在接受blinatumumab治疗的患者中,t(9;22) BCR::ABL1的b淋巴母细胞白血病/淋巴瘤向角蛋白强烈表达的未分化肿瘤的去分化

Krasimira A. Rozenova , Anja C. Roden , Christopher Hartley , Jess F. Peterson , Gregory E. Otteson , Aref Al-Kali , Harry E. Fuentes Bayne , Mithun V. Shah , Mrinal S. Patnaik , Rebecca L. King , Daniel P. Larson
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引用次数: 0

摘要

目的blinatumomab治疗B-ALL患者的谱系转换已有报道。我们报告了一例blinatumomab治疗的t(9;22)(q34.1;q11.2)(Ph+B-ALL)复发为角蛋白阳性的未分化肿瘤,结果一名47岁男性Ph+B-ALL(p190融合转录物)早期复发,接受了包括blinatumomab在内的多药治疗,并获得了完全缓解。开始治疗11个月后,他出现了胸壁肿块。活检显示一个未成熟的肿瘤,没有谱系特异性分化,但角蛋白表达和BCR::ABL1保留。随后,发现了角蛋白阳性和BCR:ABL1的骨髓复发。这些发现与Ph+B-ALL的去分化和角蛋白异常表达最为一致。结论据我们所知,我们报告了第一例急性白血病病例,该病例作为去分化肿瘤复发,第二例报告了Ph+B-AL患者的淋巴细胞性白血病,角蛋白表达异常,并接受了包括blinatumomab在内的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dedifferentiation of B-lymphoblastic leukemia/lymphoma with t(9;22) BCR::ABL1 to an undifferentiated neoplasm with strong keratin expression in a patient receiving blinatumomab

Objectives

Lineage switch in patients with B-ALL treated with blinatumomab has been previously reported. We present a case of blinatumomab-treated B-ALL with t(9;22)(q34.1;q11.2) (Ph + B-ALL) relapsing as a keratin-positive undifferentiated neoplasm with lack of B-cell, T-cell, or definitive myeloid antigens and persistent BCR::ABL1.

Results

A 47-year-old male with Ph + B-ALL (p190 fusion transcript) experienced early relapse and received multi-agent therapy including blinatumomab and achieved complete remission. Eleven months after initiation of treatment, he presented with a chest wall mass. Biopsy showed an immature- appearing neoplasm without lineage-specific differentiation, but with expression of keratin and retention of the BCR::ABL1. Subsequently, bone marrow relapse with keratin positivity and BCR::ABL1 was identified. The findings were most compatible with dedifferentiation and aberrant keratin expression of Ph + B-ALL.

Conclusions

We present, to our knowledge, the first reported case of an acute leukemia which relapsed as a dedifferentiated neoplasm and the second reported case of lymphoblastic leukemia with aberrant keratin expression in a patient with Ph + B-ALL and treatment including blinatumomab.

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