Fernández-López Cristina, Expósito-Hernández José, Arrebola-Moreno Juan Pedro, Calleja-Hernández Miguel Ángel, Expósito-Ruíz Manuela, Guerrero-Tejada Rosa, Linares Isabel, Cabeza-Barrera José
Department of Pharmacy, Biosanitary Institute of Granada (ibs.GRANADA), University Hospitals of Granada/University of Granada, Granada, Spain.
Department of Oncology, Virgen de las Nieves Universitary Hospital, Granada, Spain.
Cancer Med. 2016 Sep;5(9):2190-7. doi: 10.1002/cam4.782. Epub 2016 Jul 23.
The objective of this review was to analyze trends in outcomes and in the quality of phase III randomized controlled trials on advanced NSCLC published between 2000 and 2012, selecting 76 trials from a total of 122 retrieved in a structured search. Over the study period, the number of randomized patients per trial increased by 14 per year (P = 0.178). The sample size significantly increased between 2000 and 2012 in trials of targeted agents (460.1 vs. 740.8 patients, P = 0.009), trials of >1 drug (360.4 vs. 584.8, P = 0.014), and those including patients with good performance status (675.3 vs. 425.6; P = 0.003). Quality of life was assessed in 46 trials (60.5%), and significant improvements were reported in 10 of these (21.7%). Platinum-based regimens were the most frequently investigated (86.8% of trials). Molecular-targeted agents were studied in 25.0% of chemotherapy arms, and the percentage of trials including these agents increased each year. The median (interquartile range) overall survival (MOS) was 9.90 (3.5) months with an increase of 0.384 months per year of publication (P < 0.001). A statistically significant improvement in MOS was obtained in only 13 (18.8%) trials. The median progression-free survival was 4.9 (1.9) months, with a nonsignificant increase of 0.026 months per year (P > 0.05). There has been a continuous but modest improvement in the survival of patients with advanced NSCLC over the past 12 years. Nevertheless, the quality of clinical trials and the benefit in outcomes should be carefully considered before the incorporation of novel approaches into clinical practice.
本综述的目的是分析2000年至2012年间发表的关于晚期非小细胞肺癌(NSCLC)的III期随机对照试验的结果及质量趋势,在结构化检索中从总共检索到的122项试验中选取了76项试验。在研究期间,每项试验随机分组的患者数量每年增加14例(P = 0.178)。2000年至2012年间,靶向药物试验(460.1例对740.8例患者,P = 0.009)、一种以上药物的试验(360.4例对584.8例,P = 0.014)以及纳入体能状态良好患者的试验(675.3例对425.6例;P = 0.003)中的样本量显著增加。46项试验(60.5%)评估了生活质量,其中10项(21.7%)报告有显著改善。铂类方案是研究最频繁的(86.8%的试验)。25.0%的化疗组研究了分子靶向药物,且纳入这些药物的试验百分比逐年增加。中位(四分位间距)总生存期(MOS)为9.90(3.5)个月,每年发表的试验中MOS增加0.384个月(P < 0.001)。仅13项(18.8%)试验的MOS有统计学显著改善。中位无进展生存期为4.9(1.9)个月,每年无显著增加,仅增加0.026个月(P > 0.05)。在过去12年中,晚期NSCLC患者的生存率有持续但适度的改善。然而,在将新方法纳入临床实践之前,应仔细考虑临床试验的质量和结果的获益情况。