Zhao Yue, Siddiqi Imran, Wildes Tyler J, McCracken Jenna, Deak Kristen, Rehder Catherine, Wang Endi
Department of Pathology, The First Hospital and College of Basic Medical Sciences, China Medical University, Shenyang, China.
Department of Pathology, Duke University School of Medicine, Durham, NC, USA.
Am J Clin Pathol. 2023 Apr 4;159(4):337-351. doi: 10.1093/ajcp/aqac165.
To evaluate clinicopathologic characteristics of biclonal chronic lymphocytic leukemia (CLL).
Retrospectively analyze clinical data and pathologic features.
Ten cases were identified in which flow cytometry demonstrated an abnormal B-cell population with a CLL-like immunophenotype but showed no definitive light chain restriction. All had cytogenetic abnormalities detected, including seven with two CLL-related abnormalities. Four of these showed features suggestive of clonal evolution, all having del(13q) as a "stem-line" abnormality and three showing del(11q) as a "side-line" abnormality. Five (50%) cases demonstrated deleterious NOTCH1 mutations, in contrast to 11.8% in a control group of monoclonal CLL (P < .05). Of the 10 patients, 5 received treatment, with good/partial response in three cases and therapeutic resistance in one case. The median treatment-free survival was estimated at 68 months.
Despite a polytypic pattern of light chain expression, the neoplastic nature of biclonal CLL is suggested by a characteristic CLL phenotype and can be confirmed by cytogenetic and genomic analyses. The two clones with discordant light chain isotypes may share a "stem-line" cytogenetic abnormality, suggesting possible clonal evolution. Biclonal CLL is associated with NOTCH1 mutations, which may occur in a small subclone and gradually evolve in clonal size. Genomic analysis on light chain-sorted and/or chronologically collected samples may provide insight into clonal evolution in CLL.
评估双克隆慢性淋巴细胞白血病(CLL)的临床病理特征。
回顾性分析临床资料和病理特征。
共鉴定出10例病例,流式细胞术显示存在异常B细胞群体,具有CLL样免疫表型,但未显示明确的轻链限制。所有病例均检测到细胞遗传学异常,其中7例有两种与CLL相关的异常。其中4例显示出克隆进化的特征,所有病例均以del(13q)作为“主干线”异常,3例以del(11q)作为“分支线”异常。5例(50%)病例存在有害的NOTCH1突变,而单克隆CLL对照组的这一比例为11.8%(P < 0.05)。10例患者中,5例接受了治疗,3例获得良好/部分缓解,1例治疗耐药。估计无治疗生存期的中位数为68个月。
尽管轻链表达呈多型性模式,但特征性的CLL表型提示双克隆CLL的肿瘤性质,可通过细胞遗传学和基因组分析得以证实。具有不一致轻链同种型的两个克隆可能共享一种“主干线”细胞遗传学异常,提示可能存在克隆进化。双克隆CLL与NOTCH1突变相关,该突变可能发生在一个小的亚克隆中,并在克隆大小上逐渐演变。对轻链分选和/或按时间顺序收集的样本进行基因组分析可能有助于深入了解CLL中的克隆进化。