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Record W2898400750 · doi:10.1093/annonc/mdy272.355

LUCY: A phase IIIb, real-world study of olaparib in HER2-negative metastatic breast cancer patients with a BRCA mutation

2018· article· en· W2898400750 on OpenAlexaff
Karen A. Gelmon, G.P. Walker, Gabrielle Fisher, Susan McCutcheon

Bibliographic record

VenueAnnals of Oncology · 2018
Typearticle
Languageen
FieldMedicine
TopicAdvanced Breast Cancer Therapies
Canadian institutionsBC Cancer Agency
Fundersnot available
KeywordsMedicineOlaparibMetastatic breast cancerOncologyInternal medicineBRCA mutationBreast cancerTaxaneCohortProgression-free survivalEribulinCancerChemotherapy

Abstract

fetched live from OpenAlex

Background: The Phase III OlympiAD trial (NCT02000622) showed a significant improvement in progression-free survival (PFS) in favour of olaparib vs physician’s choice chemotherapy in patients with HER2-negative metastatic breast cancer (mBC) and a germline BRCA mutation (gBRCAm). In January 2018, the US FDA expanded the approved use of olaparib to treat patients with HER2-negative mBC and a gBRCAm. LUCY (NCT03286842) has been initiated to evaluate the clinical effectiveness of olaparib in these patients in a real-world setting, and has been expanded to include a cohort of patients with somatic BRCA mutations (sBRCAm). Trial design: LUCY is an open-label, single-arm, multicentre, international Phase IIIb trial. Patients with HER2-negative mBC and a deleterious BRCAm (gBRCAm or sBRCAm), who have received treatment with taxane or anthracycline in either the adjuvant or metastatic setting, and ≤2 prior lines of chemotherapy for metastatic disease, will be enrolled. Patients will be treated with open-label olaparib tablets (300 mg twice daily) until disease progression, unacceptable toxicity, or other discontinuation criteria. For gBRCAm patients (Cohort 1), the primary objective is to evaluate the clinical effectiveness of olaparib via investigator-assessed PFS (radiological, symptomatic, or clear progression of non-measurable disease); secondary objectives include overall survival, time to second progression, and clinical response rate. These primary and secondary objectives will be exploratory in sBRCAm patients (Cohort 2), and PFS will be assessed by RECIST 1.1. An additional key exploratory objective will be 24-week disease control rate in the subset of all patients with adequately treated, stable brain metastases at baseline. Safety and tolerability will be described. Initial screening across ∼170 sites in 16 countries will be conducted to identify a target sample of 250 patients with gBRCAm and 20 patients with sBRCAm. The first subject was enrolled in Q1 2018. Clinical trial identification: NCT03286842. Editorial acknowledgement: Stephen Paterson, Mudskipper Business Ltd. Legal entity responsible for the study: AstraZeneca. Funding: AstraZeneca. Disclosure: K.A. Gelmon: Consulting or advisory role: AstraZeneca, Eli Lilly, Merck, and Pfizer; Expert opinion: Genentech. G.P. Walker: Contracted services and stockholder; AstraZeneca. G.V. Fisher, S.C. McCutcheon: Employee and stockholder; AstraZeneca.

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)0.003
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Non-randomized trial · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.007
Threshold uncertainty score0.024

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.002
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0020.001
Bibliometrics0.0000.000
Science and technology studies0.0010.002
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0020.004
Insufficient payload (model declined to judge)0.0070.002

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 head0.058
GPT teacher head0.438
Teacher spread0.380 · 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 designNon-randomized 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

Citations5
Published2018
Admission routes1
Has abstractyes

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