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

Jean E AbrahamKaren PinillaAlimu DayimuLouise GrybowiczNikolaos DemirisCaron HarveyLynsey M DrewettRebecca LuceyAlexander FultonAnne N RobertsJoanna R WorleyAnita ChhabraWendi QianAnne-Laure VallierRichard M HardySteve ChanTamas HickishDevashish TripathiRamachandran VenkitaramanMojca PersicShahzeena AslamDaniel GlassmanSanjay RajAnnabel BorleyJeremy P BraybrookeStephanie SutherlandEmma StaplesLucy C ScottMark DaviesCheryl A PalmerMargaret MoodyMark J ChurnJacqueline C NewbyMukesh B MukeshAmitabha ChakrabartiRebecca R RoylancePhilip C SchoutenNicola C LevittKaren McAdamAnne C ArmstrongEllen R CopsonEmma McMurtryMarc TischkowitzElena ProvenzanoHelena M Earl
Published in: Nature (2024)
PARTNER is a prospective, phase II-III, randomized controlled clinical trial that recruited patients with triple-negative breast cancer 1,2 , who were germline BRCA1 and BRCA2 wild type 3 . 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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