Precision medicine for the treatment of triple negative breast cancer: opportunities and challenges

M. Sadiq, Juliette Servante, S. Madhusudan
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引用次数: 1

Abstract

ABSTRACT Introduction: Triple negative breast cancer (TNBC) is a challenging disease generally following an aggressive clinical phenotype with poor survival outcomes. Scarcity of druggable targets coupled with molecular and genetic diversity has raised barriers in effective management of this disease; however, novel therapeutic strategies are on the horizon. Areas covered: We aim to present an overview of promising drugs that have emerged from preclinical studies undergoing investigation in early and late clinical trials alongside current challenges in the implementation of these in clinic. Expert opinion: The advent of immunotherapy and PARP inhibitors has finally started to diversify the cytotoxic chemotherapy-dependent treatment portfolio for TNBC. During this process, numerous challenges around novel biomarker discovery, optimum patient selection and combinatorial toxicity have been exposed. There is a clear need to further our understanding of the molecular pathways involved in the evolution of TNBC to optimize targets and explain inadequacies of current investigational treatments. We expect progressive expansion in diagnostic and prognostic biomarker panels allowing for further personalization of TNBC treatment.
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精准医学治疗三阴性乳腺癌:机遇与挑战
摘要简介:三阴性乳腺癌(TNBC)是一种具有挑战性的疾病,通常具有侵袭性的临床表型和较差的生存结果。可药物靶点的缺乏,加上分子和遗传多样性,为有效管理这种疾病增加了障碍;然而,新的治疗策略即将出现。涵盖的领域:我们的目标是概述从临床前研究中出现的有希望的药物,这些药物正在进行早期和晚期临床试验的调查,以及在临床中实施这些药物的当前挑战。专家意见:免疫疗法和PARP抑制剂的出现终于开始使TNBC的细胞毒性化疗依赖治疗组合多样化。在这一过程中,围绕新的生物标志物发现,最佳患者选择和组合毒性的许多挑战已经暴露出来。显然,我们需要进一步了解TNBC进化过程中涉及的分子途径,以优化靶点并解释当前研究治疗的不足之处。我们期望逐步扩大诊断和预后生物标志物面板,从而进一步个性化TNBC治疗。
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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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