4.7 Article

Molecular imaging of prostate cancer: translating molecular biology approaches into the clinical realm

Journal

EUROPEAN RADIOLOGY
Volume 25, Issue 5, Pages 1294-1302

Publisher

SPRINGER
DOI: 10.1007/s00330-014-3539-5

Keywords

Prostate cancer; Molecular imaging; MRI/PET; Optical imaging; Cerenkov imaging

Funding

  1. NCI NIH HHS [P30 CA008748] Funding Source: Medline

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The epidemiology of prostate cancer has dramatically changed since the introduction of prostate-specific antigen (PSA) screening in the 1980's. Most prostate cancers today are detected at early stages of the disease and are considered 'indolent'; however, some patients' prostate cancers demonstrate a more aggressive behaviour which leads to rapid progression and death. Increasing understanding of the biology underlying the heterogeneity that characterises this disease has led to a continuously evolving role of imaging in the management of prostate cancer. Functional and metabolic imaging techniques are gaining importance as the impact on the therapeutic paradigm has shifted from structural tumour detection alone to distinguishing patients with indolent tumours that can be managed conservatively (e.g., by active surveillance) from patients with more aggressive tumours that may require definitive treatment with surgery or radiation. In this review, we discuss advanced imaging techniques that allow direct visualisation of molecular interactions relevant to prostate cancer and their potential for translation to the clinical setting in the near future. The potential use of imaging to follow molecular events during drug therapy as well as the use of imaging agents for therapeutic purposes will also be discussed. aEuro cent Advanced imaging techniques allow direct visualisation of molecular interactions in prostate cancer. aEuro cent MRI/PET, optical and Cerenkov imaging facilitate the translation of molecular biology. aEuro cent Multiple compounds targeting PSMA expression are currently undergoing clinical translation. aEuro cent Other targets (e.g., PSA, prostate-stem cell antigen, GRPR) are in development.

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