神经母细胞瘤RAS病毒癌基因同源物
克拉斯
医学
结直肠癌
肿瘤科
帕尼单抗
内科学
表皮生长因子受体
癌症
西妥昔单抗
临床试验
外显子
吉非替尼
癌症研究
基因
遗传学
生物
作者
Carmen J. Allegra,R. Bryan Rumble,Stanley R. Hamilton,Pamela B. Mangu,Nancy Roach,Alexander Hantel,Richard L. Schilsky
标识
DOI:10.1200/jco.2015.63.9674
摘要
In addition to the evidence reviewed in the original PCO, 11 systematic reviews with meta-analyses, two retrospective analyses, and two health technology assessments based on a systematic review were obtained. These evaluated the outcomes for patients with mCRC with no mutation detected or presence of mutation in additional exons in KRAS and NRAS. PCO: All patients with mCRC who are candidates for anti-EGFR antibody therapy should have their tumor tested in a Clinical Laboratory Improvement Amendments-certified laboratory for mutations in both KRAS and NRAS exons 2 (codons 12 and 13), 3 (codons 59 and 61), and 4 (codons 117 and 146). The weight of current evidence indicates that anti-EGFR MoAb therapy should only be considered for treatment of patients whose tumor is determined to not have mutations detected after such extended RAS testing.
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