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18F-FDG-PET/CT and 18F-NaF-PET/CT in men with castrate-resistant prostate cancer

To evaluate 18 F-labeled-fluorodeoxyglucose ( 18 F-FDG-) and 18 F-labeled-sodium fluoride ( 18 F-NaF-) positron emission tomography/computed tomography (PET/CT) as biomarkers in metastatic castrate-resistant prostate cancer (mCRPC). Nine men (53-75 years) in a phase 1 trial of abiraterone and caboza...

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Published in:American journal of nuclear medicine and molecular imaging 2014-12, Vol.5 (1), p.72-82
Main Authors: Zukotynski, Katherine A, Kim, Chun K, Gerbaudo, Victor H, Hainer, Jon, Taplin, Mary-Ellen, Kantoff, Philip, den Abbeele, Annick D Van, Seltzer, Steven, Sweeney, Christopher J
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container_title American journal of nuclear medicine and molecular imaging
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creator Zukotynski, Katherine A
Kim, Chun K
Gerbaudo, Victor H
Hainer, Jon
Taplin, Mary-Ellen
Kantoff, Philip
den Abbeele, Annick D Van
Seltzer, Steven
Sweeney, Christopher J
description To evaluate 18 F-labeled-fluorodeoxyglucose ( 18 F-FDG-) and 18 F-labeled-sodium fluoride ( 18 F-NaF-) positron emission tomography/computed tomography (PET/CT) as biomarkers in metastatic castrate-resistant prostate cancer (mCRPC). Nine men (53-75 years) in a phase 1 trial of abiraterone and cabozantinib had 18 F-FDG-PET/CT, 18 F-NaF-PET/CT and standard imaging ( 99m Tc-labeled-methylene-diphosphonate ( 99m Tc-MDP) bone scan and abdominal/pelvic CT) at baseline and after 8 weeks of therapy. Baseline disease was classified as widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid (1 site), or non- 18 F-FDG-avid. Metabolic response was classified using European Organisation for Research and Treatment of Cancer (EORTC) criteria. Treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, Prostate Cancer Working Group 2 (PCWG2) guidelines and days on trial (DOT) were recorded. All men were followed for 1 year or until progression. Four men had 18 F-FDG-avid disease: two with widespread (DOT 53 and 76) and two with oligometastatic disease (DOT 231 and still on trial after 742+ days). Five men had non- 18 F-FDG-avid disease; three remained stable or improved (2 still on trial while one discontinued for non-oncologic reasons; DOT 225-563+), and 2 progressed (DOT 285 and 532). Despite the small sample size, Kaplan-Meier analysis showed a significant difference in progression free survival (PFS) between men with widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid and non- 18 F-FDG-avid disease (p < 0.01). All men had 18 F-NaF-avid disease. Neither 18 F-NaF-avid disease extent nor intensity was predictive of treatment response. 18 F-FDG-PET/CT may be superior to 18 F-NaF-PET/CT and standard imaging in men with mCRPC on abiraterone and cabozantinib. 18 F-FDG-PET/CT may have potential to stratify men into 3 groups (widespread vs. oligometastatic 18 F-FDG-avid vs. non- 18 F-FDG-avid mCRPC) to tailor therapy. Further evaluation is warranted.
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Nine men (53-75 years) in a phase 1 trial of abiraterone and cabozantinib had 18 F-FDG-PET/CT, 18 F-NaF-PET/CT and standard imaging ( 99m Tc-labeled-methylene-diphosphonate ( 99m Tc-MDP) bone scan and abdominal/pelvic CT) at baseline and after 8 weeks of therapy. Baseline disease was classified as widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid (1 site), or non- 18 F-FDG-avid. Metabolic response was classified using European Organisation for Research and Treatment of Cancer (EORTC) criteria. Treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, Prostate Cancer Working Group 2 (PCWG2) guidelines and days on trial (DOT) were recorded. All men were followed for 1 year or until progression. Four men had 18 F-FDG-avid disease: two with widespread (DOT 53 and 76) and two with oligometastatic disease (DOT 231 and still on trial after 742+ days). Five men had non- 18 F-FDG-avid disease; three remained stable or improved (2 still on trial while one discontinued for non-oncologic reasons; DOT 225-563+), and 2 progressed (DOT 285 and 532). Despite the small sample size, Kaplan-Meier analysis showed a significant difference in progression free survival (PFS) between men with widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid and non- 18 F-FDG-avid disease (p &lt; 0.01). All men had 18 F-NaF-avid disease. Neither 18 F-NaF-avid disease extent nor intensity was predictive of treatment response. 18 F-FDG-PET/CT may be superior to 18 F-NaF-PET/CT and standard imaging in men with mCRPC on abiraterone and cabozantinib. 18 F-FDG-PET/CT may have potential to stratify men into 3 groups (widespread vs. oligometastatic 18 F-FDG-avid vs. non- 18 F-FDG-avid mCRPC) to tailor therapy. 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Nine men (53-75 years) in a phase 1 trial of abiraterone and cabozantinib had 18 F-FDG-PET/CT, 18 F-NaF-PET/CT and standard imaging ( 99m Tc-labeled-methylene-diphosphonate ( 99m Tc-MDP) bone scan and abdominal/pelvic CT) at baseline and after 8 weeks of therapy. Baseline disease was classified as widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid (1 site), or non- 18 F-FDG-avid. Metabolic response was classified using European Organisation for Research and Treatment of Cancer (EORTC) criteria. Treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, Prostate Cancer Working Group 2 (PCWG2) guidelines and days on trial (DOT) were recorded. All men were followed for 1 year or until progression. Four men had 18 F-FDG-avid disease: two with widespread (DOT 53 and 76) and two with oligometastatic disease (DOT 231 and still on trial after 742+ days). Five men had non- 18 F-FDG-avid disease; three remained stable or improved (2 still on trial while one discontinued for non-oncologic reasons; DOT 225-563+), and 2 progressed (DOT 285 and 532). Despite the small sample size, Kaplan-Meier analysis showed a significant difference in progression free survival (PFS) between men with widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid and non- 18 F-FDG-avid disease (p &lt; 0.01). All men had 18 F-NaF-avid disease. Neither 18 F-NaF-avid disease extent nor intensity was predictive of treatment response. 18 F-FDG-PET/CT may be superior to 18 F-NaF-PET/CT and standard imaging in men with mCRPC on abiraterone and cabozantinib. 18 F-FDG-PET/CT may have potential to stratify men into 3 groups (widespread vs. oligometastatic 18 F-FDG-avid vs. non- 18 F-FDG-avid mCRPC) to tailor therapy. 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Nine men (53-75 years) in a phase 1 trial of abiraterone and cabozantinib had 18 F-FDG-PET/CT, 18 F-NaF-PET/CT and standard imaging ( 99m Tc-labeled-methylene-diphosphonate ( 99m Tc-MDP) bone scan and abdominal/pelvic CT) at baseline and after 8 weeks of therapy. Baseline disease was classified as widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid (1 site), or non- 18 F-FDG-avid. Metabolic response was classified using European Organisation for Research and Treatment of Cancer (EORTC) criteria. Treatment response using Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, Prostate Cancer Working Group 2 (PCWG2) guidelines and days on trial (DOT) were recorded. All men were followed for 1 year or until progression. Four men had 18 F-FDG-avid disease: two with widespread (DOT 53 and 76) and two with oligometastatic disease (DOT 231 and still on trial after 742+ days). Five men had non- 18 F-FDG-avid disease; three remained stable or improved (2 still on trial while one discontinued for non-oncologic reasons; DOT 225-563+), and 2 progressed (DOT 285 and 532). Despite the small sample size, Kaplan-Meier analysis showed a significant difference in progression free survival (PFS) between men with widespread 18 F-FDG-avid, oligometastatic 18 F-FDG-avid and non- 18 F-FDG-avid disease (p &lt; 0.01). All men had 18 F-NaF-avid disease. Neither 18 F-NaF-avid disease extent nor intensity was predictive of treatment response. 18 F-FDG-PET/CT may be superior to 18 F-NaF-PET/CT and standard imaging in men with mCRPC on abiraterone and cabozantinib. 18 F-FDG-PET/CT may have potential to stratify men into 3 groups (widespread vs. oligometastatic 18 F-FDG-avid vs. non- 18 F-FDG-avid mCRPC) to tailor therapy. Further evaluation is warranted.</abstract><pub>e-Century Publishing Corporation</pub><pmid>25625029</pmid></addata></record>
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title 18F-FDG-PET/CT and 18F-NaF-PET/CT in men with castrate-resistant prostate cancer
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