Evidence map›Paper›PMID 25962846›Full record

ArticleMedical image analysis2015

Tumor growth prediction with reaction-diffusion and hyperelastic biomechanical model by physiological data fusion.

Ken C L Wong, Ronald M Summers, Electron Kebebew, Jianhua Yao

Abstract read
In one paragraph

Article in Medical image analysis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. 75 Years of Mathematical Oncology.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Estimating Glioblastoma Biophysical Growth Parameters Using Deep Learning Regression.Brainlesion : glioma, multiple sclerosis, stroke and traumatic brain injuries. BrainLes (Workshop) · 2021
    Article
  7. Towards integration ofScientific reports · 2020
    Article
  8. Review
  9. Coupling brain-tumor biophysical models and diffeomorphic image registration.Computer methods in applied mechanics and engineering · 2019
    Article
  10. Article
  11. Article
  12. Improved brain tumor segmentation by utilizing tumor growth model in longitudinal brain MRI.Proceedings of SPIE--the International Society for Optical Engineering · 2017
    Article
  13. Article
  14. Progress in Fully Automated Abdominal CT Interpretation.AJR. American journal of roentgenology · 2016
    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

4 authors.

Ken C L WongClinical Image Processing Service, Radiology and Imaging Sciences, Clinical Center, NIH, Bethesda, MD, USA. Electronic address: ken.wong@nih.gov.
Ronald M SummersClinical Image Processing Service, Radiology and Imaging Sciences, Clinical Center, NIH, Bethesda, MD, USA. Electronic address: rsummers@cc.nih.gov.
Electron KebebewEndocrine Oncology Branch, National Cancer Institute, NIH, Bethesda, MD, USA. Electronic address: kebebewe@mail.nih.gov.
Jianhua YaoClinical Image Processing Service, Radiology and Imaging Sciences, Clinical Center, NIH, Bethesda, MD, USA. Electronic address: jyao@cc.nih.gov.

Funding

Computer Aided Detection for Radiologic ImagesZIACL040004 · CLC · CLINICAL CENTER · PI SUMMERS, RONALD M. · 2009 to 2025
$0k
Intramural NIH HHS Z99 CL999999
6 · The paper itself

Abstract

The goal of tumor growth prediction is to model the tumor growth process, which can be achieved by physiological modeling and model personalization from clinical measurements. Although image-driven frameworks have been proposed with promising results, several issues such as infinitesimal strain assumptions, complicated personalization procedures, and the lack of functional information, may limit their prediction accuracy. In view of these issues, we propose a framework for pancreatic neuroendocrine tumor growth prediction, which comprises a FEM-based tumor growth model with coupled reaction-diffusion equation and nonlinear biomechanics. Physiological data fusion of structural and functional images is used to improve the subject-specificity of model personalization, and a derivative-free global optimization algorithm is adopted to facilitate the complicated model and accommodate flexible choices of objective functions. With this flexibility, we propose an objective function accounting for both the tumor volume difference and the root-mean-squared error of intracellular volume fractions. Experiments were performed on synthetic and clinical data to verify the parameter estimation capability and the prediction performance. Comparisons of using different biomechanical models and objective functions were also performed. From the experimental results of eight patient data sets, the average recall, precision, Dice coefficient, and relative volume difference between predicted and measured tumor volumes were 84.5 ± 6.9%, 85.8 ± 8.2%, 84.6 ± 1.7%, and 14.2 ± 8.4%, respectively.

Indexed as

AlgorithmsBiomechanical PhenomenaContrast MediaFluorodeoxyglucose F18HumansNeoplasmsPositron-Emission TomographyPredictive Value of TestsRadiographic Image Interpretation, Computer-AssistedRadiopharmaceuticalsSensitivity and SpecificityTomography, X-Ray ComputedContrast MediaFluorodeoxyglucose F18RadiopharmaceuticalsDerivative-free optimizationModel personalizationNonlinear solid mechanicsPhysiological data fusionTumor growth prediction

Identifiers

PMID25962846
PMCPMC4540673

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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.