异体自然杀伤细胞 MG4101 在复发或难治性急性髓性白血病患者中的应用:一项试验研究。

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2025-02-01 Epub Date: 2024-10-22 DOI:10.1080/10428194.2024.2414903
Sang-A Kim, Miyoung Jung, Hyojin Kim, Ja Min Byun, Junshik Hong, Dong-Yeop Shin, Inho Kim, Sung-Soo Yoon, Sung Yoo Cho, Yu Kyeong Hwang, Youngil Koh
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引用次数: 0

摘要

我们评估了异基因体外扩增 NK 细胞 MG4101 在难治性或复发性急性髓细胞性白血病患者中的安全性和有效性。分析了免疫学特征与临床反应之间的关系。2018年4月至2020年2月期间,11名患者(男:女=5:6)接受了MG4101治疗。在8名可评估的患者中,2人(25.0%)出现部分应答,2人(25.0%)病情稳定。中位总生存期为3.4个月(95%置信区间[95% CI],2.5-4.3个月),异基因造血干细胞移植(HSCT)删减反应持续时间为2.9个月(95% CI,1.5-4.4个月)。两名患者在MG4101治疗后接受了造血干细胞移植。除一次3级输液相关反应外,未观察到严重不良事件。应答者的激活 KIRs 总和往往高于非应答者。对NKRL和KIR的分析凸显了免疫机制在治疗髓系肿瘤中的重要性。
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MG4101, an allogeneic natural killer cell, in patients with relapsed or refractory acute myeloid leukemia: a pilot study.

We evaluated the safety and efficacy of allogeneic, ex-vivo expanded, NK cells, MG4101, in patients with refractory or relapsed AML. The relationship between immunological characteristics and clinical responses was analyzed. Between April 2018 and February 2020, 11 patients (male:female = 5:6) were treated with MG4101. Of eight evaluable patients, two (25.0%) showed partial response and two (25.0%) showed stable disease. The median overall survival was 3.4 months (95% confidence interval [95% CI], 2.5-4.3 months), and the allogeneic hematopoietic stem cell transplantation (HSCT) censored duration of response was 2.9 months (95% CI, 1.5-4.4 months). Two patients underwent HSCT after MG4101 treatment. Except for one grade 3 infusion-related reaction, no serious adverse events were observed. The sum of activating KIRs in responders tended to be higher than that in non-responders. Analyses of NKRL and KIR highlighted the importance of immunological mechanisms in treating myeloid neoplasms.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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