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[《美国国立综合癌症网络(NCCN)2017 第 1.0 版结直肠癌临床实践指南》更新解读]

[Interpretation of the updates of NCCN 2017 version 1.0 guideline for colorectal cancer].

作者信息

Chen Gong

机构信息

Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.

出版信息

Zhonghua Wei Chang Wai Ke Za Zhi. 2017 Jan 25;20(1):28-33.

Abstract

The NCCN has recently released its 2017 version 1.0 guideline for colorectal cancer. There are several updates from this new version guideline which are believed to change the current clinical practice. Update one, low-dose aspirin is recommended for patients with colorectal cancer after colectomy for secondary chemoprevention. Update two, biological agents are removed from the neoadjuvant treatment regimen for resectable metastatic colorectal cancer (mCRC). This update is based on lack of evidence to support benefits of biological agents including bevacizumab and cetuximab in the neoadjuvant setting. Both technical criteria and prognostic information should be considered for decision-making. Currently biological agents may not be excluded from the neoadjuvant setting for patients with resectable but poor prognostic disease. Update three, panitumumab and cetuximab combination therapy is only recommended for left-sided tumors in the first line therapy. The location of the primary tumor can be both prognostic and predictive in response to EGFR inhibitors in metastatic colorectal cancer. Cetuximab and panitumumab confer little benefit to patients with metastatic colorectal cancer in the primary tumor originated on the right side. On the other hand, EGFR inhibitors provide significant benefit compared with bevacizumab-containing therapy or chemotherapy alone for patients with left primary tumor. Update four, PD-1 immune checkpoint inhibitors including pembrolizumab or nivolumab are recommended as treatment options in patients with metastatic deficient mismatch repair (dMMR) colorectal cancer in second- or third-line therapy. dMMR tumors contain thousands of mutations, which can encode mutant proteins with the potential to be recognized and targeted by the immune system. It has therefore been hypothesized that dMMR tumors may be sensitive to PD-1 inhibitors.

摘要

美国国立综合癌症网络(NCCN)最近发布了其2017年第1版结直肠癌指南。该新版指南有多项更新内容,据信将改变当前的临床实践。更新一,推荐对接受结肠切除术后的结直肠癌患者使用低剂量阿司匹林进行二级化学预防。更新二,生物制剂被从可切除转移性结直肠癌(mCRC)的新辅助治疗方案中移除。这一更新是基于缺乏证据支持生物制剂(包括贝伐单抗和西妥昔单抗)在新辅助治疗中的益处。决策时应同时考虑技术标准和预后信息。目前,对于可切除但预后不良的疾病患者,新辅助治疗中可能不排除使用生物制剂。更新三,帕尼单抗和西妥昔单抗联合治疗仅推荐用于一线治疗中的左侧肿瘤。在转移性结直肠癌中,原发肿瘤的位置对表皮生长因子受体(EGFR)抑制剂的反应可能具有预后和预测价值。对于原发肿瘤起源于右侧的转移性结直肠癌患者,西妥昔单抗和帕尼单抗几乎没有益处。另一方面,对于原发肿瘤位于左侧的患者,与含贝伐单抗治疗或单纯化疗相比,EGFR抑制剂可带来显著益处。更新四,推荐将包括帕博利珠单抗或纳武利尤单抗在内的PD-1免疫检查点抑制剂作为二线或三线治疗中转移性错配修复缺陷(dMMR)结直肠癌患者的治疗选择。dMMR肿瘤含有数千种突变,这些突变可编码有可能被免疫系统识别和靶向的突变蛋白。因此,有人推测dMMR肿瘤可能对PD-1抑制剂敏感。

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