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炎症性肠病患者非黑素瘤皮肤癌风险增加。

Increased risk for non-melanoma skin cancer in patients with inflammatory bowel disease.

机构信息

Division of Gastroenterology and Hepatology, University of North Carolina, Chapel Hill, North Carolina 27599-7080, USA.

出版信息

Clin Gastroenterol Hepatol. 2010 Mar;8(3):268-74. doi: 10.1016/j.cgh.2009.11.024. Epub 2010 Jan 16.

Abstract

BACKGROUND & AIMS: Patients with inflammatory bowel disease (IBD) might be at increased risk for certain malignancies. We evaluated the risk of non-melanoma skin cancer (NMSC) in patients with IBD and determined how immunosuppressive and biologic medications affect this risk.

METHODS

We performed retrospective cohort and nested case-control studies by using administrative data from PharMetrics Patient Centric Database. In the cohort study, 26,403 patients with Crohn's disease (CD) and 26,974 patients with ulcerative colitis (UC) were each matched to 3 non-IBD controls. NMSC risk was evaluated by incidence rate ratio (IRR). In the nested case-control study, 387 CD patients and 355 UC patients with NMSC were each matched to 4 IBD patients without NMSC by using incidence density sampling. Conditional logistic regression was used to determine the association between specific IBD medication use and NMSC.

RESULTS

In the cohort study, the incidence of NMSC was higher among patients with IBD compared with controls (IRR, 1.64; 95% confidence interval [CI], 1.51-1.78). In the nested-case control study, recent thiopurine use (< or =90 days) was associated with NMSC (adjusted odds ratio [OR], 3.56; 95% CI, 2.81-4.50), as was recent biologic use among patients with CD (adjusted OR, 2.07; 95% CI, 1.28-3.33). Persistent thiopurine use (>365 days) was associated with NMSC (adjusted OR, 4.27; 95% CI, 3.08-5.92), as was persistent biologic use among patients with CD (adjusted OR, 2.18; 95% CI, 1.07-4.46).

CONCLUSIONS

Patients with IBD, especially those who receive thiopurines, are at risk for NMSC. Appropriate counseling and monitoring of such patients with IBD are recommended.

摘要

背景与目的

炎症性肠病(IBD)患者可能存在某些恶性肿瘤的高风险。我们评估了 IBD 患者罹患非黑色素瘤皮肤癌(NMSC)的风险,并确定了免疫抑制和生物药物对这种风险的影响。

方法

我们利用 PharMetrics 患者中心数据库的管理数据,进行了回顾性队列和巢式病例对照研究。在队列研究中,26403 例克罗恩病(CD)患者和 26974 例溃疡性结肠炎(UC)患者分别与 3 例非 IBD 对照相匹配。通过发病率比率(IRR)评估 NMSC 风险。在巢式病例对照研究中,使用发病率密度抽样法,387 例 CD 患者和 355 例 UC 患者的 NMSC 与 4 例 IBD 无 NMSC 患者相匹配。采用条件逻辑回归分析特定 IBD 药物使用与 NMSC 之间的关联。

结果

在队列研究中,IBD 患者的 NMSC 发生率高于对照组(IRR,1.64;95%置信区间[CI],1.51-1.78)。在巢式病例对照研究中,最近使用硫嘌呤(<或=90 天)与 NMSC 相关(调整后的比值比[OR],3.56;95%CI,2.81-4.50),CD 患者最近使用生物制剂也与 NMSC 相关(调整后的 OR,2.07;95%CI,1.28-3.33)。持续使用硫嘌呤(>365 天)与 NMSC 相关(调整后的 OR,4.27;95%CI,3.08-5.92),CD 患者持续使用生物制剂也与 NMSC 相关(调整后的 OR,2.18;95%CI,1.07-4.46)。

结论

IBD 患者,尤其是接受硫嘌呤治疗的患者,罹患 NMSC 的风险增加。建议对这类 IBD 患者进行适当的咨询和监测。

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