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造血干细胞移植后索拉非尼维持治疗改善 FLT3-ITD 突变型急性髓系白血病的预后。

Sorafenib maintenance after hematopoietic stem cell transplantation improves outcome of FLT3-ITD-mutated acute myeloid leukemia.

机构信息

Department of Oncology, Hematology, Immuno-Oncology and Rheumatology, University Hospital of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.

Department of Oncology, Hematology, A.O.U. Città Della Salute e Della Scienza, Turin, Italy.

出版信息

Int J Hematol. 2022 Dec;116(6):883-891. doi: 10.1007/s12185-022-03427-4. Epub 2022 Aug 9.

Abstract

In a retrospective analysis, 21 acute myeloid leukemia patients receiving single-agent sorafenib maintenance therapy in complete remission (CR) after hematopoietic stem cell transplantation (HSCT) were compared with a control group of 22 patients without maintenance. Sorafenib was initiated a median of 3 months (IQR: 2.3-3.5) after allogeneic HSCT with a median daily dosage of 400 mg (range: 200-800) orally, and lasted a median of 11.3 months (IQR: 3.3-24.4). No significant increase in graft versus host disease or toxicity was observed. Adverse events were reversible with dose adjustment or temporary discontinuation in 19/19 cases. With a median follow-up of 34.7 months (IQR: 16.9-79.5), sorafenib maintenance significantly improved cumulative incidence of relapse (p = 0.028) as well as overall survival (OS) (p = 0.016), especially in patients undergoing allogeneic HSCT in CR1 (p < 0.001). In conclusion, sorafenib maintenance after allogeneic HSCT is safe and may improve cumulative incidence of relapse and OS in FLT3-ITD-mutated AML.

摘要

在一项回顾性分析中,21 例接受单药索拉非尼维持治疗的急性髓系白血病(AML)患者在造血干细胞移植(HSCT)后完全缓解(CR)与 22 例未接受维持治疗的对照组患者进行了比较。在异基因 HSCT 后中位 3 个月(IQR:2.3-3.5)开始使用索拉非尼,中位日剂量为 400mg(范围:200-800)口服,中位持续时间为 11.3 个月(IQR:3.3-24.4)。未观察到移植物抗宿主病或毒性增加。19/19 例患者通过剂量调整或暂时停药可使不良事件可逆。中位随访 34.7 个月(IQR:16.9-79.5)后,索拉非尼维持治疗显著改善了累积复发率(p=0.028)和总生存率(OS)(p=0.016),特别是在 CR1 时接受异基因 HSCT 的患者(p<0.001)。总之,异基因 HSCT 后索拉非尼维持治疗是安全的,可能会降低 FLT3-ITD 突变 AML 的累积复发率和 OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96a4/9668769/1fbe42b3b306/12185_2022_3427_Fig1_HTML.jpg

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