Evaluation of the efficacy of A166 in Patients with HER2-Positive unresectable or metastatic breast cancer previously treated with TOP1 inhibitor Antibody-Drug Conjugates
This study will evaluate the efficacy of A166 in patients with HER2-positive unresectable or metastatic breast cancer previously treated with TOP1 inhibitor Antibody-Drug Conjugates. A166 will be administered every 3 weeks (Q3W) intravenous (IV) infusion.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
intravenous(IV) infusion (Q3W)
Henan Provincial Cancer Hospital
Zhenzhou, Henan, China
RECRUITINGObjective response rate(ORR)
ORR is defined as the percentage of patients who achieve complete response(CR) or partial response (PR), as assessed by investigator per RECIST 1.1
Time frame: Within 24 months of last patient enrolled
Progression-free survival (PFS)
PFS, 6-month PFS, 12-month PFS.PFS as assessed by investigator according to RECIST v 1.1
Time frame: Within 24 months of last patient enrolled
Overall survival (OS)
OS, 1-year survival rate, 1.5-year survival rate, and 2-year survival rate.OS defined as time from inclusion until death
Time frame: Within 48 months of last patient enrolled
Disease control rate(DCR)
DCR is defined as the percentage of patients who achieve CR, PR or stable disease (SD), as assessed by investigator per RECIST 1.1
Time frame: Within 24 months of last patient enrolled
Duration of response(DOR)
DoR is defined as the time from the date of first documented CR or PR until date of documented disease progression per RECIST 1.1, as assessed by investigator or death due to any cause, whichever occurs first.
Time frame: Within 24 months of last patient enrolled
Clinical Benefit Rate (CBR)
CBR is defined as a patient having a best overall response of a complete response (CR), partial response (PR), or stable disease for at least 6 months.
Time frame: Within 24 months of last patient enrolled
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