGINAL RESEARCH article

Front. Med.

Sec. Hematology

Volume 12 - 2025 | doi: 10.3389/fmed.2025.1626325

Analysis of the Efficacy of Avatrombopag for the delayed platelet engraftment after Allogeneic Hematopoietic Stem Cell Transplantation for aplastic anemia

Provisionally accepted
xinhe  Zhangxinhe Zhang1Jia  FengJia Feng1Zhengwei  TanZhengwei Tan1Herui  ZhangHerui Zhang1Huijin  HuHuijin Hu2Yuechao  ZhaoYuechao Zhao2Dijiong  WuDijiong Wu2Yu  ZhangYu Zhang2Liqiang  WuLiqiang Wu2Tonglin  HuTonglin Hu2Zhengsong  YanZhengsong Yan2Baodong  YeBaodong Ye2Wenbin  LiuWenbin Liu2*
  • 1The First Clinical College of Zhejiang Chinese Medical University, Hangzhou, China
  • 2The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China

The final, formatted version of the article will be published soon.

Background: Delayed platelet engraftment (DPE) after allo-HSCT lacks standard therapy. Avatrombopag (AVA), a second-generation TPO agonist, is often delayed until transfusion-related events occur, potentially harming high-risk recipients.We compared recombinant human thrombopoietin (rh-TPO) with early AVA switching for treating DPE in aplastic anemia (AA) patients post-allo-HSCT to optimize management strategies.Methods: This single-centre study retrospectively enrolled 154 consecutive AA patients receiving allo-HSCT at Zhejiang Provincial Hospital of Traditional Chinese Medicine (March 2019-September 2023). Of these, 39 deemed high-risk for poor platelet engraftment (advanced donor/recipient age, low CD34+ dose, etc.) were non-randomly assigned: (1) AVA group (n = 11), switched to avatrombopag if platelets remained <30×10⁹/L on day +14 or <50×10⁹/L on day +21; (2) rh-TPO group (n = 28), continued rh-TPO monotherapy. Allocation followed clinician judgment and patient consent.Results: Our findings revealed that the 1-year overall survival (OS) rate was notably higher in AVA group (100% vs 78.6%, P=0.106). And the complete remission (CR) rate in the AVA group was significantly higher than that in the rh-TPO group at 3 and 6 months after transplantation(100% vs 67.9%, P=0.032; 100% vs 71.4%, P=0.047). At 3 months post transplantation, the platelet engraftment rate in the AVA group was significantly higher than that in the rhTPO group (67.9% vs 100%, P= 0.04). The median time to achieve platelet engraftment was 20 (13, 25) days for the AVA group and 23 (10, 68) days for the rh-TPO group. Additionally, the AVA group reached platelet counts of 30, 50, and 125 × 109/L more rapidly than the rh-TPO group. Furthermore, at 3 months post-transplantation, the median platelet transfusion volume of AVA group was less than rh-TPO group(63U vs 82U, P=0.141).For patients identified as being at high risk for poor platelet engraftment following allo-HSCT, early transition to AVA can significantly reduce the duration of DPE and promote platelet recovery post-transplantation. This strategy has the potential to enhance patient survival rates and overall outcomes.

Keywords: DPE, Avatrombopag, Allo-HSCT, TPO-RA, RhTPO

Received: 10 May 2025; Accepted: 29 Jul 2025.

Copyright: © 2025 Zhang, Feng, Tan, Zhang, Hu, Zhao, Wu, Zhang, Wu, Hu, Yan, Ye and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Wenbin Liu, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.