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  2. Adebrelimab (SHR-1316) in combination with chemotherapy as perioperative treatment in patients with resectable stage II-III NSCLC: an open-label, multicenter, phase 1b trial

Adebrelimab (SHR-1316) in combination with chemotherapy as perioperative treatment in patients with resectable stage II-III NSCLC: an open-label, multicenter, phase 1b trial

  • J Thorac Oncol. 2022 Sep 30;S1556-0864(22)01822-6. doi: 10.1016/j.jtho.2022.09.222.
Wanpu Yan 1 Wen-Zhao Zhong 2 Yan-Hui Liu 2 Qixun Chen 3 Wenqun Xing 4 Qin Zhang 5 Lunxu Liu 6 Di Ge 7 Keneng Chen 1 Fan Yang 8 Xiang Lin 9 Li Song 9 Wei Shi 9 Yi-Long Wu 10
Affiliations

Affiliations

  • 1 Department of Thoracic Oncology I, Beijing Cancer Hospital, Beijing, China.
  • 2 Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, Guangzhou, China.
  • 3 Thoracic Surgery, Zhejiang Cancer Hospital, Hangzhou, China.
  • 4 Thoracic Surgery Ward, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, China.
  • 5 Department of Thoracic Surgery, Jiangsu Cancer Hospital, Nanjing, China.
  • 6 Department of Thoracic Surgery, West China Hospital of Sichuan University, Chengdu, China.
  • 7 Thoracic Surgery, Zhongshan Hospital Fudan University, Shanghai, China.
  • 8 Thoracic Surgery, Peking University People's Hospital, Beijing, China.
  • 9 Jiangsu Hengrui Pharmaceuticals Co, Ltd, Shanghai, China.
  • 10 Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, Guangzhou, China. Electronic address: syylwu@live.cn.
Abstract

Introduction: This study evaluated adebrelimab (a PD-L1 antibody) plus nab-paclitaxel and carboplatin as perioperative treatment for resectable NSCLC.

Methods: Eligible patients had resectable stage II-III NSCLCs without driver gene. Patients received neoadjuvant treatment with 3 cycles of intravenous adebrelimab (20 mg/kg on day 1), nab-paclitaxel (100 mg/m2 on days 1, 8, and 15), and carboplatin (area under the curve 5 mg/mL per min on day 1), of each 21-day cycle before surgical resection, and followed by 16 cycles of adebrelimab (20 mg/kg on day 1 in 3 weeks) Adjuvant treatment. The primary endpoint was major pathological response (MPR) per blinded independent pathological review (BIPR).

Results: A total of 37 patients were enrolled and received planned neoadjuvant therapy. Thirty-four (91.9%) patients underwent surgery. As of data cutoff on Jan 25, 2022, 19 (51.4%, 95% CI 35.9-66.6) of the 37 patients achieved MPR per BIPR and 11 (29.7%, 95% CI 17.5-45.8) patients achieved pathological complete response. Twenty-six (70.3%, 95% CI 54.2-82.5) patients had an objective response per RECIST v1.1. The 12-month event-free survival (EFS) rate was 77.8% (95% CI 54.1-90.3). Twenty-nine (78.4%) patients had grade ≥3 treatment-related adverse events (AEs) and nine (24.3%) had treatment-related serious AEs. No treatment-related deaths occurred. Grade ≥3 surgery-related AEs within 30 or 90 days after surgery were both reported in 5 (14.7%) patients.

Conclusion: Adebrelimab plus nab-paclitaxel and carboplatin as perioperative therapy led to a substantial proportion of MPR and high resectability, with manageable toxicities. Based on the phase 1b results, phase 3 trial was initiated.

Keywords

Adebrelimab; NSCLC; perioperative therapy.

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