肿瘤免疫治疗进展

IF 1 Q4 PHARMACOLOGY & PHARMACY Expert Review of Precision Medicine and Drug Development Pub Date : 2021-05-03 DOI:10.1080/23808993.2021.1911638

A. Cimadamore, A. Rizzo, V. Mollica, F. Massari, A. López-Beltran, M. Scarpelli, Liang Cheng, M. Santoni, R. Montironi

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引用次数: 2

摘要

意大利安科纳联合医院马尔凯地区理工大学医学院病理解剖科;意大利博洛尼亚国立博洛尼亚大学肿瘤学中心，意大利博洛尼亚;科尔多瓦大学医学院外科，西班牙科尔多瓦;印第安纳大学医学院病理与检验医学系，美国印第安纳波利斯;意大利马切拉塔马切拉塔医院肿瘤科

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An update on immunotherapy in uro-oncology

Section of Pathological Anatomy, Polytechnic University of the Marche Region, School of Medicine, United Hospitals, Ancona, Italy; Division of Oncology, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy; Department of Surgery, Cordoba University Medical School, Cordoba, Spain; Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, USA; Oncology department, Macerata Hospital, Macerata, Italy

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来源期刊

Expert Review of Precision Medicine and Drug Development PHARMACOLOGY & PHARMACY-

CiteScore

2.30

自引率

0.00%

发文量

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.