Cancer biomarker that are currently used in cancer therapy and under evaluation in clinical trials.

Advances in cancer research Pub Date : 2026-01-01 Epub Date: 2026-01-03 DOI:10.1016/bs.acr.2025.12.010
Lakshita Tyagi, Shreeja Mishra, Simran, Harjinder Singh, Manoj Kumar, Garima Rathi, Navneet Kaur, Satbir Singh Sehgal, Umesh Kumar
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Abstract

Cancer biomarkers significantly advance precision oncology by giving physicians guidance about treatment options based on the molecular characteristics of a person's tumor, allowing for personalized cancer care. When used collectively, the identification of these cancer biomarkers will lead to better selection of appropriate therapies, facilitate monitoring of response to treatment, and provide rapid evaluation of treatment efficacy. Genetic mutations that are frequently used as cancer biomarkers include mutant forms of particular oncogenes like EGFR (epidermal growth factor receptor), BRAF (B-Raf proto-oncogene), and NTRK (neurotrophic receptor kinase). Targeted therapies that have been successfully developed to treat EGFR mutations in lung cancer and V600E BRAF mutations in melanoma have been proven to be effective. The use of drug therapies such as imlunestrant that specifically target ESR1 mutations in advanced breast cancer cases reflects the incorporation of genetic biomarkers into routine clinical decision making. Non-invasive liquid biopsy technologies, such as the MI Cancer Seek assay, permit the identification of the driver mutations (e.g., PIK3CA, EGFR, BRAF), the presence of microsatellite instability (MSI), and the mutational burden of a tumor tissue sample, providing predictive markers for both targeted and immunotherapeutic treatment options. The further development of HRD and the viral onco-genes have widened the options available for a biomarker-based therapy. This chapter will provide an in-depth explanation of an Introduction to Cancer Biomarkers and new research developments.

目前用于癌症治疗和临床试验评估中的癌症生物标志物。
癌症生物标志物通过为医生提供基于患者肿瘤分子特征的治疗方案指导,从而实现个性化的癌症治疗,显著推进了精准肿瘤学的发展。当这些癌症生物标志物被共同使用时,将有助于更好地选择合适的治疗方法,促进对治疗反应的监测,并提供治疗效果的快速评估。经常被用作癌症生物标志物的基因突变包括特定癌基因的突变形式,如表皮生长因子受体(EGFR)、B-Raf原癌基因BRAF和神经营养受体激酶(NTRK)。已经成功开发的靶向治疗肺癌中的EGFR突变和黑色素瘤中的V600E BRAF突变已被证明是有效的。在晚期乳腺癌病例中使用特异性靶向ESR1突变的药物治疗,如imlunestrant,反映了将遗传生物标志物纳入常规临床决策。非侵入性液体活检技术,如MI Cancer Seek测定,允许识别驱动突变(例如,PIK3CA, EGFR, BRAF),微卫星不稳定性(MSI)的存在,以及肿瘤组织样本的突变负担,为靶向和免疫治疗方案提供预测标记。HRD和病毒癌基因的进一步发展扩大了基于生物标志物的治疗的选择。本章将深入介绍癌症生物标志物和新的研究进展。
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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