Taniguchi Hiroya, Yamazaki Kentaro, Yoshino Takayuki, Muro Kei, Yatabe Yasushi, Watanabe Toshiaki, Ebi Hiromichi, Ochiai Atsushi, Baba Eishi, Tsuchihara Katsuya
Department of Clinical Oncology, Aichi Cancer Center Hospital, Aichi, Japan.
Cancer Sci. 2015 Mar;106(3):324-7. doi: 10.1111/cas.12595.
The Japanese guidelines for the testing of KRAS mutations in colorectal cancer have been used for the past 5 years. However, new findings of RAS (KRAS/NRAS) mutations that can further predict the therapeutic effects of anti-epidermal growth factor receptor (EGFR) antibody therapy necessitated a revision of the guidelines. The revised guidelines included the following five basic requirements for RAS mutation testing to highlight a patient group in which anti-EGFR antibody therapy may be ineffective: First, anti-EGFR antibody therapy may not offer survival benefit and/or tumor shrinkage to patients with expanded RAS mutations. Thus, current methods to detect KRAS exon 2 (codons 12 and 13) mutations are insufficient for selecting appropriate candidates for this therapy. Additional testing of extended KRAS/NRAS mutations is recommended. Second, repeated tests are not required for the detection; tissue materials of either primary or metastatic lesions are applicable for RAS mutation testing. Evaluating RAS mutations prior to anti-EGFR antibody therapy is recommended. Third, direct sequencing with manual dissection or allele-specific PCR-based methods is currently applicable for RAS mutation testing. Fourth, thinly sliced sections of formalin-fixed, paraffin-embedded tissue blocks are applicable for RAS mutation testing. One section stained with H&E should be provided to histologically determine whether the tissue contains sufficient amount of tumor cells for testing. Finally, RAS mutation testing must be performed in laboratories with appropriate testing procedures and specimen management practices.
日本结直肠癌KRAS突变检测指南在过去5年一直被采用。然而,RAS(KRAS/NRAS)突变的新发现能够进一步预测抗表皮生长因子受体(EGFR)抗体治疗的疗效,因此有必要对该指南进行修订。修订后的指南包括RAS突变检测的以下五项基本要求,以明确抗EGFR抗体治疗可能无效的患者群体:第一,抗EGFR抗体治疗可能不会给具有扩展RAS突变的患者带来生存获益和/或肿瘤缩小。因此,目前检测KRAS外显子2(密码子12和13)突变的方法不足以筛选出该治疗的合适候选者。建议对扩展的KRAS/NRAS突变进行额外检测。第二,检测不需要重复进行;原发或转移病灶的组织材料均可用于RAS突变检测。建议在抗EGFR抗体治疗前评估RAS突变。第三,目前手动解剖直接测序或基于等位基因特异性PCR的方法适用于RAS突变检测。第四,福尔马林固定、石蜡包埋组织块的薄片适用于RAS突变检测。应提供一张苏木精-伊红(H&E)染色切片,以组织学方式确定组织中是否含有足够数量的肿瘤细胞用于检测。最后,RAS突变检测必须在具备适当检测程序和标本管理规范的实验室中进行。