MétaCan
Menu
Back to cohort
Record W4416930951 · doi:10.1055/s-0045-1812908

AHOD2131: A Randomized Phase 3 Response-Adapted Trial Comparing Standard Therapy to Immuno-oncology for Children & Adults with Newly Diagnosed Stage I and II Hodgkin Lymphoma

2025· article· W4416930951 on OpenAlexaff
Jennifer Seelisch, Boyu Hu, Lindsay A. Renfro, Frank G. Keller, Aaron DuVall, Tara O. Henderson, Yonghui Wu, S. Y. Cho, Bradford S. Hoppe, Sarah A. Milgrom, Lisa Roth, Natalie S. Grover, Ann S. LaCasce, J M Kahn, Song Yao, Susan K. Parson, Nadia Khan, Raymond B. Mailhot Vega, Pamela S. Hinds, Peter B. Allen, Andrew M. Evens, Heiko Schöder, Sharon M. Castellino, Kara M. Kelly

Bibliographic record

VenueKlinische Pädiatrie · 2025
Typearticle
Language
FieldMedicine
TopicLymphoma Diagnosis and Treatment
Canadian institutionsChildren's Hospital of Western OntarioLondon Health Sciences CentreWestern University
Fundersnot available
KeywordsStage (stratigraphy)Hodgkin lymphomaRandomized controlled trialRadiation therapyLymphomaClinical trial

Abstract

fetched live from OpenAlex

Introduction Chemotherapy with or without radiotherapy (RT) is a standard frontline treatment for early-stage (ES) classic Hodgkin lymphoma (cHL). Toxicities due to conventional chemotherapy and RT are of concern, as incidence of cHL peaks in adolescents and young adults. Novel immunotherapy (IO) agents offer new potential frontline therapies in ES cHL that aim to improve progression-free survival (PFS) and maintain overall survival (OS), while minimizing morbidity and late effects. Methods AHOD2131 was developed collaboratively between pediatric and medical oncologists in the National Cancer Institute’s National Clinical Trial Network (NCTN) groups, aiming to harmonize IO-based treatment approaches for ES cHL. Study champions from North American (NA) cooperative groups [COG, SWOG, ECOG-ACRIN, Alliance, NRG] and experts in imaging, radiation oncology, lymphoma biology and patient-reported outcomes (PRO) were included. The resulting COG-led trial represents the largest ES cHL trial in the history of NA cooperative groups and the first to enroll patients across the age continuum. Results AHOD2131 (NCT05675410) is a randomized, phase 3 trial for patients ages 5 to 60 years with newly diagnosed stage I/II cHL, comparing the addition of brentuximab vedotin (Bv) with nivolumab to standard chemotherapy+/- involved site RT (ISRT). AHOD2131 was activated in April 2023 with a target enrollment of 1875 patients over 5 years. As of 28 May 2025, 336 sites have activated and 503 participants have enrolled. 241 (49%) patients are< 18 years of age. The primary objective is to compare PFS through a response-adapted, superiority design with either standard therapy or IO (Bv+nivolumab). Enrollment is stratified based on favorable or unfavorable risk features at registration. Based on response assessment by PET/CT (central review) after 2 cycles of ABVD, patients will be designated PET2 positive (slow early response [SER]) or PET2 negative (rapid early response [RER]). Patients with SER receive systemic therapy and ISRT while those with RER receive systemic therapy only. Key secondary endpoints include a non-inferiority comparison of 12-year OS and longitudinal PRO measures assessing health related quality of life, with 11 additional secondary endpoints and 10 exploratory aims. Conclusion AHOD2131 aims to evaluate an IO approach and establish a harmonized standard of care for ES cHL across the age continuum in the NCTN. Publication History Article published online: 02 December 2025 © 2025. Thieme. All rights reserved. Georg Thieme Verlag KG Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Randomized trial · Consensus signal: Randomized trial
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.027

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0030.002
Bibliometrics0.0000.000
Science and technology studies0.0000.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0020.004
Insufficient payload (model declined to judge)0.0080.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.023
GPT teacher head0.336
Teacher spread0.314 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designRandomized trial
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractno

Explore more

Same venueKlinische PädiatrieSame topicLymphoma Diagnosis and TreatmentFrench-language works237,207