首页> 外文期刊>BMC Cancer >Multicenter phase II study on cisplatin, pemetrexed, and bevacizumab followed by maintenance with pemetrexed and bevacizumab for patients with advanced or recurrent nonsquamous non-small cell lung cancer: MAP study
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Multicenter phase II study on cisplatin, pemetrexed, and bevacizumab followed by maintenance with pemetrexed and bevacizumab for patients with advanced or recurrent nonsquamous non-small cell lung cancer: MAP study

机译:Cisplatin,Pemetrexed和Bevacizumab的多中心II期研究,然后用Pemetrexed和Bevacizumab进行维持,用于高级或复发性非小细胞肺癌的患者:地图研究

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We evaluated the safety and efficacy of induction chemotherapy with bevacizumab followed by maintenance chemotherapy with bevacizumab for advanced non-small cell lung cancer (NSCLC) in this multicenter phase II study. Chemotherapy-na?ve patient with stage IIIB-IV or recurrent nonsquamous NSCLC were eligible. We planned approximately four cycles of induction cisplatin (75?mg/m2), pemetrexed (500?mg/m2), and bevacizumab (15?mg/kg) followed by maintenance with pemetrexed (500?mg/m2) and bevacizumab (15?mg/kg) until disease progression. Progression-free survival (PFS) was the primary endpoint. Forty patients received a median of four induction chemotherapy cycles. Of them, 35 (87.5%) patients received a median of nine maintenance chemotherapy cycles. The objective response was 70.6%, and the disease control rate was 97.1%. The median PFS was 10.8 (95% CI, 9.0-12.6), and overall survival was 48.0 (95% CI, 32.9-63.1) months. Median PFS of 23 patients with epidermal growth factor receptor (EGFR) mutations and of 16 patients without EGFR mutations were 12.9 (95% CI, 9.4-16.3) and 7.9 (95% CI, 1.1-14.7) months, respectively. Toxicities graded ≥3 included neutropenia (15%), anemia (15%), hypertension (7.5%), anorexia (7.5%), fatigue (7.5%), thromboembolic events (5%), jaw osteonecrosis (5%), nausea (2.5%), oral mucositis (2.5%), tumor pain (2.5%), hyponatremia (2.5%), and gastrointestinal perforation (2.5%). Treatment-related deaths were not found. In patients with advanced or recurrent nonsquamous NSCLC, induction chemotherapy with cisplatin, pemetrexed, and bevacizumab followed by maintenance chemotherapy with pemetrexed and bevacizumab is safe and effective regardless of their EGFR mutation status. UMIN Clinical Trial Registry: UMIN000005569 . Registered date: May 8, 2011.
机译:我们评估了诱导化疗与Bevacizumab的安全性和有效性,然后用贝伐单抗进行饲养化疗,在该多中心II期研究中进行高级非小细胞肺癌(NSCLC)。患有阶段IIIB-IV或反复性不良NSCLC的化疗-NA'VE患者符合条件。我们计划大约四个感应顺铂(75×mg / m 2),培养基(500×mg / m 2),叶片(500〜mg / kg),然后用Pemetrexed(500×mg / m2)和bevacizumab进行维持(15 ?mg / kg)直到疾病进展。无进展生存(PFS)是主要终点。四十名患者接受了四个诱导化疗循环的中位数。其中,35名(87.5%)患者接受了九个维持化疗周期的中位数。客观反应为70.6%,疾病控制率为97.1%。中位数PFS为10.8(95%CI,9.0-12.6),总生存率为48.0(95%CI,32.9-63.1)个月。表皮生长因子受体(EGFR)突变的23名患者的中位数PFS分别为12.9(95%CI,9.4-16.3)和7.9(95%CI,1.1-14.7)个月。含有≥3分配的毒性(15%),贫血(15%),高血压(7.5%),厌食(7.5%),疲劳(7.5%),血栓骨折(5%),颌骨骨折(5%),恶心(2.5%),口服粘膜炎(2.5%),肿瘤疼痛(2.5%),低钠血症(2.5%)和胃肠穿孔(2.5%)。没有找到治疗相关的死亡。在先进或经常性的非调节NSCLC患者中,与顺铂,PemetreXed和Bevacizumab的诱导化疗,然后用培养基和贝伐单抗进行维持化疗,无论其EGFR突变状态如何,都是安全的,有效的。 UMIN临床试验登记处:UMIN000005569。注册日期:2011年5月8日。

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