MedPath

Phase II Clinical Trial of PD-L1 in Combination with Vinorelbine + Cyclophosphamide + Capecitabine (VEX) Metronomic Chemotherapy with or Without Radiotherapy for Advanced Triple-negative Breast Cancer.

Phase 2
Recruiting
Conditions
Advanced Triple-negative Breast Cancer
Interventions
Drug: Adebry single antibody + VEX metronomic chemotherapy + radiotherapy
Drug: debry single antibody + VEX metronomic chemotherapy
Registration Number
NCT06771609
Lead Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Brief Summary

Phase II clinical trial of PD-L1 in combination with vinorelbine + cyclophosphamide + capecitabine (VEX) metronomic chemotherapy with or without radiotherapy for advanced triple-negative breast cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Adebry single antibody + VEX metronomic chemotherapy + radiotherapyAdebry single antibody + VEX metronomic chemotherapy + radiotherapy1. Adebry antibody: 1200mg on day 1, every 3 weeks; 2. vinorelbine + cyclophosphamide + capecitabine (VEX) metronomic chemotherapy: Vinorelbine 20mg orally, once every other day, Q3W Cyclophosphamide 50mg orally, once daily, Q3W Capecitabine 500mg orally, three times daily, Q3W 3. Radiotherapy: Radiotherapy is administered within 3 weeks after the first immunotherapy. Different radiotherapy techniques are chosen based on the size and location of the metastatic lesions: Stereotactic Body Radiation Therapy (SBRT), Spatially Fractionated Radiation Therapy (SFRT), or Low-dose Radiotherapy (LDRT).
debry single antibody + VEX metronomic chemotherapydebry single antibody + VEX metronomic chemotherapy1. Adebry antibody: 1200mg on day 1, every 3 weeks; 2. VEX Metronomic Chemotherapy: Vinorelbine 20mg orally, once every other day, Q3W Cyclophosphamide 50mg orally, once daily, Q3W Capecitabine 500mg orally, three times daily, Q3W
Primary Outcome Measures
NameTimeMethod
Progression-Free Survival24 months

According to RECIST 1.1 criteria:Disease Progression (PD): Referring to the smallest sum of the diameters of all measured target lesions throughout the entire experimental study, there is a relative increase of at least 20% in the sum of the diameters (if the baseline measurement is the smallest, then the baseline value is used as the reference); in addition, there must be an absolute increase of at least 5 mm in the sum of the diameters (the appearance of one or more new lesions is also considered disease progression).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Cancer Hospital, Chinese Academy of Medical Sciences

🇨🇳

Beijing, Beijing, China

© Copyright 2025. All Rights Reserved by MedPath