Department of Oncology, Barretos Cancer Hospital, Barretos, Brazil.
Molecular Oncology Research Center, Barretos Cancer Hospital, Barretos, Brazil.
J Gastrointest Cancer. 2024 Mar;55(1):344-354. doi: 10.1007/s12029-023-00964-x. Epub 2023 Aug 23.
Evaluate overall survival (OS), RAS, BRAF, and MSI frequencies in patients with metastatic colorectal cancer (mCRC), refractory to chemotherapy, and finally treated with cetuximab.
A retrospective cohort study to evaluate 211 mCRC patients with wild-type KRAS treated with cetuximab. BRAF V600E, KRAS, NRAS gene mutations, and MSI status were identified using PCR techniques in a population of pre-treated patients who were refractory to fluoropyrimidines, oxaliplatin, and irinotecan. In addition, we evaluated the mutation frequency of the BRAF and NRAS genes and the MSI status of this population. Uni- and multivariate analyses were performed for independent prognostic factors of OS.
The median OS was 10.4 months, 6.6 months for patients with right and 11.5 months for left colon cancers (p = 0.02). The frequencies of mutations were BRAF at 3.9% (median OS of 4.9 months), NRAS at 3.38% (median OS of 6.9 months), and MSI-High status at 3.3% (median OS of 4.6 months). The OS, NRAS, and MSI frequencies were similar to those found in other studies that evaluated cetuximab in poly-treated patients and were associated with lower survival rates in univariate analyses. The frequency of BRAF mutations was lower than that found in previous studies. The only variable that remained significant for OS in the multivariate model was tumour laterality, with patients with right colon cancer presenting a worse prognosis (HR = 2.81).
Although BRAF, NRAS mutations, and MSI-High status were associated with shorter OS in univariate analyses, only tumour laterality remained an independent prognostic factor in the multivariate analysis.
评估转移性结直肠癌(mCRC)患者的总生存期(OS)、RAS、BRAF 和 MSI 频率,这些患者对化疗耐药,最后接受西妥昔单抗治疗。
这是一项回顾性队列研究,共评估了 211 例接受西妥昔单抗治疗的野生型 KRAS 转移性结直肠癌患者。采用 PCR 技术在氟嘧啶、奥沙利铂和伊立替康耐药的预处理患者人群中鉴定 BRAF V600E、KRAS、NRAS 基因突变和 MSI 状态。此外,我们还评估了该人群中 BRAF 和 NRAS 基因突变及 MSI 状态的突变频率。对 OS 的独立预后因素进行单变量和多变量分析。
中位 OS 为 10.4 个月,右半结肠癌患者为 6.6 个月,左半结肠癌患者为 11.5 个月(p=0.02)。突变频率为 BRAF 3.9%(中位 OS 为 4.9 个月),NRAS 3.38%(中位 OS 为 6.9 个月),MSI-High 状态 3.3%(中位 OS 为 4.6 个月)。OS、NRAS 和 MSI 频率与其他评估西妥昔单抗在多线治疗患者中的研究相似,且单变量分析显示这些因素与生存率较低相关。BRAF 突变的频率低于既往研究。多变量模型中唯一与 OS 显著相关的变量是肿瘤侧别,右半结肠癌患者的预后更差(HR=2.81)。
虽然 BRAF、NRAS 突变和 MSI-High 状态在单变量分析中与 OS 较短相关,但只有肿瘤侧别在多变量分析中仍是独立的预后因素。