PRODIGY: A Phase III Study of Neoadjuvant Docetaxel, Oxaliplatin, and S-1 Plus Surgery and Adjuvant S-1 Versus Surgery and Adjuvant S-1 for Resectable Advanced Gastric Cancer

医学 围手术期 四分位间距 胃切除术 癌症 佐剂 内科学 新辅助治疗 辅助化疗 多西紫杉醇 养生 化疗 阶段(地层学) 肿瘤科 外科 临床研究阶段 胃肠病学 卡培他滨 奥沙利铂 乳腺癌 结直肠癌 古生物学 生物
作者
Yoon-Koo Kang,Jeong Hwan Yook,Young-Kyu Park,Jong-Ho Lee,Young-Jin Kim,Jin-Soo Kim,Min-Hee Ryu,Sun Young Rha,Ik Joo Chung,Inho Kim,Sang Cheul Oh,Youngsoo Park,Taeil Son,Mi Ran Jung,Mi Hwa Heo,Hark Kyun Kim,Cho-Hyun Park,Chang D. Yoo,Jin-Hyuk Choi,Dae Young Zang,You Jin Jang,Ji Young Sul,Jin Won Kim,Beom Joon Kim,Seung Hoon Beom,Sang Heon Cho,Seung Ryu,Myeong-Cherl Kook,Baek-Yeol Ryoo,Hyun Jung Kim,Moon-Won Yoo,Nam Yong Lee,Sang Yup Lee,Gyunji Kim,Yeon-Ju Lee,Jee Young Lee,Sung Hoon Noh
出处
期刊:Journal of Clinical Oncology [American Society of Clinical Oncology]
卷期号:39 (26): 2903-2913 被引量:49
标识
DOI:10.1200/jco.20.02914
摘要

PURPOSE Adjuvant chemotherapy after D2 gastrectomy is standard for resectable locally advanced gastric cancer (LAGC) in Asia. Based on positive findings for perioperative chemotherapy in European phase III studies, the phase III PRODIGY study (ClinicalTrials.gov identifier: NCT01515748 ) investigated whether neoadjuvant docetaxel, oxaliplatin, and S-1 (DOS) followed by surgery and adjuvant S-1 could improve outcomes versus standard treatment in Korean patients with resectable LAGC. PATIENTS AND METHODS Patients 20-75 years of age, with Eastern Cooperative Oncology Group performance status 0-1, and with histologically confirmed primary gastric or gastroesophageal junction adenocarcinoma (clinical TNM staging: T2-3N+ or T4Nany) were randomly assigned to D2 surgery followed by adjuvant S-1 (40-60 mg orally twice a day, days 1-28 every 6 weeks for eight cycles; SC group) or neoadjuvant DOS (docetaxel 50 mg/m 2 , oxaliplatin 100 mg/m 2 intravenously day 1, S-1 40 mg/m 2 orally twice a day, days 1-14 every 3 weeks for three cycles) before D2 surgery, followed by adjuvant S-1 (CSC group). The primary objective was progression-free survival (PFS) with CSC versus SC. Two sensitivity analyses were performed: intent-to-treat and landmark PFS analysis. RESULTS Between January 18, 2012, and January 2, 2017, 266 patients were randomly assigned to CSC and 264 to SC at 18 Korean study sites; 238 and 246 patients, respectively, were treated (full analysis set). Follow-up was ongoing in 176 patients at data cutoff (January 21, 2019; median follow-up 38.6 months [interquartile range, 23.5-62.1]). CSC improved PFS versus SC (adjusted hazard ratio, 0.70; 95% CI, 0.52 to 0.95; stratified log-rank P = .023). Sensitivity analyses confirmed these findings. Treatments were well tolerated. Two grade 5 adverse events (febrile neutropenia and dyspnea) occurred during neoadjuvant treatment. CONCLUSION PRODIGY showed that neoadjuvant DOS chemotherapy, as part of perioperative chemotherapy, is effective and tolerable in Korean patients with LAGC.
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