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

Authors :
Abraham JE
Pinilla K
Dayimu A
Grybowicz L
Demiris N
Harvey C
Drewett LM
Lucey R
Fulton A
Roberts AN
Worley JR
Chhabra A
Qian W
Vallier AL
Hardy RM
Chan S
Hickish T
Tripathi D
Venkitaraman R
Persic M
Aslam S
Glassman D
Raj S
Borley A
Braybrooke JP
Sutherland S
Staples E
Scott LC
Davies M
Palmer CA
Moody M
Churn MJ
Newby JC
Mukesh MB
Chakrabarti A
Roylance RR
Schouten PC
Levitt NC
McAdam K
Armstrong AC
Copson ER
McMurtry E
Tischkowitz M
Provenzano E
Earl HM
Source :
Nature [Nature] 2024 May; Vol. 629 (8014), pp. 1142-1148. Date of Electronic Publication: 2024 Apr 08.
Publication Year :
2024

Abstract

PARTNER is a prospective, phase II-III, randomized controlled clinical trial that recruited patients with triple-negative breast cancer <superscript>1,2</superscript> , who were germline BRCA1 and BRCA2 wild type <superscript>3</superscript> . 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) <superscript>4</superscript> , and secondary end points included event-free survival (EFS) and overall survival (OS) <superscript>5</superscript> . 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 .<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1476-4687
Volume :
629
Issue :
8014
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
38588696
Full Text :
https://doi.org/10.1038/s41586-024-07384-2