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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >Primary intestinal diffuse large B-cell non-Hodgkin's lymphoma: clinical features, management, and prognosis of 66 patients.
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Primary intestinal diffuse large B-cell non-Hodgkin's lymphoma: clinical features, management, and prognosis of 66 patients.

机译:原发性肠弥漫性大B细胞非霍奇金淋巴瘤:66例患者的临床特征,治疗和预后。

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BACKGROUND: In Saudi Arabia, primary gastrointestinal non-Hodgkin's lymphoma (NHL) is common. Recently we have reported one of the largest series of primary gastric (PG) diffuse large B-cell lymphoma (DLCL). This has prompted the analysis of another series of patients with primary intestinal DLCL to depict the clinical features and the outcome of that disease and to compare those with that for PG involvement. PATIENTS AND METHODS: The data of 66 adult patients with primary intestinal NHL having DLCL histology were retrospectively reviewed. RESULTS: Patients had a median age of 45 years. Of 64 treated patients, 16% and 84%, received single and multiple modality treatment, respectively. Seventy-six percent, ten percent, and fourteen percent attained complete remission (CR), partial remission (PR), and no response/progressive disease, respectively. Multivariate analysis failed to identify any variable that predict the likelihood of attaining CR. Over a median follow-up of 81 months for all 66 patients, 32 (48%) were alive and disease-free, 5 (8%) were alive with evidence of disease, and the remaining 29 (44%) were dead. The median overall survival (OS) was 101 months and it was 58% (+/- 6%) and 48% (+/- 7%) at 5- and 10-year, respectively. Of the 54 patients who achieved CR or PR, the median event-free survival (EFS) was not reached, but the predicted 5- and 10-year EFS was 61% (+/- 7%) and 52% (+/- 7%), respectively. Only low serum albumin (<30 g/l) was associated with adverse OS and EFS in a univariate analysis, however, multivariate analysis was not possible. Our analysis showed that compared with single-modality management, multi-modality strategy attained significantly higher CR, and advantageous EFS, but without a significant superior effect on OS. In comparison with patients with PG DLCL, those with primary intestinal disease demonstrated more adverse prognostic features, but had an equivalent survival. CONCLUSIONS: This series characterized the clinico-pathologic features and outcome of patients with primary intestinal DLCL. While surgical resection in primary intestinal NHL seems beneficial, only prospective randomized studies can ascertain its precise role. Compared with patients with PG NHL, patients with primary intestinal disease had more prevalence of adverse prognostic features.
机译:背景:在沙特阿拉伯,原发性胃肠道非霍奇金淋巴瘤(NHL)很常见。最近,我们报告了最大的原发性胃(PG)弥漫性大B细胞淋巴瘤(DLCL)系列之一。这促使对另一系列原发性肠道DLCL患者进行分析,以描绘该疾病的临床特征和结局,并将其与PG受累者进行比较。患者和方法:回顾性分析66例具有DLCL组织学原发性NHL成人患者的数据。结果:患者的平均年龄为45岁。在64位接受治疗的患者中,分别接受了单模式和多模式治疗的分别为16%和84%。分别达到完全缓解(CR),部分缓解(PR)和无反应/进行性疾病的比例分别为76%,10%和14%。多变量分析未能确定任何预测达到CR可能性的变量。在对所有66位患者进行的81个月的中位随访中,有32位(48%)活着并且没有疾病,有5位(8%)活着并有疾病迹象,其余29位(44%)死亡。中位总生存期(OS)为101个月,在5年和10年时分别为58%(+/- 6%)和48%(+/- 7%)。在54位获得CR或PR的患者中,未达到无事件生存期(EFS)的中位数,但预测的5年和10年EFS分别为61%(+/- 7%)和52%(+/- 7%)。在单变量分析中,只有低血清白蛋白(<30 g / l)与不良OS和EFS相关,但是,不可能进行多变量分析。我们的分析表明,与单模式管理相比,多模式策略具有显着更高的CR和有利的EFS,但对OS没有明显的优越效果。与PG DLCL患者相比,原发性肠道疾病患者预后不良,但生存率相当。结论:本系列研究描述了原发性肠DLCL患者的临床病理特征和预后。虽然在原发性肠道NHL中进行手术切除似乎是有益的,但只有前瞻性随机研究才能确定其确切作用。与PG NHL患者相比,原发性肠道疾病患者不良预后特征的患病率更高。

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