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Biomarkers in prostate-specific membrane antigen theranostics

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Autore
Vlachostergios P.J., Zachos I., Tzortzis V.
Data
2021
Language
en
DOI
10.3390/diagnostics11061108
Soggetto
alkaline phosphatase
analgesic agent
biological marker
chromogranin A
fluorodeoxyglucose f 18
hemoglobin
lactate dehydrogenase
lutetium 177
neuroendocrine specific protein
neurotensin receptor
prostate specific antigen
prostate specific membrane antigen
alkaline phosphatase blood level
cancer prognosis
cancer survival
cancer tissue
circulating tumor cell
composite predictive score
DNA damage response
DNA repair
drug efficacy
drug therapy
Gleason score
human
lactate dehydrogenase blood level
metastasis
metastatic castration resistant prostate cancer
mutation
overall survival
pain
platelet count
positron emission tomography
progression free survival
protein expression
radioisotope therapy
Review
scoring system
standardized uptake value
theranostic nanomedicine
treatment response
tumor doubling time
tumor volume
MDPI
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Abstract
Theranostics of prostate cancer (PC) represents a growing area of development of imaging agents and targeted radionuclide therapeutics against a major target, prostate specific membrane antigen (PSMA). In view of the encouraging efficacy from the use of177 Lu and other radionuclides in metastatic castration-resistant prostate cancer (mCRPC), it is becoming increasingly important to identify surrogate markers that can help predict which patients are more likely to respond and experience improved survival. This review discusses potential predictors of efficacy of PSMA-targeted radionuclide therapies (TRT) segregated in three major categories: imaging, clinical and molecular. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/80662
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