Neoadjuvant apatinib combined with oxaliplatin and capecitabine in patients with locally advanced adenocarcinoma of stomach or gastroesophageal junction: a single-arm, open-label, phase 2 trial

被引:22
作者
Tang, Zhaoqing [1 ]
Wang, Yan [2 ]
Yu, Yiyi [2 ]
Cui, Yuehong [2 ]
Liang, Liang [3 ]
Xu, Chen [4 ]
Shen, Zhenbin [1 ]
Shen, Kuntang [1 ]
Wang, Xuefei [1 ]
Liu, Tianshu [2 ]
Sun, Yihong [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Gen Surg, 180 Fenglin Rd, Shanghai 200032, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Dept Med Oncol, 180 Fenglin Rd, Shanghai 200032, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Radiol, 180 Fenglin Rd, Shanghai 200032, Peoples R China
[4] Fudan Univ, Zhongshan Hosp, Dept Pathol, 180 Fenglin Rd, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Anti-angiogenics; Apatinib; Neoadjuvant therapy; Gastric cancer; PERIOPERATIVE CHEMOTHERAPY; GASTRIC-CANCER; D2; GASTRECTOMY; DOUBLE-BLIND; II TRIAL; SURGERY; MULTICENTER; COMPLICATIONS; BEVACIZUMAB; DISSECTION;
D O I
10.1186/s12916-022-02309-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Adding anti-angiogenics to neoadjuvant chemotherapy for localized gastric cancer is recognized as a promising strategy, but its clinical value remains to be defined. Methods: This single-center, single-arm, phase 2 trial included patients with locally advanced (cT3/4aN+M0) adenocarcinoma of the stomach or gastroesophageal junction (GEJ) who received three cycles of intravenous oxaliplatin (135 mg/m(2) on day 1), oral capecitabine (1000 mg/m(2) twice daily on days 1 to 14), and oral apatinib for 21 days (250 mg once daily in the first two cycles, and further increased to 500 mg daily in the third cycle based on whether any adverse event of grade 3 or worse occurred), and an additional cycle of oxaliplatin plus capecitabine, followed by gastrectomy with D2 lymphadenectomy. The primary endpoint was the proportion of patients who achieved an objective response according to RECIST version 1.1. Results: Between April 28, 2017, and October 23, 2019, 37 patients were screened and 35 participants were included. Of the 32 patients assessable for efficacy and safety, objective responses were achieved in 25 (78.1%; 95% confidence interval [CI], 60.0% to 90.7%) patients. Thirty-one (96.9%) patients received R0 resection, two (6.3%) patients achieved pathological complete response, and 11 (34.4%) patients achieved pathological response. At the data cutoff date (September 30, 2021), the median event-free survival was 42.6 (95% CI, 16.2 to not reached) months, and the median overall survival was not reached. The most common grade 3 or 4 treatment-emergent adverse events were hypertension (9/32, 28.1%), thrombocytopenia (7/32, 21.9%), and neutropenia (5/32, 15.6%). Seven (21.9%) patients developed surgical complications, and the most common one was intra-abdominal abscess (4/32, 12.5%). Conclusions: The concomitant use of apatinib, oxaliplatin, and capecitabine as neoadjuvant therapy showed promising efficacy and manageable safety profile in patients with locally advanced adenocarcinoma of the stomach or GEJ, and further phase 3 study is warranted.
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页数:11
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