Evidence map›Paper›PMID 41286498›Full record

ArticleNPJ precision oncology2025

Evaluating the application of dynamic prediction models in oncological prognostic studies with repeated measurement predictors.

Qian Zhou, Zhi-Hang Chen, Sui Peng

Registry-linked trialAbstract read
In one paragraph

Article in NPJ precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07644390 (Integration of Subphenotypic Lesions, Imaging-Based Healing Outcomes, and Biomarker Trajectories in a Retrospective Analysis of a Single-Center Retrospective Crohn's Disease Cohort), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT07644390 completednot on this map

Integration of Subphenotypic Lesions, Imaging-Based Healing Outcomes, and Biomarker Trajectories in a Retrospective Analysis of a Single-Center Retrospective Crohn's Disease Cohort

TypeobservationalSponsorSixth Affiliated Hospital, Sun Yat-sen UniversityRan2010 to 2026Enrolled500ConditionsCrohn Disease (CD), Dynamic Prediction Model
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

3 authors.

Qian Zhou *Department of Medical Statistics, Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. zhouq49@mail.sysu.edu.cn.
Zhi-Hang Chen *Department of Liver Surgery, Center of Hepato-pancreato-biliary Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Sui PengClinical Trials Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China. pengsui@mail.sysu.edu.cn.

Funding

National Natural Science Foundation of China 82404079
6 · The paper itself

Abstract

Recent cancer prognosis research emphasizes longitudinal data's importance for survival prediction, yet its analysis challenges researchers, often leading to oversimplified dual-timepoint comparisons (e.g., pre- vs. post-treatment). To meet precision oncology needs, this study evaluated dynamic prediction model (DPM) applications by a cross-sectional analysis of published studies. A comprehensive search of PubMed and Web of Science identified 6,549 records, from which 174 DPMs in 165 studies were analyzed. These studies covered 19 cancers and showed a rising trend in DPM usage (trend test, p < 0.001). Notably, 58.6% of studies used only one dynamic predictor. Seven DPM categories were identified: two-stage models (most common at 32.2%), joint models (28.2%), time-dependent covariate models (12.6%), multi-state models (10.3%), landmark Cox models (8.6%), artificial intelligence (4.6%), and others (3.4%). DPM distribution significantly shifted over 5 years (Chi-square test, p < 0.001), trending towards joint models and AI. We described and compared these DPMs across multiple dimensions, including principles, advantages and limitations, and clinical application scenarios. Joint models, integrating longitudinal and survival data, and artificial intelligence, extracting high-dimensional features, offer promising precision prognosis pathways. Future research should prioritize developing DPMs capable of handling high-dimensional data from smaller samples to improve treatment monitoring and prognosis.

Identifiers

PMID41286498
PMCPMC12644621

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Registered trials

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.