Protocol of OGSG 1901: a phase II trial of ramucirumab plus irinotecan for patients with early relapsed gastric cancer during or after adjuvant docetaxel plus S-1 therapy

被引:2
|
作者
Yamaguchi, Toshifumi [1 ]
Kawakami, Hisato [2 ]
Sakai, Daisuke [1 ]
Kurokawa, Yukinori [3 ]
Shimokawa, Toshio [4 ]
Goto, Masahiro [5 ]
Satoh, Taroh [1 ]
机构
[1] Osaka Univ, Dept Frontier Sci Canc & Chemotherapy, Grad Sch Med, Suita, Osaka, Japan
[2] Kindai Univ, Fac Med, Dept Med Oncol, 377-2 Ohno Higashi, Osaka 5898511, Japan
[3] Osaka Univ, Dept Gastroenterol Surg, Grad Sch Med, Osaka, Japan
[4] Wakayama Med Univ Hosp, Clin Study Support Ctr, Wakayama, Japan
[5] Osaka Med Coll, Canc Chemotherapy Ctr, Osaka, Japan
关键词
Gastric cancer; Early relapse; Docetaxel; S-1; Irinotecan; Ramucirumab; GASTROESOPHAGEAL JUNCTION; COMBINATION CHEMOTHERAPY; DOUBLE-BLIND; ADENOCARCINOMA; PACLITAXEL; PLACEBO; MULTICENTER; CISPLATIN; FOLFIRI;
D O I
10.1186/s12885-022-09844-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Although docetaxel plus S-1 adjuvant chemotherapy after gastrectomy with D2 lymphadenectomy has been a standard of treatment for stage III gastric cancer, there is no established chemotherapy for patients with recurrence during or within six months after the completion of adjuvant docetaxel plus S-1 therapy. Methods: The OGSG 1901 trial is a prospective, open-label, multicenter, phase II trial evaluating ramucirumab plus irinotecan for gastric cancer patients with early relapse after adjuvant docetaxel plus S-1 therapy. The key eligibility criteria were: 1) histologically confirmed gastric adenocarcinoma 2) patients who were on docetaxel plus S-1 adjuvant chemotherapy after the confirmation of pathological stage III, 3) patients with early relapse, i.e., recurrence during or within 6 months after the completion of docetaxel plus S-1 therapy, and 4) patient with Eastern Cooperative Oncology Group performance status of 0-1. Irinotecan (150 mg/m(2), day 1) and ramucirumab (8 mg/kg, day 1) will be administered every 2 weeks. The primary endpoint is overall survival, and the secondary endpoints are overall response rate, progression-free survival, and safety. The number of patients has been set at 40 based on the threshold and expected median survival times of 7 and 11 months, respectively, with a one-sided alpha error of 0.05 and power of 0.80. The enrollment and follow-up periods are 2 and 1.5 years, respectively. Discussion: The results of this trial will indicate whether the ramucirumab with irinotecan regimen has the potential to be a recommended treatment regimen for patients with recurrence gastric cancer during or within 6 months after the completion of adjuvant docetaxel plus S-1 therapy.
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