慢性淋巴细胞白血病中出现与治疗耐药相关的IGH::CCND1重排和TP53、BTK和BCL2突变

EJHaem Pub Date : 2024-10-08 DOI:10.1002/jha2.1024
Qing Wei, Hong Fang, James M. Jing, Roman Segura-Rivera, L. Jeffrey Medeiros, Wei Wang
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引用次数: 0

摘要

慢性淋巴细胞白血病(CLL)是一种惰性的低级别b细胞肿瘤,通常对治疗反应良好。罕见的CLL病例表现出IGH::CCND1重排,这对区分CLL内的克隆进化和独立的套细胞淋巴瘤提出了诊断挑战。我们报告一例CLL患者,在疾病进展过程中出现了与治疗耐药相关的IGH::CCND1重排和突变,包括TP53、BTK和BCL2。免疫表型、细胞遗传学和分子分析支持这些改变是CLL克隆中的次要事件。该病例显示了对治疗的动态克隆选择和扩增,这反过来又有助于治疗抗性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Emergence of IGH::CCND1 rearrangement and mutations in TP53, BTK, and BCL2 associated with therapy resistance in chronic lymphocytic leukemia

Emergence of IGH::CCND1 rearrangement and mutations in TP53, BTK, and BCL2 associated with therapy resistance in chronic lymphocytic leukemia

Chronic lymphocytic leukemia (CLL) is an indolent low-grade B-cell neoplasm that generally responds well to treatment. Rarely, CLL cases exhibit an IGH::CCND1 rearrangement, presenting a diagnostic challenge in distinguishing between clonal evolution within CLL and an independent mantle cell lymphoma. We report a case of CLL with the emergence of an IGH::CCND1 rearrangement and mutations associated with treatment resistance, including TP53, BTK, and BCL2, during disease progression. Immunophenotypic, cytogenetic, and molecular analyses support that these alterations are secondary events within the CLL clone. This case demonstrates dynamic clonal selection and expansion in response to treatments, which, in turn, contributes to treatment resistance.

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