Management of Inflammatory Bowel Disease Patients with a Cancer History

被引:18
|
作者
Beaugerie, Laurent [1 ,2 ,3 ]
机构
[1] Hop St Antoine, AP HP, Dept Gastroenterol, F-75012 Paris, France
[2] Univ Paris 06, INSERM, ERL 1057, UMRS 7203, F-75005 Paris, France
[3] Univ Paris 06, GRC UPMC 03, F-75005 Paris, France
关键词
Biologics; cancer recurrence; immunosuppressive therapy; second cancer; ORGAN TRANSPLANT RECIPIENTS; NONMELANOMA SKIN CANCERS; NECROSIS FACTOR THERAPY; RHEUMATOID-ARTHRITIS; RECEIVE THIOPURINES; BIOLOGICS REGISTER; CROHNS-DISEASE; RISK; AZATHIOPRINE; MALIGNANCIES;
D O I
10.2174/1389450115666140821113330
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In Inflammatory Bowel Disease (IBD) patients, thiopurines promote carcinogenesis of Epstein-Barr Virus (EBV)-related lymphomas, non-melanoma skin cancers and urinary tract cancers, while anti-TNF agents could promote carcinogenesis of melanomas. Patients with IBD and previous cancer are at a higher risk of developing new or recurrent cancer than IBD patients without a history of cancer, irrespective of the use of immunosuppressants. In transplant recipients, the use of thiopurines is associated with a high rate of cancer recurrence, particularly within the first two years following transplantation. In patients with chronic inflammatory disease, limited data suggest that no dramatic incidence of cancer recurrence is associated with the use of thiopurines or anti-TNF agents. However, there is a rationale for a two-year drug holiday from immunosuppressants after the diagnosis and treatment of the majority of incident cancers, as often as possible. Extending the duration of the immunosuppressant drug holiday to 5 years in patients with previous cancers associated with a high risk of recurrence in the post-transplant state should be considered. The immunosuppressants that can be initiated or resumed after cancer treatment should be chosen according to the type of the previous cancer. All individual decisions should be made on a case-by-case basis, together with the oncologist, according to characteristics and expected evolution of the index cancer, expected impact of the immunosuppressants on cancer evolution, and intrinsic severity of IBD, with its associated risks.
引用
收藏
页码:1042 / 1048
页数:7
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