Yang Zhi, Guan Fada, Bronk Lawrence, Zhao Lina
Department of Radiation Oncology, Xijing Hospital, Fourth Military Medical University, 15 West Changle Road, Xi'an, China.
Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, CT 06510, United States of America.
Pharmacol Ther. 2024 Feb;254:108591. doi: 10.1016/j.pharmthera.2024.108591. Epub 2024 Jan 28.
Neoadjuvant chemoradiotherapy (NCRT) followed by surgery has been established as the standard treatment strategy for operable locally advanced esophageal cancer (EC). However, achieving pathologic complete response (pCR) or near pCR to NCRT is significantly associated with a considerable improvement in survival outcomes, while pCR patients may help organ preservation for patients by active surveillance to avoid planned surgery. Thus, there is an urgent need for improved biomarkers to predict EC chemoradiation response in research and clinical settings. Advances in multiple high-throughput technologies such as next-generation sequencing have facilitated the discovery of novel predictive biomarkers, specifically based on multi-omics data, including genomic/transcriptomic sequencings and proteomic/metabolomic mass spectra. The application of multi-omics data has shown the benefits in improving the understanding of underlying mechanisms of NCRT sensitivity/resistance in EC. Particularly, the prominent development of artificial intelligence (AI) has introduced a new direction in cancer research. The integration of multi-omics data has significantly advanced our knowledge of the disease and enabled the identification of valuable biomarkers for predicting treatment response from diverse dimension levels, especially with rapid advances in biotechnological and AI methodologies. Herein, we summarize the current status of research on the use of multi-omics technologies in predicting NCRT response for EC patients. Current limitations, challenges, and future perspectives of these multi-omics platforms will be addressed to assist in experimental designs and clinical use for further integrated analysis.
新辅助放化疗(NCRT)后行手术已被确立为可手术的局部晚期食管癌(EC)的标准治疗策略。然而,对NCRT达到病理完全缓解(pCR)或接近pCR与生存结果的显著改善显著相关,而pCR患者可通过主动监测避免计划性手术,从而有助于患者的器官保留。因此,在研究和临床环境中迫切需要改进的生物标志物来预测EC的放化疗反应。下一代测序等多种高通量技术的进步促进了新型预测生物标志物的发现,特别是基于多组学数据,包括基因组/转录组测序和蛋白质组/代谢组质谱。多组学数据的应用已显示出有助于增进对EC中NCRT敏感性/抗性潜在机制的理解。特别是,人工智能(AI)的显著发展为癌症研究引入了新方向。多组学数据的整合极大地推进了我们对该疾病的认识,并能够从不同维度水平识别用于预测治疗反应的有价值生物标志物,尤其是随着生物技术和AI方法的快速发展。在此,我们总结了使用多组学技术预测EC患者NCRT反应的研究现状。将讨论这些多组学平台当前的局限性、挑战及未来展望,以协助进行实验设计和临床应用,以便进一步进行综合分析。