Evidence map›Paper›PMID 40836219›Full record

ArticleBMC medical research methodology2025

A multistate transition model for survival estimation in randomized trials with treatment switching and a cured subgroup.

Haixia Hu, Ling Wang, Kejian Wu, Wei Ge, Jielai Xia, Chen Li

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

Haixia HuDepartment of Health Statistics, School of Preventive Medicine, Fourth Military Medical University, Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, No.169 Changlexilu Road, Xi'an, Shaanxi, 710032, China.
Ling WangDepartment of Health Statistics, School of Preventive Medicine, Fourth Military Medical University, Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, No.169 Changlexilu Road, Xi'an, Shaanxi, 710032, China. wl.medstat@qq.com.
Kejian WuDepartment of Mathematics and Physics, Basic Medical Science Academy, Fourth Military Medical University, Xi'an, Shaanxi, China.
Wei GeDepartment of Field and Disaster Nursing, Fourth Military Medical University, Xi'an, Shaanxi, China.
Jielai XiaDepartment of Health Statistics, School of Preventive Medicine, Fourth Military Medical University, Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, No.169 Changlexilu Road, Xi'an, Shaanxi, 710032, China.
Chen LiDepartment of Health Statistics, School of Preventive Medicine, Fourth Military Medical University, Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, No.169 Changlexilu Road, Xi'an, Shaanxi, 710032, China. lc.biosta@qq.com.

Funding

National Natural Science Foundation of China 82273728National Natural Science Foundation of China 82273729National Natural Science Foundation of China 82373680
6 · The paper itself

Abstract

Although many methods have been proposed on the overall survival estimation in randomized trials permitting treatment switching after the progressive disease (PD), the cured subgroup of patients within these trials has not been fully considered. These cured patients would never experience PD and subsequent risk of treatment switching, yet they may suffer death hazard similar to those without the disease. Due to the mix of the cured subgroup, existing methods may yield biased effect estimation for the uncured patients between treatment groups. To address this limitation, we propose a multistate transition model that integrates multi-states of the cure, PD, treatment switching, and death during trials. In this model, the cure probability for all the patients and the death hazard of the cured subgroup are modeled separately. Meanwhile, the semi-competing risks model is used for the treatment effect evaluation on the uncured patients through transitional hazards between states of PD, treatment switching, and death. The particle swarm optimization algorithm is employed to estimate the model parameters. Extensive simulation studies have been conducted to assess the performance of the proposed multistate model in comparison with existing treatment switching adjustment methods. The results show that the treatment effect estimations of our proposed model are more accurate across all scenarios. Moreover, the illustration based on a simulated diffuse large B-cell lymphoma trial demonstrates the applicability and advantages of the proposed model. The robustness of the proposed multistate transition model enables it to accurately estimate the treatment effect in trials that involve a cured subgroup and the treatment switching after PD.

Indexed as

Models, StatisticalRandomized Controlled Trials as TopicAlgorithmsComputer SimulationDisease ProgressionHumansSurvival AnalysisCured subgroupEffect estimationMultistate modelSemi-competing risksTreatment switching

Identifiers

PMID40836219
PMCPMC12366173

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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.