Improved post-transplant outcomes since 2000 for Ph-positive acute lymphoblastic leukemia in first remission: A study from the EBMT Acute Leukemia Working Party

IF 7.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2025-04-13 DOI:10.1002/hem3.70117
Ali Bazarbachi, Myriam Labopin, Iman Abou Dalle, Ibrahim Yakoub-Agha, Gérard Socié, Thomas Schroeder, Didier Blaise, Xavier Poiré, Marie Balsat, Urpu Salmenniemi, Nicolaus Kröger, Alexander Kulagin, Eva Maria Wagner-Drouet, Depei Wu, Eolia Brissot, Arnon Nagler, Sebastian Giebel, Fabio Ciceri, Mohamad Mohty
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引用次数: 0

Abstract

Allogeneic hematopoietic cell transplantation (allo-HCT) remains a curative treatment for patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) in their first complete remission (CR1). Recent results using the combination of blinatumomab and second- or third-generation tyrosine kinase inhibitors have challenged the necessity of allo-HCT in CR1. Here we assessed real-world changes over time in transplant characteristics and outcomes in adult patients with Ph+ ALL in CR1, using a large dataset from the European Society for Blood and Marrow Transplantation registry. A total of 3292 patients (45% female; median age 45 years) who underwent allo-HCT from 2001 to 2020 were included. Over four periods (2001–2005, 2006–2010, 2011–2015, and 2016–2020), the 3-year cumulative incidence of relapse decreased from 41% to 19%, and non-relapse mortality decreased from 25% to 17% (p < 0.001 for both). Correspondingly, 3-year leukemia-free survival (LFS) improved from 34% to 64%, and overall survival (OS) from 47% to 75% (p < 0.001 for both). Graft versus host disease-free and relapse-free survival also improved from 26% to 49% (p < 0.001). Factors negatively affecting LFS included older age, male gender, male donor and measurable residual disease (MRD) positivity pre-transplant, while total body conditioning (TBI) positively affected LFS. OS was positively influenced by younger age, female gender, matched sibling donor, TBI, and T cell depletion. Importantly, improvement in post-transplant outcomes over time was observed regardless of pre-transplant MRD status. In conclusion, we observed an impressive improvement over time in post-transplant outcomes of Ph+ ALL. These large-scale data can serve as a benchmark for future studies.

Abstract Image

自2000年以来,首次缓解的ph阳性急性淋巴细胞白血病移植后预后改善:EBMT急性白血病工作组的一项研究
同种异体造血细胞移植(alloo - hct)仍然是费城染色体阳性急性淋巴细胞白血病(Ph+ ALL)首次完全缓解(CR1)患者的根治性治疗方法。最近使用blinatumomab和第二代或第三代酪氨酸激酶抑制剂联合治疗CR1的结果挑战了allo-HCT治疗的必要性。在这里,我们使用来自欧洲血液和骨髓移植协会注册的大型数据集,评估了CR1 Ph+ ALL成人患者移植特征和结果随时间的变化。共3292例患者(女性45%;研究对象包括2001年至2020年期间接受同种异体ct治疗的患者(中位年龄45岁)。在四个时期(2001-2005年、2006-2010年、2011-2015年和2016-2020年),3年累积复发率从41%下降到19%,非复发死亡率从25%下降到17%(两者的p <; 0.001)。相应地,3年无白血病生存率(LFS)从34%提高到64%,总生存率(OS)从47%提高到75%(两者的p <; 0.001)。移植物抗宿主无病和无复发生存率也从26%提高到49% (p < 0.001)。影响LFS的因素包括年龄、男性、男性供体和移植前可测量残留病(MRD)阳性,而total body conditioning (TBI)对LFS有积极影响。OS与年龄、女性、匹配的兄弟姐妹供体、TBI和T细胞耗竭呈正相关。重要的是,无论移植前MRD状态如何,移植后结果随时间的推移都有所改善。总之,随着时间的推移,我们观察到移植后Ph+ ALL预后的显著改善。这些大规模的数据可以作为未来研究的基准。
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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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