首页> 外文期刊>Asia-Pacific journal of clinical oncology >Comparative effectiveness of bevacizumab plus cisplatin-based chemotherapy versus pemetrexed plus cisplatin treatment in East Asian non-squamous non-small cell lung cancer patients applying real-life outcomes.
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Comparative effectiveness of bevacizumab plus cisplatin-based chemotherapy versus pemetrexed plus cisplatin treatment in East Asian non-squamous non-small cell lung cancer patients applying real-life outcomes.

机译:应用现实生活结果的东亚非鳞状非小细胞肺癌患者,贝伐单抗联合顺铂化疗与培美曲塞联合顺铂治疗的比较效果。

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AIM: To indirectly compare real-life clinical effectiveness of bevacizumab + cisplatin-based therapy from the Safety of Avastin in Lung (SAiL) phase IV clinical trial with published evidence from the phase III clinical trial for pemetrexed + cisplatin among East Asian patients with non-squamous metastatic or recurrent non-small cell lung cancer (NSCLC). METHODS: Survival outcomes were compared between subgroups of East Asian patients receiving treatments of either bevacizumab + cisplatin-based chemotherapy or pemetrexed + cisplatin using a matching-adjusted indirect comparison approach. Patient-level data were used to derive a new group with similar characteristics compared to those reported in a phase III clinical trial evaluating pemetrexed + cisplatin therapy. Exclusions to the SAiL data included those with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 2, those with mixed cell histology, non-East Asians and those who did not receive cisplatin-based chemotherapy. In total 1000 samples of the pre-matched analysis set of the SAiL data were selected that resulted in equal distributions of the ECOG PS and gender matching variables selected and evaluated for a progression-free survival (PFS) outcome. RESULTS: Median PFS was longer for patients treated with bevacizumab-based therapy (7.4 months; 95% confidence interval [CI]: 6.7-8.2) versus pemetrexed + cisplatin (6.4 months; 95% CI N/A) among non-squamous East Asian NSCLC patients. CONCLUSION: The results suggest that East Asian non-squamous NSCLC patients treated with bevacizumab-based therapy have a trend toward improved PFS outcomes compared to those treated with pemetrexed + cisplatin, even after adjusting for differences between the two trial groups.
机译:目的:为了间接比较肺炎阿瓦斯汀安全性(SAiL)第四期临床试验中贝伐单抗+顺铂治疗的实际临床疗效,与东亚非甲非西非患者中培美曲塞+顺铂三期临床试验的已发表证据进行比较-鳞状转移性或复发性非小细胞肺癌(NSCLC)。方法:采用匹配调整间接比较方法,对接受贝伐单抗+顺铂化疗或培美曲塞+顺铂治疗的东亚患者亚组之间的生存结局进行了比较。与评估培美曲塞+顺铂治疗的III期临床试验中报道的那些患者相比,使用患者水平的数据来得出一个具有相似特征的新组。 SAiL数据的排除对象包括东部合作肿瘤小组(ECOG)表现状态(PS)为2的患者,混合细胞组织学的患者,非东亚人和未接受基于顺铂化疗的患者。总共选择了1000个SAiL数据的预匹配分析集样本,这些样本可导致ECOG PS均等分布,并选择性别匹配变量并评估无进展生存(PFS)结果。结果:在非鳞状东部患者中,以贝伐单抗为基础治疗的患者中位PFS较长(7.4个月; 95%置信区间[CI]:6.7-8.2),而培美曲塞+顺铂(6.4个月; 95%CI不适用)亚洲NSCLC患者。结论:结果表明,与贝美曲塞+顺铂相比,接受贝伐单抗治疗的东亚非鳞状非小细胞肺癌患者的PFS结局有改善的趋势,即使在调整了两个试验组之间的差异之后也是如此。

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