Evidence map›Paper›PMID 41906079›Full record

ArticleBMC medical research methodology2026

Rationale for incorporating short-term endpoints in interim futility analysis of phase 3 oncology trials: a simulation study.

Shuhan Liu, Zhihao Cheng, Ben Zhang, Fangrong Yan, Bosheng Li, Tao Zhang

Abstract read
In one paragraph

Article in BMC medical research methodology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shuhan Liu *Department of Biostatistics, China Pharmaceutical University, 639 Longmian Dadao, Nanjing, 211198, China.
Zhihao Cheng *Innovative Clinical Research and Development Centre, Qilu Pharmaceutical Co., Ltd, No.8888 Lvyou Road, High-tech Zone, Jinan, 250100, China.
Ben ZhangInnovative Clinical Research and Development Centre, Qilu Pharmaceutical Co., Ltd, No.8888 Lvyou Road, High-tech Zone, Jinan, 250100, China.
Fangrong YanDepartment of Biostatistics, China Pharmaceutical University, 639 Longmian Dadao, Nanjing, 211198, China.
Bosheng LiDepartment of Biostatistics, China Pharmaceutical University, 639 Longmian Dadao, Nanjing, 211198, China. boshengli@foxmail.com.
Tao ZhangInnovative Clinical Research and Development Centre, Qilu Pharmaceutical Co., Ltd, No.8888 Lvyou Road, High-tech Zone, Jinan, 250100, China. tao26.zhang@qilu-pharma.com.

Funding

Fundamental Research Funds for the Central Universities No. 2632023FY05National Natural Science Foundation of China No. 82273735the General Program of China Postdoctoral Science Foundation No. 2025M780727
6 · The paper itself

Abstract

backgroundFutility analysis is a critical component of phase III oncology trials, enabling early termination of ineffective treatments to save resources and time. However, these interim analyses are often challenged by insufficient data for long-term primary endpoints, such as overall survival.

methodsA comprehensive simulation study was conducted to model various phase III trial scenarios. This simulation study investigates the benefits of utilizing mixture models to incorporate short-term endpoint information for enhancing futility stopping decisions across various scenarios.

resultsWhen the short-term endpoint was strongly predictive of the long-term endpoint, its inclusion via mixture models increases trial power and the probability of correctly stopping for futility, leading to reduced expected trial duration and sample size. In scenarios with delayed treatment effects, simple mixture models perform poorly; however, by employing mixture segmented hazards models to account for the delays, the benefits of integrating short-term endpoints remain evident. Importantly, when the short-term endpoint was non-predictive or contradictory, its inclusion did not inflate the Type I error rate or otherwise negatively impact the trial’s integrity.

conclusionsIncorporating short-term endpoint information into futility analysis through appropriately specified mixture models is a robust and efficient strategy. Our findings provide evidence-based guidance for the design of adaptive clinical trials.

Indexed as

Clinical Trials, Phase III as TopicEndpoint DeterminationMedical FutilityMedical OncologyNeoplasmsComputer SimulationHumansModels, StatisticalResearch DesignSample SizeDelayed Treatment EffectFutility AnalysisInterim AnalysisMixture ModelsShort-term Endpoint

Identifiers

PMID41906079
PMCPMC13220472

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.