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Accès ouvert déclaré 2024 article

The PARTNER trial of neoadjuvant olaparib with chemotherapy in triple-negative breast cancer

51Citations signalées, ce qui n’est pas une note de qualité
46Institutions déclarées
2Pays d’affiliation déclarés

Rattachement africain : gb, gr. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

Abstract PARTNER is a prospective, phase II–III, randomized controlled clinical trial that recruited patients with triple-negative breast cancer1,2, who were germline BRCA1 and BRCA2 wild type3. Here we report the results of the trial. Patients (n = 559) were randomized on a 1:1 basis to receive neoadjuvant carboplatin–paclitaxel with or without 150 mg olaparib twice daily, on days 3 to 14, of each of four cycles (gap schedule olaparib, research arm) followed by three cycles of anthracycline-based chemotherapy before surgery. The primary end point was pathologic complete response (pCR)4, and secondary end points included event-free survival (EFS) and overall survival (OS)5. pCR was achieved in 51% of patients in the research arm and 52% in the control arm (P = 0.753). Estimated EFS at 36 months in the research and control arms was 80% and 79% (log-rank P > 0.9), respectively; OS was 90% and 87.2% (log-rank P = 0.8), respectively. In patients with pCR, estimated EFS at 36 months was 90%, and in those with non-pCR it was 70% (log-rank P < 0.001), and OS was 96% and 83% (log-rank P < 0.001), respectively. Neoadjuvant olaparib did not improve pCR rates, EFS or OS when added to carboplatin–paclitaxel and anthracycline-based chemotherapy in patients with triple-negative breast cancer who were germline BRCA1 and BRCA2 wild type. ClinicalTrials.gov ID: NCT03150576 .

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
The PARTNER trial of neoadjuvant olaparib with chemotherapy in triple-negative breast cancer
Date Crossref
08/04/2024
Éditeur
Springer Science and Business Media LLC
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Les institutions déclarées

University of CambridgeCancer Research UKCancer Research UK Cambridge CenterCambridge University Hospitals NHS Foundation TrustAthens University of Economics and BusinessRoyal Devon & Exeter NHS Foundation TrustNottingham University Hospitals NHS TrustRoyal Bournemouth HospitalRussells Hall HospitalThe Royal Wolverhampton NHS TrustEast Suffolk and North Essex NHS Foundation TrustIpswich HospitalBedford HospitalMid Yorkshire Hospitals NHS TrustPinderfields HospitalRoyal Hampshire County HospitalUniversity Hospital Southampton NHS Foundation TrustBasingstoke and North Hampshire HospitalVelindre Cancer CentreUniversity Hospitals Bristol NHS Foundation TrustUniversity Hospitals Bristol and Weston NHS Foundation TrustMount Vernon Cancer CentreBarking, Havering And Redbridge University Hospitals NHS TrustQueen's HospitalBeatson West of Scotland Cancer CentreSwansea Bay University Health BoardHinchingbrooke HospitalWest Suffolk NHS Foundation TrustWest Suffolk HospitalWorcestershire Acute Hospitals NHS TrustAlexandra HospitalKidderminster Hospital and Treatment CentreRoyal Free London NHS Foundation TrustColchester HospitalPoole HospitalUniversity Hospitals Dorset NHS Foundation TrustUniversity College London Hospitals NHS Foundation TrustUniversity College LondonAddenbrooke's HospitalOxford Health NHS Foundation TrustUniversity of OxfordPeterborough City HospitalThe Christie NHS Foundation TrustUniversity of Southampton21c Consultancy (United Kingdom)National Institute for Health and Care Research

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

PARP inhibition in cancer therapyBRCA gene mutations in cancerAdvanced Breast Cancer Therapies

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