代表SFGM-TC:高危骨髓增生异常综合征和急性髓系白血病同种异体干细胞移植患者的预防性供体淋巴细胞输注。

IF 1.7 4区 医学 Q3 HEMATOLOGY Acta Haematologica Pub Date : 2023-01-01 DOI:10.1159/000528184
Charles Guisnel, Luciane Schirmer, Stéphane Morisset, Marie Robin, Hélène Labussière-Wallet, Rémy Duléry, Patrice Ceballos, Edouard Forcade, Stéphanie Nguyen, Xavier Poiré, Johan Maertens, Sylvain Chantepie, Patrice Chevallier, Etienne Daguindau, Alban Villate, Amandine Charbonnier, Cristina Castilla-Llorente, Nathalie Contentin, Anne Huynh, Ibrahim Yakoub-Agha, Claude Eric Bulabois, Marie-Thérèse Rubio, Maud D'Aveni
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引用次数: 0

摘要

同种异体造血干细胞移植(allo-HSCT)仍然是治疗高危骨髓增生异常综合征(MDS)和急性髓系白血病(AML)的最佳选择。不幸的是,由于逃避同种异体反应性T细胞控制的机制,它仍然与复发的显著风险相关。重复辅助供体淋巴细胞输注(DLI),称为预防性DLI (proDLI),作为预防复发的有效策略仍存在争议。方法:我们进行了一项回顾性多中心研究,以评估proDLI在同种异体移植AML和MDS中的疗效。我们确定了56例接受proDLI治疗的患者(计划在没有任何疾病复发迹象的完全嵌合体中进行DLI),并根据相似的年龄、初始疾病、细胞遗传学预后和调节强度,将他们与对照组的167例患者(混合嵌合体或阳性微小残留疾病进行DLI)进行匹配。结果:在单因素分析中,两组患者在同种异体造血干细胞移植后100天的严重aGVHD发生率和1年后所有级别的慢性GVHD发生率相似。我们还观察到proDLI组的3年RI(52.61%[95%可信区间25.99-79.23])高于对照组(29.31% [20.28-38.34],p = 0.067)。然而,两组的3年总生存率(p = 0.892)、无进展生存率(p = 0.239)和非复发死亡率(p = 0.343)相似。在多变量分析中,影响总生存率和无进展生存率的唯一因素是调节方案中抗胸腺细胞球蛋白的使用。结论:与先发制人的策略相比,proDLI策略具有可接受的毒性,但并没有改善患者的预后。
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On Behalf of the SFGM-TC: Prophylactic Donor Lymphocyte Infusion in Patients Treated with Allogeneic Stem-Cell Transplantation for High-Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia.

Introduction: Allogeneic hematopoietic stem-cell transplantation (allo-HSCT) remains the best curative option for high-risk myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). Unfortunately, it is still associated with a significant risk of relapse due to mechanisms of escape from the control of alloreactive T cells. Repetitive adjuvant donor lymphocyte infusion (DLI), termed prophylactic DLI (proDLI), as an effective strategy in preventing relapse is still debated.

Methods: We performed a retrospective multicenter study to evaluate the efficacy of proDLI in allografted AML and MDS. We identified 56 patients treated with proDLI (DLI planned in full chimeras without any sign of disease relapse) and matched them to 167 patients in control group, (DLI performed for mixed chimerism or positive minimal residual disease) based on similar age, initial disease, cytogenetic prognosis, and conditioning intensity.

Results: In univariate analysis, the incidence of severe aGVHD at 100 days and incidence of all grades of chronic GVHD 1 year after allo-HSCT were similar in the two groups. We also observed a trend of higher 3-year RI (52.61% [95% confidence interval 25.99-79.23]) in the proDLI group versus the control group (29.31% [20.28-38.34], p = 0.067). However, 3-year overall survival (p = 0.892), progression-free survival (p = 0.239), and nonrelapse mortality (p = 0.343) were similar between the two groups. In multivariate analysis, the only factor influencing overall and progression-free survival was anti-thymocyte globulin administration during the conditioning regimen.

Conclusion: The proDLI strategy had an acceptable toxicity profile but did not improve patient outcomes compared to the pre-emptive strategy.

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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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