主要研究结果:
• 207例患者中,2例(0.96%)的FIL CDx检测无ctDNA
• 没有患者肿瘤分数(TF)<1%,而68.3%(140/206)的ctDNA升高(TF≥10%)
• 发现了1013个基因变异
• FIL CDx发现19例有KRAS/NRAS/BRAF V600E变异,本地实验室则分类为RAS/BRAF V600E WT
• 80%(164/205)的患者同时可获得F1 CDx & F1L CDx,一致率为61.4%
• TF≥10%的F1L CDx一致率升高到72.7%
• 潜在参与抗EGFR耐药基因的一致率为83%(137/164),TF≥10%的F1L CDx中该比例增加到91.5%
• F1L CDx检测到的基因变异数多于F1 CDx,包括6例KRAS/NRAS变异
• 根据ESMO的分子靶点临床可操作性量表(ESCAT),53.2%(109/205)的患者有至少一个可操作的基因变异(I-IIIB)
参考文献:
Ciardiello D, Bielo LB, Napolitano S, Martinelli E, Troiani T, Nicastro A, Latiano TP, Parente P, Maiello E, Avallone A, Normanno N, Pisconti S, Nisi C, Bordonaro R, Russo AE, Tamburrini E, Toma I, Lotesoriere C, Vallarelli S, Zampino MG, Fazio N, Curigliano G, De Vita F, Ciardiello F, Martini G; CAPRI-2 GOIM study Group.. Comprehensive genomic profiling by liquid biopsy captures tumor heterogeneity and identifies cancer vulnerabilities in patients with RAS/BRAFV600E wild type metastatic colorectal cancer in the CAPRI 2-GOIM trial. Ann Oncol. 2024 Aug 28:S0923-7534(24)03914-0. doi: 10.1016/j.annonc.2024.08.2334. Epub ahead of print. PMID: 39214459.