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1
Refractory celiac disease and EATL patients show severe malnutrition and malabsorption at diagnosis.难治性乳糜泻和肠病相关T细胞淋巴瘤患者在诊断时表现出严重营养不良和吸收不良。
Clin Nutr. 2016 Jun;35(3):685-91. doi: 10.1016/j.clnu.2015.04.014. Epub 2015 Apr 30.
2
The composition and differentiation potential of the duodenal intraepithelial innate lymphocyte compartment is altered in coeliac disease.乳糜泻患者十二指肠上皮固有淋巴细胞区的组成和分化潜能发生改变。
Gut. 2016 Aug;65(8):1269-78. doi: 10.1136/gutjnl-2014-308153. Epub 2015 May 12.
3
Mucosal histopathology in celiac disease: a rebuttal of Oberhuber's sub-division of Marsh III.乳糜泻的黏膜组织病理学:对奥伯胡伯对马什III型细分的反驳
Gastroenterol Hepatol Bed Bench. 2015 Spring;8(2):99-109.
4
Video capsule endoscopy in patients with nonresponsive celiac disease.视频胶囊内镜在对不耐受的腹腔疾病患者中的应用。
J Clin Gastroenterol. 2013 May-Jun;47(5):393-9. doi: 10.1097/MCG.0b013e31826bea12.
5
Refractory celiac disease: from bench to bedside.难治性乳糜泻:从基础到临床。
Semin Immunopathol. 2012 Jul;34(4):601-13. doi: 10.1007/s00281-012-0322-z. Epub 2012 Jul 19.
6
MR enteroclysis in refractory celiac disease: proposal and validation of a severity scoring system.磁共振肠造影术在难治性乳糜泻中的应用:严重程度评分系统的提出与验证。
Radiology. 2011 Apr;259(1):151-61. doi: 10.1148/radiol.11101808. Epub 2011 Feb 17.
7
Evaluation of Cladribine treatment in refractory celiac disease type II.评估克拉屈滨治疗难治性 II 型乳糜泻的效果。
World J Gastroenterol. 2011 Jan 28;17(4):506-13. doi: 10.3748/wjg.v17.i4.506.
8
Auto-SCT in refractory celiac disease type II patients unresponsive to cladribine therapy.自身造血干细胞移植治疗对克拉屈滨治疗无反应的难治性 II 型乳糜泻患者。
Bone Marrow Transplant. 2011 Jun;46(6):840-6. doi: 10.1038/bmt.2010.199. Epub 2010 Sep 6.
9
Novel approaches in the management of refractory celiac disease.难治性乳糜泻的治疗新方法。
Expert Rev Clin Immunol. 2008 Mar;4(2):205-19. doi: 10.1586/1744666X.4.2.205.
10
Double-balloon endoscopy as the primary method for small-bowel video capsule endoscope retrieval.双气囊内镜作为小肠胶囊内镜取出的主要方法。
Gastrointest Endosc. 2010 Mar;71(3):535-41. doi: 10.1016/j.gie.2009.10.029.

II型难治性乳糜泻中的淋巴瘤发生与生存:组织学反应作为预后因素

Lymphoma development and survival in refractory coeliac disease type II: Histological response as prognostic factor.

作者信息

Nijeboer P, van Wanrooij Rlj, van Gils T, Wierdsma N J, Tack G J, Witte B I, Bontkes H J, Visser O, Mulder Cjj, Bouma G

机构信息

Department of Gastroenterology, VU University Medical Centre, Amsterdam, The Netherlands.

Department of Nutrition and Dietetics, VU University Medical Centre, Amsterdam, The Netherlands.

出版信息

United European Gastroenterol J. 2017 Mar;5(2):208-217. doi: 10.1177/2050640616646529. Epub 2016 Jun 23.

DOI:10.1177/2050640616646529
PMID:28344788
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5349358/
Abstract

BACKGROUND

Refractory coeliac disease type II (RCDII) frequently transforms into an enteropathy-associated T-cell lymphoma (EATL) and therefore requires intensive treatment. Current evaluated treatment strategies for RCDII include cladribine (2-CdA) and autologous stem cell transplantation (auSCT).

OBJECTIVE

The purpose of this study was to evaluate long-term survival and define clear prognostic criteria for EATL development comparing two treatment strategies.

METHODS

A total of 45 patients were retrospectively analysed. All patients received 2-CdA, after which they were either closely monitored (monotherapy,  = 30) or a step-up approach was used including auSCT (step-up therapy,  = 15).

RESULTS

Ten patients (22%) ultimately developed EATL; nine of these had received monotherapy. Absence of histological remission after monotherapy was associated with EATL development ( = 0.010). Overall, 20 patients (44%) died with a median survival of 84 months. Overall survival (OS) within the monotherapy group was significantly worse in those without histological remission compared to those with complete histological remission( = 0.030). The monotherapy group who achieved complete histological remission showed comparable EATL occurrence and OS as compared to the step-up therapy group ( = 0.80 and  = 0.14 respectively).

CONCLUSION

Histological response is an accurate parameter to evaluate the effect of 2-CdA therapy and this parameter should be leading in the decisions whether or not to perform a step-up treatment approach in RCDII.

摘要

背景

II型难治性乳糜泻(RCDII)常转变为肠病相关T细胞淋巴瘤(EATL),因此需要强化治疗。目前评估的RCDII治疗策略包括克拉屈滨(2-CdA)和自体干细胞移植(auSCT)。

目的

本研究旨在比较两种治疗策略,评估EATL发生的长期生存率并确定明确的预后标准。

方法

对45例患者进行回顾性分析。所有患者均接受2-CdA治疗,之后要么密切监测(单一疗法,n = 30),要么采用包括auSCT的逐步治疗方法(逐步治疗,n = 15)。

结果

10例患者(22%)最终发生EATL;其中9例接受单一疗法。单一疗法后组织学未缓解与EATL发生相关(P = 0.010)。总体而言,20例患者(44%)死亡,中位生存期为84个月。单一疗法组中,组织学未缓解者的总生存期(OS)明显差于组织学完全缓解者(P = 0.030)。与逐步治疗组相比,组织学完全缓解的单一疗法组的EATL发生率和OS相当(分别为P = 0.80和P = 0.14)。

结论

组织学反应是评估2-CdA治疗效果的准确参数,该参数应作为决定是否对RCDII进行逐步治疗的主导因素。