Proteomics-inspired precision medicine for treating and understanding multiple myeloma.

IF 1 Q4 PHARMACOLOGY & PHARMACY
Matthew Ho, Giada Bianchi, Kenneth C Anderson
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引用次数: 5

Abstract

Introduction: Remarkable progress in molecular characterization methods has led to significant improvements in how we manage multiple myeloma (MM). The introduction of novel therapies has led to significant improvements in overall survival over the past 10 years. However, MM remains incurable and treatment choice is largely based on outdated risk-adaptive strategies that do not factor in improved treatment outcomes in the context of modern therapies.

Areas covered: This review discusses current risk-adaptive strategies in MM and the clinical application of proteomics in the monitoring of treatment response, disease progression, and minimal residual disease (MRD). We also discuss promising biomarkers of disease progression, treatment response, and chemoresistance. Finally, we will discuss an immunomics-based approach to monoclonal antibody (mAb), vaccine, and CAR-T cell development.

Expert opinion: It is an exciting era in oncology with basic scientific knowledge translating in novel therapeutic approaches to improve patient outcomes. With the advent of effective immunotherapies and targeted therapies, it has become crucial to identify biomarkers to aid in the stratification of patients based on anticipated sensitivity to chemotherapy. As a paradigm of diseases highly dependent on protein homeostasis, multiple myeloma provides the perfect opportunity to investigate the use of proteomics to aid in precision medicine.

蛋白质组学启发的精准医学治疗和理解多发性骨髓瘤。
简介:分子表征方法的显著进步导致了我们如何管理多发性骨髓瘤(MM)的显着改进。在过去的10年里,新疗法的引入导致了总体生存率的显著提高。然而,多发性骨髓瘤仍然无法治愈,治疗选择主要基于过时的风险适应策略,在现代治疗背景下,这些策略没有考虑到改善的治疗结果。涵盖领域:本综述讨论了目前MM的风险适应策略以及蛋白质组学在监测治疗反应、疾病进展和最小残留病(MRD)中的临床应用。我们还讨论了有希望的疾病进展、治疗反应和化疗耐药的生物标志物。最后,我们将讨论基于免疫组学的单克隆抗体(mAb)、疫苗和CAR-T细胞发育方法。专家意见:这是肿瘤学的一个激动人心的时代,基础科学知识转化为新的治疗方法,以改善患者的预后。随着有效的免疫疗法和靶向治疗的出现,识别生物标志物以帮助基于化疗预期敏感性的患者分层变得至关重要。作为一种高度依赖蛋白质稳态的疾病范例,多发性骨髓瘤为研究蛋白质组学在精准医学中的应用提供了绝佳的机会。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
9
期刊介绍: Expert Review of Precision Medicine and Drug Development publishes primarily review articles covering the development and clinical application of medicine to be used in a personalized therapy setting; in addition, the journal also publishes original research and commentary-style articles. In an era where medicine is recognizing that a one-size-fits-all approach is not always appropriate, it has become necessary to identify patients responsive to treatments and treat patient populations using a tailored approach. Areas covered include: Development and application of drugs targeted to specific genotypes and populations, as well as advanced diagnostic technologies and significant biomarkers that aid in this. Clinical trials and case studies within personalized therapy and drug development. Screening, prediction and prevention of disease, prediction of adverse events, treatment monitoring, effects of metabolomics and microbiomics on treatment. Secondary population research, genome-wide association studies, disease–gene association studies, personal genome technologies. Ethical and cost–benefit issues, the impact to healthcare and business infrastructure, and regulatory issues.
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