Enteropathy-associated T-cell lymphoma: A review on clinical presentation, diagnosis, therapeutic strategies and perspectives

M.-O. Chandesris , G. Malamut , V. Verkarre , B. Meresse , E. Macintyre , R. Delarue , M.-T. Rubio , F. Suarez , B. Deau-Fischer , N. Cerf-Bensussan , N. Brousse , C. Cellier , O. Hermine
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引用次数: 40

Abstract

Introduction

Enteropathy-associated T-cell lymphoma (EATL) is a rare complication of celiac disease (<1% of lymphomas) and has a poor prognosis.

Methods

International literature review with PubMed search (up to January 2009) of pathophysiological, clinical and therapeutic data.

Results

EATL is found in patients with a mean age of 59 years, often with a complication that signals its diagnosis. Refractory celiac disease (RCD), equivalent to low-grade intraepithelial T-cell lymphoma, could be an intermediary between celiac disease and high-grade invasive T-cell lymphoma. The median survival is 7 months, with no significant difference between stages; the cumulative 5-year survival is less than 20%. The poor prognosis is determined by disease that has often spread before it is diagnosed (50%), multifocal involvement of the small bowel (50%), poor general health status and undernutrition, and recurrence of complications (infections, perforations, gastrointestinal haemorrhages, occlusions), thus delaying the chemotherapy and contributing to frequent chemotherapy resistance. There is currently no effective and consensual treatment: preventive surgery for complications is controversial, and the results of chemotherapy are disappointing. The classic CHOP protocol (combination of doxorubicin–cyclophosphamide–vincristine–prednisone) does not have satisfactory results and survival remains poor, especially in patients with underlying RCD. High-dose chemotherapy with autotransplantion seems to only improve the prognosis in localised forms. Allogeneic bone marrow transplantation was not evaluated. In all, 1/3 of patients, being unfit for treatment, die before 3 months and half of treated patients stop chemotherapy prematurely due to inefficacy, intolerance and/or complications.

Conclusion

Improvement of the prognosis requires collaboration in order to compose a national cohort, to evaluate new diagnostic and therapeutic strategies and to define prognostic factors.

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肠病相关t细胞淋巴瘤:临床表现,诊断,治疗策略和观点的综述
肠病相关t细胞淋巴瘤(enteropathy -associated T-cell lymphoma, EATL)是一种罕见的腹腔疾病并发症(占淋巴瘤的1%),预后较差。方法采用PubMed检索(截至2009年1月)的国际文献综述,检索病理生理、临床和治疗数据。结果seatl见于平均年龄59岁的患者,常伴有并发症。难治性乳糜泻(RCD),相当于低级别上皮内t细胞淋巴瘤,可能是乳糜泻和高级别侵袭性t细胞淋巴瘤之间的中介。中位生存期为7个月,分期间无显著差异;累计5年生存率低于20%。不良预后是由以下因素决定的:疾病往往在确诊前就已经扩散(50%)、小肠多灶性受累(50%)、一般健康状况不佳和营养不良、并发症(感染、穿孔、胃肠道出血、闭塞)复发,从而推迟化疗时间并导致化疗频繁产生耐药性。目前还没有有效和双方同意的治疗方法:并发症的预防性手术是有争议的,化疗的结果令人失望。经典CHOP方案(多柔比星-环磷酰胺-长春新碱-泼尼松联合治疗)没有令人满意的结果,生存率仍然很低,特别是对于有潜在RCD的患者。自体移植的大剂量化疗似乎只能改善局部形式的预后。异体骨髓移植未被评估。总而言之,1/3不适合治疗的患者在3个月内死亡,一半接受治疗的患者因无效、不耐受和/或并发症而过早停止化疗。结论改善预后需要合作,以组成一个国家队列,评估新的诊断和治疗策略,并确定预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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