首页> 美国卫生研究院文献>Oncology Letters >The efficacy and safety of bevacizumab in addition to platinum-based chemotherapy for the first-line treatment of patients with advanced nonsquamous non-small-cell lung cancer: Final results of AVALANCHE an observational cohort study
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The efficacy and safety of bevacizumab in addition to platinum-based chemotherapy for the first-line treatment of patients with advanced nonsquamous non-small-cell lung cancer: Final results of AVALANCHE an observational cohort study

机译:贝伐单抗和铂类化疗联合用于一线治疗晚期非鳞状非小细胞肺癌患者的疗效和安全性:一项观察性队列研究AVALANCHE的最终结果

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摘要

The previous results of former clinical studies confirmed that first-line bevacizumab (BEV) in combination with chemotherapy improves clinical outcomes in patients with advanced non-squamous non-small cell lung cancer. The AVALANCHE study ( Identifier ) was undertaken to assess the clinical outcomes of first-line BEV combined with standard platinum-based regimens in the Hungarian clinical practice. This observational study was conducted in 28 Hungarian sites, with patients enrolled between July 2008 and April 2011. Patients with untreated locally advanced, metastatic or recurrent lung adenocarcinoma received BEV (7.5 mg/kg, q3w) with any platinum-doublet for up to 6 cycles, and then non-progressors proceeded to receive BEV until disease progression or unacceptable toxicity. The primary endpoint was time-to-progression, and secondary endpoints included overall survival (OS), tumour control rate and safety. Patients were also analysed as two cohorts (non-progressors vs. progressors) based on whether or not they received BEV maintenance therapy following completion of first-line chemotherapy plus BEV. The study enrolled 283 patients (median age: 58.2 (18–78) years; males: 50.5%; stage: III/B: 18.4%, IV: 79.9%; adenocarcinoma/other: 95.8/4.2%; ECOG PS 0/1/2/≥3: 30.8/59.7/2.6/1.4%). Centrally located tumours were reported in 21.6%. Cisplatin/carboplatin-based regimens: 53.8/46.2%. A total of 43% of patients received BEV maintenance therapy. The median number of BEV cycles was 6. Median progression-free survival (PFS) was 7.2 months and OS was 15.2 months for the entire cohort. Longer PFS and OS were observed in patients who received BEV maintenance therapy [median OS, 26.2 vs. 10.2 months (P<0.001); median PFS, 9.2 vs. 5.8 months (P<0.001)]. Contrary to the results of previous OCS no significant difference was recorded in the different age groups or gender. Best tumour response: Complete remission/partial remission/stable disease/progressive diseaseot reported were: 1.5/29.9/26.9/9.1/32.6% of all patients. In conclusion, clinical outcomes obtained in this real-life population were consistent with pivotal studies. BEV maintenance treatment was associated with a significantly longer PFS and OS.
机译:先前临床研究的先前结果证实,一线贝伐单抗(BEV)联合化疗可改善晚期非鳞状非小细胞肺癌患者的临床结局。进行AVALANCHE研究(标识符)以评估匈牙利临床实践中一线BEV与标准铂类疗法相结合的临床结果。这项观察性研究在2008年7月至2011年4月期间在匈牙利的28个地点进行。未治疗的局部晚期,转移性或复发性肺腺癌患者接受BEV(7.5 mg / kg,q3w)配任何双铂治疗,最多6次周期,然后非进展者开始接受BEV,直到疾病进展或不可接受的毒性。主要终点是进展时间,次要终点包括总生存期(OS),肿瘤控制率和安全性。还根据一线化疗加BEV后是否接受BEV维持治疗,将患者分为两个队列(非进展者与进展者)进行分析。该研究招募了283名患者(中位年龄:58.2(18-78)岁;男性:50.5%;阶段:III / B:18.4%,IV:79.9%;腺癌/其他:95.8 / 4.2%; ECOG PS 0/1) /2/≥3:30.8/59.7/2.6/1.4%)。据报道位于中心的肿瘤占21.6%。基于顺铂/卡铂的方案:53.8 / 46.2%。共有43%的患者接受了BEV维持治疗。 BEV周期的中位数为6。整个队列的中位无进展生存期(PFS)为7.2个月,OS为15.2个月。接受BEV维持治疗的患者观察到更长的PFS和OS [中位OS,中位26.2 vs. 10.2个月(P <0.001); PFS中位数分别为9.2个月和5.8个月(P <0.001)]。与以前的OCS结果相反,在不同年龄组或性别中均未发现明显差异。最佳肿瘤反应:完全缓解/部分缓解/稳定疾病/进行性疾病/未报告的患者:1.5 / 29.9 / 26.9 / 9.1 / 32.6%。总之,在这一现实生活中获得的临床结果与关键性研究一致。 BEV维持治疗与更长的PFS和OS相关。

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