4.7 Article

Trastuzumab Plus Endocrine Therapy or Chemotherapy as First-line Treatment for Patients with Hormone Receptor-Positive and HER2-Positive Metastatic Breast Cancer (SYSUCC-002)

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CLINICAL CANCER RESEARCH
卷 28, 期 4, 页码 637-645

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-21-3435

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  1. Sci-Tech Project Foundation of Guangzhou City [202002020033]
  2. Natural Science Foundation of Guangdong Province [2019A151011781]
  3. cultivation foundation for the junior teachers in Sun Yat-sen University [20ykpy164]

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This study aimed to compare the efficacy of endocrine therapy and chemotherapy as partner strategies with anti-HER2 therapy for first-line treatment of HR(+)HER2(+) metastatic breast cancer. The results showed that trastuzumab plus endocrine therapy was noninferior to trastuzumab plus chemotherapy in terms of progression-free survival, with a significantly higher prevalence of toxicity in the chemotherapy group.
Purpose: There is no research evidence demonstrate which is the better partner strategy, endocrine therapy or chemotherapy, to combine with anti-HER2 therapy as the first-line management of hormone receptor (HR)-positive (HR+) and HER2-positive (HER2(+)) metastatic breast cancer (MBC). We wished to ascertain if trastuzumab plus endocrine therapy is noninferior to trastuzumab plus chemotherapy. Patients and Methods: We conducted an open-label, noninferiority, phase III, randomized, controlled trial (NCT01950182) at nine hospitals in China. Participants, stratified by previous adjuvant endocrine therapy and disease status (recurrent disease vs. de novo metastasis), were assigned randomly (1:1) to receive trastuzumab plus endocrine therapy (per investigator's choice of oestrogen receptor modulators or aromatase inhibitor, with/without concurrent ovarian suppression) or chemotherapy (per investigator's choice of taxanes, capecitabine, or vinorelbine). The primary end point was progression-free survival (PFS) with a noninferiority upper margin of 1.35 for the HR. The intention-to-treat population was used in primary and safety analyses. Results: A total of 392 patients were enrolled and assigned randomly to receive trastuzumab plus endocrine therapy (ET group, n = 196) or trastuzumab plus chemotherapy (CT group, n = 196). After a median follow-up of 30.2 months [interquartile range (IQR) 15.0-44.7], the median PFS was 19.2 months [95% confidence interval (CI), 16.7-21.7)] in the ET group and 14.8 months (12.8-16.8) in the CT group (hazard ratio, 0.88; 95% CI, 0.71-1.09; P-noninferiority < 0.0001). A significantly higher prevalence of toxicity was observed in the CT group compared with the ET group. Conclusions: Trastuzumab plus endocrine therapy was noninferior to trastuzumab plus chemotherapy in patients with HR(+)HER2(+) MBC.

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