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首页> 外文期刊>Thoracic cancer. >Long‐term results of a randomized, double‐blind, and placebo‐controlled phase III trial: Endostar (rh‐endostatin) versus placebo in combination with vinorelbine and cisplatin in advanced non‐small cell lung cancer
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Long‐term results of a randomized, double‐blind, and placebo‐controlled phase III trial: Endostar (rh‐endostatin) versus placebo in combination with vinorelbine and cisplatin in advanced non‐small cell lung cancer

机译:一项随机,双盲和安慰剂对照的III期临床试验的长期结果:Endostar(rh-endostatin)与安慰剂联合长春瑞滨和顺铂治疗晚期非小细胞肺癌

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AbstractBackground: 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.MethodsFour 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.Results: 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).Conclusion: 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.
机译:摘要背景:在未经治疗和先前接受过治疗的局部晚期或非小细胞肺癌(NSCLC)患者的II-III期试验中,Endostar能够增强铂类化学疗法(NP方案)的疗效并具有可耐受的不良反应。 186例患者被随机分为两组:研究组A:NP加Endostar(n = 322;长春瑞滨,顺铂,Endostar),研究组B:NP加安慰剂(n = 164;长春瑞滨,顺铂,0.9%钠氯化物)。患者每三周接受2至6个周期的治疗。结果:A组的总缓解率为35.4%,B组的总缓解率为19.5%(P = 0.0003)。 A组的中位进展时间分别为6.3个月和B组的3.6个月(P <0.001)。 A组的临床受益率为73.3%,B组的为64.0%(P = 0.035)。 A组的3/4级中性粒细胞减少,贫血和恶心/呕吐分别为28.5%,3.4%和8.0%,而B组的分别为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例死亡(P> 0.05)。结论:长期随访发现,NP方案加用Endostar可以使晚期NSCLC患者获得显着的临床和生存获益,这是A组患者的中位总生存期长于B组的患者(P <0.0001)。 ,与仅NP相比。

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