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吉非替尼或卡铂-紫杉醇用于治疗肺腺癌。

Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma.

作者信息

Mok Tony S, Wu Yi-Long, Thongprasert Sumitra, Yang Chih-Hsin, Chu Da-Tong, Saijo Nagahiro, Sunpaweravong Patrapim, Han Baohui, Margono Benjamin, Ichinose Yukito, Nishiwaki Yutaka, Ohe Yuichiro, Yang Jin-Ji, Chewaskulyong Busyamas, Jiang Haiyi, Duffield Emma L, Watkins Claire L, Armour Alison A, Fukuoka Masahiro

机构信息

State Key Laboratory in Oncology in South China, Sir YK Pao Centre for Cancer, Department of Clinical Oncology, Chinese University of Hong Kong, Hong Kong.

出版信息

N Engl J Med. 2009 Sep 3;361(10):947-57. doi: 10.1056/NEJMoa0810699. Epub 2009 Aug 19.

Abstract

BACKGROUND

Previous, uncontrolled studies have suggested that first-line treatment with gefitinib would be efficacious in selected patients with non-small-cell lung cancer.

METHODS

In this phase 3, open-label study, we randomly assigned previously untreated patients in East Asia who had advanced pulmonary adenocarcinoma and who were nonsmokers or former light smokers to receive gefitinib (250 mg per day) (609 patients) or carboplatin (at a dose calculated to produce an area under the curve of 5 or 6 mg per milliliter per minute) plus paclitaxel (200 mg per square meter of body-surface area) (608 patients). The primary end point was progression-free survival.

RESULTS

The 12-month rates of progression-free survival were 24.9% with gefitinib and 6.7% with carboplatin-paclitaxel. The study met its primary objective of showing the noninferiority of gefitinib and also showed its superiority, as compared with carboplatin-paclitaxel, with respect to progression-free survival in the intention-to-treat population (hazard ratio for progression or death, 0.74; 95% confidence interval [CI], 0.65 to 0.85; P<0.001). In the subgroup of 261 patients who were positive for the epidermal growth factor receptor gene (EGFR) mutation, progression-free survival was significantly longer among those who received gefitinib than among those who received carboplatin-paclitaxel (hazard ratio for progression or death, 0.48; 95% CI, 0.36 to 0.64; P<0.001), whereas in the subgroup of 176 patients who were negative for the mutation, progression-free survival was significantly longer among those who received carboplatin-paclitaxel (hazard ratio for progression or death with gefitinib, 2.85; 95% CI, 2.05 to 3.98; P<0.001). The most common adverse events were rash or acne (in 66.2% of patients) and diarrhea (46.6%) in the gefitinib group and neurotoxic effects (69.9%), neutropenia (67.1%), and alopecia (58.4%) in the carboplatin-paclitaxel group.

CONCLUSIONS

Gefitinib is superior to carboplatin-paclitaxel as an initial treatment for pulmonary adenocarcinoma among nonsmokers or former light smokers in East Asia. The presence in the tumor of a mutation of the EGFR gene is a strong predictor of a better outcome with gefitinib. (ClinicalTrials.gov number, NCT00322452.)

摘要

背景

既往非对照研究提示,吉非替尼一线治疗对部分非小细胞肺癌患者有效。

方法

在这项3期开放标签研究中,我们将东亚地区既往未接受过治疗、患有晚期肺腺癌、不吸烟或既往轻度吸烟的患者随机分组,分别接受吉非替尼(每日250 mg)(609例患者)或卡铂(剂量按体表面积计算,曲线下面积为5或6 mg·min/ml)加紫杉醇(200 mg/m²体表面积)(608例患者)治疗。主要终点为无进展生存期。

结果

吉非替尼组和卡铂 - 紫杉醇组的12个月无进展生存率分别为24.9%和6.7%。该研究达到了其主要目标,即证明吉非替尼的非劣效性,并且在意向性治疗人群中,与卡铂 - 紫杉醇相比,吉非替尼在无进展生存期方面还显示出优势(疾病进展或死亡的风险比为0.74;95%置信区间[CI]为0.65至0.85;P<0.001)。在261例表皮生长因子受体基因(EGFR)突变阳性的患者亚组中,接受吉非替尼治疗的患者无进展生存期显著长于接受卡铂 - 紫杉醇治疗的患者(疾病进展或死亡的风险比为0.48;95%CI为0.36至0.64;P<0.001),而在176例突变阴性的患者亚组中,接受卡铂 - 紫杉醇治疗的患者无进展生存期显著更长(吉非替尼治疗患者疾病进展或死亡的风险比为2.85;95%CI为2.05至3.98;P<0.001)。吉非替尼组最常见的不良事件为皮疹或痤疮(66.2%的患者)和腹泻(46.6%),卡铂 - 紫杉醇组为神经毒性作用(69.9%)、中性粒细胞减少(67.1%)和脱发(58.4%)。

结论

在东亚地区不吸烟或既往轻度吸烟的患者中,吉非替尼作为肺腺癌的初始治疗优于卡铂 - 紫杉醇。肿瘤中EGFR基因突变的存在是吉非替尼治疗预后较好的有力预测指标。(ClinicalTrials.gov编号,NCT00322452。)

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