Perioperative toripalimab and chemotherapy in locally advanced gastric or gastro-esophageal junction cancer: a randomized phase 2 trial.
Shu-Qiang YuanRun-Cong NieYing JinCheng-Cai LiangYuan-Fang LiRui JianXiao-Wei SunYing-Bo ChenWen-Long GuanZi-Xian WangHai-Bo QiuWei WangShi ChenDong-Sheng ZhangYi-Hong LingShao-Yan XiMu-Yan CaiChun-Yu HuangQiu-Xia YangZhi-Min LiuYuan-Xiang GuanYong-Ming ChenWeiwei XiaoXiong-Wen TangJun-Sheng PengZhou-Wei ZhouRui-Hua XuFeng-Hua WangPublished in: Nature medicine (2024)
Perioperative chemotherapy is the standard treatment for locally advanced gastric or gastro-esophageal junction cancer, and the addition of programmed cell death 1 (PD-1) inhibitor is under investigation. In this randomized, open-label, phase 2 study (NEOSUMMIT-01), patients with resectable gastric or gastro-esophageal junction cancer clinically staged as cT3-4aN + M0 were randomized (1:1) to receive either three preoperative and five postoperative 3-week cycles of SOX/XELOX (chemotherapy group, n = 54) or PD-1 inhibitor toripalimab plus SOX/XELOX, followed by toripalimab monotherapy for up to 6 months (toripalimab plus chemotherapy group, n = 54). The primary endpoint was pathological complete response or near-complete response rate (tumor regression grade (TRG) 0/1). The results showed that patients in the toripalimab plus chemotherapy group achieved a higher proportion of TRG 0/1 than those in the chemotherapy group (44.4% (24 of 54, 95% confidence interval (CI): 30.9%-58.6%) versus 20.4% (11 of 54, 95% CI: 10.6%-33.5%)), and the risk difference of TRG 0/1 between toripalimab plus chemotherapy group and chemotherapy group was 22.7% (95% CI: 5.8%-39.6%; P = 0.009), meeting a prespecified endpoint. In addition, a higher pathological complete response rate (ypT0N0) was observed in the toripalimab plus chemotherapy group (22.2% (12 of 54, 95% CI: 12.0%-35.6%) versus 7.4% (4 of 54, 95% CI: 2.1%-17.9%); P = 0.030), and surgical morbidity (11.8% in the toripalimab plus chemotherapy group versus 13.5% in the chemotherapy group) and mortality (1.9% versus 0%), and treatment-related grade 3-4 adverse events (35.2% versus 29.6%) were comparable between the treatment groups. In conclusion, the addition of toripalimab to chemotherapy significantly increased the proportion of patients achieving TRG 0/1 compared to chemotherapy alone and showed a manageable safety profile. ClinicalTrials.gov registration: NCT04250948 .
Keyphrases
- locally advanced
- open label
- rectal cancer
- neoadjuvant chemotherapy
- squamous cell carcinoma
- phase ii study
- end stage renal disease
- stem cells
- patients undergoing
- newly diagnosed
- randomized controlled trial
- computed tomography
- clinical trial
- chemotherapy induced
- ejection fraction
- papillary thyroid
- transcription factor
- chronic kidney disease
- magnetic resonance imaging
- cardiac surgery
- phase iii
- acute kidney injury
- patient reported
- replacement therapy
- liver metastases