Survival in refractory coeliac disease and enteropathy-associated T-cell lymphoma: retrospective evaluation of single-centre experience
Top Cited Papers
- 1 October 2007
- Vol. 56 (10) , 1373-1378
- https://doi.org/10.1136/gut.2006.114512
Abstract
Background: Coeliac disease may be regarded as refractory disease (RCD) when symptoms persist or recur despite strict adherence to a gluten-free diet. RCD may be subdivided into types I and II with a phenotypically normal and aberrant intraepithelial T-cell population, respectively. RCD I seems to respond well to azathioprine/prednisone therapy. RCD II is usually resistant to any known therapy and transition into enteropathy-associated T-cell lymphoma (EATL) is common. Aim: To provide further insight into RCD and the development of EATL, by reporting on long-term survival and risk of transition of RCD into EATL in a large cohort of patients with complicated coeliac disease. Design and Methods: Retrospective comparison of responses to therapy in four groups of patients with complicated coeliac disease: 43, RCD I; 50, RCD II (total), of whom 26 with RCD II developed EATL after a period of refractoriness to a gluten-free diet (secondary EATL) and 13 were EATL patients without preceding history of complicated coeliac disease (de novo EATL). Results: No coeliac-disease-related mortality was recognised in the RCD I group. The overall 5-year survival in the RCD I group it was 96%; in the RCD II (total) group was 58%; and in the RCD II group after developing EATL it was only 8%. The 2-year survival in the de novo EATL group was 20% versus 15% in secondary EATL group (p = 0.63). Twenty-eight (56%) of the 50 patients with RCD II died, 23 (46%) due to EATL, 4 due to a progressive refractory state with emaciation and 1 from neurocoeliac disease. Conclusion: Remarkably, no patient with RCD I developed RCD II or EATL within the mean follow-up period of 5 years (range 2–15 years). A total of 52% of the RCD II patients developed EATL within 4–6 years after the diagnosis of RCD II. More aggressive and targeted therapies seem necessary in RCD II and EATL.Keywords
This publication has 44 references indexed in Scilit:
- Cladribine Therapy in Refractory Celiac Disease With Aberrant T CellsClinical Gastroenterology and Hepatology, 2006
- Autologous hematopoietic stem cell transplantation in refractory celiac disease with aberrant T cellsBlood, 2006
- Double-Balloon Enteroscopy: Indications, Diagnostic Yield, and Complications in a Series of 275 Patients with Suspected Small-Bowel DiseaseEndoscopy, 2006
- Transformation and progression of Waldenström's macroglobulinemia following cladribine therapy in two cases: natural evolution or iatrogenic causation?American Journal of Hematology, 2006
- Refractory sprue, coeliac disease, and enteropathy-associated T-cell lymphomaThe Lancet, 2000
- Distinction between coeliac disease and refractory sprue: a simple immunohistochemical methodHistopathology, 2000
- Intestinal lymphoma and enteropathyThe Journal of Pathology, 1995
- A gene dosage effect of the DQA1∗0501/DQB1∗0201 allelic combination influences the clinical heterogeneity of celiac diseaseHuman Immunology, 1994
- Primary Lymphoma of the Small Intestine A. Clinicopathological Study of 119 CasesThe American Journal of Surgical Pathology, 1993
- Typing of HLA-DQA1 and DQB1 using DNA single-strand conformation polymorphismHuman Immunology, 1992