Nakajima T, Kinoshita T, Nashimoto A, Sairenji M, Yamaguchi T, Sakamoto J, Fujiya T, Inada T, Sasako M, Ohashi Y
Department of Gastrointestinal Surgery, Cancer Institute Hospital, Tokyo, Japan.
Br J Surg. 2007 Dec;94(12):1468-76. doi: 10.1002/bjs.5996.
This prospective randomized study compared the survival of patients with tumour node metastasis (TNM) stage T2 N1-2 gastric cancer treated by gastrectomy alone or gastrectomy followed by uracil-tegafur.
Patients were randomly assigned to surgery alone or to surgery and postoperative uracil-tegafur 360 mg per m(2) per day orally for 16 months. The primary endpoint was overall survival. Relapse-free survival and site of recurrence were secondary endpoints.
Of 190 registered patients, 95 were randomized to each group; two patients with early cancer were subsequently excluded from the chemotherapy group. The trial was terminated before the target number of patients was reached because accrual was slower than expected. Drug-related adverse effects were mild, with no treatment-related deaths. At a median follow-up of 6.2 years, overall and relapse-free survival rates were significantly higher in the chemotherapy group (hazard ratio for overall survival 0.48, P = 0.017; hazard ratio for relapse-free survival 0.44, P = 0.005), confirming the survival benefit shown in an interim analysis performed 2 years earlier.
Interim and final analyses revealed a significant survival benefit for postoperative adjuvant chemotherapy with uracil-tegafur in patients with serosa-negative, node-positive gastric cancer.
NCT00152243 (http://www.clinicaltrials.gov).
本前瞻性随机研究比较了单纯胃切除术或胃切除术后使用替加氟尿嘧啶治疗的肿瘤淋巴结转移(TNM)分期为T2 N1 - 2的胃癌患者的生存率。
患者被随机分配至单纯手术组或手术加术后口服替加氟尿嘧啶360 mg/m²/天,共16个月。主要终点为总生存期。无复发生存期和复发部位为次要终点。
190例登记患者中,每组随机分配95例;化疗组随后排除了2例早期癌症患者。由于入组速度慢于预期,试验在达到目标患者数量之前终止。药物相关不良反应较轻,无治疗相关死亡。中位随访6.2年时,化疗组的总生存期和无复发生存率显著更高(总生存期风险比0.48,P = 0.017;无复发生存期风险比0.44,P = 0.005),证实了2年前中期分析中显示的生存获益。
中期和最终分析显示,对于浆膜阴性、淋巴结阳性的胃癌患者,术后使用替加氟尿嘧啶辅助化疗有显著的生存获益。
NCT00152243(http://www.clinicaltrials.gov)