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Phenotypic and genotypic infidelity in B-lineage neoplasms, including transdifferentiation following targeted therapy: Report from the 2021 SH/EAHP Workshop

血液病理学 转分化 CDKN2A 谱系标记 谱系(遗传) 生物 髓样 淋巴瘤 靶向治疗 白血病 癌症研究 表型 免疫学 癌症 干细胞 基因 遗传学 细胞遗传学 染色体
作者
John R. Goodlad,Wenbin Xiao,Catalina Amador,James R. Cook,Lanie E. Happ,Devang Thakkar,Sandeep S. Davé,Ahmet Doğan,Amy S. Duffield,Reza Nejati,German Ott,Mariusz A Wasik,Magdalena Czader
出处
期刊:American Journal of Clinical Pathology [Oxford University Press]
卷期号:159 (6): 538-553 被引量:2
标识
DOI:10.1093/ajcp/aqad035
摘要

Session 2 of the 2021 Society for Hematopathology and European Association for Haematopathology Workshop collected examples of lineage infidelity and transdifferentiation in B-lineage neoplasms, including after targeted therapy.Twenty cases were submitted. Whole-exome sequencing and genome-wide RNA expression analysis were available on a limited subsample.A diagnosis of B-cell acute lymphoblastic leukemia (B-ALL) was rendered on at least 1 biopsy from 13 patients. There was 1 case of acute myeloid leukemia (AML); the remaining 6 cases were mature B-cell neoplasms. Targeted therapy was administered in 7 cases of B-ALL and 4 cases of mature B-cell neoplasms. Six cases of B-ALL underwent lineage switch to AML or mixed-phenotype acute leukemia at relapse, 5 of which had rearranged KMT2A. Changes in maturational state without lineage switch were observed in 2 cases. Examples of de novo aberrant T-cell antigen expression (n = 2) were seen among the mature B-cell lymphoma cohort, and their presence correlated with alterations in tumor cell gene expression patterns.This cohort of cases enabled us to illustrate, discuss, and review current concepts of lineage switch and aberrant antigen expression in a variety of B-cell neoplasms and draw attention to the role targeted therapies may have in predisposing neoplasms to transdifferentiation as well as other, less expected changes in maturational status.

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