Suppr超能文献

原发性胃肠道套细胞淋巴瘤:一项回顾性研究。

Primary gastrointestinal mantle cell lymphoma: a retrospective study.

作者信息

Dasappa Lokanatha, Suresh Babu M C, Sirsath Nagesh T, Suresh T M, Govind Babu K, Sathyanarayna Vishwanatha, Lokesh K N, Lakshmaiah K C

机构信息

Department of Medical Oncology, Kidwai Memorial Institute of Oncology, M.H. Mari Gowda Road, Banglore, Karnataka, 560029, India.

出版信息

J Gastrointest Cancer. 2014 Dec;45(4):481-6. doi: 10.1007/s12029-014-9655-2.

Abstract

INTRODUCTION

Primary gastrointestinal tract mantle cell lymphoma is very rare. There is paucity of literature regarding natural history and outcome of this unusual entity.

AIMS AND OBJECTIVES

The aim of the present study was to analyze clinical profile, epidemiological parameters, and outcome of primary gastrointestinal mantle cell lymphoma patients treated at our institute.

MATERIALS AND METHODS

This was a retrospective observational study of consecutive patients diagnosed with primary gastrointestinal mantle cell lymphoma at our institute between 2001 and 2012.

RESULTS

A total of seven patients, all males with a median age of 67.7 years, were diagnosed with primary gastrointestinal mantle cell lymphoma. Sites involved were the stomach, colon, and rectum. Blastoid and diffuse variants were observed in three patients each, and one patient had nodular pattern. Five patients received cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP) chemotherapy. Only one patient achieved complete remission and remained disease free for 21 months before being lost to follow up. The remaining four patients had inadequate response to CHOP chemotherapy with a median survival of 6 months. Cyclophosphamide, vincristine, prednisolone (CVP) was given to one patient in view of poor performance status. He had progressive disease and died after first cycle of chemotherapy. One patient is currently undergoing treatment and receiving rituximab with chemotherapy.

CONCLUSIONS

Primary gastrointestinal mantle cell lymphoma is highly aggressive with the Mantle Cell Lymphoma International Prognostic Index (MIPI) scores in high-risk group; survival is poor compared to nodal mantle cell lymphoma involving the gastrointestinal tract; patients respond poorly to CHOP chemotherapy. As majority of patients are elderly and not eligible for transplant, the use of rituximab in remission induction and maintenance should be considered to improve outcome of these patients.

摘要

引言

原发性胃肠道套细胞淋巴瘤非常罕见。关于这一特殊实体的自然病史和转归的文献较少。

目的

本研究旨在分析我院治疗的原发性胃肠道套细胞淋巴瘤患者的临床特征、流行病学参数及转归。

材料与方法

这是一项对2001年至2012年间在我院连续诊断为原发性胃肠道套细胞淋巴瘤的患者进行的回顾性观察研究。

结果

共有7例患者被诊断为原发性胃肠道套细胞淋巴瘤,均为男性,中位年龄67.7岁。受累部位为胃、结肠和直肠。3例患者观察到母细胞样和弥漫性变异型,1例患者为结节型。5例患者接受了环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗。仅1例患者达到完全缓解,在失访前无病生存21个月。其余4例患者对CHOP化疗反应不佳,中位生存期为6个月。鉴于患者身体状况较差,1例患者给予环磷酰胺、长春新碱、泼尼松(CVP)化疗。他病情进展,在化疗第一周期后死亡。1例患者目前正在接受治疗,接受利妥昔单抗联合化疗。

结论

原发性胃肠道套细胞淋巴瘤侵袭性强,根据套细胞淋巴瘤国际预后指数(MIPI)评分属于高危组;与累及胃肠道的结外型套细胞淋巴瘤相比,生存率较低;患者对CHOP化疗反应不佳。由于大多数患者为老年人且不符合移植条件,应考虑在缓解诱导和维持治疗中使用利妥昔单抗以改善这些患者的转归。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验