Evaluating the Efficacy and Safety of PD-L1 Monoclonal Antibody Combined With VEX Metronomic Chemotherapy and Concurrent or Delayed Radiotherapy in Patients With Advanced HER2-Negative Breast Cancer With Brain Metastasis

A Prospective, multicenter, randomized controlled phase II study to evaluate the efficacy and safety of PD-L1 monoclonal antibody combined with vinorelbine + cyclophosphamide + capecitabine (VEX) metronomic chemotherapy and concurrent or delayed radiotherapy in patients with advanced HER2-negative breast cancer with brain metastasis

Trial Details

NCT ID
NCT06839560
Phase
PHASE2
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Status
RECRUITING
Cancer Type
Breast Cancer
Interventions
  • Adebrelimab+VEX Metronomic Chemotherapy+Concurrent Radiotherapy
  • Adebrelimab+VEX Metronomic Chemotherapy+Delayed Radiotherapy
Locations (sample)
  • Beijing, Beijing Municipality, China|39.9075,116.39723

Key Eligibility Criteria

  • Males or females who are at least 18 years of age on the day of signing the informed consent form.
  • Patients with metastatic HER2-negative breast cancer brain metastasis, with clear clinical documentation; specific criteria refer to the guidelines…
  • Patients who have received no more than one line of chemotherapy during the metastatic stage of breast cancer.
  • Patients with brain metastasis should not require immediate local therapy during the trial and meet at least one of the following criteria:

For full eligibility, visit ClinicalTrials.gov.

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