Precision Breast Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
Cancer Research UK Cambridge Centre, University of Cambridge, Cambridge, UK.
Nature. 2024 May;629(8014):1142-1148. doi: 10.1038/s41586-024-07384-2. Epub 2024 Apr 8.
PARTNER is a prospective, phase II-III, randomized controlled clinical trial that recruited patients with triple-negative breast cancer, who were germline BRCA1 and BRCA2 wild type. 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), and secondary end points included event-free survival (EFS) and overall survival (OS). 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 .
PARTNER 是一项前瞻性的 II-III 期随机对照临床试验,招募了三阴性乳腺癌且胚系 BRCA1 和 BRCA2 野生型的患者。在此,我们报告该试验的结果。患者(n=559)按 1:1 比例随机分为接受新辅助卡铂紫杉醇联合或不联合每日两次 150mg 奥拉帕利的两组(奥拉帕利间隙方案,研究组),每 21 天为一个周期,共 4 个周期,随后在手术前进行三个周期的蒽环类药物化疗。主要终点是病理完全缓解(pCR),次要终点包括无事件生存(EFS)和总生存(OS)。研究组 51%的患者达到 pCR,对照组为 52%(P=0.753)。研究组和对照组的 36 个月 EFS 估计值分别为 80%和 79%(对数秩 P>0.9);OS 分别为 90%和 87.2%(对数秩 P=0.8)。在 pCR 患者中,36 个月时的估计 EFS 为 90%,非 pCR 患者为 70%(对数秩 P<0.001),OS 分别为 96%和 83%(对数秩 P<0.001)。在三阴性乳腺癌且胚系 BRCA1 和 BRCA2 野生型的患者中,与卡铂紫杉醇和蒽环类药物化疗联合使用新辅助奥拉帕利并未提高 pCR 率、EFS 或 OS。ClinicalTrials.gov ID:NCT03150576。