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术前 S-1 联合顺铂治疗初治局部进展期不可切除胃癌的 II 期临床试验。

Phase II trial of preoperative S-1 plus cisplatin followed by surgery for initially unresectable locally advanced gastric cancer.

机构信息

Department of Surgery, Kansai Medical University, Shinmachi 2-3-1, Hirakata city, Osaka 573-1191, Japan.

出版信息

Eur J Surg Oncol. 2012 Feb;38(2):143-9. doi: 10.1016/j.ejso.2011.11.009. Epub 2011 Dec 9.

Abstract

BACKGROUND

The aim of this study was to evaluate the efficacy and feasibility of preoperative chemotherapy with S-1 plus cisplatin in patients with initially unresectable locally advanced gastric cancer.

METHODS

We enrolled patients with initially unresectable locally advanced gastric cancer because of severe lymph node metastases or invasion of adjacent structures. Preoperative chemotherapy consisted of S-1 at 80 mg/m(2) divided in two daily doses for 21 days and cisplatin at 60 mg/m(2) intravenously on day 8, repeated every 35 days. If a tumor decreased in size, patients received 1 or 2 more courses. Surgery involved radical resection with D2 lymphadenectomy.

RESULTS

Between December 2000 and December 2007, 27 patients were enrolled on the study. No CR was obtained, but PR was seen in 17 cases, and the response rate was 63.0%. Thirteen patients (48.1%) had R0 resections. There were no treatment related deaths. The median overall survival time (MST) and the 3-year overall survival (OS) of all patients were 31.4 months and 31.0%, respectively. Among the 13 patients who underwent curative resection, the median disease-free survival (DFS) and the 3-year DFS were 17.4 months and 23.1%, respectively. The MST and the 3-year OS were 50.1 months and 53.8%, respectively. The most common site of initial recurrence after the R0 resection was the para-aortic lymph nodes.

CONCLUSIONS

Preoperative S-1 plus cisplatin can be safely delivered to patients undergoing radical gastrectomy. This regimen is promising as neoadjuvant chemotherapy for resectable gastric cancer. For initially unresectable locally advanced gastric cancer, new trials using more effective regimens along with extended lymph node dissection are necessary.

摘要

背景

本研究旨在评估 S-1 联合顺铂术前化疗对初始不可切除局部进展期胃癌患者的疗效和可行性。

方法

我们纳入了因严重淋巴结转移或邻近结构侵犯而初始不可切除的局部进展期胃癌患者。术前化疗方案为 S-1 80mg/m2,每日两次,共 21 天,顺铂 60mg/m2 静脉滴注,第 8 天,每 35 天重复一次。如果肿瘤缩小,患者接受 1 或 2 个疗程。手术采用根治性切除术和 D2 淋巴结清扫术。

结果

2000 年 12 月至 2007 年 12 月期间,共纳入 27 例患者。未获得完全缓解(CR),但有 17 例患者获得部分缓解(PR),缓解率为 63.0%。13 例患者(48.1%)接受了 R0 切除术。无治疗相关死亡。所有患者的中位总生存期(MST)和 3 年总生存率(OS)分别为 31.4 个月和 31.0%。在 13 例接受根治性切除术的患者中,中位无病生存期(DFS)和 3 年 DFS 分别为 17.4 个月和 23.1%。MST 和 3 年 OS 分别为 50.1 个月和 53.8%。R0 切除后最初复发的最常见部位是腹主动脉旁淋巴结。

结论

术前 S-1 联合顺铂可安全用于接受根治性胃切除术的患者。该方案有望成为可切除胃癌的新辅助化疗方案。对于初始不可切除的局部进展期胃癌,需要新的试验采用更有效的方案和扩大淋巴结清扫术。

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