Evidence map›Paper›PMID 41806695›Full record

ArticleComputers in biology and medicine2026

Empirical evaluation of variability and multi-institutional generalizability of deep learning survival models: application to renal cancer CT scans.

Brennan Flannery, Thomas DeSilvio, Mohsen Hariri, Amir Reza Sadri, Nicholas Heller, Christopher Weight, Satish E Viswanath

Abstract readMulticenter Study
In one paragraph

Article in Computers in biology and medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

7 authors.

Brennan FlanneryCase Western Reserve University, Department of Biomedical Engineering, 10900 Euclid Ave, Cleveland, OH 44106, USA. Electronic address: bxf169@case.edu.
Thomas DeSilvioCase Western Reserve University, Department of Biomedical Engineering, 10900 Euclid Ave, Cleveland, OH 44106, USA.
Mohsen HaririCase Western Reserve University, Department of Computer and Data Sciences, 10900 Euclid Ave, Cleveland, OH 44106, USA.
Amir Reza SadriCase Western Reserve University, Department of Biomedical Engineering, 10900 Euclid Ave, Cleveland, OH 44106, USA.
Nicholas HellerCleveland Clinic, Department of Urology, 9500 Euclid Ave, Cleveland, OH 44106, USA.
Christopher WeightCleveland Clinic, Department of Urology, 9500 Euclid Ave, Cleveland, OH 44106, USA.
Satish E ViswanathCase Western Reserve University, Department of Biomedical Engineering, 10900 Euclid Ave, Cleveland, OH 44106, USA; Louis Stokes Veteran Affairs Medical Center, 10701 East Blvd, Cleveland, OH 44106, USA. Electronic address: satish.viswanath@emory.edu.

Funding

Interdisciplinary Biomedical Imaging Training ProgramT32EB007509 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI DAVID Lynn WILSON, Xin Yu · 2007 to 2026
$5.6M
Cardiovascular risk from comprehensive evaluation of the CT calcium score examR01HL165218 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI Sanjay Rajagopalan, DAVID Lynn WILSON · 2023 to 2026
$3.8M
OPtimizing Technology to Improve Medication Adherence and BP Control (OPTIMA-BP).R01NR019585 · NINR · CASE WESTERN RESERVE UNIVERSITY · PI STILL, CAROLYN HARMON · 2021 to 2025
$3.4M
Novel radiomic signatures for treatment response to neoadjuvant therapy in rectal cancersR01CA280981 · NCI · EMORY UNIVERSITY · PI ANDREI SARAIVA PURYSKO, Emily Steinhagen · 2024 to 2026
$1.7M
AI-Driven Digital Pathology Tool for Evaluating Inflammation and Therapeutic Efficacy in Preclinical ModelsR01EB037526 · NIBIB · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Maneesh Dave · 2025 to 2026
$1.4M
Image informatics tools for curation and prognostic modeling in pediatric brain tumorsU01CA294415 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Pallavi Tiwari, Satish Easwar Viswanath · 2025 to 2026
$783k
Pathologically Interpretable Computational Imaging Predictor for Response to Total Neoadjuvant Treatment in Rectal CancersF31CA291057 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI DESILVIO, THOMAS · 2025 to 2025
$50k
BLRD VA I01 BX006439NCI NIH HHS F31 CA291057NCI NIH HHS R01 CA280981NCI NIH HHS U01 CA294415NHLBI NIH HHS R01 HL165218NIBIB NIH HHS R01 EB037526NIBIB NIH HHS T32 EB007509NINR NIH HHS R01 NR019585
6 · The paper itself

Abstract

Deep learning survival (DLS) modeling has shown significant promise across multiple disease conditions for predicting patient outcomes via biomedical data, but remain relatively under-explored in conjunction with medical imaging. This poses the question of what methodological choices promote model generalization, especially when predicting continuous survival outcomes in external validation cohorts. In this work, we systematically examined the impact of data partitioning, data order, model initialization, and augmentation strategies on the generalization of CT-based DLS survival models in renal cancers. A multi-institutional CT cohort was assembled, leveraging public repositories such as TCGA-KIRC, TCGA-KICH, TCGA-KIRP, and KITS19; totaling 525 patients from across 9 institutions. A 3D ResNet-18 model was trained to predict overall patient survival with a Cox loss function and evaluated across three controlled experiments: (i) random versus covariate-balanced data partitioning, (ii) randomizing vs fixing data ordering and initial model weights, and (iii) varying intensity, spatial, and noise based augmentations; evaluated in terms of concordance index (c-index) and hazard ratio (HR). Intelligent covariate-balanced data partitioning demonstrated optimal performance on an external validation set (c-index 0.74, HR 5.08) compared to random partitioning (c-index 0.56, HR 0.29). Different model initializations significantly impacted the average performance and variance across replicate trainings, while data ordering had little to no effect. Combining multiple augmentations produced the best performance on external validation (c-index +4.76%, HR +44.39%) compared to no augmentations, while most impactful individual augmentation type was additive gaussian noise (c-index +3.17%, HR +23.47%). Our results demonstrate that careful selection of strategies for data partitioning and ordering, weight initialization, and image augmentation are critical for developing robust and generalizable DL models for continuous survival prediction using medical imaging data.

Indexed as

Deep LearningKidney NeoplasmsTomography, X-Ray ComputedFemaleHumansMaleSurvival AnalysisCTDeep learningRadiologySurvivalVariability

Identifiers

PMID41806695
PMCPMC13054227

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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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.