Inferior Overall Survival After Haploidentical Donor Lymphocyte Infusions in Relapsed Myeloid Neoplasms.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-11-05 DOI:10.1111/ejh.14340
Tobias Matthieu Benoit, Adrian Bachofner, Nathan Wolfensberger, Yvonne Zaugg-Berger, Markus Gabriel Manz, Dominik Schneidawind
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Abstract

Objectives: Allogeneic hematopoietic stem cell transplantation (HSCT) effectively treats high-risk myeloid neoplasms, but relapses post-HSCT, particularly in acute myeloid leukemia (AML) and myelodysplastic neoplasms (MDS), pose significant challenges. Donor lymphocyte infusion (DLI) has been utilized, but its effectiveness, especially in haploidentical settings, remains insufficiently clarified, and graft-versus-host disease (GvHD) poses a substantial risk.

Methods: In this retrospective cohort study, 57 patients with AML or MDS who received DLI after allogeneic HSCT at our center from 2002 to 2023 were analyzed. Herein, only preemptively or therapeutically applied DLI were included, and endpoints included overall survival (OS), progression-free survival (PFS), and GvHD incidence post-DLI.

Results: Median OS after DLI was 517 days, with a 1-year OS of 62.5%. Factors associated with longer OS included patient age, HLA-identical donor, post-HSCT treatment naivety, and preemptive DLI indication. Haploidentical DLI was associated with inferior OS compared to HLA-identical DLI; however, PFS and GvHD incidence post-DLI did not differ significantly.

Conclusions: Our study findings indicate that OS rate is inferior in patients with relapsed AML or MDS treated with haploidentical DLI in comparison to those who received HLA-identical DLI. Given the limitations of haploidentical DLI, alternative strategies, such as higher cell doses or combination treatment approaches, warrant further investigation.

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复发性髓系肿瘤患者接受同种异体淋巴细胞输注后的总体生存率较低。
目标:异基因造血干细胞移植(HSCT)可有效治疗高风险髓系肿瘤,但HSCT后复发,尤其是急性髓性白血病(AML)和骨髓增生异常肿瘤(MDS)的复发,带来了巨大挑战。捐献淋巴细胞输注(DLI)已得到应用,但其有效性,尤其是在单倍体情况下的有效性仍未得到充分阐明,移植物抗宿主病(GvHD)也构成了巨大风险:在这项回顾性队列研究中,我们分析了2002年至2023年在本中心接受异基因造血干细胞移植后接受DLI的57例AML或MDS患者。结果:DLI后的中位OS为1.5年,PFS为1.5年,GvHD为1.5年:DLI后的中位OS为517天,1年OS为62.5%。与较长的OS相关的因素包括患者年龄、HLA相同的供体、HSCT后治疗的天真程度以及先期DLI适应症。与HLA相同的DLI相比,同种异体DLI与较差的OS相关;然而,DLI后的PFS和GvHD发生率并无显著差异:我们的研究结果表明,与接受HLA相同DLI治疗的患者相比,接受单倍体DLI治疗的复发AML或MDS患者的OS率较低。鉴于单倍体 DLI 的局限性,需要进一步研究其他策略,如更高的细胞剂量或联合治疗方法。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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