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Patterns of progression and subsequent management of patients with <i>BRCA1/2</i> mutated platinum-sensitive recurrent epithelial ovarian cancer (EOC) progressing on olaparib versus placebo: the SOLO2/ENGOT Ov-21 trial (NCT01874353).

2020· article· en· W3029321131 on OpenAlexaff
Jean‐Sébastien Frenel, Jae‐Weon Kim, Dominique Berton, Rebecca Asher, Laura Vidal, Patricia Pautier, Jonathan A. Ledermann, Richard T. Penson, Amit M. Oza, Jacob Korach, Tomasz Huzarski, Sandro Pignata, Nicoletta Colombo, Tjoung‐Won Park‐Simon, Kenji Tamura, Gabe S. Sonke, Elizabeth Lowe, Alison Freimund, Chee Khoon Lee, Éric Pujade-Lauraine

Bibliographic record

VenueJournal of Clinical Oncology · 2020
Typearticle
Languageen
FieldMedicine
TopicPARP inhibition in cancer therapy
Canadian institutionsPrincess Margaret Cancer Centre
Fundersnot available
KeywordsMedicineOlaparibInternal medicinePlaceboClinical endpointOvarian cancerProgression-free survivalOncologyProgressive diseaseGastroenterologySurgeryCancerUrologyChemotherapyClinical trialPathology

Abstract

fetched live from OpenAlex

6070 Background: Olaparib maintenance is a standard treatment of BRCA1/2 mutated platinum-sensitive recurrent EOC. Despite improvement in PFS, olaparib (O) resistance often occurs and the optimal management of post-olaparib progression remains undefined. Methods: Data of patients who participated in the SOLO-2 trial and progressed were analyzed. Primary objective was to depict the patterns of progression of patients treated with O compared to placebo (P). Secondary objectives include description of post-progression treatments. Results: 106/195 (54%) and 80/99 (81%) patients had a RECIST progression in the O and P arms respectively. As permitted in the protocol, 37 (35%) pts continued O despite a RECIST progression and 10 remained on treatment at the date of data base cut-off of the primary endpoint. Median duration of O post progression was 3.2 months (range: 1 to 19.4). In the placebo arm, only 20% of the patients with progressive disease continued placebo during a median of 1.6 months (range:1.1 to 16.1). Patterns of sites of progressive disease were similar in the O and P arms respectively in terms of liver (21% vs 18%), lung (4% vs 3%), lymph node (20% vs 16%) peritoneal (48% vs 32%) or brain metastases (0% vs 2%). Number of sites of relapsing disease were similar in the O and P arm respectively (1 (68% vs 64), ≥2 (32% vs 36%). A total of 54 (51%) patients in the O arm and 42 (53%) in the P arm received subsequent platinum-based therapy. In both arms, 8% received bevacizumab and 6% received no further treatment. Median PFS with first post-study platinum-based and non platinum-based therapy were 7.1 months and 5.6 months respectively. In the P arm, 18 (23) patients received PARP inhibitors following the first subsequent chemotherapy. Conclusions: Patterns of disease progression and subsequent chemotherapy were similar in patients receiving O or P in the SOLO2 trial. Instead of switching to chemotherapy, continuing O at the time of RECIST progression was an option for 35% of the patients. Clinical trial information: NCT01874353.

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 score0.001
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

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 head0.128
GPT teacher head0.453
Teacher spread0.324 · 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".

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Citations4
Published2020
Admission routes1
Has abstractyes

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