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SOBIC 试验:含奥沙利铂和贝伐珠单抗的 S-1 为基础序贯联合化疗方案加或不加西妥昔单抗治疗转移性结直肠癌的Ⅱ期临床研究。

Phase II study of S-1-based sequential combination chemotherapy including oxaliplatin plus bevacizumab and irinotecan with or without cetuximab for metastatic colorectal cancer: the SOBIC trial.

机构信息

Department of Surgery, Meiwa Hospital, Nishinomiya, Hyogo, 663-8186, Japan.

Division of Lower GI Surgery, Department of Surgery, Hyogo College of Medicine, Nishinomiya, Japan.

出版信息

Int J Clin Oncol. 2020 Jul;25(7):1285-1290. doi: 10.1007/s10147-020-01657-2. Epub 2020 Mar 21.

Abstract

BACKGROUND

Fluorouracil and leucovorin combined with oxaliplatin or irinotecan plus bevacizumab (Bmab) or cetuximab (Cmab) are now widely accepted treatment options as first-line or second-line chemotherapy for metastatic colorectal cancer (mCRC). Sequential chemotherapy with oral 5-FU backbone for mCRC without using central venous ports is beneficial for both patients and physicians. We designed the SOBIC trial to validate the effectiveness of the first- and second-line oral combination chemotherapy for mCRC.

PATIENTS AND METHODS

From May 2010 through March 2013, 52 patients were enrolled from 47 institutions in the Hyogo Colorectal Cancer Surgery Group. First-line chemotherapy was S-1 + oxaliplatin (SOX) plus Bmab, and second-line chemotherapy after first-line failure was irinotecan + S-1 (IRIS) + Cmab, IRIS + Bmab, or IRIS based on the KRAS status.

RESULTS

The 50 finally included patients received first-line chemotherapy. Second-line therapy was administered to 20 patients (40%): 12 patients received IRIS + Cmab and 8 patients received IRIS + Bmab. The median follow-up period was 48.6 months (range 35-67 months). The median second progression-free survival was 24.2 months (95% confidence interval [CI] 17.7-35.2). The response rate after first- and second-line chemotherapy was 46.7% and 15%, respectively. The median overall survival was 35.2 months (95% CI: 27.8 to not reached). The main grade 3-4 adverse events were sensory neuropathy (18%) and fatigue (10%). There were no treatment-related deaths.

CONCLUSION

Sequential S-1-based combination regimens including oxaliplatin, irinotecan, Bmab, and Cmab were beneficial for patients with mCRC.

摘要

背景

氟尿嘧啶和亚叶酸钙联合奥沙利铂或伊立替康加贝伐珠单抗(Bmab)或西妥昔单抗(Cmab)现已被广泛接受为转移性结直肠癌(mCRC)的一线或二线化疗选择。对于 mCRC 患者,不使用中心静脉置管,采用口服氟尿嘧啶为基础的序贯化疗对患者和医生都有益。我们设计 SOBIC 试验是为了验证 mCRC 一线和二线口服联合化疗的有效性。

患者和方法

2010 年 5 月至 2013 年 3 月,来自兵库县结直肠癌外科组的 47 家机构共招募了 52 名患者。一线化疗采用 S-1+奥沙利铂(SOX)加 Bmab,一线治疗失败后,二线治疗采用伊立替康+S-1(IRIS)加 Cmab、IRIS+Bmab 或基于 KRAS 状态的 IRIS。

结果

50 名最终纳入的患者接受了一线化疗。20 名患者(40%)接受了二线治疗:12 名患者接受了 IRIS+Cmab,8 名患者接受了 IRIS+Bmab。中位随访时间为 48.6 个月(范围 35-67 个月)。中位二线无进展生存期为 24.2 个月(95%置信区间[CI]:17.7-35.2)。一线和二线化疗后的客观缓解率分别为 46.7%和 15%。中位总生存期为 35.2 个月(95%CI:27.8-未达到)。主要的 3-4 级不良事件是感觉神经病变(18%)和疲劳(10%)。无治疗相关死亡。

结论

包括奥沙利铂、伊立替康、Bmab 和 Cmab 的以 S-1 为基础的序贯联合方案对 mCRC 患者有益。

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