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