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Record W4415507443 · doi:10.1016/j.eclinm.2025.103539

Avasopasem manganese treatment for severe oral mucositis from chemoradiotherapy for locally advanced head and neck cancer: phase 3 randomized controlled trial (ROMAN)

2025· article· en· W4415507443 on OpenAlexaff
Carryn M. Anderson, Christopher M. Lee, Joseph Randall Kelley, Gary V. Walker, Neal Dunlap, Voichita Bar‐Ad, Douglas A. Miller, Vernon King, Abhinand Peddada, D. Ciuba, F. Vincent, Brian C. Muzyka, Amanda Gillespie-Twardy, Stephen T. Sonis, Jon Holmlund, Robert A. Beardsley, Eugene P. Kennedy, Deborah Saunders

Bibliographic record

VenueEClinicalMedicine · 2025
Typearticle
Languageen
FieldMedicine
TopicOral health in cancer treatment
Canadian institutionsNortheast Cancer CentreHealth Sciences NorthCentre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec
Fundersnot available
KeywordsRandomized controlled trialMucositisChemoradiotherapyHead and neckPhases of clinical researchManganese

Abstract

fetched live from OpenAlex

Background Of patients who receive standard concomitant chemoradiation (CRT; intensity-modulated radiation therapy [IMRT] plus cisplatin) for locally advanced head and neck cancer (HNC), approximately two-thirds will develop severe oral mucositis (SOM), limiting their ability to eat solids (WHO grade 3) or drink liquids (WHO grade 4). In a randomized, double-blind phase 2b trial, avasopasem manganese substantially reduced duration and incidence of SOM versus placebo. This phase 3 trial further assessed avasopasem's reduction of SOM due to CRT. Methods In this double-blind, placebo-controlled trial (Clinicaltrials.gov: NCT03689712), patients receiving 60–72 Gy IMRT (>50 Gy to ≥2 oral mucosal sites) plus cisplatin (Q3W or QW) were randomized 3:2 to avasopasem 90 mg or placebo before each RT fraction. SOM was assessed twice weekly during IMRT, then weekly for 2 weeks. First subject was enrolled 03 October 2018 and last subject completed OM follow-up 13 September 2021. Last subject completed long-term follow-up 30 August 2021. Primary endpoint was SOM incidence through end of IMRT. Secondary endpoints included SOM duration, time to onset, grade 4 incidence and duration, tumor outcomes, and renal function. Findings 455 patients were randomized; 407 (241 avasopasem/166 placebo) were included in the primary analysis population. Statistically significant reductions in SOM incidence (54% vs 64%; relative risk=0·84, p = 0·045, 95% CI 0·71, 1·00) and SOM duration ( p = 0·002; median, 8 vs 18 days) were observed. SOM onset was nominally delayed ( p = 0·002; median, 49 vs 38 days). Grade 4 OM incidence and days were not significantly reduced by avasopasem, 27% ( p = 0·052) and 24% ( p = 0·143), respectively. Adverse event frequencies were comparable between treatments. After 1 year, tumor outcomes were maintained and two-year overall survival showed: avasopasem 89% (95% CI: 84–93) versus placebo 93% (95% CI: 88–96). Interpretation The primary endpoint of incidence was not as improved as predicted by the Phase 2b trial and avasopasem's contribution to adverse events could not be excluded. For these reasons and others discussed, ROMAN did not provide a sufficiently favorable benefit-risk determination for FDA approval. A confirmatory phase 3 trial was requested. Funding Provided by Galera Therapeutics, Inc.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
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 score0.140
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0050.001
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.044
GPT teacher head0.455
Teacher spread0.411 · 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 teacher head, not a consensus.

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

Citations3
Published2025
Admission routes1
Has abstractyes

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