Ding Ping'an, Yang Peigang, Tian Yuan, Guo Honghai, Liu Yang, Zhang Ze, Zheng Tao, Tan Bibo, Zhang Zhidong, Wang Dong, Li Yong, Zhao Qun
The Third Department of Surgery, the Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
J Gastrointest Oncol. 2021 Aug;12(4):1416-1427. doi: 10.21037/jgo-21-375.
To explore the efficacy and safety of neoadjuvant intraperitoneal and systemic (NIPS) paclitaxel chemotherapy combined with apatinib and S-1 in the treatment of gastric cancer patients with positive exfoliative cytology.
Patients with gastric cancer (PCY) who were confirmed to have free cancer cells (FCCs) in the abdominal cavity after laparoscopic exploration from April 2018 to August 2019 were enrolled. All patients underwent NIPS chemotherapy using paclitaxel combined with apatinib and S-1 treatment. Laparoscopic exploration was performed after 3 cycles of conversion therapy. The primary study endpoint was the FCC negative rate, and the secondary study endpoints were overall survival time (OS), progression-free survival time (PFS), objective response rate (ORR), disease control rate (DCR), and safety indicators.
Out of 312 advanced gastric cancer patients who underwent laparoscopic exploration, 36 patients with PCY gastric cancer were identified and enrolled in this study. After 3 cycles of conversion therapy, the ORR was 80.56% and the DCR was 94.44%. All patients underwent secondary laparoscopic exploration, and the FCC conversion rate was 77.78%. All patients with negative FCC underwent R0 surgical resection, with a median follow-up time of 11.4 months. The median survival time was 15.5 months, and the 1-year OS was 80.55%. The median PFS was 14.4 months, and the 1-year PFS was 75.00%. Treatment-related grade 3 adverse reactions were mainly leukopenia and neutropenia. No grade 4 adverse reactions were observed. There were no reported deaths related to chemotherapy or surgery in the study cohort.
NIPS with paclitaxel combined with apatinib and S-1 treatment may increase the FCC negative rate of PCY gastric cancer patients.
探讨新辅助腹腔及全身(NIPS)紫杉醇化疗联合阿帕替尼及S-1治疗胃癌脱落细胞学阳性患者的疗效及安全性。
纳入2018年4月至2019年8月间经腹腔镜探查腹腔内有游离癌细胞(FCCs)的胃癌患者。所有患者接受NIPS化疗,采用紫杉醇联合阿帕替尼及S-1治疗。转化治疗3个周期后进行腹腔镜探查。主要研究终点为FCC阴性率,次要研究终点为总生存时间(OS)、无进展生存时间(PFS)、客观缓解率(ORR)、疾病控制率(DCR)及安全性指标。
312例接受腹腔镜探查的晚期胃癌患者中,36例PCY胃癌患者被纳入本研究。转化治疗3个周期后,ORR为80.56%,DCR为94.44%。所有患者均接受了二次腹腔镜探查,FCC转化率为77.78%。所有FCC阴性的患者均接受了R0手术切除,中位随访时间为11.4个月。中位生存时间为15.5个月,1年OS为80.55%。中位PFS为14.4个月,1年PFS为75.00%。与治疗相关的3级不良反应主要为白细胞减少和中性粒细胞减少。未观察到4级不良反应。研究队列中未报告与化疗或手术相关的死亡病例。
NIPS紫杉醇联合阿帕替尼及S-1治疗可能提高PCY胃癌患者的FCC阴性率。