Bone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, 310003, Zhejiang, People's Republic of China.
Institute of Hematology, Zhejiang University, Hangzhou, Zhejiang, People's Republic of China.
Ann Hematol. 2020 Nov;99(11):2679-2687. doi: 10.1007/s00277-020-04106-2. Epub 2020 Jun 9.
Post-transplantation thrombocytopenia (PT) is a common and severe complication which usually leads to poor prognosis. Eltrombopag (EPAG), a novel oral thrombopoietin (TPO) receptor agonist, has shown promising effects in thrombocytopenia due to immune thrombocytopenic purpura (ITP) and refractory severe aplastic anemia (rSAA), while the effectiveness of EPAG for PT patients still needs to be evaluated. A total of 32 PT patients receiving EPAG were retrospectively analyzed between September 2017 and July 2019, including 15 patients with poor graft function (PGF) and 17 patients with secondary failure of platelet recovery (SFPR). To date, 21 (65.6%) patients achieved overall recovery (OR) and 14 (43.8%) patients achieved complete recovery (CR). Among responders, 18 (85.7%) patients discontinued or tapered the drug and 16 (76.2%) patients successfully maintained their best response. During the EPAG treatment, responders received much lower median platelet transfusion units than non-responders (11 vs. 95, P < 0.001). After a median follow-up time of 364 days (range, 24-842), the overall survival in these patients was 78.1% (100% for responders and 36.4% for non-responders, P < 0.001). In the univariate and multivariate analysis, PGF was identified as the independent risk factor for OR (P = 0.041, HR = 5.333). Megakaryocyte (Megk) amounts (P = 0.025, HR = 14.638) and splenomegaly (P = 0.042, HR = 11.278) were identified as independent risk factors for CR. Besides, PGF patients tended to take a longer time to achieve PR and CR than SFPR patients. In conclusion, our data suggest that EPAG can promote platelet recovery and reduce platelet transfusion in PT patients.
移植后血小板减少症(PT)是一种常见且严重的并发症,通常导致预后不良。艾曲泊帕(EPAG)是一种新型的口服血小板生成素(TPO)受体激动剂,在免疫性血小板减少性紫癜(ITP)和难治性重型再生障碍性贫血(rSAA)引起的血小板减少症中显示出良好的疗效,而 EPAG 对 PT 患者的疗效仍需进一步评估。回顾性分析了 2017 年 9 月至 2019 年 7 月期间接受 EPAG 治疗的 32 例 PT 患者,其中 15 例为移植物功能不良(PGF)患者,17 例为血小板恢复不良的继发性失败(SFPR)患者。截至目前,21 例(65.6%)患者获得总缓解(OR),14 例(43.8%)患者获得完全缓解(CR)。在缓解者中,18 例(85.7%)患者停用或减少了药物剂量,16 例(76.2%)患者成功维持了最佳反应。在 EPAG 治疗期间,缓解者接受的中位血小板输注单位明显低于未缓解者(11 对 95,P<0.001)。中位随访时间为 364 天(范围,24-842 天)后,这些患者的总生存率为 78.1%(缓解者为 100%,未缓解者为 36.4%,P<0.001)。单因素和多因素分析显示,PGF 是 OR 的独立危险因素(P=0.041,HR=5.333)。巨核细胞(Megk)数量(P=0.025,HR=14.638)和脾肿大(P=0.042,HR=11.278)是 CR 的独立危险因素。此外,PGF 患者达到 PR 和 CR 的时间长于 SFPR 患者。总之,我们的数据表明,EPAG 可促进血小板恢复,减少 PT 患者的血小板输注。