scholarly journals TCH-030 PET/CT Imaging with [11C]Choline as a Radiopharmaceutical For the Detection of Recurrent Prostate Cancer: A Reliable Production Method and Quality Control

2013 ◽  
Vol 20 (Suppl 1) ◽  
pp. A79.2-A79
Author(s):  
M Riondato ◽  
A Democrito ◽  
MC Bagnara ◽  
M Massollo ◽  
GM Sambuceti
2018 ◽  
Vol 14 (11) ◽  
pp. 1101-1115 ◽  
Author(s):  
Lucia Zanoni ◽  
Irene Bossert ◽  
Antonella Matti ◽  
Riccardo Schiavina ◽  
Cristian Pultrone ◽  
...  

2019 ◽  
Vol 61 (6) ◽  
pp. 881-889 ◽  
Author(s):  
Esther Mena ◽  
Maria Liza Lindenberg ◽  
Ismail Baris Turkbey ◽  
Joanna H. Shih ◽  
Stephanie A. Harmon ◽  
...  

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Avira Som ◽  
Preet Ayoub Shaikh ◽  
Daniel Lenihan ◽  
Kathleen W Zhang

Background: Men who receive androgen deprivation therapy for prostate cancer may be at increased risk for cardiovascular events. Vascular calcification is predictive of coronary events in the general population. The prevalence of vascular calcification in men with prostate cancer is not known. Methods: 211 consecutive patients who underwent 18F-fluciclovine positron emission tomography (PET) /computed tomography (CT) at Washington University School of Medicine for recurrent prostate cancer were retrospectively identified. Clinical, demographic, and cardiac biomarker data were obtained from the medical record. Coronary and aortic calcification were qualitatively assessed on non-gated CT scans using standardized scoring systems. Results: Among 211 men with recurrent prostate cancer, median age was 69 (IQR 64, 75) years. Cardiovascular comorbidities were common (70% hypertension, 65% hyperlipidemia, 20% diabetes mellitus, 47% current or former smoking). 21% carried a clinical diagnosis of coronary artery disease while 6% had peripheral vascular disease. On CT imaging, 147 patients (70%) had coronary artery calcification of whom 29 (20%) had severe calcification. Additionally, 189 patients (90%) had aortic calcification on CT imaging of whom 48 (25%) had severe thoracic aortic calcification and 109 (58%) had severe calcification at the aortoiliac bifurcation. Conclusions: Coronary and peripheral vascular calcification are common on PET/CT imaging in men with prostate cancer. Vascular calcification on CT imaging may have utility for cardiovascular risk stratification and guiding implementation of cardiovascular therapies in men receiving androgen deprivation therapy.


2017 ◽  
Vol 45 (1) ◽  
pp. 4-11 ◽  
Author(s):  
Esther Mena ◽  
Maria L. Lindenberg ◽  
Joanna H. Shih ◽  
Stephen Adler ◽  
Stephanie Harmon ◽  
...  

2018 ◽  
Vol 37 (5) ◽  
pp. 813-821 ◽  
Author(s):  
Elif Neslihan Akdemir ◽  
Murat Tuncel ◽  
Fadıl Akyol ◽  
Cenk Yucel Bilen ◽  
Dilek Ertoy Baydar ◽  
...  

2014 ◽  
Vol 42 (2) ◽  
pp. 197-209 ◽  
Author(s):  
Ali Afshar-Oromieh ◽  
Eleni Avtzi ◽  
Frederik L. Giesel ◽  
Tim Holland-Letz ◽  
Heinz G. Linhart ◽  
...  

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Avira Som ◽  
Preet Ayoub Shaikh ◽  
Daniel Lenihan ◽  
Melissa Reimers ◽  
Brian Baumann ◽  
...  

Background: Gonadotropin releasing hormone (GnRH) agonist therapy is associated with major adverse cardiovascular (CV) events in men with prostate cancer. The effect of GnRH agonists on vascular calcification is not known. Methods: Consecutive patients who underwent 18F-fluciclovine positron emission tomography (PET) /computed tomography (CT) at our institution for recurrent prostate cancer were retrospectively identified. Clinical and demographic data were obtained from the medical record. Patients without available data on prior prostate cancer therapies received were excluded (n=25). Coronary calcification was qualitatively assessed on non-gated CT scans using a published scoring system. The association of prior GnRH agonist therapy with coronary calcification was evaluated using stratified odds ratio (OR) analysis in a 2x2 contingency table. Results: Among 186 men included, median age was 69.0 years (IQR 64.3, 74.5) and CV comorbidities were common (72% hypertension, 68% hyperlipidemia, 43% current or former smoking, and 21% diabetes mellitus). 55 patients (30%) received prior hormone therapy, 50 of whom received a GnRH agonist either as single- or multi-agent therapy. Men with prior GnRH agonists were older than those without prior GnRH agonists (71.4 vs. 68.4 years, p=0.025). There were no significant differences in prevalence of CV comorbidities between the two groups. Men with at least mild coronary calcification were more likely to have received prior GnRH agonist therapy (OR=3.0, 95% CI 1.2-7.1, p=0.015 by Fisher’s exact test), with a stronger association seen in younger men (OR=3.9, age <69 years) than in older men (OR=1.8, age ≥69). Conclusions: Coronary calcification is associated with prior GnRH agonist therapy in men with recurrent prostate cancer undergoing PET/CT imaging. The utility of vascular protective therapies including aspirin and statin to mitigate the adverse CV effects of GnRH agonists requires further study.


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