Evidence map›Paper›PMID 41604602›Full record

ArticleJCO clinical cancer informatics2026

Improving Survival Models in Health Care by Balancing Imbalanced Cohorts: A Novel Approach.

Catherine Ning, Dimitris Bertsimas, Per Eystein Lønning, Federico N Auecio, Richard Burkhart, Felix Balzer, Stefan Buettner, Hideo Baba, Itaru Endo, Georgios Stasinos and 4 more

Abstract read
In one paragraph

Article in JCO clinical cancer informatics, 2026. 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

14 authors.

Catherine NingOperations Research Center, Massachusetts Institute of Technology, Cambridge, MA.ORCID 0009-0004-9979-5743
Dimitris BertsimasOperations Research Center, Massachusetts Institute of Technology, Cambridge, MA.
Per Eystein LønningDepartment of Clinical Science, University of Bergen, Department of Oncology, Haukeland University Hospital, Bergen, Norway.ORCID 0000-0002-8890-6303
Federico N AuecioDepartment of General Surgery, Digestive Disease Institute, Cleveland Clinic, Cleveland, OH.
Richard BurkhartDepartment of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
Felix BalzerCharité-Universitätsmedizin Berlin, Berlin, Germany.
Stefan BuettnerDepartment of Surgery, Erasmus MC University Medical Centre, Rotterdam, the Netherlands.ORCID 0000-0002-0942-127X
Hideo BabaDepartment of Gastroenterological Surgery, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.ORCID 0000-0002-3474-2550
Itaru EndoDepartment of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan.ORCID 0000-0001-5520-8114
Georgios StasinosTechnical Chamber of Greece, Athens, Greece.
Johan GagnièreDepartment of Digestive and Hepatobiliary Surgery-Liver Transplantation U1071 Inserm/Clermont-Auvergne University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.ORCID 0000-0002-1820-3362
Cornelis VerhoefDepartment of Surgery, Erasmus MC University Medical Centre, Rotterdam, the Netherlands.
Martin E KreisDepartment of General and Visceral Surgery, Charité Campus Benjamin Franklin, Berlin, Germany.
Georgios Antonios MargonisDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-4894-5743

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

purposeWe explore whether survival model performance in underrepresented high- and low-risk subgroups-regions of the prognostic spectrum where clinical decisions are most consequential-can be improved through targeted restructuring of the training data set. Rather than modifying model architecture, we propose a novel risk-stratified sampling method that addresses imbalances in prognostic subgroup density to support more reliable learning in underrepresented tail strata.

methodsWe introduce a novel methodology that partitions patients by baseline prognostic risk and applies matching within each stratum to equalize representation across the risk distribution. We implement this framework on a cohort of 1,799 patients with resected colorectal liver metastases (CRLM), including 1,197 who received adjuvant chemotherapy and 602 who did not. All models used in this study are Cox proportional hazards models trained on the same set of selected variables. Model performance is assessed via Harrell's C index and Integrated Calibration Index, with internal validation using Efron's bias-corrected bootstrapping. External validation is conducted on two independent CRLM data sets.

resultsCox models trained on risk-balanced cohorts showed consistent improvements in internal validation compared with models trained on the full data set. The proposed approach preserved overall model calibration while noticeably improving stratified C index values in underrepresented high- and low-risk strata of the external cohorts.

conclusionOur findings suggest that survival model performance in observational oncology cohorts can be meaningfully improved through targeted rebalancing of the training data across prognostic risk strata. This approach offers a practical and model-agnostic complement to existing methods, especially in applications where predictive reliability across the full risk continuum is critical to downstream clinical decisions.

Indexed as

Colorectal NeoplasmsDelivery of Health CareLiver NeoplasmsAgedCohort StudiesFemaleHumansMaleMiddle AgedPrognosisProportional Hazards ModelsSurvival Analysis

Identifiers

PMID41604602
PMCPMC12854512

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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.