Department of Respiratory Medicine, Tohoku University Hospital, Sendai, Japan.
Ann Oncol. 2013 Jan;24(1):54-9. doi: 10.1093/annonc/mds214. Epub 2012 Sep 11.
NEJ002 study, comparing gefitinib with carboplatin (CBDCA) and paclitaxel (PTX; Taxol) as the first-line treatment for advanced non-small cell lung cancer (NSCLC) harboring an epidermal growth factor receptor (EGFR) mutation, previously reported superiority of gefitinib over CBDCA/PTX on progression-free survival (PFS). Subsequent analysis was carried out mainly regarding overall survival (OS).
For all 228 patients in NEJ002, survival data were updated in December, 2010. Detailed information regarding subsequent chemotherapy after the protocol treatment was also assessed retrospectively and the impact of some key drugs on OS was evaluated.
The median survival time (MST) was 27.7 months for the gefitinib group, and was 26.6 months for the CBDCA/PTX group (HR, 0.887; P=0.483). The OS of patients who received platinum throughout their treatment (n=186) was not statistically different from that of patients who never received platinum (n=40). The MST of patients treated with gefitinib, platinum, and pemetrexed (PEM) or docetaxel (DOC, Taxotere; n=76) was around 3 years.
No significant difference in OS was observed between gefitinib and CBDCA/PTX in the NEJ002 study, probably due to a high crossover use of gefitinib in the CBDCA/PTX group. Considering the many benefits and the risk of missing an opportunity to use the most effective agent for EGFR-mutated NSCLC, the first-line gefitinib is strongly recommended.
NEJ002 研究比较了吉非替尼与卡铂(CBDCA)联合紫杉醇(PTX;紫杉醇)作为表皮生长因子受体(EGFR)突变型晚期非小细胞肺癌(NSCLC)一线治疗药物,先前报告显示吉非替尼在无进展生存期(PFS)方面优于 CBDCA/PTX。随后的分析主要针对总生存期(OS)进行。
对 NEJ002 中的所有 228 例患者,于 2010 年 12 月更新生存数据。回顾性评估了方案治疗后后续化疗的详细信息,并评估了一些关键药物对 OS 的影响。
吉非替尼组的中位生存时间(MST)为 27.7 个月,CBDCA/PTX 组为 26.6 个月(HR,0.887;P=0.483)。接受全程铂类治疗(n=186)的患者 OS 与从未接受过铂类治疗(n=40)的患者无统计学差异。接受吉非替尼、铂类和培美曲塞(PEM)或多西他赛(DOC,泰索帝)治疗的患者(n=76)的 MST 约为 3 年。
在 NEJ002 研究中,吉非替尼与 CBDCA/PTX 的 OS 无显著差异,可能是由于 CBDCA/PTX 组中吉非替尼的高交叉使用。考虑到众多获益和错失使用针对 EGFR 突变型 NSCLC 最有效药物的机会的风险,强烈推荐一线使用吉非替尼。