免疫检查点抑制剂健康经济评价研究报告质量:系统综述。

IF 2.7 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2025-05-01 Epub Date: 2025-03-27 DOI:10.1007/s40261-025-01435-w
Takashi Yoshioka, Shintaro Azuma, Satoshi Funada, Takahiro Itaya, Rei Goto
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引用次数: 0

摘要

背景和目的:在肿瘤学中引入免疫检查点抑制剂(ICIs),由于其巨大的经济负担,对资源分配提出了关键的医疗保健政策挑战。本研究评估了ici健康经济评价(HEE)研究的报告质量。方法:本研究对2014年1月1日至2022年12月31日期间发表的4个数据库(PubMed、EMBASE、Cochrane CENTRAL和International HTA Database)进行了系统的文献检索。截至2022年12月31日,在美国、欧盟、中国和日本批准的所有ICIs都包括在内。报告质量采用2013年发布的《综合卫生经济评估报告标准》(CHEERS 2013)进行评估,该标准是HEE研究中得到最广泛认可和实施的报告指南。根据赞助偏倚风险或引用CHEERS 2013进行亚组分析。结果:共检索到5368条记录,经全文审阅后纳入252条记录。研究设计、设置和最常观察到的ICIs分别是成本-效果和成本-效用分析(63.5%)、美国(46.0%)和派姆单抗(38.1%)。在2013年的24个项目中,充分报告的项目是有限的,特别是在方法部分。94.4%的记录未报告设置和位置。分组分析还显示方法部分的项目报告不足,特别是“设置和位置”。结论:无论赞助偏倚风险或引用情况如何,2014年至2022年期间关于ICIs的健康经济评价研究在2013年CHEERS的24个项目中报告有限。方法部分关于设置和地点的项目特别少报,强调了在ICIs的HEE研究中透明报告的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Reporting Quality in Health Economic Evaluation Studies of Immune Checkpoint Inhibitors: A Systematic Review.

Reporting Quality in Health Economic Evaluation Studies of Immune Checkpoint Inhibitors: A Systematic Review.

Reporting Quality in Health Economic Evaluation Studies of Immune Checkpoint Inhibitors: A Systematic Review.

Reporting Quality in Health Economic Evaluation Studies of Immune Checkpoint Inhibitors: A Systematic Review.

Background and objective: The introduction of immune checkpoint inhibitors (ICIs) in oncology presents a critical healthcare policy challenge for resource allocation due to their substantial financial burden. This study assessed the reporting quality of health economic evaluation (HEE) studies of ICIs.

Methods: This study conducted a systematic literature search of four databases (PubMed, EMBASE, Cochrane CENTRAL, and the International HTA Database) for studies published between January 1, 2014 and December 31, 2022. All ICIs approved up to December 31, 2022, in the USA, EU, China, and Japan were included. Reporting quality was assessed using the Consolidated Health Economic Evaluation Reporting Standards published in 2013 (CHEERS 2013), which is the most widely recognised and implemented reporting guideline for HEE studies. Subgroup analyses were also performed based on the risk of sponsorship bias or citation of CHEERS 2013.

Results: A total of 5368 records were identified, 252 of which were included after full-text review. The study design, setting, and ICIs most frequently observed were cost-effectiveness and cost-utility analyses (63.5%), the USA (46.0%), and pembrolizumab (38.1%), respectively. Of the 24 items of CHEERS 2013, fully reported items were limited, particularly in the Methods section. Setting and location were not reported in 94.4% of the records. Subgroup analyses also revealed insufficient reporting of items in the Methods section, particularly "Setting and location".

Conclusion: Health economic evaluation studies on ICIs between 2014 and 2022 had limited reporting across the 24 items of CHEERS 2013, regardless of sponsorship bias risk or citations. The items on setting and location in the Methods section were particularly underreported, emphasising the need for transparent reporting in HEE studies of ICIs.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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