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CD19导向治疗后MLL重排婴儿白血病中的谱系转换

Lineage Switch in MLL-Rearranged Infant Leukemia Following CD19-Directed Therapy.

作者信息

Rayes Ahmad, McMasters Richard L, O'Brien Maureen M

机构信息

Division of Oncology, Cancer and Blood Disease Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

出版信息

Pediatr Blood Cancer. 2016 Jun;63(6):1113-5. doi: 10.1002/pbc.25953. Epub 2016 Feb 23.

Abstract

Rearrangements of the mixed lineage leukemia (MLL) gene occur frequently in infants with both acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). Conversions of leukemia cell lineage are rare, but occur most commonly in the setting of MLL-rearrangement. Blinatumomab is a bidirectional antibody targeting CD19 with significant activity in relapsed B-precursor ALL. We report an infant with ALL with t(4;11)(q21;q23) refractory to cytotoxic chemotherapy who was treated with blinatumomab. Following rapid initial clearance of peripheral lymphoblasts, bone marrow evaluation demonstrated a leukemic lineage switch to CD19-negative monoblastic AML. Complete remission was achieved with myeloid-directed chemotherapy.

摘要

混合谱系白血病(MLL)基因重排在急性淋巴细胞白血病(ALL)和急性髓细胞白血病(AML)婴儿中频繁发生。白血病细胞系的转化很少见,但最常发生在MLL重排的情况下。博纳吐单抗是一种靶向CD19的双向抗体,对复发的B前体ALL具有显著活性。我们报告了一名患有t(4;11)(q21;q23)的ALL婴儿,对细胞毒性化疗耐药,接受了博纳吐单抗治疗。在外周淋巴细胞迅速初始清除后,骨髓评估显示白血病细胞系转变为CD19阴性单核细胞AML。采用髓系定向化疗实现了完全缓解。

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