Sun Yan, Wang Jin Wan, Liu Yong Yu, Yu Qi Tao, Zhang Yi Ping, Li Kai, Xu Li Yan, Luo Su Xia, Qin Feng Zhan, Chen Zheng Tang, Liu Wen Chao, Zhou Qing Hua, Chen Qiang, Nan Ke Jun, Liu Xiao Qing, Liu Wei, Liang Hou Jie, Lu Hui Shan, Wang Xiu Wen, Wang Jie Jun, Song Shu Ping, Tu Yuan Rong, Zhou Jing Min, Li Wei Lian, Yao Chen
Cancer Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Liaoning Provincial Cancer Hospital, Shenyang, China.
Thorac Cancer. 2013 Nov;4(4):440-448. doi: 10.1111/1759-7714.12050.
: Phase II-III trials in patients with untreated and previously treated locally advanced or non-small cell lung cancer (NSCLC) suggested that Endostar was able to enhance the effect of platinum-based chemotherapy (NP regimen) with tolerable adverse effects.
Four hundred and eighty six patients were randomized into two arms: study arm A: NP plus Endostar (n = 322; vinorelbine, cisplatin, Endostar), and study arm B: NP plus placebo (n = 164; vinorelbine, cisplatin, 0.9% sodium chloride). Patients were treated every third week for two to six cycles.
: Overall response rates were 35.4% in arm A and 19.5% in arm B (P = 0.0003). The median time to progression was 6.3 months for arm A and 3.6 months for B, respectively (P < 0.001). The clinical benefit rates were 73.3% in arm A and 64.0% in arm B (P = 0.035). Grade 3/4 neutropenia, anemia, and nausea/vomiting were 28.5%, 3.4%, and 8.0%, respectively, in Arm A compared with 28.2%, 3.0%, and 6.6%, respectively, in Arm B (P > 0.05). There were two treatment related deaths in arm A and one in arm B (P > 0.05). The median overall survival was longer in arm A than in arm B (P < 0.0001).
: Long-term follow-up revealed that the addition of Endostar to an NP regimen can result in a significant clinical and survival benefit in advanced NSCLC patients, compared with NP alone.
针对未经治疗及先前接受过治疗的局部晚期或非小细胞肺癌(NSCLC)患者开展的II-III期试验表明,恩度能够增强铂类化疗(NP方案)的疗效,且不良反应可耐受。
486例患者被随机分为两组:研究组A:NP加恩度(n = 322;长春瑞滨、顺铂、恩度),研究组B:NP加安慰剂(n = 164;长春瑞滨、顺铂、0.9%氯化钠)。患者每三周接受一次治疗,共进行2至6个周期。
A组的总缓解率为35.4%,B组为19.5%(P = 0.0003)。A组的中位疾病进展时间分别为6.3个月,B组为3.6个月(P < 0.001)。A组的临床获益率为73.3%,B组为64.0%(P = 0.035)。A组3/4级中性粒细胞减少、贫血和恶心/呕吐的发生率分别为28.5%、3.4%和8.0%,B组分别为28.2%、3.0%和6.6%(P > 0.05)。A组有2例与治疗相关的死亡,B组有1例(P > 0.05)。A组的中位总生存期长于B组(P < 0.0001)。
长期随访显示,与单纯NP方案相比,在NP方案中添加恩度可使晚期NSCLC患者获得显著的临床和生存获益。