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结直肠黏膜相关淋巴组织(MALT)淋巴瘤的临床特征、治疗及转归:1993年至2017年发表的英文文献综述

Clinical features, treatment and outcomes of colorectal mucosa-associated lymphoid tissue (MALT) lymphoma: literature reviews published in English between 1993 and 2017.

作者信息

Won Jae Hee, Kim Sung Min, Kim Jong Wan, Park Jun Ho, Kim Jeong Yeon

机构信息

Department of Surgery, Dongtan Sacred Hospital, Hallym University College of Medicine, KyungKee, Korea.

Department of Surgery, Kangdong Sacred Hospital, Hallym University College of Medicine, KyungKee, Korea.

出版信息

Cancer Manag Res. 2019 Sep 20;11:8577-8587. doi: 10.2147/CMAR.S214197. eCollection 2019.

Abstract

BACKGROUND

Colorectal mucosa-associated lymphoid tissue (MALT) lymphoma (cMALToma) is rare and comprises only 2.5% of the MALT lymphomas. Its etiology and treatment have not been well established. The aim of this systematic literature review was to try to characterize cMALToma and analyze the risk factors for treatment failure with various therapeutic strategies.

METHODS

We retrospectively reviewed 50 case reports from 1993 to 2017 through a PubMed search of English medical literature, describing cMALToma. We included 67 patients from previous case reports and we added 6 patients treated for cMALToma in our multicenter institutes. Risk factor analysis was done for treatment failure, defined as remission failure and recurrence.

RESULTS

Of 73 patients diagnosed with cMALToma, tumors were located in 54 patients (74.0%) in the rectum, in 10 patients (13.6%) in the right colon, in 3 patients (4.1%) in the transverse colon, and in 6 patients (8.2%) in the sigmoid colon. In first-line treatment, patients achieved complete remission (CR) with surgery (18/19 cases), local resection (18/19 cases), chemotherapy (12/13 cases), radiation therapy (4/5 cases), antibiotics therapy including eradication (12/15 cases), and no treatment (1/2 cases). Among these, eight cases (10.9%) needed second-line treatment, and there was overall remission failure in 3 cases (4.1%). Of the remaining 70 patients with CR, the tumor recurred in 5 patients (6.8%). The multivariable analysis showed that male sex, multiple tumors, and first-line treatment failure were significantly related to treatment failure (=0.03, =0.05, =0.03, respectively).

CONCLUSION

CR of primary cMALToma was achieved using various therapeutic strategies. First-line treatment failure and multiple tumors were associated with treatment failure, although the numbers of cases that failed are too small to draw definitive conclusions.

摘要

背景

结直肠黏膜相关淋巴组织(MALT)淋巴瘤(cMALToma)较为罕见,仅占MALT淋巴瘤的2.5%。其病因及治疗方法尚未完全明确。本系统文献综述的目的是试图描述cMALToma的特征,并分析采用各种治疗策略时治疗失败的危险因素。

方法

我们通过在PubMed上检索1993年至2017年的英文医学文献,回顾了50例描述cMALToma的病例报告。我们纳入了先前病例报告中的67例患者,并增加了在我们多中心机构接受cMALToma治疗的6例患者。对治疗失败进行危险因素分析,治疗失败定义为缓解失败和复发。

结果

在73例诊断为cMALToma的患者中,肿瘤位于直肠的有54例(74.0%),右结肠的有10例(13.6%),横结肠的有3例(4.1%),乙状结肠的有6例(8.2%)。在一线治疗中,患者通过手术(18/19例)、局部切除(18/19例)、化疗(12/13例)、放疗(4/5例)、包括根除治疗的抗生素治疗(12/15例)以及未治疗(1/2例)实现了完全缓解(CR)。其中,8例(10.9%)需要二线治疗,3例(4.1%)总体缓解失败。在其余70例CR患者中,5例(6.8%)肿瘤复发。多变量分析显示,男性、多发肿瘤和一线治疗失败与治疗失败显著相关(分别为P = 0.03、P = 0.05、P = 0.03)。

结论

采用各种治疗策略可实现原发性cMALToma的CR。一线治疗失败和多发肿瘤与治疗失败相关,尽管失败病例数过少,无法得出明确结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b1b/6759223/3b97aa7f2306/CMAR-11-8577-g0001.jpg

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