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Abstract P2-16-06: Final Overall Survival Results, Including Analysis of Patients with Triple-Negative Disease and Aged ≥70 Years, from the ATHENA Study Evaluating First-Line Bevacizumab-Containing Therapy for Locally Recurrent/Metastatic Breast Cancer

2010· article· en· W2143498161 on OpenAlexaff
Kathleen I. Pritchard, Christoph Thomssen, J-Y Pierga, H. Cortés-Funes, Laura Biganzoli, Zhong Guan, Г. М. Манихас, D Jendiroba, Beatrice Uziely, F Boyle, Agnieszka Jagiełło-Gruszfeld, Cynthia van Arkel, Y Tung, AA Dünne, IE. Smith

Bibliographic record

VenueCancer Research · 2010
Typearticle
Languageen
FieldMedicine
TopicCancer Treatment and Pharmacology
Canadian institutionsHealth Sciences CentreSunnybrook Health Science Centre
Fundersnot available
KeywordsBevacizumabMedicineTaxaneDocetaxelInternal medicineRegimenChemotherapyClinical endpointMetastatic breast cancerOncologyPopulationChemotherapy regimenSurgeryProgression-free survivalAnthracyclineCancerBreast cancerRandomized controlled trial

Abstract

fetched live from OpenAlex

Abstract Background: First-line bevacizumab combined with chemotherapy significantly improves efficacy versus chemotherapy alone in HER2-negative locally recurrent/metastatic breast cancer (LR/mBC). ATHENA, a multinational, open-label, single-arm study, further evaluated first-line bevacizumab in combination with standard chemotherapy in patients treated in routine oncology practice. Patients and methods: Eligible patients had HER2-negative LR/mBC, ECOG performance status 0-2, and had received no prior chemotherapy for LR/mBC. They received bevacizumab 10 mg/kg q2w or 15 mg/kg q3w in combination with taxane-based chemotherapy (or other non-anthracycline chemotherapy) until disease progression, unacceptable toxicity, or patient withdrawal. The primary endpoint was safety; secondary endpoints included time to progression (TTP) and overall survival (OS). Results: Between September 2006 and March 2009, 2264 patients began therapy with bevacizumab, combined with single-agent paclitaxel (34%), single-agent docetaxel (33%), taxane-based combination therapy (11%), non-taxane-containing therapy (10%), or sequential chemotherapy (switching chemotherapy regimen before disease progression while continuing on bevacizumab; 12%). After final data cut-off in July 2010, the median duration of follow-up was 20.1 months (range 0.1-43.6 months). Bevacizumab therapy was continued for ≥1 year in 473 patients (21%). The safety profile and median TTP were very similar to those previously reported after median follow-up of 12.7 months and are consistent with findings from randomized phase III trials. Final OS results in the overall population and in clinically important subgroups are reported below for the first time. Conclusion: Median OS in the overall population is consistent with OS results reported from three randomized phase III trials in the first-line setting (25.2-30.2 months). OS results in subsets of patients with TN disease or aged ≥70 years suggest that bevacizumab-containing therapy is an effective option for these patients, who typically have fewer treatment options available. Citation Information: Cancer Res 2010;70(24 Suppl):Abstract nr P2-16-06.

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)0.002
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: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.010

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.002
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.001

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 head0.184
GPT teacher head0.478
Teacher spread0.294 · 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 designObservational
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

Citations4
Published2010
Admission routes1
Has abstractyes

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