Mok Tony, Wu Yi-Long, Zhang Li
Department of Clinical Oncology, The Chinese University of Hong Kong, Hong Kong, China.
Discov Med. 2009 Dec;8(43):227-31.
Treatment outcome for advanced-stage non-small cell lung cancer (NSCLC) is limited by empiric administration of cytotoxic chemotherapy. Recent advances in molecular genomics have revolutionized cancer management and, specifically, epidermal growth factor receptor (EGFR) mutation has become a potent biomarker for lung cancer, which predicts tumor response to and prolonged duration of disease control by EGFR tyrosine kinase inhibitors (TKI). The Iressa Pan-Asia Study (IPASS) is a randomized phase III study comparing gefitinib (EGFR TKI) with paclitaxel/carboplatin (standard chemotherapy) in Asian non-/light smokers with adenocarcinoma. Progression-free survival (PFS) in EGFR mutation-positive patients was longer with gefitinib than with chemotherapy (hazard ratio [HR], 0.48; 95% confidence interval [CI], 0.36-0.64; p<0.0001); in EGFR mutation-negative patients, PFS was longer with chemotherapy than with gefitinib (HR 2.85; 95% CI 2.05-3.98; p<0.0001). The findings are confirmed by one single-arm study and three other randomized studies. It has become clear that personalized medicine for NSCLC is feasible. This small step towards personalized medicine represents a paradigm shift in the management of NSCLC.
晚期非小细胞肺癌(NSCLC)的治疗效果受细胞毒性化疗经验性给药的限制。分子基因组学的最新进展彻底改变了癌症治疗方式,具体而言,表皮生长因子受体(EGFR)突变已成为肺癌的一种有效生物标志物,可预测肿瘤对EGFR酪氨酸激酶抑制剂(TKI)的反应以及疾病控制的延长时间。易瑞沙泛亚研究(IPASS)是一项III期随机研究,比较了吉非替尼(EGFR TKI)与紫杉醇/卡铂(标准化疗)在亚洲非/轻度吸烟腺癌患者中的疗效。EGFR突变阳性患者使用吉非替尼的无进展生存期(PFS)比化疗更长(风险比[HR],0.48;95%置信区间[CI],0.36 - 0.64;p<0.0001);在EGFR突变阴性患者中,化疗的PFS比吉非替尼更长(HR 2.85;95% CI 2.05 - 3.98;p<0.0001)。一项单臂研究和其他三项随机研究证实了这些发现。很明显,NSCLC的个性化医疗是可行的。这向个性化医疗迈出的一小步代表了NSCLC治疗模式的转变。