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首页> 外文期刊>Gastric cancer: official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association >Early tumor shrinkage and depth of response in patients with advanced gastric cancer: a retrospective analysis of a randomized phase III study of first-line S-1 plus oxaliplatin vs. S-1 plus cisplatin
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Early tumor shrinkage and depth of response in patients with advanced gastric cancer: a retrospective analysis of a randomized phase III study of first-line S-1 plus oxaliplatin vs. S-1 plus cisplatin

机译:晚期胃癌患者的早期肿瘤收缩和响应深度:一行初级S-1加上奥沙利铂的随机阶段III研究的回顾性分析与S-1加顺铂

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摘要

BackgroundWe investigated early tumor shrinkage (ETS) and depth of response (DpR) using data from the G-SOX study comparing S-1 plus oxaliplatin with S-1 plus cisplatin as the first-line treatment for advanced gastric cancer (AGC).MethodsETS was determined as % decrease in the sum of the longest diameters of the target lesions at the first evaluation of week 6 compared to baseline. DpR was the maximum % shrinkage during the study treatment. The impact of ETS (cutoff value 20%) and DpR (continuous value) on progression-free survival (PFS) and overall survival (OS) were assessed by the log-rank test and Cox regression analysis including prognostic factors obtained in the G-SOX study; ECOG performance status, baseline sum of tumor diameters, disease status (recurrent/unresectable), and histology (diffuse/intestinal).ResultsAmong 685 patients enrolled in the G-SOX study, 632 patients who had the first tumor evaluation were analyzed. Patients with ETS20% had longer PFS (median 4.5 vs. 2.8 months, p0.0001) and OS (median 14.8 vs. 10.5 months, p0.0001) than those with ETS20%. Adjusted hazard ratios of ETS20 vs. 20% were 0.606 (95% confidence interval (CI) 0.506-0.725) for PFS and 0.589 (95% CI 0.492-0.704) for OS. DpR was also significantly associated with PFS and OS (both p0.0001). These results were similar between the SOX and CS groups.ConclusionsIn AGC patients receiving the first-line therapy, ETS and DpR might be predictors for PFS and OS.
机译:BackgroundWe使用来自G-SOX研究的数据进行研究,研究了早期肿瘤收缩(ETS)和深度(DPR)比较S-1加顺铂作为晚期胃癌(AGC)的第一线治疗.methodsets与基线相比,在第6周的第一次评估中被确定为靶病变的最长直径之和的百分比。 DPR是研究治疗期间的最大%收缩。 ETS(截止值20%)和DPR(连续值)对无进展存活(PFS)和总存活(OS)的影响进行评估通过LOG-ange试验和COX回归分析,包括在G-中获得的预后因素SOX学习; ECOG性能状态,肿瘤直径的基线和,疾病状态(复发/不可切除)和组织学(弥漫性/肠)。评入G-SOX研究的患者,分析了第一个肿瘤评估的632名患者。 ETS20%的患者具有较长的PFS(中位数4.5对2.8个月,P&LT; 0.0001)和OS(中位数14.8与10.5个月,P <0.0001)比具有ETS的ETS& 20%。调整的ETS的危险比为0.606(95%置信区间(CI)0.506-0.725),OS的0.589(95%CI 0.492-0.704)。 DPR也与PFS和OS显着相关(P <0.0001)。这些结果在SOx和Cs组之间类似。蛋白蛋白接受一线治疗的患者,ETS和DPR可能是PFS和OS的预测因子。

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