Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Graduate School of Medical Sciences, Weill Cornell Medicine, New York, NY 10065, USA.
Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Marie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Trends Cancer. 2024 Sep;10(9):781-791. doi: 10.1016/j.trecan.2024.06.009. Epub 2024 Jul 19.
Genomic profiling of hundreds of cancer-associated genes is now a component of routine cancer care. DNA sequencing can identify mutations, mutational signatures, and structural alterations predictive of therapy response and assess for heritable cancer risk, but it has been less useful for identifying predictive biomarkers of sensitivity to cytotoxic chemotherapies, antibody drug conjugates, and immunotherapies. The clinical adoption of molecular profiling platforms such as RNA sequencing better suited to identifying those patients most likely to respond to immunotherapies and drug combinations will be critical to expanding the benefits of precision oncology. This review discusses the potential advantages of innovative molecular and functional profiling platforms designed to replace or complement targeted DNA sequencing and the major hurdles to their clinical adoption.
现在,对数百个与癌症相关的基因进行基因组分析已成为常规癌症治疗的一部分。DNA 测序可以识别突变、突变特征和结构改变,这些改变可预测治疗反应,并评估遗传性癌症风险,但它在识别细胞毒性化疗药物、抗体药物偶联物和免疫疗法的敏感性预测生物标志物方面的作用不大。采用更适合识别最有可能对免疫疗法和药物组合有反应的患者的分子分析平台(如 RNA 测序),对于扩大精准肿瘤学的益处至关重要。这篇综述讨论了旨在替代或补充靶向 DNA 测序的创新分子和功能分析平台的潜在优势,以及它们在临床应用中面临的主要障碍。