唐氏综合征患者复发性急性淋巴细胞白血病的治疗:1例报告

IF 0.9 Q4 HEMATOLOGY
Eman Almatar, Sondus Alsharidah, Omnia A. Hashem
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引用次数: 0

摘要

患有唐氏综合症(DS)的儿童患急性淋巴细胞白血病(ALL)的风险增加10 - 20倍,化疗毒性增加。Blinatumomab是一种双特异性CD19 × CD3 t细胞参与剂,提供降低骨髓毒性的靶向免疫治疗。我们描述了一名患有DS的9岁女孩,她在2021年初被诊断为b细胞前体ALL,并于2023年9月在维持期间复发。再诱导后,她接受了两个28天的blinatumumab周期:第一个周期导致5%的细胞和无法检测到的微小残留病(MRD),第二个周期耐受性良好。她仍处于缓解期,等待异体造血干细胞移植,这突出了blinatumomab作为移植桥梁的有效性和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of relapsed acute lymphoblastic leukemia in a patient with down syndrome: A case report
Children with Down syndrome (DS) have a 10–20-fold increased risk of acute lymphoblastic leukemia (ALL) and heightened chemotherapy toxicity. Blinatumomab, a bispecific CD19 × CD3 T-cell engager, offers targeted immunotherapy with reduced myelotoxicity. We describe a 9-year-old girl with DS diagnosed with B-cell precursor ALL in early 2021 who relapsed during maintenance in September 2023. After reinduction, she received two 28-day blinatumomab cycles: the first resulted in <5 % blasts and undetectable minimal residual disease (MRD), and the second was well tolerated. She remains in remission pending allogeneic hematopoietic stem cell transplantation, highlighting blinatumomab’s efficacy and safety as a bridge to transplantation.
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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