Donor Lymphocyte Infusion Is a Feasible Way to Improve Survival in Patients with Acute Myeloid Leukemia and Myelodysplastic Syndromes Who Relapse after Allogeneic Stem Cell Transplantation.

IF 1.7 4区 医学 Q3 HEMATOLOGY Acta Haematologica Pub Date : 2024-01-01 Epub Date: 2023-10-12 DOI:10.1159/000534315
Lia Minculescu, Joanne Reekie, Soeren Lykke Petersen, Brian Thomas Kornblit, Ida Schjoedt, Niels Smedegaard Andersen, Lisbeth Pernille Andersen, Anne Fischer-Nielsen, Eva Kannik Haastrup, Lone Smidstrup Friis, Henrik Sengelov
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Abstract

Introduction: Donor lymphocyte infusion (DLI) is used to induce remission in patients who relapse after allogeneic stem cell transplantation (allo-HSCT). During the last decade, the hypomethylating agent Azacitidine has been used together with DLI for a synergistic graft-versus-leukemia (GVL) effect. Here, we report results of DLI/Azacitidine treatment from a retrospective single-center study.

Methods: Fifty AML/MDS patients treated for relapse after allo-HSCT between 2001 and 2020 with DLI at the Department of Hematology, at Rigshospitalet, Copenhagen University Hospital were included for analyses. A subgroup of patients who obtained complete remission (CR) after reinduction chemotherapy, received DLI in combination with low-dose (32 mg/m2) Azacitidine.

Results: Overall survival in all patients after DLI treatment was 59% at 2 years and 20% at 5 years. Relapse-free survival in patients in CR prior to DLI was 32% after 2 years and 7% after 5 years. In the DLI + low-dose-Azacitidine group, 5-year relapse-free survival was 40%.

Conclusion: DLI remains an effective treatment in post-transplant relapse leaving one-fifth of patients' long-term survivors. Our results support the concomitant use of low-dose Azacitidine in the future use of DLI in order to enhance the GVL effect of donor lymphocytes.

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供体淋巴细胞输注是提高异基因干细胞移植后复发的急性髓细胞白血病和骨髓增生异常综合征患者生存率的可行方法。
引言:供体淋巴细胞输注(DLI)用于诱导异基因干细胞移植(allo-HSCT)后复发的患者病情缓解。在过去的十年中,低甲基化剂阿扎胞苷与DLI一起用于协同移植物抗白血病(GVL)效果。在此,我们报告了DLI/阿扎胞苷治疗的一项回顾性单中心研究结果。方法:纳入哥本哈根大学医院Rigshospitalet血液科2001年至2020年间接受异基因造血干细胞移植后复发DLI治疗的50名AML/MDS患者进行分析。一组患者在再次诱导化疗后获得完全缓解(CR),接受DLI联合低剂量(32 mg/m2)阿扎胞苷治疗。结果:所有患者在DLI治疗后的总生存率在2年时为59%,在5年时为20%。DLI前CR患者的无复发生存率在2年后为32%,在5年后为7%。DLI+低剂量阿扎胞苷组5年无复发生存率为40%。结论:DLI仍然是治疗移植后复发的有效方法,使五分之一的患者长期存活。我们的研究结果支持在DLI的未来使用中同时使用低剂量阿扎胞苷,以增强供体淋巴细胞的GVL效应。
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来源期刊
Acta Haematologica
Acta Haematologica 医学-血液学
CiteScore
4.90
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: ''Acta Haematologica'' is a well-established and internationally recognized clinically-oriented journal featuring balanced, wide-ranging coverage of current hematology research. A wealth of information on such problems as anemia, leukemia, lymphoma, multiple myeloma, hereditary disorders, blood coagulation, growth factors, hematopoiesis and differentiation is contained in first-rate basic and clinical papers some of which are accompanied by editorial comments by eminent experts. These are supplemented by short state-of-the-art communications, reviews and correspondence as well as occasional special issues devoted to ‘hot topics’ in hematology. These will keep the practicing hematologist well informed of the new developments in the field.
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