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儿童和青少年慢性髓性白血病患者接受低强度预处理的造血干细胞移植:国际血液和骨髓移植研究组的前瞻性多中心试验。

Haematopoietic stem cell transplantation after reduced intensity conditioning in children and adolescents with chronic myeloid leukaemia: A prospective multicentre trial of the I-BFM Study Group.

机构信息

Department of Paediatric Haematology and Oncology, St. Anna Children's Hospital, Vienna, Austria.

Department of Paediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Br J Haematol. 2024 Jul;205(1):268-279. doi: 10.1111/bjh.19535. Epub 2024 May 27.

DOI:10.1111/bjh.19535
PMID:38803040
Abstract

This prospective multicentre trial evaluated the safety and the efficacy of a thiotepa/melphalan-based reduced intensity conditioning (RIC) haematopoietic stem cell transplantation (HSCT) in children and adolescents with chronic myeloid leukaemia (CML) in chronic phase (CP). Thirty-two patients were transplanted from matched siblings or matched unrelated donors. In 22 patients, HSCT was performed due to insufficient molecular response or loss of response to first- or second-generation tyrosine kinase inhibitor (TKI), with pretransplant BCR::ABL1 transcripts ranging between 0.001% and 33%. The protocol included a BCR::ABL1-guided intervention with TKI retreatment in the first year and donor lymphocyte infusions (DLI) in the second-year post-transplant. All patients engrafted. The 1-year transplant-related mortality was 3% (confidence interval [CI]: 0%-6%). After a median follow-up of 6.3 years, 5-year overall survival and event-free survival are 97% (CI: 93%-100%) and 91% (CI: 79%-100%) respectively. The current 5-year leukaemia-free survival with BCR::ABL1 <0.01% is 97% (CI: 88%-100%) and the current TKI- and DLI-free survival is 95% (CI: 85%-100%). The incidence of chronic graft-versus-host disease (GvHD) was 32%, being severe in four patients (13%). At last follow-up, 31 patients are GvHD-free and have stopped immunosuppression. RIC HSCT following pretreatment with TKI is feasible and effective in children and adolescents with CP-CML with an excellent disease-free and TKI-free survival.

摘要

这项前瞻性多中心试验评估了在慢性期(CP)慢性髓性白血病(CML)儿童和青少年中,基于噻替哌/美法仑的低强度预处理(RIC)造血干细胞移植(HSCT)的安全性和疗效。32 名患者接受了匹配的同胞或无关供者的移植。在 22 名患者中,由于对第一代或第二代酪氨酸激酶抑制剂(TKI)的分子反应不足或丧失反应,在移植前,BCR::ABL1 转录本的范围在 0.001%至 33%之间,进行了 HSCT。该方案包括 BCR::ABL1 指导的干预,第一年使用 TKI 重新治疗,第二年进行供者淋巴细胞输注(DLI)。所有患者均植入。1 年移植相关死亡率为 3%(置信区间[CI]:0%-6%)。中位随访 6.3 年后,5 年总生存率和无事件生存率分别为 97%(CI:93%-100%)和 91%(CI:79%-100%)。目前 BCR::ABL1<0.01%的白血病无复发生存率为 97%(CI:88%-100%),目前 TKI 和 DLI 无复发生存率为 95%(CI:85%-100%)。慢性移植物抗宿主病(GvHD)的发生率为 32%,其中 4 名患者(13%)病情严重。在最后一次随访时,31 名患者无 GvHD,且已停止免疫抑制。在 CP-CML 儿童和青少年中,在 TKI 预处理后进行 RIC HSCT 是可行且有效的,具有出色的无疾病和无 TKI 生存。

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