@article{bb6cd20b574445abb79232e1b3624b00,
title = "Prostate cancer",
abstract = "The management of prostate cancer continues to evolve rapidly, with substantial advances being made in understanding the genomic landscape and biology underpinning both primary and metastatic prostate cancer. Similarly, the emergence of more sensitive imaging methods has improved diagnostic and staging accuracy and refined surveillance strategies. These advances have introduced personalised therapeutics to clinical practice, with treatments targeting genomic alterations in DNA repair pathways now clinically validated. An important shift in the therapeutic framework for metastatic disease has taken place, with metastatic-directed therapies being evaluated for oligometastatic disease, aggressive management of the primary lesion shown to benefit patients with low-volume metastatic disease, and with several novel androgen pathway inhibitors significantly improving survival when used as a first-line therapy for metastatic disease. Research into the molecular characterisation of localised, recurrent, and progressive disease will undoubtedly have an impact on clinical management. Similarly, emerging research into novel therapeutics, such as targeted radioisotopes and immunotherapy, holds much promise for improving the lives of patients with prostate cancer.",
keywords = "Androgen Antagonists/therapeutic use, Disease Management, Genomics/trends, Humans, Immunotherapy/trends, Magnetic Resonance Imaging, Male, Neoplasm Grading, Prostatic Neoplasms/drug therapy",
author = "Shahneen Sandhu and Moore, {Caroline M} and Edmund Chiong and Himisha Beltran and Bristow, {Robert G} and Williams, {Scott G}",
note = "Funding Information: SGW is supported by the Prostate Cancer Foundation, Prostate Cancer Foundation Australia, Peter MacCallum Cancer Foundation, Cancer Council Victoria, and Victoria Cancer Agency. SS has received support from the Prostate Cancer Foundation, Victoria Cancer Agency, Medical Research Future Fund, and Peter MacCallum Cancer Foundation. RGB is supported by the Cancer Research UK Manchester Institute and RadNet funding programmes, the Manchester NIHR Biomedical Research Centre, and Prostate Cancer UK. HB has received support from the National Cancer Institute and National Institutes of Health (R37CA241486 , P50 CA211024), US Department of Defense (PC160264), and the Prostate Cancer Foundation. Funding Information: SGW reports grant support from Bristol-Myers Squibb; consultancy fees and travel support from Astellas Pharma, Janssen, Bayer, Amgen, and Noxopharm paid to institution; and chaired the prostate cancer subcommittee of the Australia and New Zealand Urogenital and Prostate clinical trials group, during which time he received scientific grant support from Bayer and Astellas Pharma. SS reports advisory board fees paid to institution and grant support from AstraZeneca, Merck Sharp & Dohme, Amgen, Endocyte, Bristol-Myers Squibb, and Genentech. EC reports speaker honorarium and advisory board fees from Beckman Coulter Singapore, Janssen, Astellas Pharma, Bayer, Ipsen, AstraZeneca, Ferring, Amgen, and grant support from Janssen and Astellas Pharma. HB reports research support from AbbVie, Janssen, Millennium, Eli Lilly, and Astellas Pharma; and has served as advisor or consultant for Janssen, Astellas Pharma, Sanofi Genzyme, Merck Sharp & Dohme, Pfizer, Amgen, and Blue Earth. CMM reports speaker fees from Astellas Pharma, Janssen, and Steba Biotech; and grant support from SpectraCure. RGB reports no competing interests. Publisher Copyright: {\textcopyright} 2021 Elsevier Ltd",
year = "2021",
month = sep,
day = "18",
doi = "10.1016/S0140-6736(21)00950-8",
language = "English",
volume = "398",
pages = "1075--1090",
journal = "Lancet (London, England)",
issn = "0140-6736",
publisher = "Elsevier BV",
number = "10305",
}