Pyrotinib after trastuzumab-based adjuvant therapy in patients with HER2-positive breast cancer (PERSIST): A multicenter phase II trial
Background: Approximately one-third of patients with HER2-positive breast cancer experienced recurrence within 10 years after receiving 1 year of adjuvant trastuzumab. The ExteNET study showed that 1 year of extended adjuvant neratinib after trastuzumab-based adjuvant therapy could reduce invasive disease-free survival (iDFS) events compared with placebo. This study investigated the efficacy and safety of pyrotinib, an irreversible pan-HER receptor tyrosine kinase inhibitor, after trastuzumab-based adjuvant therapy in patients with high-risk, HER2-positive early or locally advanced breast cancer. Methods: This multicenter phase II trial was conducted at 23 centers in China. After enrollment, patients received 1 year of extended adjuvant pyrotinib (400 mg/day), which should be initiated within 6 months after the completion of 1-year adjuvant therapy (trastuzumab alone or plus pertuzumab). The primary endpoint was 2-year iDFS rate. Results: Between January 2019 and February 2022, 141 eligible women were enrolled and treated. As of October 10, 2022, the median follow-up was 24 (interquartile range, 18.0–34.0) months. The 2-year iDFS rate was 94.59% (95% confidence interval [CI]: 88.97–97.38) in all patients, 94.90% (95% CI: 86.97–98.06) in patients who completed 1-year treatment, 90.32% (95% CI: 72.93–96.77) in patients who completed only 6-month treatment, 96.74% (95% CI: 87.57–99.18) in the hormone receptor (HR)-positive subgroup, 92.77% (95% CI: 83.48–96.93) in the HR-negative subgroup, 96.88% (95% CI: 79.82–99.55) in the lymph node-negative subgroup, 93.85% (95% CI: 86.81–97.20) in the lymph node-positive subgroup, 97.30% (95% CI: 82.32–99.61) in patients with adjuvant trastuzumab plus pertuzumab, and 93.48% (95% CI: 86.06–97.02) in patients with adjuvant trastuzumab. The most common adverse events were diarrhea (79.4%), fatigue (36.9%), lymphocyte count decreased (36.9%), nausea (33.3%), and hand-foot syndrome (33.3%). Conclusions: Extended adjuvant pyrotinib administrated after trastuzumab-based adjuvant therapy showed promising efficacy in patients with high-risk HER2-positive breast cancer. The follow-up is ongoing to determine the long-term benefit. Funding: No external funding was received for this work. Clinical trial number: ClinicalTrials.gov: NCT05880927
Authors
- Zhaosheng Ma
- Jichun Zhou (ORCID: https://orcid.org/0000-0002-0727-4034)
- Dongbo Shi (ORCID: https://orcid.org/0000-0002-4408-3042)
- Jingde Shu
- Feilin Cao (ORCID: https://orcid.org/0009-0002-5083-1462)
- Qingjing Feng
- Deyou Tao
- Weizhu Wu (ORCID: https://orcid.org/0000-0002-5064-0685)
- Shifen Huang
- Zhanwen Li
- Wei Lin (ORCID: https://orcid.org/0000-0002-7506-3466)
- Zenggui Wu
- Xiaotao Zhu
- Xiaochun Ji (ORCID: https://orcid.org/0000-0002-4771-5017)
- Ouchen Wang (ORCID: https://orcid.org/0000-0001-5382-5178)
- Binbin Cui (ORCID: https://orcid.org/0000-0003-2368-5519)
- Jing Hao (ORCID: https://orcid.org/0009-0000-9809-2596)
Institutions
- Ningbo University (CN)
- Wenzhou Medical University (CN)
- Women's and Children's Hospital (AU)
- First Affiliated Hospital of Wenzhou Medical University (CN)
- Sir Run Run Shaw Hospital (CN)
- Quzhou City People's Hospital (CN)
- Ningbo Medical Center Lihuili Hospital (CN)
- Yichang Central People's Hospital (CN)
- Jinhua Central Hospital (CN)
- Zhejiang University (CN)
Publication Details
- Journal
- eLife
- Published
- 2025-03-25
- DOI
- https://doi.org/10.7554/elife.101724.3
- Primary Topic
- HER2/EGFR in Cancer Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00