Evidence map›Paper›PMID 41085870›Full record

ArticleLifetime data analysis2025

Assessing delayed treatment benefits of immunotherapy using long-term average hazard: a novel test/estimation approach.

Miki Horiguchi, Lu Tian, Kenneth L Kehl, Hajime Uno

Abstract read
In one paragraph

Article in Lifetime data analysis, 2025. 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

4 authors.

Miki HoriguchiDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.ORCID 0000-0002-9800-1954
Lu TianDepartment of Biomedical Data Science, Stanford University, Stanford, CA, 94305, USA.ORCID 0000-0002-5893-0169
Kenneth L KehlDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA.
Hajime UnoDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA, 02215, USA. huno@ds.dfci.harvard.edu.ORCID 0000-0003-0622-8471

Funding

Statistical Methods for Optimizing Personalized Treatment SelectionR01HL089778 · NHLBI · STANFORD UNIVERSITY · PI LU TIAN · 2008 to 2026
$4.8M
Survival Data Analysis using general censoring-free incident rateR01GM152499 · NIGMS · DANA-FARBER CANCER INST · PI Hajime Uno · 2024 to 2026
$1.0M
NHLBI NIH HHS R01 HL089778NHLBI NIH HHS R01HL089778NIGMS NIH HHS R01GM15249NIGMS NIH HHS R01 GM152499
6 · The paper itself

Abstract

Delayed treatment effects on time-to-event outcomes are commonly observed in randomized controlled trials of cancer immunotherapies. When the treatment effect has a delayed onset, the conventional test/estimation approach-using the log-rank test for between-group comparison and Cox's hazard ratio to quantify the treatment effect-can be suboptimal. The log-rank test may lack power in such scenarios, and the interpretation of the hazard ratio is often ambiguous. Recently, alternative test/estimation approaches have been proposed to address these limitations. One such approach is based on long-term restricted mean survival time (LT-RMST), while another is based on average hazard with survival weight (AH-SW). This paper integrates these two concepts and introduces a novel long-term average hazard (LT-AH) approach with survival weight for both hypothesis testing and estimation. Numerical studies highlight specific scenarios where the proposed LT-AH method achieves higher power than the existing alternatives. The LT-AH for each group can be estimated nonparametrically, and the proposed between-group comparison maintains test/estimation coherency. Because the difference and ratio of LT-AH do not rely on model assumptions about the relationship between two groups, the LT-AH approach provides a robust framework for estimating the magnitude of between-group differences. Furthermore, LT-AH allows for treatment effect quantification in both absolute (difference in LT-AH) and relative (ratio of LT-AH) terms, aligning with guideline recommendations and addressing practical needs. Given its interpretability and improved power in certain settings, the proposed LT-AH approach offers a useful alternative to conventional hazard-based methods, particularly when delayed treatment effects are expected.

Indexed as

ImmunotherapyNeoplasmsHumansProportional Hazards ModelsRandomized Controlled Trials as TopicSurvival AnalysisTime FactorsTreatment DelayTreatment OutcomeAverage intensityGeneral censoring-free incidence rateImmunotherapyNon-proportional hazardsRestricted mean survival timeT-year event rate

Identifiers

PMID41085870
PMCPMC12586407

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.