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Record W2439102632 · doi:10.1093/neuonc/now073.124

HG-128BO25041 - A PHASE II OPEN-LABEL, RANDOMIZED, MULTI CENTRE COMPARATIVE STUDY OF BEVACIZUMAB BASED THERAPY IN PAEDIATRIC PATIENTS WITH NEWLY DIAGNOSED SUPRATENTORIAL, INFRATENTORIAL CEREBELLAR, OR PEDUNCULAR HIGH GRADE GLIOMA

2016· article· en· W2439102632 on OpenAlexaffabout
Jacques Grill, Darren Hargrave, Maura Massimino, Éric Bouffet, Amedeo A. Azizi, Geoffrey McCowage, Adela Cañete, Frank Saran, Marie‐Cécile Le Deley, Pascale Varlet, Paul S. Morgan, Tim Jaspan, Chris Jones, Helen Smith, Josep Garcia, Magalie Hilton, Lauren E. Abrey, Raphaël F. Rousseau, Gilles Vassal

Bibliographic record

VenueNeuro-Oncology · 2016
Typearticle
Languageen
FieldMedicine
TopicGlioma Diagnosis and Treatment
Canadian institutionsHospital for Sick Children
Fundersnot available
KeywordsBevacizumabMedicineOpen labelGliomaRandomized controlled trialSurgeryChemotherapyCancer research

Abstract

fetched live from OpenAlex

The prognosis for paediatric patients with newly diagnosed HGG remains poor; there is an unmet clinical need for new therapies. Bevacizumab is an anti-VEGF-A monoclonal antibody, which has been shown to improve PFS of newly diagnosed glioblastoma in adults and has been approved for use in adult patients with recurrent glioblastoma. The randomized phase II HERBY trial (BO25041; NCT01390948) evaluated the efficacy and safety of bevacizumab in addition to standard of care (RT/TMZ) in paediatric and adolescent patients with newly diagnosed HGG. Study patients were aged ≥3 and <18 years (median 10.5 years). Patients with gliomatosis cerebri, multifocal or metastatic high-grade gliomas were not included in the trial. Randomization was stratified on age, extent of resection, and tumor grade. Online central pathology review was requested to confirm the diagnosis before study entry. Online central radiology review was performed in case pseudoprogression was suspected before treatment discontinuation. Histone status was determined by Sanger sequencing. Hundred and twenty one patients were enrolled from October 2011 to February 2015 in 70 centers distributed in Europe, Australia ans Canada. Fifty percent of patients had a total/near total resection. The two arms did not show a difference in event-free survival (EFS), the primary efficacy endpoint (HR: 1.44 (95% CI: 0.90, 2.30), p-value: 0.13 (log-rank test)) after central review. Similar results were shown when considering the local investigator's evaluations. One year-EFS rate was 38% (95% CI: 26, 51) in the experimental arm vs 48% (95% CI: 35, 61) in the standard arm. The two arms did not show a difference in overall survival (OS), the secondary efficacy endpoint (HR: 1.23 (95% CI: 0.72, 2.09), p-value: 0.46 (log-rank test)). No new safety signals was identified. The incidence of Grade 3-5 AEs was comparable between the two treatment arms (42% vs. 38% in the experimental and standard arms, respectively). Proteinuria was observed in 13.3% of patients in the Bevacizumab arm (compared to 8.1% reported in the whole previous experience with bevacizumab). Twelve patients (20%) had to discontinue bevacizumab because of toxicity. More patients had to discontinue any component of the treatment due to toxicity in the experimental arm compared to the standard arm (22% vs 5%, respectively). In conclusion, these results do not support the use of bevacizumab in the routine management of pediatric HGG as an adjunct to the standard radiochemotherapy with temozolomide.

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 score0.335
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0030.000
Bibliometrics0.0010.001
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 head0.047
GPT teacher head0.337
Teacher spread0.290 · 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
Published2016
Admission routes2
Has abstractyes

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