Khuri Fadlo R, Lee J Jack, Lippman Scott M, Kim Edward S, Cooper Jay S, Benner Steven E, Winn Rodger, Pajak Thomas F, Williams Brendell, Shenouda George, Hodson Ian, Fu Karen, Shin Dong M, Vokes Everett E, Feng Lei, Goepfert Helmuth, Hong Waun Ki
Winship Cancer Institute/Emory University School of Medicine, Atlanta, GA 30322, USA.
J Natl Cancer Inst. 2006 Apr 5;98(7):441-50. doi: 10.1093/jnci/djj091.
Isotretinoin (13-cis-retinoic acid) is a synthetic vitamin A derivative, or retinoid, widely used in the treatment of cystic acne. Preclinical and clinical studies of high-dose isotretinoin in patients with head and neck squamous cell cancer (HNSCC) have produced encouraging results. We conducted a phase III randomized trial of low-dose isotretinoin versus placebo in early-stage HNSCC patients to assess its effect on second primary tumor incidence and survival.
We randomly assigned 1190 patients who had been treated for stage I or II HNSCC to receive either low-dose isotretinoin (30 mg/day) or placebo for 3 years. The patients were monitored for up to 4 more years. Survival was analyzed by the Kaplan-Meier method, and Cox proportional hazards models were used for multivariable survival analysis. All statistical tests were two-sided.
Isotretinoin did not statistically significantly reduce the rate of second primary tumors (hazard ratio [HR] = 1.06, 95% confidence interval [CI] = 0.83 to 1.35) or increase survival (HR = 1.03, 95% CI = 0.81 to 1.32) compared with placebo in patients with early-stage HNSCC. Current smokers had a higher rate of second primary tumors than that of never (HR = 1.64, 95% CI = 1.08 to 2.50) or former (HR = 1.32, 95% CI = 1.01 to 1.71) smokers. The hazard ratio of death from any cause for current smokers versus never smokers was 2.51 (95% CI = 1.54 to 4.10) and for current smokers versus former smokers was 1.60 (95% CI = 1.23 to 2.07). Major sites of second primary tumors (n = 261) included lung (31%), oral cavity (17%), larynx (8%), and pharynx (5%).
Low-dose isotretinoin was not effective in reducing the rate of second primary tumors or death or smoking-related disease. Smoking statistically significantly increased the rate of second primary tumors and death. Ongoing trials are testing higher doses of isotretinoin as part of combination bioadjuvant therapeutic methods for patients with locally advanced HNSCC.
异维A酸(13 - 顺式维甲酸)是一种合成的维生素A衍生物,即类视黄醇,广泛用于治疗囊肿性痤疮。对头颈部鳞状细胞癌(HNSCC)患者进行的高剂量异维A酸的临床前和临床研究已产生了令人鼓舞的结果。我们开展了一项III期随机试验,比较低剂量异维A酸与安慰剂对早期HNSCC患者第二原发性肿瘤发生率和生存率的影响。
我们将1190例已接受I期或II期HNSCC治疗的患者随机分配,使其接受低剂量异维A酸(30毫克/天)或安慰剂治疗3年。对患者进行长达4年的监测。采用Kaplan - Meier方法分析生存率,并使用Cox比例风险模型进行多变量生存分析。所有统计检验均为双侧检验。
与安慰剂相比,对于早期HNSCC患者,异维A酸在统计学上未显著降低第二原发性肿瘤的发生率(风险比[HR]=1.06,95%置信区间[CI]=0.83至1.35),也未提高生存率(HR = 1.03,95% CI = 0.81至1.32)。目前吸烟者的第二原发性肿瘤发生率高于从不吸烟者(HR = 1.64,95% CI = 1.08至2.50)或既往吸烟者(HR = 1.32,95% CI = 1.01至1.71)。目前吸烟者与从不吸烟者相比,任何原因导致死亡的风险比为2.51(95% CI = 1.54至4.10),目前吸烟者与既往吸烟者相比为1.60(95% CI = 1.23至2.07)。第二原发性肿瘤的主要部位(n = 261)包括肺部(31%)、口腔(17%)、喉部(8%)和咽部(5%)。
低剂量异维A酸在降低第二原发性肿瘤发生率、死亡率或吸烟相关疾病方面无效。吸烟在统计学上显著增加了第二原发性肿瘤的发生率和死亡率。正在进行的试验正在测试更高剂量的异维A酸,作为局部晚期HNSCC患者联合生物辅助治疗方法的一部分。