The Efficacy and Safety of Anlotinib Combined With Fulvestrant in Patients With Advanced Breast Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorZhejiang Cancer Hospital

About this trial

The management of HR-positive, HER2-negative metastatic breast cancer includes endocrine monotherapy or combination regimens, both with benefit diminishing as resistance develops. Nowadays, various studies have demonstrated that estrogen interacts with many angiogenic pathways and is an important mechanism for resistance leading to the question of whether combination with antiangiogenesis and antiestrogen therapies could be an appropriate therapeutic modality. Anlotinib is a novel multi-target tyrosine kinase inhibitor that effectively inhibit VEGFR, FGFR, PDGFR, c-KIT, c-MET and RET. Previous studies have proven the efficacy of both anlotinib monotherapy and combination regimens in advanced breast cancer. This phase II study aims to preliminarily evaluate the efficacy and safety of anlotinib combined with endocrine therapy.

Eligibility criteria

Qualifiers

Aged 18 years or older female;

ECOG score 0-1;

Life expectancy is not less than 12 weeks;

Histology confirmed HR-positive and HER2-negative locally advanced or metastatic breast cancer;

Disqualifiers

Have received prior fulvestrant or anti-angiogenic drug treatment, or known to be allergic to any excipients in the study;

Visceral crisis;

Uncontrolled or high-burden CNS metastases;

Unable to swallow;

Trial design

Treatments tested in this trial

  • anlotinib, fulvestrant

Treatment groups

40 Participants
are divided into 1 treatment group

Sponsors and collaborators