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Association Between Use of Thiopurines or Tumor Necrosis Factor Antagonists Alone or in Combination and Risk of Lymphoma in Patients With Inflammatory Bowel Disease

医学 硫嘌呤甲基转移酶 内科学 四分位间距 炎症性肠病 入射(几何) 联合疗法 淋巴瘤 克罗恩病 胃肠病学 回顾性队列研究 疾病 光学 物理
作者
Magali Lemaître,Julien Kirchgesner,Annie Rudnichi,Fabrice Carrat,Mahmoud Zureik,Franck Carbonnel,Rosemary Dray‐Spira
出处
期刊:JAMA [American Medical Association]
卷期号:318 (17): 1679-1679 被引量:419
标识
DOI:10.1001/jama.2017.16071
摘要

Importance

An increased risk of lymphoma has been reported among patients receiving thiopurines for inflammatory bowel disease (IBD). The risk of lymphoma associated with anti–tumor necrosis factor (TNF) agents either alone or in combination with thiopurines is uncertain.

Objective

To assess the risk of lymphoma associated with thiopurines and anti-TNF agents, used alone or in combination, for the management of IBD.

Design, Setting, and Participants

Nationwide cohort study based on French National Health Insurance databases. Patients aged 18 years or older identified with IBD were included from January 1, 2009, through December 31, 2013, and followed up until December 31, 2015.

Exposures

At each time of the follow-up, patients were categorized as being exposed to thiopurine monotherapy, anti-TNF monotherapy, or combination therapy, or being unexposed.

Main Outcomes and Measures

The primary outcome was incident lymphoma.

Results

Among the 189 289 patients included (54% women; median age, 43 years [interquartile range, 32-56 years]) and followed up for a median of 6.7 years, 123 069 were never exposed during follow-up, 50 405 were exposed to thiopurine monotherapy, 30 294 to anti-TNF monotherapy, and 14 229 to combination therapy. Overall, 336 lymphoma cases occurred: 220 in unexposed patients (incidence rate [IR] per 1000 person-years, 0.26; 95% CI, 0.23-0.29), 70 in patients exposed to thiopurine monotherapy (IR, 0.54; 95% CI, 0.41-0.67), 32 in patients exposed to anti-TNF monotherapy (IR, 0.41; 95% CI, 0.27-0.55), and 14 in patients exposed to combination therapy (IR, 0.95; 95% CI, 0.45-1.45). In a multivariable Cox model, compared with unexposed patients, the risk of lymphoma was higher among those exposed to thiopurine monotherapy (adjusted hazard ratio [aHR], 2.60; 95% CI, 1.96-3.44;P < .001), anti-TNF monotherapy (aHR, 2.41; 95% CI, 1.60-3.64;P < .001), or combination therapy (aHR, 6.11; 95% CI, 3.46-10.8;P < .001). The risk was higher in patients exposed to combination therapy vs those exposed to thiopurine monotherapy (aHR, 2.35; 95% CI, 1.31-4.22;P < .001) or anti-TNF monotherapy (aHR, 2.53; 95% CI, 1.35-4.77;P < .001).

Conclusions and Relevance

Among adults with IBD, the use of thiopurine monotherapy or anti-TNF monotherapy was associated with a small but statistically significant increased risk of lymphoma compared with exposure to neither medication, and this risk was higher with combination therapy than with each of these treatments used alone. These findings may inform decisions regarding the benefits and risks of treatment.
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