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CD10与BCL-6共表达的套细胞淋巴瘤患者的临床和生物学特征:一项回顾性研究

Clinical and biological features of mantle cell lymphoma patients with co-expression of CD10 and BCL-6: a retrospective study.

作者信息

Chen Wanzi, Liu Hangmin, Wang Pengcheng, Li Guoping

机构信息

Fujian Institute of Hematology, Fujian Provincial Key Laboratory on Hematology, Fujian Medical University Union Hospital, Fuzhou, China.

Clinical Laboratory, Fujian Medical University Union Hospital, Fuzhou, China.

出版信息

Transl Cancer Res. 2021 Nov;10(11):4786-4793. doi: 10.21037/tcr-21-882.

Abstract

BACKGROUND

Mantle cell lymphoma (MCL) with co-expression of CD10 and BCL-6 was scarcely reported, and its biological features were largely remained unknown. Thus, this study aimed to describe the clinical and biological features, as well as outcome of MCL patients with co-expression of CD10 and BCL-6.

METHODS

A total of 104 cases of MCL who were admitted to our hospital between January 2011 and October 2018 were recruited. Those patients were diagnosed according to the 2016 World Health Organization (WHO) classification system for tumors of the hematopoietic and lymphoid tissues, in compliance with the results of cytomorphology and immunohistochemical analysis. Patients were followed up through telephone interviews, medical records. Differences in age, gender, leukocyte count, lactate dehydrogenase (LDH) level, beta-2 microglobulin (β2-MG) level and results of immunohistochemistry were analyzed. Then the event-free survival (EFS) rate and overall survival (OS) rate were performed by the Kaplan-Meier method and log-rank test.

RESULTS

The results showed that, in total, 5 patients had superficial lymph node enlargement, 2 patients suffered from abdominal discomfort, and 1 patient's red blood cell (RBC) count was abnormal at the time of diagnosis. All patients were in stage IV, 75% had bone marrow involvement, and 75% and 100% of patients had elevated levels of LDH and β2-MG, respectively. Three classic genes and five variants were involved in the 8 patients. MCL patients with the co-expression of CD10 and BCL-6 had higher Ki-67 index, white blood cell (WBC) count, LDH level, and β2-MG level than those of without co-expression of CD10 and BCL-6 (P=0.025, 0.038, 0.015, and 0.021, respectively). Besides, MCL patients with CD10 and BCL-6 co-expression had shorter OS and EFS (χ=6.401 and 5.975; P=0.011 and 0.015, respectively), indicating patients' susceptibility to get complex karyotype and TP53 abnormality.

CONCLUSIONS

MCL patients with co-expression of CD10 and BCL-6 were more likely to have bone marrow involvement, higher Ki-67 index, increased WBC count, and elevated levels of LDH and β2-MG at the time of diagnosis, then might has complex cytogenetic and poor prognosis.

摘要

背景

CD10和BCL-6共表达的套细胞淋巴瘤(MCL)鲜有报道,其生物学特征在很大程度上仍不清楚。因此,本研究旨在描述CD10和BCL-6共表达的MCL患者的临床和生物学特征以及预后。

方法

招募了2011年1月至2018年10月期间我院收治的104例MCL患者。这些患者根据2016年世界卫生组织(WHO)造血与淋巴组织肿瘤分类系统,结合细胞形态学和免疫组化分析结果进行诊断。通过电话访谈、病历对患者进行随访。分析患者年龄、性别、白细胞计数、乳酸脱氢酶(LDH)水平、β2微球蛋白(β2-MG)水平及免疫组化结果的差异。然后采用Kaplan-Meier法和对数秩检验计算无事件生存(EFS)率和总生存(OS)率。

结果

结果显示,诊断时共有5例患者出现浅表淋巴结肿大,2例患者有腹部不适,1例患者红细胞(RBC)计数异常。所有患者均为IV期,75%有骨髓受累,75%和100%的患者LDH和β2-MG水平升高。8例患者涉及3个经典基因和5个变异。CD10和BCL-6共表达的MCL患者的Ki-67指数、白细胞(WBC)计数、LDH水平和β2-MG水平高于未共表达CD10和BCL-6的患者(P分别为0.025、0.038、0.015和0.021)。此外,CD10和BCL-6共表达的MCL患者的OS和EFS较短(χ=6.401和5.975;P分别为0.011和0.015),表明患者易出现复杂核型和TP53异常。

结论

CD10和BCL-6共表达的MCL患者在诊断时更易出现骨髓受累、Ki-67指数更高、白细胞计数增加、LDH和β2-MG水平升高,可能具有复杂的细胞遗传学特征和不良预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52b7/8798977/f6b3ca999c8f/tcr-10-11-4786-f1.jpg

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