Evidence map›Paper›PMID 41391612›Full record

ArticleInternational journal of radiation oncology, biology, physics2026

Multimodality Artificial Intelligence for Involved-Site Radiation Therapy: Clinical Target Volume Delineation in High-Risk Pediatric Hodgkin Lymphoma.

Xin Tie, Sarah A Milgrom, Andrea C Lo, Anne-Marie Charpentier, Michael J LaRiviere, Danyal Maqbool, Steve Y Cho, Kara M Kelly, David Hodgson, Sharon M Castellino and 2 more

Abstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Xin TieDepartment of Radiology, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin.
Sarah A MilgromDepartment of Radiation Oncology, University of Colorado School of Medicine, Aurora, Colorado.
Andrea C LoDepartment of Radiation Oncology, BC Cancer, Vancouver Center, Vancouver, Canada.
Anne-Marie CharpentierDepartment of Radiation Oncology, Centre Hospitalier de l'Universite de Montreal, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.
Michael J LaRiviereDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
Danyal MaqboolDepartment of Radiology, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin.
Steve Y ChoDepartment of Radiology, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin; University of Wisconsin Carbone Comprehensive Cancer Center, Madison, Wisconsin.
Kara M KellyDepartment of Pediatric Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New York; Department of Pediatrics, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York.
David HodgsonRadiation Medicine Program, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Sharon M CastellinoDepartment of Pediatrics, Emory University School of Medicine, Atlanta, Georgia; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Bradford S HoppeDepartment of Radiation Oncology, Mayo Clinic, Jacksonville, Florida.
Tyler J BradshawDepartment of Radiology, School of Medicine and Public Health, University of Wisconsin, Madison, Wisconsin. Electronic address: tbradshaw@wisc.edu.

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
IROC: Enhancing local enrolling site radiological data capture capabilities for NCTN trialsU24CA180803 · NCI · AMERICAN COLLEGE OF RADIOLOGY · PI Thomas J. FitzGerald, MICHAEL V KNOPP · 2014 to 2026
$116.2M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
QUALITY ASSURANCE REVIEW CENTER (QARC)U10CA029511 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FITZGERALD, THOMAS J. · 1985 to 2013
$23.4M
Multimodal Learning for Contextually-Aware Longitudinal PET/CT image analysisR01EB033782 · NIBIB · UNIVERSITY OF WISCONSIN-MADISON · PI Tyler J Bradshaw · 2024 to 2026
$1.7M
Advancing novel therapeutics and translational science to close the survivorship gap in pediatric, adolescent and young adult (AYA) lymphomaR50CA285492 · NCI · EMORY UNIVERSITY · PI SHARON MARIE CASTELLINO · 2024 to 2026
$537k
NCI NIH HHS R50 CA285492NCI NIH HHS U10 CA029511NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA180803NIBIB NIH HHS R01 EB033782
6 · The paper itself

Abstract

purposeClinical target volume (CTV) delineation for involved-site radiation therapy (ISRT) in Hodgkin lymphoma (HL) is time-consuming because of the need to analyze multi-timepoint positron emission tomography (PET)/computed tomography (CT) scans coregistered to the planning CT. Our goal was to develop automated CTV segmentation algorithms that integrated multimodality imaging to facilitate ISRT planning. METHODS AND MATERIALS: This study included planning CT, baseline PET/CT (PET1), and interim PET/CT (PET2) scans from 288 pediatric patients with high-risk HL enrolled in the Children's Oncology Group AHOD 1331 trial. Data from 58 patients across 24 institutions were held out for external testing, while the remaining 230 cases from 95 institutions were used for model development. We investigated 3 deep learning (DL) architectures (SegResNet, ResUNet, and SwinUNETR) and evaluated the impact of incorporating PET1 and PET2 images along with the planning CT. Performance was assessed using the Dice similarity coefficient (DSC) and 95% Hausdorff distance (HD95). Interobserver variability was estimated by comparing original institutional CTVs with those newly delineated by 4 radiation oncologists on 10 cases. The quality of CTVs generated by the top-performing model was independently assessed by radiation oncologists in 40 other cases using a 5-point Likert scale and compared against the original institutional CTVs.

resultsIn the external cohort, a SwinUNETR model incorporating planning CT, PET1, and PET2 images achieved the highest performance, with a DSC of 0.72 and HD95 of 34.43 mm. All models incorporating PET/CT images were significantly better (P < .01) than planning CT-only models. Interobserver variability analysis yielded a DSC of 0.70 and HD95 of 30.14 mm. In clinical evaluation, DL-generated CTVs received a mean quality score of 3.38 out of 5, comparable to original physician-delineated CTVs (3.13; P = .13)

conclusionsThe DL model was able to generate clinically useful CTVs with quality comparable to manually delineated CTVs, suggesting its potential to improve physician efficiency in ISRT planning.

Indexed as

Artificial IntelligenceDeep LearningHodgkin DiseasePositron Emission Tomography Computed TomographyRadiotherapy Planning, Computer-AssistedAdolescentAlgorithmsChildFemaleHumans

Identifiers

PMID41391612
PMCPMC12991415

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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.