NTRK融合:一种新的癌症诊断和治疗方法

Rishika Singh, Nupur Singh, G. Vidal
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摘要

这篇评论讨论了来自出版物“转移性三阴性乳腺癌与组织上的NTRK基因融合,而不是ctDNA分子谱”的病例。本文强调了分子谱分析的重要性,以发现特征突变,如NTRK基因融合,增加治疗选择,包括酪氨酸受体激酶抑制剂,如larorectinib和entrectinib。本文还讨论了当前的分析技术,并对其优点和局限性进行了讨论。与当前药物治疗相关的基因组检测将塑造癌症诊断和治疗的未来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NTRK fusions: A novel diagnostic and therapeutic methodology for cancer
This commentary discusses the case from the publication “Metastatic Triple Negative Breast Cancer with NTRK Gene Fusion on Tissue but not on ctDNA Molecular Profile.” This paper stresses the importance of molecular profiling to find characteristic mutations such as NTRK gene fusions which increase therapeutic options including tyrosine receptor kinase inhibitors such as Larotrectinib and entrectinib. The current profiling techniques are also discussed with both advantages and limitations discussed. Genomic testing in relation to current pharmaceutical therapies will shape the future of cancer diagnosis and treatment.
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