Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models01:06

Model Approaches for Pharmacokinetic Data: Distributed Parameter Models

333
Pharmacokinetic models are mathematical constructs that represent and predict the time course of drug concentrations in the body, providing meaningful pharmacokinetic parameters. These models are categorized into compartment, physiological, and distributed parameter models.
The distributed parameter models are specifically designed to account for variations and differences in some drug classes. This model is particularly useful for assessing regional concentrations of anticancer or...
333
Pharmacokinetic Models: Comparison and Selection Criterion01:26

Pharmacokinetic Models: Comparison and Selection Criterion

490
Physiological and compartmental models are valuable tools used in studying biological systems. These models rely on differential equations to maintain mass balance within the system, ensuring an accurate representation of the dynamic processes at play.
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.
490

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Diagnostic performance of commercial AI systems versus participating radiologists for pulmonary nodule detection in routine clinical practice.

Japanese journal of radiology·2026
Same author

Radiation-Based Multimodal Strategies for Esophageal Squamous Cell Carcinoma: From Definitive Chemoradiotherapy to Salvage Treatment.

Cancers·2026
Same author

Photon beam energy selection for scalp dose reduction in whole-brain radiotherapy: a benchmark phantom study.

Radiological physics and technology·2026
Same author

A model-based selection of oral cancer patient for passive scattering proton beam therapy.

Journal of radiation research·2026
Same author

Development of a practical and high-speed deep learning-based dose calculation model in boron neutron capture therapy for head and neck cancer.

Medical physics·2026
Same author

Feasibility of retrieval-augmented generation for large language models with Japanese input in radiotherapy.

Journal of radiation research·2026

Related Experiment Video

Updated: May 2, 2026

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
08:34

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies

Published on: February 6, 2019

21.2K

Generalizability of deep learning-based dose conversion model in proton beam therapy.

Ryohei Kato1,2, Noriyuki Kadoya2, Takahiro Kato3

  • 1Department of Radiation Physics and Technology, Southern Tohoku Proton Therapy Center, Koriyama, Fukushima, Japan.

Journal of Applied Clinical Medical Physics
|February 27, 2026
PubMed
Summary

Deep learning models can accurately convert proton beam therapy (PBT) doses to Monte Carlo (MC) equivalent doses, improving treatment planning speed and accuracy across various tumor sites.

Keywords:
Monte Carlodeep learningproton therapy

More Related Videos

A Whole Body Dosimetry Protocol for Peptide-Receptor Radionuclide Therapy PRRT: 2D Planar Image and Hybrid 2D+3D SPECT/CT Image Methods
09:49

A Whole Body Dosimetry Protocol for Peptide-Receptor Radionuclide Therapy PRRT: 2D Planar Image and Hybrid 2D+3D SPECT/CT Image Methods

Published on: April 24, 2020

10.5K
Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform
07:57

Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform

Published on: March 24, 2022

3.3K

Related Experiment Videos

Last Updated: May 2, 2026

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies
08:34

Proton Therapy Delivery and Its Clinical Application in Select Solid Tumor Malignancies

Published on: February 6, 2019

21.2K
A Whole Body Dosimetry Protocol for Peptide-Receptor Radionuclide Therapy PRRT: 2D Planar Image and Hybrid 2D+3D SPECT/CT Image Methods
09:49

A Whole Body Dosimetry Protocol for Peptide-Receptor Radionuclide Therapy PRRT: 2D Planar Image and Hybrid 2D+3D SPECT/CT Image Methods

Published on: April 24, 2020

10.5K
Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform
07:57

Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform

Published on: March 24, 2022

3.3K

Area of Science:

  • Medical Physics
  • Radiotherapy
  • Computational Biology

Background:

  • Proton beam therapy (PBT) faces dose uncertainties in inhomogeneous regions with analytical pencil beam (PB) algorithms.
  • Accurate Monte Carlo (MC) dose calculations are time-consuming, creating a trade-off between speed and precision.
  • Deep learning (DL) offers a solution by converting PB doses to MC-equivalent distributions, but generalizability across tumor sites requires investigation.

Purpose of the Study:

  • To develop and evaluate a DL-based dose conversion model for PBT.
  • To assess the model's generalizability across diverse and previously untrained tumor sites.

Main Methods:

  • A DL model was trained on PBT data from 339 patients across four tumor sites (head and neck, lung, liver, prostate).
  • The model inputs CT images and PB doses to output MC-equivalent doses.
  • Generalizability was tested on seven untrained tumor sites, with performance assessed using 3D γ-analysis and Dice Similarity Coefficient (DSC).

Main Results:

  • The DL model achieved high accuracy (≥90% γ-passing rate with 3%/2mm criteria) for most untrained tumor sites.
  • Slightly lower passing rates were observed for esophagus (91.3%), breast (85.9%), and limb bone/soft tissue (89.1%).
  • Average DSC values exceeded 0.8 for most untrained sites, indicating good performance.

Conclusions:

  • The developed DL model demonstrates significant accuracy and generalizability for MC-equivalent dose conversion in PBT.
  • The model's adaptability extends to various tumor sites, including those not included in the initial training.
  • This approach can aid PBT centers in handling diverse patient data and rare diseases.