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首页> 外文期刊>Oncology letters >Bevacizumab, pemetrexed and carboplatin in first-line treatment of non-small cell lung cancer patients: Focus on patients with brain metastases
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Bevacizumab, pemetrexed and carboplatin in first-line treatment of non-small cell lung cancer patients: Focus on patients with brain metastases

机译:贝伐单抗,培美曲塞和卡铂在非小细胞肺癌患者的一线治疗中:关注脑转移患者

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Data concerning bevacizumab plus pemetrexed plus carboplatin as first-line treatment for patients with non-squamous non-small cell lung cancer (NSCLC) with or without brain metastases (BM) are lacking. The present study analyzed the efficacy and safety of this combination as induction therapy, followed by maintenance therapy with bevacizumab plus pemetrexed in non-squamous NSCLC patients with or without BM. Treatment-naive patients with advanced non-squamous NSCLC and an Eastern Cooperative Oncology Group performance status score of 0-2 were eligible. Treatment consisted of carboplatin (area under the curve of 5), pemetrexed (500 mg/m(2)) and bevacizumab (15 mg/kg) every 3 weeks for 6 cycles. Responders and patients with stable disease received maintenance therapy with bevacizumab plus pemetrexed until disease progression, which was evaluated every 3 cycles, or unacceptable toxicity. Kaplan-Meier median progression-free survival (PFS) and overall survival (OS) times were the primary endpoints, and safety was the secondary endpoint. In total, 39 patients, aged 44-78 years (median, 60 years), were treated; 11 (28.2%) of whom presented with BM. The majority of patients (56.4%) completed 6 cycles of induction therapy, and 26 patients continued on to maintenance therapy. The median PFS time was 8.2 months [95% confidence interval (CI), 7.05-9.35] and the median OS time was 14.0 months (95% CI, 8.46-19.54). Median PFS and OS times did not differ significantly between patients with or without BM (log rank (Mantel-Cox): PFS, P=0.748 and OS, P=0.447). The majority of patients (76.9%) did not experience adverse events during treatment. Overall, bevacizumab plus pemetrexed plus carboplatin as induction therapy, followed by bevacizumab plus pemetrexed as maintenance therapy was effective and well tolerated in advanced NSCLC, whether brain metastases were present or not.
机译:缺乏关于贝伐单抗加培美曲塞加卡铂作为有或无脑转移瘤(BM)的非鳞状非小细胞肺癌(NSCLC)患者的一线治疗的数据。本研究分析了该组合作为诱导疗法的有效性和安全性,然后对贝伐单抗联合培美曲塞维持治疗在有或无BM的非鳞状NSCLC患者中进行。初治的非鳞状上皮非小细胞肺癌和东部合作肿瘤小组的工作状态评分为0-2的未接受治疗的患者是合格的。每3周一次,由卡铂(5点以下的面积),培美曲塞(500 mg / m(2))和贝伐单抗(15 mg / kg)组成,治疗6个周期。响应者和病情稳定的患者接受贝伐单抗联合培美曲塞的维持治疗,直至疾病进展,每3个周期评估其毒性或出现不可接受的毒性。 Kaplan-Meier中位无进展生存期(PFS)和总生存期(OS)时间是主要终点,安全性是次要终点。总共治疗了39例年龄在44-78岁(中位数为60岁)的患者;其中11人(占28.2%)接受BM培训。大多数患者(56.4%)完成了6个周期的诱导治疗,还有26个患者继续接受维持治疗。 PFS时间中位数为8.2个月[95%置信区间(CI),7.05-9.35],OS时间中位数为14.0个月(95%CI,8.46-19.54)。有或没有BM的患者之间的中位PFS和OS时间无显着差异(对数等级(Mantel-Cox):PFS,P = 0.748和OS,P = 0.447)。大多数患者(76.9%)在治疗期间未发生不良事件。总体而言,贝伐单抗联合培美曲塞加卡铂作为诱导治疗,然后贝伐单抗联合培美曲塞作为维持治疗对晚期NSCLC有效且耐受性良好,无论是否存在脑转移。

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