Evidence map›Paper›PMID 41655816›Full record

ArticleInternational journal of radiation oncology, biology, physics2026

Subsequent Neoplasm Risk After Modern Mediastinal Radiation Therapy for Pediatric Hodgkin Lymphoma: Insights From a Multi-Institutional Children's Oncology Group Trial.

Sarah A Milgrom, Harald Paganetti, Hitesh Dama, Lindsay Renfro, Yue Wu, Isaac Meyer, Meenakshi Jeeva, Susan K Parsons, Angela Punnett, Anne-Marie Charpentier and 7 more

Abstract readMulticenter Study
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

17 authors.

Sarah A MilgromDepartment of Radiation Oncology, University of Colorado, Aurora, California.
Harald PaganettiDepartment of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Hitesh DamaDepartment of Radiation Oncology, Princess Margaret Cancer Centre and University of Toronto, Toronto, Ontario, Canada.
Lindsay RenfroDivision of Biostatistics, University of Southern California, Los Angeles, California; Children's Oncology Group, Monrovia, California.
Yue WuDepartment of Biostatistics, Children's Oncology Group, Statistics and Data Center, University of Florida, Gainesville, Florida.
Isaac MeyerDepartment of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
Meenakshi JeevaDepartment of Radiation Oncology, Princess Margaret Cancer Centre and University of Toronto, Toronto, Ontario, Canada.
Susan K ParsonsDivision of Hematology/Oncology and Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, Massachusetts.
Angela PunnettDivision of Hematology/Oncology, SickKids Hospital, University of Toronto, Toronto, Ontario, Canada.
Anne-Marie CharpentierDepartment of Radiation Oncology, Centre hospitalier de l'Université de Montréal, Montreal, Québec, Canada.
Andrea C LoDepartment of Radiation Oncology, British Columbia Cancer, Vancouver, British Columbia, Canada.
Raymond Mailhot VegaDepartment of Radiation Oncology, University of Florida, Jacksonville, Florida.
Frank G KellerDepartment of Pediatrics, Emory University, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Kara M KellyDepartment of Pediatric Oncology, Roswell Park Comprehensive Cancer Center and University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York.
Bradford S HoppeDepartment of Radiation Oncology, Mayo Clinic Florida, Jacksonville, Florida.
Sharon M CastellinoDepartment of Pediatrics, Emory University, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
David HodgsonDepartment of Radiation Oncology, Princess Margaret Cancer Centre and University of Toronto, Toronto, Ontario, Canada.

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
QUALITY ASSURANCE REVIEW CENTER (QARC)U10CA029511 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FITZGERALD, THOMAS J. · 1985 to 2013
$23.4M
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 CA098543NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA180803
6 · The paper itself

Abstract

purposeThe reported incidence of subsequent malignant neoplasms (SMNs) in long-term survivors of pediatric classic Hodgkin lymphoma (cHL) is based on patients treated with outdated radiation therapy (RT) doses and techniques. The risk associated with modern mediastinal RT in pediatric cHL is unknown. METHODS AND MATERIALS: We modeled the risk of SMN in children with cHL who enrolled in the multi-institutional Children's Oncology Group AHOD1331 trial (2015-2019) and received mediastinal RT.

resultsAmong 587 trial patients, 296 (50%) received mediastinal RT and were eligible for this analysis. Proton therapy was used for 25%, photon intensity modulated RT (IMRT) for 46%, and photon 3-dimensional conformal RT (3D-CRT) for 28%. The RT prescription dose was 21 Gy in 83% and 30 Gy in 16%. The estimated mean lifetime attributable risk at 70 years of age of breast carcinoma (females) was 2.92% (1.45% proton; 4.36% IMRT; 1.82% 3D-CRT; P < .0001), lung carcinoma was 5.37% (4.15% proton; 6.24% IMRT; 5.07% 3D-CRT; P < .0001), and thyroid carcinoma was 0.17% (0.25% proton; 0.17% IMRT; 0.12% 3D-CRT; P = .271). The predicted risk of breast carcinoma was higher among female patients treated with their arms raised versus arms down (P < .0001).

conclusionsNormal tissue doses associated with contemporary mediastinal RT produce lower predicted SMN risks than were observed in cohorts treated with historical RT approaches, with substantial variation among individuals. On average, proton therapy is associated with a lower predicted risk. These findings have implications for the selection of therapies, counseling of patients, planning of RT, and recommendations for SMN screening.

Indexed as

Hodgkin DiseaseNeoplasms, Radiation-InducedNeoplasms, Second PrimaryAdolescentBreast NeoplasmsChildChild, PreschoolFemaleHumansLung NeoplasmsMaleMediastinumProton TherapyRadiotherapy, ConformalRadiotherapy DosageRadiotherapy, Intensity-Modulated

Identifiers

PMID41655816
PMCPMC13089109

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.