Department of Epidemiology and Biostatistics, VU Medical Centre, Amsterdam, the Netherlands.
Pharmacoeconomics. 2012 Jan;30(1):17-34. doi: 10.2165/11595000-000000000-00000.
In past decades, studies focusing on new chemotherapeutic agents for patients with inoperable non-small-cell lung cancer have reported only modest gains in survival. These health gains are achieved at considerable cost, but economic evidence is lacking on superiority of one agent in terms of cost effectiveness. The objective of this systematic review was to assess fully published cost-effectiveness studies comparing the new agents docetaxel, paclitaxel, vinorelbine, gemcitabine and pemetrexed, and the targeted therapies erlotinib and gefitinib with one another. We performed systematic searches in the bibliographic databases PubMed, EMBASE and Health Economic Evaluations (HEED) [via the Cochrane Library] for fully published studies from the past 10 years. Studies were screened by two independent reviewers according to a priori inclusion criteria. The methodological quality of the included studies was evaluated by two independent reviewers using standardized assessment tools. A total of 222 potential studies were identified; 11 studies and six reviews were included. The methodological quality of the full economic evaluations was fairly good. Transparency in costs and resource use, details on statistical tests and sensitivity analysis were points for improvement. In first-line treatment, gemcitabine+cisplatin was cost effective compared with other platinum-based regimens (paclitaxel, docetaxel and vinorelbine). In one study, pemetrexed+cisplatin was cost effective compared with gemcitabine+cisplatin in patients with non-squamous-cell carcinoma. In second-line treatment, docetaxel was cost effective compared with best supportive care; erlotinib was cost effective compared with placebo; and docetaxel and pemetrexed were dominated by erlotinib. We found indications of superiority in terms of cost effectiveness for gemcitabine+cisplatin in a first-line setting, and for erlotinib in a second-line setting.
在过去的几十年中,针对无法手术的非小细胞肺癌患者的新化疗药物的研究报告仅显示生存获益略有增加。这些健康收益是付出了相当大的代价才实现的,但缺乏关于一种药物在成本效益方面优于另一种药物的经济证据。本系统评价的目的是全面评估比较新药物多西他赛、紫杉醇、长春瑞滨、吉西他滨和培美曲塞以及靶向治疗药物厄洛替尼和吉非替尼的已发表的成本效益研究。我们在文献数据库 PubMed、EMBASE 和健康经济评估(HEED)[通过 Cochrane 图书馆]中进行了系统搜索,以查找过去 10 年中已发表的研究。研究由两名独立审查员根据预先确定的纳入标准进行筛选。两名独立审查员使用标准化评估工具评估纳入研究的方法学质量。共确定了 222 项潜在研究,纳入了 11 项研究和 6 项综述。全经济评估的方法学质量相当好。在成本和资源使用方面的透明度、统计检验和敏感性分析的详细信息是需要改进的地方。在一线治疗中,吉西他滨+顺铂与其他铂类方案(紫杉醇、多西他赛和长春瑞滨)相比具有成本效益。在一项研究中,培美曲塞+顺铂在非鳞状细胞癌患者中与吉西他滨+顺铂相比具有成本效益。在二线治疗中,多西他赛与最佳支持治疗相比具有成本效益;厄洛替尼与安慰剂相比具有成本效益;多西他赛和培美曲塞被厄洛替尼所主导。我们发现吉西他滨+顺铂在一线治疗中具有成本效益优势的迹象,以及厄洛替尼在二线治疗中的成本效益优势的迹象。