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平台试验与传统试验的成本和所需时间的经济评估。

Economic Evaluation of Cost and Time Required for a Platform Trial vs Conventional Trials.

机构信息

Experimental Medicine, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.

Department of Health Research Methods, Evidence, and Impact, McMaster University Health Sciences Centre, Hamilton, Ontario, Canada.

出版信息

JAMA Netw Open. 2022 Jul 1;5(7):e2221140. doi: 10.1001/jamanetworkopen.2022.21140.

Abstract

IMPORTANCE

Platform trial design allows the introduction of new interventions after the trial is initiated and offers efficiencies to clinical research. However, limited guidance exists on the economic resources required to establish and maintain platform trials.

OBJECTIVE

To compare cost (US dollars) and time requirements of conducting a platform trial vs a series of conventional (nonplatform) trials using a real-life example.

DESIGN, SETTING, AND PARTICIPANTS: For this economic evaluation, an online survey was administered to a group of international experts (146 participants) with publication records of platform trials to elicit their opinions on cost and time to set up and conduct platform, multigroup, and 2-group trials. Using the reported entry dates of 10 interventions into Systemic Therapy in Advancing Metastatic Prostate Cancer: Evaluation of Drug Efficacy, the longest ongoing platform trial, 3 scenarios were designed involving a single platform trial (scenario 1), 1 multigroup followed by 5 2-group trials (scenario 2), and a series of 10 2-group trials (scenario 3). All scenarios started with 5 interventions, then 5 more interventions were either added to the platform or evaluated independently. Simulations with the survey results as inputs were used to compare the platform vs conventional trial designs. Data were analyzed from July to September 2021.

EXPOSURE

Platform trial design.

MAIN OUTCOMES AND MEASURES

Total trial setup and conduct cost and cumulative duration.

RESULTS

Although setup time and cost requirements of a single trial were highest for the platform trial, cumulative requirements of setting up a series of multiple trials in scenarios 2 and 3 were larger. Compared with the platform trial, there was a median (IQR) increase of 216.7% (202.2%-242.5%) in cumulative setup costs for scenario 2 and 391.1% (365.3%-437.9%) for scenario 3. In terms of total cost, there was a median (IQR) increase of 17.4% (12.1%-22.5%) for scenario 2 and 57.5% (43.1%-69.9%) for scenario 3. There was a median (IQR) increase in cumulative trial duration of 171.1% (158.3%-184.3%) for scenario 2 and 311.9% (282.0%-349.1%) for scenario 3. Cost and time reductions in the platform trial were observed in both the initial and subsequently evaluated interventions.

CONCLUSIONS AND RELEVANCE

Although setting up platform trials can take longer and be costly, the findings of this study suggest that having a single infrastructure can improve efficiencies with respect to costs and efforts.

摘要

重要性

平台试验设计允许在试验启动后引入新的干预措施,并为临床研究提供效率。然而,关于建立和维持平台试验所需的经济资源,目前的指导意见有限。

目的

使用实际示例比较进行平台试验与一系列常规(非平台)试验的成本(美元)和时间要求。

设计、设置和参与者:在这项经济评估中,向一群具有平台试验发表记录的国际专家(146 名参与者)进行了在线调查,以征求他们对平台、多组和 2 组试验的设立和进行成本和时间的意见。利用报告的 10 种干预措施进入系统治疗进展期前列腺癌的最早日期:药物疗效评估,这是最长的正在进行的平台试验,设计了 3 种情况,涉及单一平台试验(情况 1)、1 个多组试验后再进行 5 个 2 组试验(情况 2)和一系列 10 个 2 组试验(情况 3)。所有情况均从 5 个干预措施开始,然后向平台添加或独立评估另外 5 个干预措施。使用调查结果作为输入的模拟用于比较平台与常规试验设计。数据于 2021 年 7 月至 9 月进行分析。

暴露

平台试验设计。

主要结果和措施

总试验设置和进行成本和累积持续时间。

结果

虽然平台试验的单个试验设置和成本要求最高,但在情况 2 和 3 中设置一系列多个试验的累积要求更大。与平台试验相比,情况 2 和 3 的累积设置成本中位数(IQR)分别增加了 216.7%(202.2%-242.5%)和 391.1%(365.3%-437.9%)。就总费用而言,情况 2 的中位数(IQR)增加了 17.4%(12.1%-22.5%),情况 3 的中位数(IQR)增加了 57.5%(43.1%-69.9%)。情况 2 的累积试验持续时间中位数(IQR)增加了 171.1%(158.3%-184.3%),情况 3 的累积试验持续时间中位数(IQR)增加了 311.9%(282.0%-349.1%)。在初始和随后评估的干预措施中都观察到平台试验的成本和时间减少。

结论和相关性

尽管建立平台试验可能需要更长的时间并且成本更高,但这项研究的结果表明,拥有单一基础设施可以提高成本和努力方面的效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61b7/9277502/fffc7d422b08/jamanetwopen-e2221140-g001.jpg

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