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首页> 外文期刊>Annals of hematology >A retrospective analysis of primary gastric diffuse large B-cell lymphoma with or without concomitant mucosa-associated lymphoid tissue (MALT) lymphoma components
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A retrospective analysis of primary gastric diffuse large B-cell lymphoma with or without concomitant mucosa-associated lymphoid tissue (MALT) lymphoma components

机译:胃原发性弥漫性大B细胞淋巴瘤伴或不伴黏膜相关淋巴组织(MALT)淋巴瘤成分的回顾性分析

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摘要

Primary gastric diffuse large B-cell lymphoma (DLBCL) is a heterogeneous disease entity that includes patients with (DLBCL/MALT) and without detectable mucosa-associated lymphoid tissue (MALT) lymphoma components (de novo DLBCL). We sought to evaluate the clinical characteristics and outcome of this disease in a large number of cases. Patients with primary gastric DLBCL (n = 162) seen on 2001-2011 at the Tianjin Medical University Cancer Institute and Hospital and the First affiliated Hospital of Chinese PLA General Hospital were retrospectively reviewed. The distribution of sex, age, Lugano staging, and other main clinical characteristics was similar between the de novo DLBCL and DLBCL/MALT groups (p > 0.05). However, the proportion of patients with a stage-modified international prognostic index (m-IPI) ≥ 2 was higher in the de novo DLBCL (34 %) than the DLBCL/MALT group (17 %) (p = 0.026). In addition, the Helicobacter pylori infection rates were higher in the DLBCL/MALT (75 %) than the de novo DLBCL group (36 %) (p < 0.001). Five-year progression-free survival (PFS) and overall survival (OS) estimates were similar for patients in the de novo DLBCL (p = 0.705) and DLBCL/MALT groups (p = 0.846). Surgical treatment did not offer survival benefits when compared with chemotherapy for 5-year PFS (p = 0.607) and OS estimates (p = 0.554). There were no significant differences in 5-year PFS and OS estimates for patients treated with rituximab-chemotherapy (p = 0.261) or conventional chemotherapy (p = 0.227). Non-GCB subtype and m-IPI ≥ 2 were independently associated with shorter OS, and advanced stages of lymphoma were independently associated with shorter PFS.
机译:原发性胃弥漫性大B细胞淋巴瘤(DLBCL)是一种异质性疾病实体,包括患有(DLBCL / MALT)且没有可检测到的粘膜相关淋巴样组织(MALT)淋巴瘤成分(de novo DLBCL)的患者。我们试图评估在许多情况下该疾病的临床特征和结局。回顾性分析2001-2011年在天津医科大学附属肿瘤医院和中国人民解放军总医院第一附属医院收治的原发性胃DLBCL患者(n = 162)。从头DLBCL组和DLBCL / MALT组之间的性别,年龄,卢加诺分期和其他主要临床特征分布相似(p> 0.05)。但是,从头开始的DLBCL(34%)患者的国际预后指数(m-IPI)≥2的患者比例高于DLBCL / MALT组(17%)(p = 0.026)。此外,DLBCL / MALT中的幽门螺杆菌感染率(75%)高于新生的DLBCL组(36%)(p <0.001)。从头开始的DLBCL(p = 0.705)和DLBCL / MALT组(p = 0.846)的患者五年无进展生存期(PFS)和总体生存期(OS)估算值相似。与5年PFS(p = 0.607)和OS估计值(p = 0.554)相比,手术治疗没有提供生存益处。对于接受利妥昔单抗(p = 0.261)或常规化疗(p = 0.227)治疗的患者,其5年PFS和OS估计值无显着差异。非GCB亚型和m-IPI≥2与较短的OS独立相关,而淋巴瘤的晚期则与较短的PFS独立相关。

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