Loftus E V, Tremaine W J, Habermann T M, Harmsen W S, Zinsmeister A R, Sandborn W J
Inflammatory Bowel Disease Clinic, Division of Gastroenterology and Hepatology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
Am J Gastroenterol. 2000 Sep;95(9):2308-12. doi: 10.1111/j.1572-0241.2000.02316.x.
Inflammatory bowel disease with a subsequent diagnosis of non-Hodgkin's lymphoma has been reported. There is concern that the risk of developing lymphoma will rise with increasing use of immune modifier therapy. We determined the risk of non-Hodgkin's lymphoma in an U.S. population-based inception cohort, and evaluated the association between inflammatory bowel disease and lymphoma in our referral practice.
The records of all incidence cases of inflammatory bowel disease in Olmsted County, Minnesota, between 1950 and 1993 were reviewed for the diagnosis of lymphoma. Standardized incidence ratios (observed/expected) were used to estimate relative risk. In addition, the clinical features and outcomes of all patients with inflammatory bowel disease and lymphoma seen at Mayo Clinic between 1976 and 1997 were reviewed.
Among 454 county residents diagnosed with inflammatory bowel disease, a single non-Hodgkin's lymphoma occurred in a patient with Crohn's disease. No cases were seen with ulcerative colitis. The estimated relative risk of lymphoma was 2.4 in Crohn's disease (95% confidence interval, 0.1-13), 0 in ulcerative colitis (0-6), and 1.0 in inflammatory bowel disease overall (0.03-6). Between 1976 and June 1997, 61 patients with inflammatory bowel disease and lymphoma (approximately 0.41%) were seen in the referral practice. In four patients with Crohn's disease (13%), potential neoplastic risk factors were identified-therapeutic radiation in 1, and use of purine analogs in 3 (median length of use, 11 months).
Our population-based cohort study demonstrated that the absolute risk of non-Hodgkin's lymphoma remains quite small (0.01% per person-year). This risk may not exceed that in the general population. In our referral practice, immune modifier therapy could be potentially implicated in only 5% of cases of lymphoma occurring in the setting of inflammatory bowel disease.
有报道称炎性肠病患者随后被诊断为非霍奇金淋巴瘤。人们担心随着免疫调节剂治疗的使用增加,患淋巴瘤的风险会上升。我们确定了美国一个基于人群的起始队列中非霍奇金淋巴瘤的风险,并评估了在我们的转诊实践中炎性肠病与淋巴瘤之间的关联。
回顾了明尼苏达州奥尔姆斯特德县1950年至1993年间所有炎性肠病发病病例的记录以诊断淋巴瘤。使用标准化发病比(观察值/期望值)来估计相对风险。此外,还回顾了1976年至1997年间在梅奥诊所就诊的所有炎性肠病合并淋巴瘤患者的临床特征和结局。
在454名被诊断为炎性肠病的县居民中,1例克罗恩病患者发生了1例非霍奇金淋巴瘤。溃疡性结肠炎患者未出现病例。克罗恩病患者淋巴瘤的估计相对风险为2.4(95%置信区间,0.1 - 13),溃疡性结肠炎患者为0(0 - 6),总体炎性肠病患者为1.0(0.03 - 6)。在1976年至1997年6月期间,转诊实践中见到了第61例炎性肠病合并淋巴瘤患者(约0.41%)。在4例克罗恩病患者(13%)中,确定了潜在的肿瘤危险因素——1例接受过治疗性放疗,3例使用过嘌呤类似物(使用中位时长为11个月)。
我们基于人群的队列研究表明,非霍奇金淋巴瘤的绝对风险仍然相当小(每人年0.01%)。这种风险可能不超过一般人群。在我们的转诊实践中,免疫调节剂治疗可能仅与5%的炎性肠病背景下发生的淋巴瘤病例有关。