Effects of neoadjuvant stereotactic body radiotherapy plus adebrelimab and chemotherapy for triple-negative breast cancer: A pilot study

Author:

Chen Guanglei123,Gu Xi123,Xue Jinqi123,Zhang Xu1,Yu Xiaopeng1,Zhang Yu14,Li Ailin1,Zhao Yi1,He Guijin1,Tang Meiyue1,Xing Fei1,Yin Jianqiao1,Bian Xiaobo1,Han Ye1ORCID,Cao Shuo1,Liu Chao123,Jiang Xiaofan123,Zhang Keliang5,Xia Yan6,Li Huajun6,Niu Nan123,Liu Caigang123ORCID,

Affiliation:

1. Department of Oncology, Shengjing Hospital of China Medical University

2. Cancer Stem Cell and Translational Medicine Laboratory, Shengjing Hospital of China Medical University

3. Innovative Cancer Drug Research and Development Engineering Center of Liaoning Province

4. Department of Gastrointestinal Surgery, Yantai Affiliated Hospital of Binzhou Medical University

5. Liaoning Center for Drug Evaluation and Inspection

6. Jiangsu Hengrui Pharmaceuticals

Abstract

Background:Emerging data have supported the immunostimulatory role of radiotherapy, which could exert a synergistic effect with immune checkpoint inhibitors (ICIs). With proven effective but suboptimal effect of ICI and chemotherapy in triple-negative breast cancer (TNBC), we designed a pilot study to explore the efficacy and safety of neoadjuvant stereotactic body radiotherapy (SBRT) plus adebrelimab and chemotherapy in TNBC patients.Methods:Treatment-naïve TNBC patients received two cycles of intravenous adebrelimab (20 mg/kg, every 3 weeks), and SBRT (24 Gy/3 f, every other day) started at the second cycle, then followed by six cycles of adebrelimab plus nab-paclitaxel (125 mg/m² on days 1 and 8) and carboplatin (area under the curve 6 mg/mL per min on day 1) every 3 weeks. The surgery was performed within 3–5 weeks after the end of neoadjuvant therapy. Primary endpoint was pathological complete response (pCR, ypT0/is ypN0). Secondary endpoints included objective response rate (ORR), residual cancer burden (RCB) 0-I, and safety.Results:13 patients were enrolled and received at least one dose of therapy. 10 (76.9%) patients completed SBRT and were included in efficacy analysis. 90% (9/10) of patients achieved pCR, both RCB 0-I and ORR reached 100% with three patients achieved complete remission. Adverse events (AEs) of all-grade and grade 3–4 occurred in 92.3% and 53.8%, respectively. One (7.7%) patient had treatment-related serious AEs. No radiation-related dermatitis or death occurred.Conclusions:Adding SBRT to adebrelimab and neoadjuvant chemotherapy led to a substantial proportion of pCR with acceptable toxicities, supporting further exploration of this combination in TNBC patients.Funding:None.Clinical trial number:NCT05132790.

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference30 articles.

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