Department of Surgery, Yonsei University College of Medicine, Seoul, South Korea.
Gastric Cancer Branch, Research Institute and Hospital, National Cancer Center, Goyang, South Korea.
Lancet Oncol. 2014 Nov;15(12):1389-96. doi: 10.1016/S1470-2045(14)70473-5. Epub 2014 Oct 15.
The CLASSIC trial was done to compare adjuvant capecitabine plus oxaliplatin versus observation after D2 gastrectomy for patients with stage II or III gastric cancer. The planned interim analysis of CLASSIC (median follow-up 34 months) showed that adjuvant capecitabine plus oxaliplatin significantly improved disease-free survival, the primary endpoint, compared with observation after D2 gastrectomy. We report the 5-year follow-up data from the trial.
CLASSIC was a phase 3, randomised, open-label study done at 35 cancer centres, medical centres, and hospitals in China, South Korea, and Taiwan. Patients with stage II-IIIB gastric cancer who underwent curative D2 gastrectomy were randomly assigned (1:1) after surgery to receive adjuvant chemotherapy with capecitabine and oxaliplatin (eight 3-week cycles of oral capecitabine 1000 mg/m(2) twice daily on days 1-14 plus intravenous oxaliplatin 130 mg/m(2) on day 1) for 6 months or observation alone. Randomisation was stratified by country and disease stage with a permuted block (size four) design. Neither patients nor investigators were masked to treatment assignment. The primary outcome was 3-year disease-free survival in the intention-to-treat population. This analysis presents the final preplanned assessment of outcomes after 5 years. The study is registered with ClinicalTrials.gov, NCT00411229.
We enrolled 1035 patients: 520 were randomly assigned to adjuvant capecitabine and oxaliplatin, and 515 to observation. Median follow-up for this analysis in the intention-to-treat population was 62·4 months (IQR 54-70). 139 (27%) patients had disease-free survival events in the adjuvant capecitabine and oxaliplatin group versus 203 (39%) patients in the observation group (stratified hazard ratio [HR] 0·58, 95% CI 0·47-0·72; p<0·0001). Estimated 5-year disease-free survival was 68% (95% CI 63-73) in the adjuvant capecitabine and oxaliplatin group versus 53% (47-58) in the observation alone group. By the clinical cutoff date, 103 patients (20%) had died in the adjuvant capecitabine and oxaliplatin group versus 141 patients (27%) in the observation group (stratified HR 0·66, 95% CI 0·51-0·85; p=0·0015). Estimated 5-year overall survival was 78% (95% CI 74-82) in the adjuvant capecitabine and oxaliplatin group versus 69% (64-73) in the observation group. Adverse event data were not collected after the primary analysis.
Adjuvant treatment with capecitabine plus oxaliplatin after D2 gastrectomy should be considered for patients with operable stage II or III gastric cancer.
F Hoffmann La-Roche and Sanofi.
CLASSIC 试验旨在比较 II 期或 III 期胃癌患者接受 D2 胃切除术后辅助卡培他滨联合奥沙利铂与观察的疗效。CLASSIC 的计划中期分析(中位随访 34 个月)显示,与 D2 胃切除术后观察相比,卡培他滨联合奥沙利铂辅助治疗显著改善了无病生存期,这是主要终点。我们报告了该试验的 5 年随访数据。
CLASSIC 是一项在中国、韩国和中国台湾的 35 个癌症中心、医疗中心和医院进行的 III 期、随机、开放性标签研究。接受根治性 D2 胃切除术的 II 期-IIIB 胃癌患者在手术后按 1:1 随机分配接受卡培他滨和奥沙利铂辅助化疗(口服卡培他滨 1000mg/m²,每日 2 次,第 1-14 天,静脉注射奥沙利铂 130mg/m²,第 1 天),共 6 个月或单独观察。随机化按国家和疾病分期分层,采用置换块(大小为 4)设计。患者和研究者均未对治疗分组进行设盲。主要结局为意向治疗人群的 3 年无病生存率。这是在 5 年后对预先计划的结局进行的最终评估。该研究在 ClinicalTrials.gov 上注册,编号为 NCT00411229。
我们共纳入了 1035 例患者:520 例随机分配接受卡培他滨联合奥沙利铂辅助治疗,515 例接受观察。意向治疗人群的中位随访时间为 62.4 个月(IQR 54-70)。在卡培他滨联合奥沙利铂组中,有 139 例(27%)患者发生无病生存事件,而在观察组中有 203 例(39%)患者(分层风险比[HR]0.58,95%CI 0.47-0.72;p<0.0001)。卡培他滨联合奥沙利铂组的 5 年无病生存率为 68%(95%CI 63-73),而观察组为 53%(47-58)。截至临床截止日期,卡培他滨联合奥沙利铂组有 103 例(20%)患者死亡,而观察组有 141 例(27%)患者死亡(分层 HR 0.66,95%CI 0.51-0.85;p=0.0015)。卡培他滨联合奥沙利铂组的 5 年总生存率为 78%(95%CI 74-82),而观察组为 69%(64-73)。主要分析后未收集不良事件数据。
对于可手术的 II 期或 III 期胃癌患者,应考虑在 D2 胃切除术后进行卡培他滨联合奥沙利铂辅助治疗。
罗氏公司和赛诺菲公司。