Donor Cell-Derived Chronic Lymphocytic Leukemia Presenting After Allogenic Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia.

IF 1.3 Q4 HEMATOLOGY
Journal of hematology Pub Date : 2025-04-01 Epub Date: 2025-02-21 DOI:10.14740/jh2022
Katarzyna Czempik, Izabela Noster, Joanna Dziaczkowska-Suszek, Magdalena Glowala-Kosinska, Dariusz Kata, Anna Kopinska, Grzegorz Helbig
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Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative approach for many hematologic disorders, and donor cell leukemia (DCL) remains a complication rarely observed after HSCT. The number of reported cases of DCL slightly exceeds 100, with acute myeloid leukemia (AML) being the most common type. To date, only a few cases of chronic lymphocytic leukemia (CLL) emerging from donor cells have been described in the literature. Here, we report two cases of CLL of donor origin, which emerged in patients after HSCT for AML. In the reported cases, patients maintained complete remission of AML after HSCT. Both donors were free of CLL before transplantation. Several years after HSCT (9 and 3 years, respectively), lymphocytosis with proven B-cell clonality was detected in recipients prompting a detailed blood analysis to be performed also in donors. CLL population was demonstrated in both cases. The first donor-recipient pair did not meet criteria for CLL treatment and eventually died from causes not related to underlying hematologic malignancy. The second couple received Bruton's tyrosine kinase inhibitors with good disease control. The presented cases raise the question of possible clonal evolution of B-lymphocytes in donor-origin cells. Prospective screening of potential donors for pre-malignant alterations remains a matter of discussion.

同种异体造血干细胞移植治疗急性髓性白血病后出现供体细胞来源的慢性淋巴细胞白血病。
同种异体造血干细胞移植(HSCT)是许多血液疾病的治疗方法,供体细胞白血病(DCL)仍然是HSCT后罕见的并发症。报告的DCL病例数略超过100例,其中急性髓性白血病(AML)是最常见的类型。迄今为止,只有少数病例慢性淋巴细胞白血病(CLL)出现供体细胞已在文献中描述。在这里,我们报告了两例供体来源的CLL,它们出现在AML的HSCT患者中。在报告的病例中,患者在移植后AML保持完全缓解。两名供者在移植前均无CLL。移植后数年(分别为9年和3年),在受者中检测到证实有b细胞克隆的淋巴细胞增多症,促使对供者也进行详细的血液分析。两例均有CLL人群。第一对供体-受体不符合CLL治疗标准,最终死于与潜在的血液恶性肿瘤无关的原因。第二组接受布鲁顿酪氨酸激酶抑制剂治疗,病情得到良好控制。这些病例提出了供体源细胞中b淋巴细胞克隆进化的可能性问题。对潜在供体进行癌前病变的前瞻性筛查仍有待讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of hematology
Journal of hematology HEMATOLOGY-
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