Goodman G E, Omenn G S, Thornquist M D, Lund B, Metch B, Gylys-Colwell I
Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.
Cancer Epidemiol Biomarkers Prev. 1993 Jul-Aug;2(4):389-96.
In preparation for a phase IV lung cancer chemoprevention trial, we conducted a pilot trial of beta-carotene and retinol in high-risk smokers. Eligibility criteria were ages of 50-69 years, a smoking history of at least 20 pack-years, and either being a current smoker or having quit within the past 6 years. Participants were recruited by mailing an interest survey to 29,928 age-selected members of King County Medical Blue Shield. We randomized 1,029 women and men to one of four intervention arms: placebo, retinol, 25,000 international units/day; beta-carotene, 30 mg/day; or retinol plus beta-carotene. Participants were followed for side effects and adherence every 2 months either by a telephone call or a clinic visit. Blood was sampled for retinoid, carotenoid, and liver function analyses annually. beta-carotene and retinol were well tolerated during the follow-up period, which had a median of 1.5 years and a maximum of 3.3 years. Yellowing of the skin was seen in both beta-carotene arms. No differences were seen among arms or over time in incidence or severity of the other 15 monitored symptoms and signs or in serum liver function tests. Adherence was good: 83% of participants remained active on study at 1 year and 75% at 2 years. Serum beta-carotene increased from a prerandomization median concentration of 170 to 2100 ng/ml after 4 months of supplementation, and retinyl palmitate median levels more than tripled.(ABSTRACT TRUNCATED AT 250 WORDS)
为筹备一项IV期肺癌化学预防试验,我们对高危吸烟者开展了一项β-胡萝卜素和视黄醇的试点试验。入选标准为年龄在50至69岁之间、吸烟史至少20包年,且为当前吸烟者或在过去6年内戒烟者。通过向金县医疗蓝盾29928名按年龄挑选的会员邮寄兴趣调查问卷来招募参与者。我们将1029名男性和女性随机分为四个干预组之一:安慰剂组、视黄醇组(25000国际单位/天)、β-胡萝卜素组(30毫克/天)或视黄醇加β-胡萝卜素组。每2个月通过电话或门诊随访参与者的副作用和依从性情况。每年采集血样进行类视黄醇、类胡萝卜素和肝功能分析。在中位时间为1.5年、最长为3.3年的随访期内,β-胡萝卜素和视黄醇耐受性良好。两个β-胡萝卜素组均出现皮肤发黄现象。在其他15种监测的症状和体征的发生率或严重程度以及血清肝功能检查方面,各干预组之间或随时间推移均未发现差异。依从性良好:83%的参与者在1年时仍积极参与研究,75%在2年时仍积极参与。补充4个月后,血清β-胡萝卜素从随机分组前的中位浓度170纳克/毫升增至2100纳克/毫升,视黄醇棕榈酸酯的中位水平增加了两倍多。(摘要截选至250字)