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Study on ctDNA-guided Treatment Decision-making for HER2-negative Metastatic Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is an exploratory, ctDNA-guided, multi-stage clinical study designed to evaluate the clinical value of treatment decision-making based on circulating tumor DNA (ctDNA) variant allele frequency (VAF) dynamics in patients with HER2-negative metastatic breast cancer. All enrolled patients will receive antibody-drug conjugate (ADC) therapy for two cycles in Stage 1, with serial ctDNA assessments performed prior to Cycle 1 and Cycle 2. In Stage 2, patients without disease progression will be assigned to different treatment strategies based on the percentage reduction in mean ctDNA VAF. The study aims to assess whether ctDNA VAF dynamics can serve as an early biomarker to guide treatment intensification and improve clinical outcomes in metastatic breast cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Age 18-75 years;ECOG performance status 0-1; Histologically or cytologically confirmed HER2-negative metastatic breast cancer; At least one measurable lesion per RECIST v1.1; Eligible for ADC therapy; Adequate organ and bone marrow function; Life expectancy ≥3 months; Willingness to provide tumor tissue and blood samples; Signed informed consent

Locations
Other Locations
China
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Contact Information
Primary
Hongxia WANG
whx365@126.com
86-138196379
Time Frame
Start Date: 2025-12-24
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 122
Treatments
Experimental: ADC + Ivonescimab
Patients with \<50% mean ctDNA VAF reduction receive ADC combined with ivonescimab.
Active_comparator: ADC Monotherapy
Patients with \<50% mean ctDNA VAF reduction receive continued ADC monotherapy.
Active_comparator: ADC Monotherapy (ctDNA responder cohort)
Patients with ≥50% mean ctDNA VAF reduction continue ADC monotherapy.
Related Therapeutic Areas
Sponsors
Leads: Fudan University

This content was sourced from clinicaltrials.gov