系统评价:从国家健康保险的角度对人上皮生长因子受体2阳性转移性乳腺癌治疗的经济评价

Gita Mir, A. Warsito, D. Susanna, Popy Yuniar
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引用次数: 0

摘要

背景:经济评价通常是从社会角度出发的。即使它很重要,因为治疗对患者的社会生活影响很大,从付款人的角度进行经济评估,也很重要,因为它可以帮助国民健康保险(NHI)作为付款人避免预算赤字,正如在印度尼西亚所观察到的那样。不幸的是,从付款人的角度进行经济评估是非常罕见的。本文汇编和回顾了关于人类上皮生长因子受体2阳性转移性乳腺癌(mBC)作为曲妥珠单抗治疗的替代疗法的经济评估的研究文章,曲妥珠单抗最近已从印度尼西亚的国民健康保险覆盖范围中删除。方法:根据系统评价和荟萃分析首选报告项目(PRISMA)建议和PICO方法(人口、干预、比较和结果)进行文献检索。相关文章从在线生物医学数据库Scopus、PubMed、ScienceDirect和SAGE期刊中检索。使用标准化的检查表进行质量评估,该检查表由CHEC检查表中的项目组成。结果:共回顾了从NHI角度对her2阳性mBC治疗进行经济评估的六篇文章(期间:2008-2018)。曲妥珠单抗+化疗的总生存期最长(OS, 37.8个月),无进展生存期(PFS)为12.7个月。曲妥珠单抗+多西他赛作为一线治疗与最长的PFS(19个月)相关,总成本为12,732美元。关于治疗顺序,一线,曲妥珠单抗+帕妥珠单抗+多西他赛;二线,曲妥珠单抗+恩坦辛;第三线,拉帕替尼+卡培他滨与最高质量调整生命年(QALY;1.81美元),但总成本和增量成本也最高(分别为360 880美元和197 250美元)。第一行序列,曲妥珠单抗/多西他赛;2线,T-DM1;在三线治疗中,曲妥珠单抗/拉帕替尼的QALY最低(1.27),但最具成本效益(总成本:158,293美元)。拉帕替尼+卡培他滨作为二线治疗和依西美坦单药治疗的总成本最低(3,190美元)。结论:拉帕替尼+卡培他滨作为二线治疗和依西美坦单药治疗对于HER-2阳性mBC具有替代曲妥珠单抗治疗的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic Review: Economic Evaluation of Treatment for Human Epithelial Growth Factor Receptor 2-positive Metastatic Breast Cancer from a National Health Insurance Perspective
Background: Economic evaluation is often held from the societal perspective. Even it is important, as the therapy affects greatly to the patients’ life in society, economic evaluation from the payer perspective, is as important as it may help National Health Insurance (NHI) as the payer avert budget deficit as was observed in Indonesia. Unfortunately economic evaluation from the payer’s perspective is very rare to be done. This article compiles and reviews research articles of economic evaluation of therapy for human epithelial growth factor receptor 2-positive metastatic Breast Cancer (mBC) as an alternative to trastuzumab therapy, which has recently been removed from Indonesia’s National Health Insurance coverage. Methods: The literature search was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) recommendations and PICO methodology (Population, Intervention, Comparison, and Outcome). Relevant articles were retrieved from online biomedical databases Scopus, PubMed, ScienceDirect, and SAGE Journals. Quality appraisal was performed using a standardized checklist which consisted of items in the CHEC checklist. Results: A total of six articles pertaining to economic evaluation of therapy for HER2-positive mBC from the NHI perspective (period: 2008–2018) were reviewed. Trastuzumab+chemotherapy showed the longest overall survival (OS, 37.8 months) with Progression-free Survival (PFS) of 12.7 months. Trastuzumab+docetaxel as 1st line therapy were associated with the longest PFS (19 months) with a total cost of US$ 12,732. With respect to therapy sequence, 1st line, trastuzumab+pertuzumab+docetaxel; 2nd line, trastuzumab+emtansine ; and 3rd line, lapatinib+capecitabine was associated with the highest quality-adjusted life year (QALY; 1.81) but also the highest total cost and incremental cost (US$360,880 and US$197,250, respectively). The sequence of 1st line, trastuzumab/docetaxel; 2nd line, T-DM1; and 3rd line, trastuzumab/lapatinib was associated the lowest QALY (1.27) but was the most cost-effective (total cost: $158,293). Lapatinib+capecitabine as 2nd line therapy and exemestane monotherapy were associated with the lowest total cost (US$3,190). Conclusion: Lapatinib+capecitabine as 2nd line therapy and exemestane monotherapy show potential as alternatives to trastuzumab therapy for HER-2 positive mBC.
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