PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
March 6, 2026Journal of Clinical Oncology1 citations

Phase II Clinical Study of Adebrelimab and Bevacizumab Combined With Cisplatin/Carboplatin in Patients With Triple-Negative Breast Cancer With Brain Metastases (ABC Study)

View Full Paper
TLT. LIZTZhou TlBWBiyun Wang

Key Points

  • This study aims to evaluate the efficacy and safety of a combination therapy for triple-negative breast cancer with brain metastases.
  • Conducted a phase II clinical trial with patients diagnosed with triple-negative breast cancer and active brain metastases.
  • Administered adebrelimab, bevacizumab, and cisplatin/carboplatin until disease progression or significant side effects occurred.
  • Measured primary endpoint as objective response rate in the central nervous system (CNS) and secondary endpoints related to survival and safety.
  • Confirmed CNS objective response rate was 77.1% with 28 out of 35 patients showing improvement.
  • Clinical benefit rate in the CNS was 80.0%.
  • Median overall progression-free survival was 8.3 months and median overall survival was 21.1 months.
  • 65.7% of patients experienced grade ≥3 treatment-related adverse events, with no treatment-related deaths.

Abstract

PURPOSE Brain metastases (BMs) of triple-negative breast cancer (TNBC) are lethal, often associated with a limited life span and lack of effective antitumor agents. Here we reported a triple combination therapy consisting of adebrelimab, bevacizumab, and cisplatin/carboplatin in BMs of TNBC. METHODS This phase II clinical trial involved patients with TNBC with active BMs. Participants were administered with adebrelimab, bevacizumab, and cisplatin/carboplatin until disease progression or unacceptable toxic effects. The primary end point was the objective response rate in CNS (CNS-ORR) according to the Response Assessment in Neuro-Oncology BMs criteria, and the secondary end points included the clinical benefit rate in CNS (CNS-CBR), progression-free survival (PFS), overall survival (OS), the first progression site, and safety. RESULTS A total of 35 patients were enrolled and treated, and the median lines of previous treatment were 2 (range, 0-4). The confirmed CNS-ORR was 77.1% (27/35, 95% CI, 59.9 to 89.6), and the CNS-CBR was 80.0% (28/35, 95% CI, 63.1 to 91.6). The median overall PFS was 8.3 months (95% CI, 5.8 to 11.5), whereas the median CNS-PFS was 10.3 months (95% CI, 7.4 to 14.3) and the median OS was 21.1 months (95% CI, 13.2 to not reached). Among the 28 patients who progressed, progression was intracranial-only in 32.1% (9/28) patients, extracranial-only in 35.7% (10/28) patients, and both in 32.1% (9/28) patients. The incidence of grade ≥3 treatment-related adverse events was 65.7% (23/35). Treatment-related serious adverse events occurred in five patients (14.3%), and no treatment-related deaths were reported. CONCLUSION The combination of adebrelimab, bevacizumab, and cisplatin/carboplatin was the first regimen to demonstrate promising intracranial antitumor activity and prolonged PFS and CNS-PFS, along with a manageable safety profile, warranting further investigation.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

LI et al. (2026) studied this question.

synapsesocial.com/papers/69aa70f8531e4c4a9ff5b4cahttps://doi.org/10.1200/jco-25-02021
Ask AI
Helpful
Bookmark
Share
View Full Paper