Long-term outcome of 2-year survivors after allogeneic hematopoietic cell transplantation for acute leukemia

IF 7.6 2区 医学 Q1 HEMATOLOGY HemaSphere Pub Date : 2024-10-22 DOI:10.1002/hem3.70026
Marion Larue, Myriam Labopin, Thomas Schroeder, Xiao-jun Huang, Igor W. Blau, Johannes Schetelig, Arnold Ganser, Rose-Marie Hamladji, Wolfgang Bethge, Nicolaus Kröger, Gerard Socié, Urpu Salmenniemi, Henrik Sengeloev, Bhagirathbhai Dholaria, Bipin N. Savani, Arnon Nagler, Fabio Ciceri, Mohamad Mohty
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Abstract

Information on late complications in patients with acute leukemia who have undergone allogeneic hematopoietic cell transplantation (HCT) is limited. We performed a left-truncated analysis of long-term survival in patients with acute leukemia who were alive and disease-free 2 years after HCT. We included 2701 patients with acute lymphoblastic leukemia (ALL) and 9027 patients with acute myeloid leukemia (AML) who underwent HCT between 2005 and 2012. The 10-year overall survival (OS) rate was 81.3% for ALL and 76.2% for AML, with the main causes of late mortality being relapse (ALL-33.9%, AML-44.9%) and chronic graft-versus-host disease (ALL-29%, AML-18%). At 10 years, HCT-related mortality was 16.8% and 20.4%, respectively. Older age and unrelated donor transplantation were associated with a worse prognosis for both types of leukemia. In addition, transplantation in the second or third complete remission and peripheral blood HSC for ALL are associated with worse outcomes. Similarly, adverse cytogenetics, female donor to male patient combination, and reduced intensity conditioning in AML contribute to poor prognosis. We conclude that 2-year survival in remission after HCT for acute leukemia is encouraging, with OS of nearly 80% at 10 years. However, the long-term mortality risk of HCT survivors remains significantly higher than that of the age-matched general population. These findings underscore the importance of tailoring transplantation strategies to improve long-term outcomes in patients with acute leukemia undergoing HCT.

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急性白血病异基因造血细胞移植后两年幸存者的长期预后。
有关接受异基因造血细胞移植(HCT)的急性白血病患者晚期并发症的信息非常有限。我们对 HCT 术后 2 年存活且无病的急性白血病患者的长期生存情况进行了左截断分析。我们纳入了 2005 年至 2012 年期间接受 HCT 的 2701 名急性淋巴细胞白血病(ALL)患者和 9027 名急性髓性白血病(AML)患者。ALL患者的10年总生存率(OS)为81.3%,AML患者为76.2%,晚期死亡的主要原因是复发(ALL-33.9%,AML-44.9%)和慢性移植物抗宿主疾病(ALL-29%,AML-18%)。10年后,HCT相关死亡率分别为16.8%和20.4%。高龄和非亲缘供体移植与两种类型白血病的较差预后有关。此外,在第二次或第三次完全缓解时进行移植以及外周血造血干细胞用于 ALL 与较差的预后有关。同样,不良细胞遗传学、女性供者与男性患者的组合以及急性髓细胞白血病的减量调理也会导致预后不良。我们的结论是,急性白血病造血干细胞移植后的2年缓解期生存率令人鼓舞,10年的OS接近80%。然而,HCT 幸存者的长期死亡风险仍明显高于年龄匹配的普通人群。这些发现强调了调整移植策略以改善接受 HCT 的急性白血病患者长期预后的重要性。
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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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