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基于吡咯替尼的双靶点疗法用于her2阳性乳腺癌患者新辅助治疗的可行性研究
Received 19 August 2024
Accepted for publication 6 November 2024
Published 29 November 2024 Volume 2024:16 Pages 845—853
DOI https://doi.org/10.2147/BCTT.S481236
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Robert Clarke
Feng Zhao,1 Hongzhen Zhang2
1The First Hospital of Anhui University of Science and Technology, Huainan, Anhui, People’s Republic of China; 2Anhui University of Science and Technology, Huainan, Anhui, People’s Republic of China
Correspondence: Hongzhen Zhang, Anhui University of Science and Technology, Huainan, Anhui, People’s Republic of China, Tel +8613155438639, Email zhanghongzhen5621@163.com
Background: HER2-positive breast cancer is one of the high-risk subtypes of breast cancer for which dual-targeted therapy has become an important treatment option. However, for some patients, complete control of the disease is still not possible and additional treatment is required. Pyrrolitinib, an inhibitor of ALK and MET, has shown promising efficacy in breast cancer treatment. The aim of this study was to investigate the feasibility of adjuvant intensive therapy with pyrrolitinib in the treatment of HER2-positive breast cancer tumors.
Materials and Methods: Twenty-eight patients with HER2-positive breast cancer who were treated at the Breast Surgery Department of the Provincial Hospital of Weihai City, Shandong Province, China, between January 1, 2019, and January 1, 2023, were selected for this study. All of these patients received dual-targeted therapy with the addition of pyrrolitinib therapy adjuvant intensive therapy. We recorded data on the patients’ basic information, pathological characteristics, treatment regimens, effects of treatment regimens, and adverse reactions, and statistically analyzed them.
Results: Of the 28 patients with HER2-positive breast cancer, all of them were added to adjuvant intensive therapy with pyrrolitinib. After examination of the samples during treatment, the breast cancer mass had been significantly reduced with the assistance of pyrrolitinib. In addition, no serious adverse reactions were found.
Conclusion: Adjuvant intensification of pyrrolitinib in the treatment of HER2-positive breast cancer tumors is feasible. The results of this study suggest that pyrrolitinib is a safe and effective therapeutic option that can significantly improve the outcome of HER2-positive breast cancer. More studies are needed to further validate this finding.
Keywords: HER2-positive breast cancer, dual-target therapy, pyrrolitinib, adjuvant intensive therapy, feasibility study