Evidence map›Paper›PMID 40123326›Full record

ArticleBiometrical journal. Biometrische Zeitschrift2025

On Sample Size Determination for Augmented Tests Based on Restricted Mean Survival Time in Randomized Clinical Trials.

Satoshi Hattori, Hajime Uno

Abstract read
In one paragraph

Article in Biometrical journal. Biometrische Zeitschrift, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

2 authors.

Satoshi HattoriDepartment of Biomedical Statistics, Graduate School of Medicine and Integrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives (OTRI), Osaka University, Suita City, Osaka, Japan.ORCID 0000-0002-0200-1408
Hajime UnoDepartment of Medical Oncology, Division of Population Sciences, Dana-Farber Cancer Institute, Department of Medicine, Harvard Medical School, Massachusetts, USA.ORCID 0000-0003-0622-8471

Funding

Survival Data Analysis using general censoring-free incident rateR01GM152499 · NIGMS · DANA-FARBER CANCER INST · PI Hajime Uno · 2024 to 2026
$1.0M
McGraw/Patterson Research Fund (HU)Ministory of Education, Science, Sports and Technology 16H06299Ministory of Education, Science, Sports and Technology 16K12403Ministory of Education, Science, Sports and Technology 18H03208National Institute of General Medical Sciences of the National Institutes of Health R01GM152499NIGMS NIH HHS R01 GM152499
6 · The paper itself

Abstract

Restricted mean survival time (RMST) is gaining attention as a measure to quantify the treatment effect on survival outcomes in randomized clinical trials. Several methods to determine sample size based on the RMST-based tests have been proposed. However, to the best of our knowledge, there is no discussion about the power and sample size regarding the augmented version of RMST-based tests, which utilize baseline covariates for a gain in estimation efficiency and in power for testing no treatment effect. The conventional event-driven study design based on the logrank test allows us to calculate the power for a given hazard ratio without specifying the survival functions. In contrast, the existing sample size determination methods for the RMST-based tests relies on the adequacy of the assumptions of the entire survival curves of two groups. Furthermore, to handle the augmented test, the correlation between the baseline covariates and the martingale residuals must be handled. To address these issues, we propose an approximated sample size formula for the augmented version of the RMST-based test, which does not require specifying the entire survival curve in the treatment group, and also a sample size recalculation approach to update the correlations between the baseline covariates and the martingale residuals with the blinded data. The proposed procedure will enable the studies to have the target power for a given RMST difference even when correct survival functions cannot be specified at the design stage.

Indexed as

BiometryRandomized Controlled Trials as TopicHumansSample SizeSurvival Analysisaugmentationblinded sample size re‐estimationmartingale residualnonproportional hazards

Identifiers

PMID40123326
PMCPMC11931358

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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.