估计平均治疗效果对生存结果的匹配加回归调整:mosunetuzumab治疗复发/难治性滤泡性淋巴瘤的案例研究

IF 3.7 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES BMC Medical Research Methodology Pub Date : 2025-02-01 DOI:10.1186/s12874-025-02456-x
Danilo Di Maio, S A Mitchell, S Batson, E Keeney, Howard H Z Thom
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引用次数: 0

摘要

背景和目的:国家健康和护理卓越研究所(英格兰的卫生技术评估机构)建议使用平均治疗效果(ATE)作为经济评估的估计。然而,关于估计ATE的方法的文献有限,特别是在生存结果的情况下。单臂试验和实际数据在卫生技术评估中发挥着越来越大的作用,特别是在肿瘤学/罕见疾病方面,因此需要新的ATE估计方法。本研究旨在展示该方法对生存结果的适应性和实用性。方法:该方法基于“双鲁棒”方法,结合匹配和回归调整(Austin 2020),使用威布尔模型(最低Akaike信息标准[AIC]规范)估计反事实事件时间。作为一个案例研究,我们比较了mosunetuzumab与利妥昔单抗/苯达莫司汀,作为利妥昔单抗/化疗的代理,治疗3L+复发/难治性滤泡性淋巴瘤。使用了mosunetuzumab (NCT02500407)和两个利妥昔单抗/苯达莫司汀3L+滤泡性淋巴瘤队列(NCT02187861/NCT02257567)的个体患者数据。终点包括总生存期(OS)和无进展生存期(PFS)。进行敏感性分析以检验事件时间对不同分布假设(对数正态、对数逻辑和指数)或模型规范(第二、第三和第四最低AIC)的稳健性。结果:病例研究发现mosunetuzumab改善了PFS(风险比[HR] 0.43[95%可信区间(CI): 0.13, 0.91])和OS (HR 0.30 [95% CI: 0.05, 5.28])。在敏感性分析中观察到一致的结果(HR范围分别为0.25-0.47和0.21-0.50,所有ci不包括/包括PFS/OS的1)。讨论/结论:拟议的调整扩大了使用“双重稳健”方法估计卫生技术评估中生存结果的(当地)ATE的可用方法范围。在我们的案例研究中,这种方法对于建模决策显得相对稳健。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Matching plus regression adjustment for the estimation of the average treatment effect on survival outcomes: a case study with mosunetuzumab in relapsed/refractory follicular lymphoma.

Background and objectives: The National Institute for Health and Care Excellence (England's health technology assessment body) recommend the use of the average treatment effect (ATE) as an estimand for economic evaluations. However there is limited literature on methods to estimate the ATE, particularly in the case of survival outcomes. Single-arm trials and real-world data are playing an increasing role in health technology assessments, particularly in oncology/rare diseases, generating a need for new ATE estimation methods. This study aimed to present the adaptation and utility of this methodology for survival outcomes.

Methods: The approach is based on a "doubly robust" method combining matching with regression adjustment (Austin 2020) using a Weibull model (lowest Akaike information criteria [AIC] specification) to estimate counterfactual event times. As a case study, we compared mosunetuzumab versus rituximab/bendamustine, as a proxy for rituximab/chemotherapy, in 3L+ relapsed/refractory follicular lymphoma. Individual patient data for mosunetuzumab (NCT02500407) and a combination of two rituximab/bendamustine 3L+ follicular lymphoma cohorts (NCT02187861/NCT02257567) were used. Endpoints included overall survival (OS) and progression-free survival (PFS). Sensitivity analyses were performed to test robustness to different distributional assumptions (log-normal, log-logistic and exponential) or model specifications (second, third and fourth lowest AIC) for event times.

Results: The case study found improved PFS (hazard ratio [HR] 0.43 [95% confidence interval (CI): 0.13, 0.91]) and OS (HR 0.30 [95% CI: 0.05, 5.28]) for mosunetuzumab. Consistent findings (HR range 0.25-0.47 and 0.21-0.50 with all CIs excluding/including 1 for PFS/OS, respectively) were observed in sensitivity analyses.

Discussion/conclusions: The proposed adaptation expands the range of available approaches for the estimation of the (local) ATE for survival outcomes in health technology assessments using "doubly robust" methods. This approach appeared relatively robust to modelling decisions in our case study.

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来源期刊
BMC Medical Research Methodology
BMC Medical Research Methodology 医学-卫生保健
CiteScore
6.50
自引率
2.50%
发文量
298
审稿时长
3-8 weeks
期刊介绍: BMC Medical Research Methodology is an open access journal publishing original peer-reviewed research articles in methodological approaches to healthcare research. Articles on the methodology of epidemiological research, clinical trials and meta-analysis/systematic review are particularly encouraged, as are empirical studies of the associations between choice of methodology and study outcomes. BMC Medical Research Methodology does not aim to publish articles describing scientific methods or techniques: these should be directed to the BMC journal covering the relevant biomedical subject area.
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