Department of Gastric Surgery, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, P. R. China.
Department of Medical Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University, Guangzhou, P. R. China.
Nat Med. 2024 Feb;30(2):552-559. doi: 10.1038/s41591-023-02721-w. Epub 2024 Jan 2.
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 .
围手术期化疗是局部晚期胃或胃食管交界癌的标准治疗方法,而程序性细胞死亡 1(PD-1)抑制剂的加入正在研究中。在这项随机、开放标签、二期研究(NEOSUMMIT-01)中,临床分期为 cT3-4aN+M0 的可切除胃或胃食管交界癌患者按 1:1 随机分配接受术前 3 个周期和术后 5 个周期的 SOX/XELOX(化疗组,n=54)或 PD-1 抑制剂特瑞普利单抗联合 SOX/XELOX,然后特瑞普利单抗单药治疗最长 6 个月(特瑞普利单抗加化疗组,n=54)。主要终点是病理完全缓解或接近完全缓解率(肿瘤退缩分级(TRG)0/1)。结果显示,特瑞普利单抗加化疗组患者的 TRG 0/1 比例高于化疗组(44.4%(24/54,95%置信区间(CI):30.9%-58.6%)比 20.4%(11/54,95%CI:10.6%-33.5%)),特瑞普利单抗加化疗组与化疗组的 TRG 0/1 风险差异为 22.7%(95%CI:5.8%-39.6%;P=0.009),达到了预设终点。此外,特瑞普利单抗加化疗组的病理完全缓解率(ypT0N0)更高(22.2%(12/54,95%CI:12.0%-35.6%)比 7.4%(4/54,95%CI:2.1%-17.9%);P=0.030),手术发病率(特瑞普利单抗加化疗组 11.8%,化疗组 13.5%)和死亡率(特瑞普利单抗加化疗组 1.9%,化疗组 0%),以及治疗相关的 3-4 级不良事件(特瑞普利单抗加化疗组 35.2%,化疗组 29.6%)在两组之间相当。总之,与单独化疗相比,特瑞普利单抗联合化疗显著增加了 TRG 0/1 的患者比例,且具有可管理的安全性。临床试验注册:NCT04250948。