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The PARTNER trial of neoadjuvant olaparib with chemotherapy in triple-negative breast cancer.
Abraham, Jean E; Pinilla, Karen; Dayimu, Alimu; Grybowicz, Louise; Demiris, Nikolaos; Harvey, Caron; Drewett, Lynsey M; Lucey, Rebecca; Fulton, Alexander; Roberts, Anne N; Worley, Joanna R; Chhabra, Anita; Qian, Wendi; Vallier, Anne-Laure; Hardy, Richard M; Chan, Steve; Hickish, Tamas; Tripathi, Devashish; Venkitaraman, Ramachandran; Persic, Mojca; Aslam, Shahzeena; Glassman, Daniel; Raj, Sanjay; Borley, Annabel; Braybrooke, Jeremy P; Sutherland, Stephanie; Staples, Emma; Scott, Lucy C; Davies, Mark; Palmer, Cheryl A; Moody, Margaret; Churn, Mark J; Newby, Jacqueline C; Mukesh, Mukesh B; Chakrabarti, Amitabha; Roylance, Rebecca R; Schouten, Philip C; Levitt, Nicola C; McAdam, Karen; Armstrong, Anne C; Copson, Ellen R; McMurtry, Emma; Tischkowitz, Marc; Provenzano, Elena; Earl, Helena M.
Afiliação
  • Abraham JE; Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK. ja344@cam.ac.uk.
  • Pinilla K; Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK. ja344@cam.ac.uk.
  • Dayimu A; Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Grybowicz L; Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
  • Demiris N; Cambridge Cancer Trials Centre, University of Cambridge, Cambridge, UK.
  • Harvey C; Cambridge Cancer Trials Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Drewett LM; Department of Statistics, Athens University of Economics and Business, Athens, Greece.
  • Lucey R; Cambridge Cancer Trials Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Fulton A; Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.
  • Roberts AN; Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Worley JR; Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
  • Chhabra A; Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Qian W; Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
  • Vallier AL; Cambridge Cancer Trials Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Hardy RM; Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
  • Chan S; Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
  • Hickish T; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Tripathi D; Cambridge Clinical Trials Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Venkitaraman R; Cambridge Cancer Trials Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Persic M; Cambridge Cancer Trials Centre, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Aslam S; The City Hospital, Nottingham University Hospitals NHS Trust, Nottingham, UK.
  • Glassman D; Royal Bournemouth General Hospital, Bournemouth, UK.
  • Raj S; Royal Wolverhampton NHS Trust, Wolverhampton, UK.
  • Borley A; Russells Hall Hospital, Dudley, UK.
  • Braybrooke JP; Ipswich Hospital, East Suffolk and North Essex NHS Foundation Trust, Ipswich, UK.
  • Sutherland S; University Hospital of Derby and Burton, Derby, UK.
  • Staples E; Bedford Hospital, Bedfordshire Hospitals NHS Foundation Trust, Bedford, UK.
  • Scott LC; Pinderfields Hospital, Mid Yorkshire Teaching NHS Trust, Wakefield, UK.
  • Davies M; University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Palmer CA; Basingstoke & North Hampshire Hospital, Basingstoke, UK.
  • Moody M; Royal Hampshire Hospital, Winchester, UK.
  • Churn MJ; Velindre Cancer Centre, Cardiff, UK.
  • Newby JC; University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
  • Mukesh MB; Mount Vernon Cancer Centre, Northwood, UK.
  • Chakrabarti A; Queens Hospital, Barking, Havering and Redbridge University Hospitals NHS Trust, Romford, UK.
  • Roylance RR; Beatson West Of Scotland Cancer Centre, Glasgow, UK.
  • Schouten PC; Swansea Bay University Health Board, Swansea, UK.
  • Levitt NC; Hinchingbrooke Hospital, North West Anglia NHS Foundation Trust, Huntingdon, UK.
  • McAdam K; Macmillan Unit, West Suffolk Hospital NHS Foundation Trust, Bury Saint Edmunds, UK.
  • Armstrong AC; Worcestershire Acute Hospitals NHS Trust, Worcester, UK.
  • Copson ER; Alexandra Redditch Hospital, Redditch, UK.
  • McMurtry E; Kidderminster Hospital, Kidderminster, Worcestershire, UK.
  • Tischkowitz M; Royal Free London NHS Foundation Trust, London, UK.
  • Provenzano E; Oncology Department, Colchester General Hospital, East Suffolk & North Essex NHS Trust, Colchester, UK.
  • Earl HM; University Hospitals Dorset NHS Foundation Trust, Poole, UK.
Nature ; 629(8014): 1142-1148, 2024 May.
Article em En | MEDLINE | ID: mdl-38588696
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 11 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 .
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ftalazinas / Piperazinas / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Limite: Adolescent / Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Nature Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ftalazinas / Piperazinas / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadjuvante / Neoplasias de Mama Triplo Negativas Limite: Adolescent / Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Nature Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido