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腹腔内化疗作为4型硬癌性胃癌患者的辅助或围手术期化疗:PHOENIX-GC2试验

Intraperitoneal Chemotherapy as Adjuvant or Perioperative Chemotherapy for Patients with Type 4 Scirrhous Gastric Cancer: PHOENIX-GC2 Trial.

作者信息

Ishigami Hironori, Tsuji Yasushi, Shinohara Hisashi, Kodera Yasuhiro, Kanda Mitsuro, Yabusaki Hiroshi, Ito Seiji, Imano Motohiro, Yamashita Hiroharu, Hidemura Akio, Yamaguchi Hironori, Fukagawa Takeo, Oba Koji, Kitayama Joji, Seto Yasuyuki

机构信息

Department of Chemotherapy, The University of Tokyo Hospital, Tokyo 113-8655, Japan.

Department of Gastrointestinal Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo 113-8655, Japan.

出版信息

J Clin Med. 2021 Nov 30;10(23):5666. doi: 10.3390/jcm10235666.

Abstract

The prognosis of patients with type 4 scirrhous gastric cancer remains poor due to a high risk of peritoneal metastasis. We have previously developed combined chemotherapy regimens of intraperitoneal (IP) paclitaxel (PTX) and systemic chemotherapy, and promising clinical efficacy was reported in gastric cancer with peritoneal metastasis. Herein, a randomized, phase III study is proposed to verify the efficacy of IP PTX to prevent peritoneal recurrence. Gastric cancer patients with type 4 tumors and without apparent distant metastasis, including peritoneal metastasis, will be randomized for standard systemic chemotherapy or combined IP and systemic chemotherapy based on peritoneal lavage cytology findings. Those with negative peritoneal cytology will receive radical gastrectomy and adjuvant chemotherapy of S-1 plus docetaxel (control arm), or S-1 plus intravenous and IP PTX (experimental arm). Those with positive peritoneal cytology will receive three courses of S-1 plus oxaliplatin (control arm), or S-1 plus oxaliplatin and IP PTX (experimental arm). Subsequently, they undergo gastrectomy and receive postoperative chemotherapy of S-1 plus docetaxel (control arm), or S-1 plus intravenous and IP PTX (experimental arm). The primary endpoint is disease free survival after a 3-year follow-up period. Secondary endpoints are overall survival, survival without peritoneal metastasis, safety, completion rate, curative resection rate, and histological response of preoperative chemotherapy. A total of 300 patients are to be enrolled.

摘要

由于腹膜转移风险高,4型硬癌性胃癌患者的预后仍然很差。我们之前已经开发了腹腔内(IP)紫杉醇(PTX)与全身化疗联合的化疗方案,并且在伴有腹膜转移的胃癌中报告了有前景的临床疗效。在此,我们提出一项随机III期研究以验证IP PTX预防腹膜复发的疗效。4型肿瘤且无明显远处转移(包括腹膜转移)的胃癌患者将根据腹腔灌洗细胞学检查结果随机接受标准全身化疗或IP与全身联合化疗。腹腔细胞学检查阴性的患者将接受根治性胃切除术及S-1加多西他赛的辅助化疗(对照组),或S-1加静脉及IP PTX(试验组)。腹腔细胞学检查阳性的患者将接受三个疗程的S-1加奥沙利铂(对照组),或S-1加奥沙利铂及IP PTX(试验组)。随后,他们接受胃切除术,并接受S-1加多西他赛的术后化疗(对照组),或S-1加静脉及IP PTX(试验组)。主要终点是3年随访期后的无病生存期。次要终点包括总生存期、无腹膜转移生存期、安全性、完成率、根治性切除率以及术前化疗的组织学反应。总共将招募300名患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9786/8658657/7c959033d06c/jcm-10-05666-g001.jpg

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