This is an prospective, open label, multicenter study to evaluate the efficacy and safety of neoadjuvant Iparomlimab and Tuvonralimab (QL1706) in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative breast cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
55
5.0mg/kg qw, start from C1D15
80mg/m\^2 qw
AUC=1.5, D1, 8, 15, every 28 days
Renji Hospital, School of Medicine, Shanghai Jiaotong University
Shanghai, China
Proportion of patients with pCR
Number of patients with pathological complete response/Number of all eligible patients
Time frame: 1-2 weeks after surgery
Proportion of patients with adverse events
Number of patients with adverse events during neoadjuvant therapy assessed according to the NCI CTCAE v5.0/Number of all eligible patients
Time frame: From the date of starting neoadjuvant therapy to the end of the treatment (up to approximately 1 year)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.