Cosnes Jacques
Department of Gastroenterology, St.-Antoine Hospital, Université Paris VI, Paris, France.
Dig Dis. 2017;35(1-2):50-55. doi: 10.1159/000449083. Epub 2017 Feb 1.
Treatment of inflammatory bowel disease (IBD) in patients with prior malignancy is challenging because therapeutic immunosuppression required for controlling IBD activity may increase the risk of cancer recurrence. Key Messages: Contrary to the observations in the post-transplant population, retrospective observational studies of IBD patients with prior malignancy have not demonstrated that immunosuppressive drugs increased significantly the risk of new or recurrent cancer. However, these studies are highly biased and do not permit the use of these drugs. Factors like the time since treatment completion, severity, and subtype of prior cancer should be weighed along with the current IBD activity before choosing the best therapeutic strategy. In practice, most cases of prior cancer require a delay of at least 2 years before starting or resuming immunosuppressants, including anti-TNF agents. This delay should be extended to 5 years in cancer with a high risk of recurrence including cancer of the urinary tract, gastrointestinal cancer, leukemias, and multiple myeloma. A special attention should be paid to cancers with a high risk of late metastasis (breast, melanoma, renal cell carcinoma). Enteral nutrition, Budesonide, mesalamine, and limited intestinal resection should be considered following the completion of cancer treatment and prior to the safe initiation of immunosuppressive treatment for IBD. Thiopurines should be avoided in case of prior Epstein-Barr virus-related lymphoma, HPV-related carcinomas, and cancer of the urinary tract. Methotrexate and anti-TNF agents seem to be safe except for the risk of recurrent melanoma for the latter.
IBD patients with prior malignancy should benefit from individual decisions made on a case-by-case basis.
对既往有恶性肿瘤的炎症性肠病(IBD)患者进行治疗具有挑战性,因为控制IBD活动所需的治疗性免疫抑制可能会增加癌症复发的风险。关键信息:与移植后人群的观察结果相反,对既往有恶性肿瘤的IBD患者进行的回顾性观察研究并未表明免疫抑制药物会显著增加新发或复发性癌症的风险。然而,这些研究存在高度偏倚,且不允许使用这些药物。在选择最佳治疗策略之前,应综合考虑自治疗结束后的时间、既往癌症的严重程度和亚型以及当前的IBD活动等因素。在实际操作中,大多数既往有癌症的病例在开始或恢复使用免疫抑制剂(包括抗TNF药物)之前需要至少延迟2年。对于复发风险高的癌症,包括泌尿系统癌症、胃肠道癌症、白血病和多发性骨髓瘤,这种延迟应延长至5年。应特别关注有高晚期转移风险的癌症(乳腺癌、黑色素瘤、肾细胞癌)。在完成癌症治疗后且在安全启动IBD免疫抑制治疗之前,应考虑肠内营养、布地奈德、美沙拉嗪和有限的肠切除术。如果既往有EB病毒相关淋巴瘤、人乳头瘤病毒相关癌和泌尿系统癌症,则应避免使用硫唑嘌呤。甲氨蝶呤和抗TNF药物似乎是安全的,但后者有复发性黑色素瘤的风险。
既往有恶性肿瘤的IBD患者应从逐案做出个性化决策中获益。