Clinical biomarkers directing the management of patients with colon and lung cancer (beyond oncogene-addicted NSCLC)

Q4 Medicine
I. Ntanasis-Stathopoulos, A. Kyriazoglou, M. Dimopoulos, M. Gavriatopoulou
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引用次数: 2

Abstract

Abstract Treatment personalisation plays a key role in the current management of patients with cancer. Several biomarkers have shown clinical utility and may guide therapeutic decisions. Amongst patients with lung cancer, the level of expression of programmed death ligand 1 (PD-L1) has both prognostic and predictive values in terms of response to the inhibition of programmed cell death protein 1 (PD-1). Depending on the clinical setting, the expression of PD-L1 ≥1% or ≥50% has been associated with improved outcomes amongst patients receiving pembrolizumab. Regarding patients with colorectal carcinoma, mutations in the KRAS oncogene predict the responsiveness to the inhibition of epidermal growth factor receptor (EGFR). Only patients with wild-type KRAS tumours derive benefit from cetuximab and panitumumab in terms of response and survival. In conclusion, future research should aim in the optimisation of the use of biomarker in the clinical practice in order to provide the optimal drug combination to each individual patient.
指导结肠癌和肺癌癌症患者治疗的临床生物标志物(除致癌物成瘾NSCLC外)
个性化治疗在当前癌症患者的治疗中起着关键作用。一些生物标志物已经显示出临床效用,并可能指导治疗决策。在肺癌患者中,程序性死亡配体1 (PD-L1)的表达水平在对程序性细胞死亡蛋白1 (PD-1)抑制的反应方面具有预后和预测价值。根据临床情况,PD-L1表达≥1%或≥50%与接受派姆单抗的患者预后改善相关。对于结直肠癌患者,KRAS癌基因突变预测对表皮生长因子受体(EGFR)抑制的反应性。只有野生型KRAS肿瘤患者从西妥昔单抗和帕尼单抗的反应和生存方面获益。总之,未来的研究应着眼于在临床实践中优化生物标志物的使用,以便为每位患者提供最佳的药物组合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Forum of Clinical Oncology
Forum of Clinical Oncology Medicine-Oncology
CiteScore
0.50
自引率
0.00%
发文量
3
审稿时长
6 weeks
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