Evidence map›Paper›PMID 42549628›Full record

ArticleStatistics in medicine2026

Conditional Estimations for Seamless Phase II/III Clinical Trials Involving Multi-Stage Early Stopping.

Siyu Zhu, Yuxuan Yang, Minggang Yin, Yixin Luo, Xueqing Liang, Shijie Yu, Chongyang Duan

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Siyu ZhuState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0009-0005-3977-4542
Yuxuan YangState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
Minggang YinState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0000-0002-4195-9360
Yixin LuoState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
Xueqing LiangState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0009-0004-2993-2722
Shijie YuState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.
Chongyang DuanState Key Laboratory of Multi-Organ Injury Prevention and Treatment, Department of Biostatistics, School of Public Health, Southern Medical University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0000-0001-7973-0353

Funding

National Natural Science Foundation of China 82273727
6 · The paper itself

Abstract

To avoid unnecessary resource expenditure resulting from the sample size overestimation in seamless phase II/III designs, multi-stage early stopping may be incorporated in the phase III component. However, existing estimation methods for seamless phase II/III designs are primarily developed for two-stage settings and do not directly accommodate designs with multi-stage early stopping in phase III. In this paper, we develop a Score-statistics-based framework for point and interval estimation in this specific class of designs. The framework provides a design-specific formulation of conditional bias adjustment, conditional median-unbiased estimation, and Rao-Blackwellization for seamless phase II/III designs with multi-stage early stopping. Conditional on the trial continuing to phase III, the proposed framework targets valid and efficient estimation of the treatment effect for the selected arm and is applicable to a range of common endpoint distributions. Within this framework, we formulate and evaluate several representative conditional estimation procedures: the multiple iterations-based conditional bias-adjusted estimator (CBAE-MI), the single iteration-based conditional bias-adjusted estimator (CBAE-SI), the conditional median unbiased estimators with the unselected treatment group effects be estimated by their maximum likelihood estimators (CMUE-MLE) or set as zero (CMUE-ZERO), and the Rao-Blackwellized (RB) estimator. In addition, to properly quantify uncertainty around the point estimates, we derive confidence intervals based on CMUE-MLE, CMUE-ZERO, and RB. Through simulation under various endpoint types and parameter configurations, we recommend employing RB for point estimation and confidence interval, as it demonstrates superior robustness and conservative coverage probability across treatment selection and trial design settings.

Indexed as

Clinical Trials, Phase II as TopicClinical Trials, Phase III as TopicEarly Termination of Clinical TrialsBiasComputer SimulationHumansModels, StatisticalResearch DesignSample Sizeconfidence intervalphase II/III designpoint estimationseamless sequential designselected treatment

Identifiers

PMID42549628
PMCPMC13435242

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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.