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参加ALL-SCT 2003/2007试验的急性淋巴细胞白血病儿童异基因造血干细胞移植后的复发结局。

Outcome of relapse after allogeneic HSCT in children with ALL enrolled in the ALL-SCT 2003/2007 trial.

作者信息

Kuhlen Michaela, Willasch Andre M, Dalle Jean-Hugues, Wachowiak Jacek, Yaniv Isaac, Ifversen Marianne, Sedlacek Petr, Guengoer Tayfun, Lang Peter, Bader Peter, Sufliarska Sabina, Balduzzi Adriana, Strahm Brigitte, von Luettichau Irene, Hoell Jessica I, Borkhardt Arndt, Klingebiel Thomas, Schrappe Martin, von Stackelberg Arend, Glogova Evgenia, Poetschger Ulrike, Meisel Roland, Peters Christina

机构信息

Department of Paediatric Oncology, Haematology and Clinical Immunology, Medical Faculty, University Children's Hospital, Heinrich Heine University, Duesseldorf, Germany.

Department for Children and Adolescents, Division for Stem Cell Transplantation and Immunology, University Hospital Frankfurt, Goethe University, Frankfurt, Germany.

出版信息

Br J Haematol. 2018 Jan;180(1):82-89. doi: 10.1111/bjh.14965. Epub 2017 Nov 28.

Abstract

Relapse remains the major cause of treatment failure in children with high-risk acute lymphoblastic leukaemia (ALL) undergoing allogeneic haematopoietic stem-cell transplantation (allo-SCT). Prognosis is considered dismal but data on risk factors and outcome are lacking from prospective studies. We analysed 242 children with recurrence of ALL after first allo-SCT enrolled in the Berlin-Frankfurt-Munster (BFM) ALL-SCT-BFM 2003 and ALL-SCT-BFM international 2007 studies. Median time from allo-SCT to relapse was 7·7 months; median follow-up from relapse after allo-SCT until last follow-up was 3·4 years. The 3-year event-free survival (EFS) was 15% and overall survival (OS) was 20%. The main cause of death was disease progression or relapse (86·5%). The majority of children (48%) received salvage therapy without second allo-SCT, 26% of the children underwent a second allo-SCT and 25% received palliative treatment only. In multivariate analyses, age, site of relapse, time to relapse and type of salvage therapy were identified as significant prognostic factors for OS and EFS, whereas factors associated with first SCT were not statistically significant. Combined approaches incorporating novel immunotherapeutic treatment options and second allo-SCT hold promise to improve outcome in children with post allo-SCT relapse.

摘要

复发仍然是接受异基因造血干细胞移植(allo-SCT)的高危急性淋巴细胞白血病(ALL)患儿治疗失败的主要原因。预后被认为很差,但前瞻性研究缺乏关于危险因素和结局的数据。我们分析了242例在首次allo-SCT后复发ALL的患儿,这些患儿纳入了柏林-法兰克福-明斯特(BFM)ALL-SCT-BFM 2003研究和ALL-SCT-BFM国际2007研究。从allo-SCT到复发的中位时间为7.7个月;从allo-SCT后复发到最后一次随访的中位随访时间为3.4年。3年无事件生存率(EFS)为15%,总生存率(OS)为20%。主要死亡原因是疾病进展或复发(86.5%)。大多数患儿(48%)接受了挽救治疗但未进行第二次allo-SCT,26%的患儿接受了第二次allo-SCT,25%的患儿仅接受了姑息治疗。在多变量分析中,年龄、复发部位、复发时间和挽救治疗类型被确定为OS和EFS的显著预后因素,而与首次SCT相关的因素无统计学意义。结合新型免疫治疗选择和第二次allo-SCT的联合方法有望改善allo-SCT后复发患儿的结局。

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