Site Editor

William J. Gradishar, MD, FACP, FASCO

Advertisement
Advertisement

Ivonescimab Plus Chemotherapy for Triple-Negative Breast Cancer

By: Justine Landin, PhD
Posted: Monday, October 28, 2024

The bispecific antibody ivonescimab combined with chemotherapy may improve clinical outcomes for patients with locally advanced unresectable or metastatic triple-negative breast cancer, according to Xiaojia Wang, MD, PhD, of Zhejiang Cancer Hospital, Hangzhou, China, and colleagues. Ivonescimab targets both PD-1 and VEGF, and when combined with chemotherapy, it yielded antitumor activity in these patients, including a disease control rate of 100%. The findings of this open-label, multicenter phase II study were presented at the European Society of Medical Oncology (ESMO) Congress 2024 (Abstract 347MO).

“Locally advanced unresectable or metastatic triple-negative breast cancer is highly aggressive and has a poor prognosis. Ivonescimab, a tetrameric bispecific antibody targeting PD-1 and VEGF, has the potential to produce complementary and synergistic antitumor effects through both pathways via cooperative binding,” stated the investigators.

Patients with locally advanced unresectable or metastatic triple-negative breast cancer received ivonescimab (20 mg/kg every 2 weeks) and paclitaxel (90 mg/m2) or nab-paclitaxel (100 mg/m2) on days 1, 8, and 15 of each 4-week treatment cycle (n = 30). The median age of patients was 54, 80% had a PD-L1 combined positive score (CPS) of < 10, and 60% had previously received taxane-based neoadjuvant therapy.

At the median follow-up of 7.2 months, the objective response rate in 29 evaluable patients was 72.4%, with a disease control rate of 100%. The objective response rates for patients with a PD-L1 CPS ≥ 10 and < 10 were 83.3% and 69.6%, respectively. Progression-free survival rate at 6 months was 68.4%, although median progression-free survival and overall survival data are not yet mature.

A total of 14 of 30 patients (46.7%) experienced at least one grade ≥ 3 treatment-related adverse event. No treatment-related adverse events led to treatment discontinuation or death.

Disclosure: For full disclosures of the study authors, visit cslide.ctimeetingtech.com.


By continuing to browse this site you permit us and our partners to place identification cookies on your browser and agree to our use of cookies to identify you for marketing. Read our Privacy Policy to learn more.