A successful second allogeneic hematopoietic stem cell transplantation from an alternative donor in a patient with loss of HLA heterozygosity relapse of juvenile myelomonocytic leukemia: case series analysis

Q4 Medicine
L. A. Tsvetkova, A. A. Osipova, A. V. Evdokimov, P. V. Kozhokar, Zh. Z. Rakhmanova, I. M. Barkhatov, O. V. Paina, O. S. Epifanovskaya, E. V. Babenko, N. E. Ivanova, D. V. Kozlov, T. L. Gindina, T. А. Bykova, E. V. Semenova, L. S. Zubarovskaya
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Abstract

Juvenile myelomonocytic leukemia (JMML) is a rare and aggressive myeloproliferative/myelodysplastic neoplasm of early childhood characterized by activation of the Ras signaling pathway. Allogeneic hematopoietic stem cell transplantation (alloHSCT) is the only proven curative treatment for JMML. However, the 5-year overall survival is about 52–64%. In this work, we analyzed 4 clinical cases of patients with relapses of JMML with loss of heterozygosity in HLA (LoH) after allo-HSCT. The patients' parents gave their consent to the use of their children's data, including photographs, for research purposes and in publications. Two patients received a second allo-HSCT from an alternative donor, two patients – from the same donor. A positive result in the form of a durable remission was observed in one patient who underwent a second allo-HSCT from an alternative donor and restored HLA genetic heterozygosity. At the same time, immunotherapy with infusions of donor lymphocytes led to the development of graft-versus-host disease without potentiating the antileukemic effect. Thus, a second allo-HSCT from an alternative donor for the treatment of relapsed JMML with HLA LoH is necessary to restore the “graft-versus-JMML” response. The study was approved by the Independent Ethics Committee and the Scientific Council of the I.P. Pavlov First Saint Petersburg State Medical University of Ministry of Healthcare of the Russian Federation.
在HLA杂合性丧失的青少年髓细胞白血病复发患者中成功的第二次异基因造血干细胞移植:病例系列分析
少年髓单细胞白血病(JMML)是一种罕见的侵袭性早期儿童骨髓增生性/骨髓增生异常肿瘤,其特征是Ras信号通路的激活。同种异体造血干细胞移植(alloHSCT)是唯一被证实的治疗JMML的方法。然而,5年总生存率约为52-64%。在这项工作中,我们分析了4例在同种异体造血干细胞移植后HLA (LoH)杂合性丧失的JMML复发患者的临床病例。患者的父母同意使用他们孩子的数据,包括照片,用于研究目的和出版物。两名患者接受了来自另一名供者的第二次同种异体造血干细胞移植,两名患者来自同一供者。一名患者接受了来自另一供体的第二次同种异体造血干细胞移植,并恢复了HLA遗传杂合性,结果出现了持久缓解的阳性结果。同时,输注供体淋巴细胞的免疫治疗导致移植物抗宿主病的发展,而没有增强抗白血病的作用。因此,从另一个供者处进行第二次同种异体造血干细胞移植,以治疗HLA - LoH复发的JMML,对于恢复“移植物抗JMML”反应是必要的。该研究得到了俄罗斯联邦卫生部巴甫洛夫第一圣彼得堡国立医科大学独立伦理委员会和科学委员会的批准。
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来源期刊
Pediatric Hematology/Oncology and Immunopathology
Pediatric Hematology/Oncology and Immunopathology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
49
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