Inflammatory Bowel Disease Center, Children's Hospital Boston, Boston, Massachusetts 02115, USA.
Inflamm Bowel Dis. 2012 May;18(5):838-43. doi: 10.1002/ibd.21844. Epub 2011 Sep 1.
Prior studies suggest an increased risk of lymphoma in adults with inflammatory bowel disease (IBD). Cases of lymphoma have also been reported in children with IBD. However, the precise risk of lymphoma in relation to drug exposure has not been ascertained in children.
We conducted a single-center, retrospective study of 1560 children and young adults with IBD evaluated at Children's Hospital Boston between 1979 and 2008. Of this group, 186 patients were excluded due to incorrect diagnosis, one-time second-opinion visits, or missing hospital records. The remaining 1374 patients had charts reviewed to determine whether lymphoma developed while they were receiving their clinical care at our institution and the duration of exposure to various IBD medications. The rate of lymphoma was calculated in patient-years of exposure for each class of medications utilized in IBD.
Of 1374 patients (741 male; age at diagnosis 12.1 ± 4.0 years; 791 Crohn's disease [CD], 535 ulcerative colitis [UC], 48 IBD unclassified), we identified two patients who developed lymphoma (one Hodgkin, one anaplastic large cell), in 6624 patient-years of follow-up (mean duration follow-up 4.8 years per patient). Both patients were males (ages 12 and 18 years at time of lymphoma onset) and were receiving thiopurines but had not yet received biologics at the time of their cancer diagnosis. They were both treated with chemotherapy and are alive without cancer 32+ and 76+ months since diagnosis. The absolute incidence rate of lymphoma for patients having received thiopurines was 4.5 per 10,000 patient-years compared to the expected rate of 0.58 per 10,000 patient-years, with a standardized incidence ratio (SIR) of 7.51 (95% confidence interval [CI] 0.74-41.98).
The overall risk of lymphoma in children with IBD is low, with only two cases seen in our hospital over a 30-year period. The lymphoma risk (as estimated by SIR) in children receiving thiopurines is comparable to that reported in studies of adults. While there may be an increased risk of lymphoma in children treated with thiopurines, the risk did not reach statistical significance in this large cohort.
先前的研究表明,炎症性肠病(IBD)患者发生淋巴瘤的风险增加。也有报道称儿童 IBD 患者发生淋巴瘤。然而,儿童中与药物暴露相关的淋巴瘤的确切风险尚未确定。
我们对 1979 年至 2008 年在波士顿儿童医院接受评估的 1560 名 IBD 儿童和青少年进行了单中心回顾性研究。其中 186 例患者由于诊断错误、单次会诊或缺失住院记录而被排除在外。其余 1374 例患者的病历被审查,以确定他们在我院接受临床治疗期间是否发生淋巴瘤,以及他们接受各种 IBD 药物治疗的时间。利用在 IBD 中使用的各类药物的患者年暴露率计算淋巴瘤的发生率。
在 1374 例患者(741 例男性;诊断时年龄 12.1±4.0 岁;791 例克罗恩病[CD],535 例溃疡性结肠炎[UC],48 例 IBD 未分类)中,我们在 6624 患者年的随访中发现了 2 例淋巴瘤患者(1 例霍奇金淋巴瘤,1 例间变性大细胞淋巴瘤)(每位患者的平均随访时间为 4.8 年)。这两名患者均为男性(淋巴瘤发病时年龄分别为 12 岁和 18 岁),正在接受硫嘌呤治疗,但在癌症诊断时尚未接受生物制剂治疗。他们均接受了化疗,自诊断以来无癌生存 32+和 76+个月。接受硫嘌呤治疗的患者淋巴瘤的绝对发病率为每 10000 患者年 4.5 例,而预期发病率为每 10000 患者年 0.58 例,标准化发病率比(SIR)为 7.51(95%置信区间[CI]为 0.74-41.98)。
IBD 儿童的总体淋巴瘤风险较低,在我们医院 30 年的时间内仅发现了两例。接受硫嘌呤治疗的儿童的淋巴瘤风险(通过 SIR 估计)与成人研究报告的风险相当。虽然接受硫嘌呤治疗的儿童发生淋巴瘤的风险可能增加,但在这个大型队列中未达到统计学意义。