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高肿瘤突变负荷(TMB-H)晚期实体恶性肿瘤管理中的挑战与未来方向

Challenges and Future Directions in the Management of Tumor Mutational Burden-High (TMB-H) Advanced Solid Malignancies.

作者信息

Ahmed Jibran, Das Biswajit, Shin Sarah, Chen Alice

机构信息

Developmental Therapeutics Clinic (DTC), National Cancer Institute (NCI), National Institute of Health (NIH), Bethesda, MD 20892, USA.

Molecular Characterization Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.

出版信息

Cancers (Basel). 2023 Dec 14;15(24):5841. doi: 10.3390/cancers15245841.

Abstract

A standardized assessment of Tumor Mutational Burden (TMB) poses challenges across diverse tumor histologies, treatment modalities, and testing platforms, requiring careful consideration to ensure consistency and reproducibility. Despite clinical trials demonstrating favorable responses to immune checkpoint inhibitors (ICIs), not all patients with elevated TMB exhibit benefits, and certain tumors with a normal TMB may respond to ICIs. Therefore, a comprehensive understanding of the intricate interplay between TMB and the tumor microenvironment, as well as genomic features, is crucial to refine its predictive value. Bioinformatics advancements hold potential to improve the precision and cost-effectiveness of TMB assessments, addressing existing challenges. Similarly, integrating TMB with other biomarkers and employing comprehensive, multiomics approaches could further enhance its predictive value. Ongoing collaborative endeavors in research, standardization, and clinical validation are pivotal in harnessing the full potential of TMB as a biomarker in the clinic settings.

摘要

对肿瘤突变负荷(TMB)进行标准化评估,在不同的肿瘤组织学类型、治疗方式和检测平台中都面临挑战,需要仔细考量以确保一致性和可重复性。尽管临床试验表明免疫检查点抑制剂(ICI)有良好疗效,但并非所有TMB升高的患者都能从中获益,而某些TMB正常的肿瘤也可能对ICI产生反应。因此,全面了解TMB与肿瘤微环境以及基因组特征之间复杂的相互作用,对于提升其预测价值至关重要。生物信息学的进步有望提高TMB评估的准确性和成本效益,解决现有挑战。同样,将TMB与其他生物标志物整合,并采用全面的多组学方法,可进一步增强其预测价值。目前在研究、标准化和临床验证方面的合作努力,对于在临床环境中充分发挥TMB作为生物标志物的潜力至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a758/10741991/2902690baf99/cancers-15-05841-g001.jpg

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