Matula Sierra, Croog Victoria, Itzkowitz Steven, Harpaz Noam, Bodian Carol, Hossain Sabera, Ullman Thomas
Dr. Henry D. Janowitz Division of Gastroenterology, Department of Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.
Clin Gastroenterol Hepatol. 2005 Oct;3(10):1015-21. doi: 10.1016/s1542-3565(05)00738-x.
BACKGROUND & AIMS: Evidence suggests that mesalamine-based anti-inflammatory medicines may prevent colorectal cancer (CRC) in ulcerative colitis (UC). If mesalamine exerts its chemopreventive effect by its anti-inflammatory activity, then other medications that reduce colitis activity also should possess chemopreventive properties. Our aim was to determine the effect of the immunomodulators 6-mercaptopurine (6MP) and azathioprine (AZA) in preventing the development of dysplasia or CRC in UC.
Patients with UC who underwent a surveillance colonoscopy in 1996-1997 were identified from a gastrointestinal pathology database. A proportional hazards analysis assessing 6MP/AZA use as a time-changing covariate was performed to evaluate the effect of 6MP/AZA on: (1) progression to any neoplasia (low-grade dysplasia, high-grade dysplasia, or CRC), and (2) progression to advanced neoplasia (high-grade dysplasia or CRC).
A total of 315 subjects met inclusion criteria and were followed for an average of 8 years from their first surveillance examination. There were no significant differences in rates of progression to advanced neoplasia or to any neoplasia between 6MP/AZA users and never-users by log-rank testing. The proportional hazards analysis resulted in hazard ratios of 1.06 (95% confidence interval, .59-1.93) and 1.30 (95% confidence interval, .45-3.75) when considering the effect of exposure to 6MP/AZA on progression to any or to advanced neoplasia, respectively. The results were unaffected by known potential confounders.
In UC patients with no initial history of dysplasia, 6MP/AZA use appears to have little or no effect on the rate of neoplastic transformation in the colon. Importantly, the use of 6MP/AZA did not increase malignant transformation in UC.
有证据表明,基于美沙拉嗪的抗炎药物可能预防溃疡性结肠炎(UC)患者发生结直肠癌(CRC)。如果美沙拉嗪通过其抗炎活性发挥化学预防作用,那么其他降低结肠炎活动度的药物也应具有化学预防特性。我们的目的是确定免疫调节剂6-巯基嘌呤(6MP)和硫唑嘌呤(AZA)在预防UC患者发育异常或CRC方面的作用。
从胃肠病理数据库中识别出1996 - 1997年接受监测结肠镜检查的UC患者。进行比例风险分析,将6MP/AZA的使用作为随时间变化的协变量,以评估6MP/AZA对以下方面的影响:(1)进展为任何肿瘤(低级别发育异常、高级别发育异常或CRC),以及(2)进展为高级别肿瘤(高级别发育异常或CRC)。
共有315名受试者符合纳入标准,从首次监测检查开始平均随访8年。通过对数秩检验,6MP/AZA使用者和从未使用者在进展为高级别肿瘤或任何肿瘤的发生率上没有显著差异。在考虑6MP/AZA暴露对进展为任何肿瘤或高级别肿瘤的影响时,比例风险分析得出的风险比分别为1.06(95%置信区间,0.59 - 1.93)和1.30(95%置信区间,0.45 - 3.75)。结果不受已知潜在混杂因素的影响。
在无初始发育异常病史的UC患者中,使用6MP/AZA似乎对结肠肿瘤转化速率几乎没有影响或无影响。重要的是,使用6MP/AZA并未增加UC患者的恶性转化。