| Literature DB >> 32233990 |
Li Danni1,2,3,4, Zhang Lingyun1,2,3,4, Wang Jian5, Yan Hongfei1,2,3,4, Xu Lu1,2,3,4, Yang Peng6, Qu Xiujuan1,2,3,4, Liu Yunpeng1,2,3,4, Teng Yuee1,2,3,4.
Abstract
Although HER2-targeted therapy has been shown to prolong the survival of patients with HER2-positive breast cancer, most patients eventually progress due to drug resistance. Novel treatment options are urgently needed to overcome resistance to HER2-targeted therapy. The VEGF/VEGFR (Vascular endothelial growth factor and its receptors) pathway is essential in tumor angiogenesis, which may be a promising target in HER2-positive breast cancer providing a rationale for the use of tyrosine kinase inhibitors (TKIs) targeting VEGFR. Here, we present a case of a heavily pretreated advanced breast cancer patient who did not respond to HER2-targeted therapy and developed resistance to multiple lines of HER2-targeted treatment. The patient was treated with apatinib at a dose of 500 mg daily, and obtained partial remission (PR) with a progression-free-stage (PFS) of 6 months. Our case indicates that apatinib might have anti-tumor activity in patients with HER2-positive breast cancer with HER2-targeted resistance. This case is of value which may provide new insights into strategies for HER2-targeted therapy resistance options in the clinic.Entities:
Keywords: Apatinib; HER2; VEGFR2; angiogenesis; breast cancer; case report
Year: 2020 PMID: 32233990 PMCID: PMC7515454 DOI: 10.1080/15384047.2020.1743159
Source DB: PubMed Journal: Cancer Biol Ther ISSN: 1538-4047 Impact factor: 4.742