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马来西亚弥漫性大B细胞淋巴瘤中CD10、BCL-6和多发性骨髓瘤-1表达的临床相关性

Clinical relevance of CD10, BCL-6 and multiple myeloma-1 expression in diffuse large B-cell lymphomas in Malaysia.

作者信息

Peh Suat-Cheng, Gan Gin-Gin, Lee Lin-Kiat, Eow Geok-Im

机构信息

Department of Pathology, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia.

出版信息

Pathol Int. 2008 Sep;58(9):572-9. doi: 10.1111/j.1440-1827.2008.02273.x.

DOI:10.1111/j.1440-1827.2008.02273.x
PMID:18801072
Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of non-Hodgkin lymphoma, and it is recognized to constitute a heterogenous group of neoplasms. It can be divided into germinal center B-cell-like (GCB) and non-GCB subgroups. The aim of the present study was to evaluate the utility of immunophenotype subgrouping of DLBCL in a cohort of multi-ethnic Asian patients. A total of 84 reconfirmed de novo DLBCL were immunostained for the expression of CD10, BCL-2, BCL-6 and multiple myeloma-1. Thirty-three (39.3%) had the GCB phenotype, and the remainder (60.7%), the non-GCB phenotype. The results concur with most reports using a similar method of stratification. Forty-five patients had complete demographic and phenotype studies and 42 patients did not have rituximab treatment and had sufficient data for survival rate analysis. Similar to other studies, patients with combined low and low-intermediate International Prognostic Index score had better overall survival (P = 0.006). But patients with GCB phenotype did not have better prognosis, and BCL-2 expression was not associated with better prognosis. The expression of BCL-6 was associated with lower overall survival rate (P = 0.038). No apparent difference in overall and disease-free survival was noted between patients with GCB and non-GCB disease. BCL-6 expression by tumor cells appears to be associated with poorer prognosis.

摘要

弥漫性大B细胞淋巴瘤(DLBCL)是非霍奇金淋巴瘤最常见的亚型,被认为是一组异质性肿瘤。它可分为生发中心B细胞样(GCB)和非GCB亚组。本研究的目的是评估DLBCL免疫表型亚组在多民族亚洲患者队列中的实用性。对84例再次确诊的初发性DLBCL进行免疫染色,检测CD10、BCL-2、BCL-6和多发性骨髓瘤-1的表达。33例(39.3%)具有GCB表型,其余(60.7%)为非GCB表型。结果与大多数采用类似分层方法的报告一致。45例患者进行了完整的人口统计学和表型研究,42例患者未接受利妥昔单抗治疗且有足够的数据进行生存率分析。与其他研究相似,国际预后指数评分为低和低-中组合的患者总生存期更好(P = 0.006)。但GCB表型的患者预后并未更好,BCL-2表达与更好的预后无关。BCL-6表达与较低的总生存率相关(P = 0.038)。GCB和非GCB疾病患者的总生存期和无病生存期无明显差异。肿瘤细胞的BCL-6表达似乎与较差的预后相关。

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