Farrell R J, Ang Y, Kileen P, O'Briain D S, Kelleher D, Keeling P W, Weir D G
Department of Clinical Medicine and Gastroenterology, St James's Hospital, Trinity College Dublin, Republic of Ireland.
Gut. 2000 Oct;47(4):514-9. doi: 10.1136/gut.47.4.514.
There is concern that the incidence of non-Hodgkin's lymphoma (NHL) will rise with increasing use of immunosuppressive therapy.
Our aim was to determine the risk of NHL in a large cohort of patients with inflammatory bowel disease (IBD), and to study the association between IBD, NHL, and immunosuppressive therapy.
We studied 782 IBD patients (238 of whom received immunosuppressive therapy) who attended our medical centre between 1990 and 1999 (median follow up 8.0 years). Standardised incidence ratios (SIRs) and 95% confidence intervals (CI) were calculated. Expected cases were derived from 1995 age and sex specific incidence rates recorded by the National Cancer Registry of Ireland.
There were four cases of NHL in our IBD cohort (SIR 31.2; 95% CI 2.0-85; p=0.0001), all of whom had received immunosuppressive therapy: azathioprine (n=2), methotrexate (n=1), and methotrexate and cyclosporin (n=1). Our immunosuppressive group had a significantly (59 times) higher risk of NHL compared with that expected in the general population (p=0.0001). Three cases were intestinal NHL and one was mesenteric. Mean age at NHL diagnosis was 49 years, mean duration of IBD at the time of NHL diagnosis was 3.1 years, and mean duration between initiation of immunosuppressive therapy and diagnosis of NHL was 20 months.
Although underlying IBD may be a causal factor in the development of intestinal NHL, our experience suggests that immunosuppressive drugs can significantly increase the risk of NHL in IBD. This must be weighed against the improved quality of life and clinical benefit immunosuppressive therapy provides for IBD patients.
人们担心随着免疫抑制疗法使用的增加,非霍奇金淋巴瘤(NHL)的发病率会上升。
我们的目的是确定一大群炎症性肠病(IBD)患者患NHL的风险,并研究IBD、NHL和免疫抑制疗法之间的关联。
我们研究了1990年至1999年间在我们医疗中心就诊的782例IBD患者(其中238例接受了免疫抑制疗法)(中位随访时间8.0年)。计算了标准化发病率(SIRs)和95%置信区间(CI)。预期病例来自爱尔兰国家癌症登记处记录的1995年年龄和性别特异性发病率。
我们的IBD队列中有4例NHL(SIR 31.2;95%CI 2.0 - 85;p = 0.0001),所有患者均接受了免疫抑制疗法:硫唑嘌呤(n = 2)、甲氨蝶呤(n = 1)以及甲氨蝶呤和环孢素(n = 1)。与普通人群预期相比,我们的免疫抑制组患NHL的风险显著高(59倍)(p = 0.0001)。3例为肠道NHL,1例为肠系膜NHL。NHL诊断时的平均年龄为49岁,NHL诊断时IBD的平均病程为3.1年,免疫抑制疗法开始至NHL诊断的平均时间为20个月。
虽然潜在的IBD可能是肠道NHL发生的一个病因,但我们的经验表明免疫抑制药物可显著增加IBD患者患NHL的风险。这必须与免疫抑制疗法为IBD患者带来的生活质量改善和临床益处相权衡。