Allogeneic Hematopoietic Stem Cell Transplantation for Elderly Acute Lymphoblastic Leukemia Patients: A Registry Study From the Société Francophone de Greffe de Moelle et Thérapie Cellulaire (SFGM-TC)

IF 9.9 1区 医学 Q1 HEMATOLOGY
Yves Chalandon, Raynier Devillier, Ariane Boumendil, Stephanie Nguyen, Claude-Eric Bulabois, Patrice Ceballos, Eolia Brissot, Marie-Thérèse Rubio, Hélène Labussière-Wallet, Johan Maertens, Patrice Chevallier, Natacha Maillard, Xavier Poiré, Cristina Castilla-Llorente, Yves Beguin, Jérôme Cornillon, Sébastien Maury, Tony Marchand, Etienne Daguindau, Jacques-Olivier Bay, Pascal Turlure, Magalie Joris, Anne-Lise Menard, Karin Bilger, Gaelle Guillerm, Sylvie François, Ali Bazarbachi, Sylvain Chantepie, Philippe Lewalle, Ambroise Marçais, Michael Loschi, Malek Benakli, Paul Chauvet, Edouard Forcade, Anne Huynh, Marie Robin, Stavroula Masouridi-Levrat
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引用次数: 0

Abstract

There are very limited data regarding the outcomes of elderly patients with acute lymphoblastic leukemia (ALL) who undergo allogeneic hematopoietic stem cell transplantation (alloHSCT). A total of 316 ALL patients aged ≥ 60 years who underwent alloHSCT between 2010 to 2022 were identified in the SFGM-TC registry. The primary objective was to evaluate progression-free survival (PFS), non-relapse mortality (NRM), relapse incidence (RI), and graft-versus-host disease (GvHD)-free relapse-free survival (GRFS), as well as their risk factors. The median age was 63.8 years (range 60–75.8), 49.8% of patients had Philadelphia-positive B-ALL (Ph + ALL), and 70.9% were in first complete remission (CR1) at transplantation. The donor was an unrelated donor in 52.1%, a matched related donor (MRD) in 26.3%, and a haplo-identical donor in 17.7%. Reduced-intensity conditioning (RIC) was administered to 64.6% of patients, while total body irradiation (TBI) was used in 35.8%. The 3-year overall survival (OS) was 46% (95% CI 40%–53%). The 3-year PFS, NRM, RI, and GRFS were 41% (95% CI 35%–48%), 23% (95% CI 18%–28%), 36% (95% CI 31%–42%), and 30% (95% CI 25%–37%), respectively. Multivariable analyses confirmed poorer OS and PFS in patients with advanced disease, with an HR of 1.79 (95% CI 1.22–2.64), p = 0.0032. Additionally, the ALL subtype significantly impacted outcomes, with an HR of 1.99 (95% CI 1.42–2.79) for non-Ph + ALL. This study suggests that alloHSCT is a viable option for elderly ALL patients, as age itself did not impact outcomes. However, advanced disease and non-Ph + ALL were associated with significantly worse survival.

老年急性淋巴母细胞白血病患者的同源造血干细胞移植:法语骨髓移植和细胞治疗学会(SFGM-TC)的注册研究。
关于老年急性淋巴细胞白血病(ALL)患者接受同种异体造血干细胞移植(alloHSCT)的结果的数据非常有限。在SFGM-TC登记中,共有316名年龄≥60岁的ALL患者在2010年至2022年期间接受了同种异体造血干细胞移植。主要目的是评估无进展生存期(PFS)、非复发死亡率(NRM)、复发率(RI)、移植物抗宿主病(GvHD)无复发生存期(GRFS)及其危险因素。中位年龄为63.8岁(60-75.8岁),49.8%的患者为费城B-ALL阳性(Ph + ALL), 70.9%的患者在移植时首次完全缓解(CR1)。无亲缘关系供者占52.1%,有匹配亲缘关系供者(MRD)占26.3%,单倍体相同供者占17.7%。64.6%的患者接受了降低强度调节(RIC)治疗,35.8%的患者接受了全身照射(TBI)治疗。3年总生存率(OS)为46% (95% CI 40%-53%)。3年PFS、NRM、RI和GRFS分别为41% (95% CI 35%-48%)、23% (95% CI 18%-28%)、36% (95% CI 31%-42%)和30% (95% CI 25%-37%)。多变量分析证实,晚期疾病患者的OS和PFS较差,风险比为1.79 (95% CI 1.22-2.64), p = 0.0032。此外,ALL亚型显著影响预后,非ph + ALL的风险比为1.99 (95% CI 1.42-2.79)。这项研究表明,对于老年ALL患者来说,同种异体造血干细胞移植是一个可行的选择,因为年龄本身并不影响结果。然而,晚期疾病和非ph + ALL与明显较差的生存率相关。
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来源期刊
CiteScore
15.70
自引率
3.90%
发文量
363
审稿时长
3-6 weeks
期刊介绍: The American Journal of Hematology offers extensive coverage of experimental and clinical aspects of blood diseases in humans and animal models. The journal publishes original contributions in both non-malignant and malignant hematological diseases, encompassing clinical and basic studies in areas such as hemostasis, thrombosis, immunology, blood banking, and stem cell biology. Clinical translational reports highlighting innovative therapeutic approaches for the diagnosis and treatment of hematological diseases are actively encouraged.The American Journal of Hematology features regular original laboratory and clinical research articles, brief research reports, critical reviews, images in hematology, as well as letters and correspondence.
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