Meyskens Frank L, McLaren Christine E, Pelot Daniel, Fujikawa-Brooks Sharon, Carpenter Philip M, Hawk Ernest, Kelloff Gary, Lawson Michael J, Kidao Jayashri, McCracken John, Albers C Gregory, Ahnen Dennis J, Turgeon D Kim, Goldschmid Steven, Lance Peter, Hagedorn Curt H, Gillen Daniel L, Gerner Eugene W
Chao Family Comprehensive Cancer Center, University of California Irvine, Irvine, California, USA.
Cancer Prev Res (Phila). 2008 Jun;1(1):32-8. doi: 10.1158/1940-6207.CAPR-08-0042.
Preclinical studies of chemoprevention drugs given in combination at low doses show remarkable efficacy in preventing adenomas with little additional toxicities, suggesting a strategy to improve risk to benefit ratios for preventing recurrent adenomas. Three hundred seventy-five patients with history of resected (> or =3 mm) adenomas were randomly assigned to receive oral difluoromethylornithine (DFMO) 500 mg and sulindac 150 mg once daily or matched placebos for 36 months, stratified by use of low-dose aspirin (81 mg) at baseline and clinical site. Follow-up colonoscopy was done 3 years after randomization or off-study. Colorectal adenoma recurrence was compared among the groups with log-binomial regression. Comparing the outcome in patients receiving placebos to those receiving active intervention, (a) the recurrence of one or more adenomas was 41.1% and 12.3% (risk ratio, 0.30; 95% confidence interval, 0.18-0.49; P < 0.001); (b) 8.5% had one or more advanced adenomas, compared with 0.7% of patients (risk ratio, 0.085; 95% confidence interval, 0.011-0.65; P < 0.001); and (c) 17 (13.2%) patients had multiple adenomas (>1) at the final colonoscopy, compared with 1 (0.7%; risk ratio, 0.055; 0.0074-0.41; P < 0.001). Serious adverse events (grade > or =3) occurred in 8.2% of patients in the placebo group, compared with 11% in the active intervention group (P = 0.35). There was no significant difference in the proportion of patients reporting hearing changes from baseline. Recurrent adenomatous polyps can be markedly reduced by a combination of low oral doses of DFMO and sulindac and with few side effects.
低剂量联合使用化学预防药物的临床前研究表明,其在预防腺瘤方面具有显著疗效,且几乎没有额外的毒性,这提示了一种改善预防复发性腺瘤风险效益比的策略。375例有切除(≥3毫米)腺瘤病史的患者被随机分配,每天口服500毫克二氟甲基鸟氨酸(DFMO)和150毫克舒林酸,或服用匹配的安慰剂,为期36个月,根据基线时是否使用低剂量阿司匹林(81毫克)和临床部位进行分层。随机分组3年后或研究结束后进行随访结肠镜检查。采用对数二项回归比较各组结直肠腺瘤复发情况。将接受安慰剂治疗的患者与接受积极干预的患者的结果进行比较,(a)一个或多个腺瘤的复发率分别为41.1%和12.3%(风险比,0.30;95%置信区间,0.18 - 0.49;P < 0.001);(b)8.5%的患者有一个或多个高级别腺瘤,而患者中这一比例为0.7%(风险比,0.085;95%置信区间,0.011 - 0.65;P < 0.001);(c)在最后一次结肠镜检查时,17例(13.2%)患者有多个(>1个)腺瘤,而在安慰剂组中这一比例为1例(0.7%;风险比,0.055;0.0074 - 0.41;P < 0.001)。安慰剂组8.2%的患者发生严重不良事件(≥3级),积极干预组为11%(P = 0.35)。报告听力与基线相比有变化的患者比例无显著差异。口服低剂量DFMO和舒林酸联合使用可显著减少复发性腺瘤性息肉,且副作用很少。