MRI findings in men on active surveillance for prostate cancer: does dutasteride make MRI visible lesions less conspicuous? Results from a placebo-controlled, randomised clinical trial

Objectives To investigate changes in the Apparent Diffusion Coefficient (ADC) using diffusion-weighted imaging (DWI) in men on active surveillance for prostate cancer taking dutasteride 0.5 mg or placebo . Methods We analysed 37 men, randomised to 6 months of daily dutasteride (n = 18) or placebo (n...

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Veröffentlicht in:European radiology 2017-11, Vol.27 (11), p.4767-4774
Hauptverfasser: Giganti, Francesco, Moore, Caroline M., Robertson, Nicola L., McCartan, Neil, Jameson, Charles, Bott, Simon R. J., Winkler, Mathias, Gambarota, Giulio, Whitcher, Brandon, Castro, Ramiro, Emberton, Mark, Allen, Clare, Kirkham, Alex
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container_end_page 4774
container_issue 11
container_start_page 4767
container_title European radiology
container_volume 27
creator Giganti, Francesco
Moore, Caroline M.
Robertson, Nicola L.
McCartan, Neil
Jameson, Charles
Bott, Simon R. J.
Winkler, Mathias
Gambarota, Giulio
Whitcher, Brandon
Castro, Ramiro
Emberton, Mark
Allen, Clare
Kirkham, Alex
description Objectives To investigate changes in the Apparent Diffusion Coefficient (ADC) using diffusion-weighted imaging (DWI) in men on active surveillance for prostate cancer taking dutasteride 0.5 mg or placebo . Methods We analysed 37 men, randomised to 6 months of daily dutasteride (n = 18) or placebo (n = 19), undergoing 3T multi-parametric Magnetic Resonance Imaging (mpMRI) scans at baseline and 6 months. Images were reviewed blind to treatment allocation and clinical information. Mean ADC of peripheral (PZ) and transition (TZ) zones, and MR-suspicious lesions were compared between groups over 6 months. Conspicuity was defined as the PZ divided by tumour ADC, and its change over 6 months was assessed. Results A decrease in mean conspicuity in the dutasteride group (but not the controls) was seen over 6 months (1.54 vs 1.38; p = 0.025). Absolute changes in ADC and conspicuity were significantly different between placebo and dutasteride groups at 6 months: (-0.03 vs 0.08, p = 0.033) and (0.11 vs –0.16, p = 0.012), as were percentage changes in the same parameters: (-2.27% vs 8.56% p = 0.048) and (9.25% vs -9.89% p = 0.013). Conclusions Dutasteride was associated with increased tumour ADC and reduced conspicuity . A lower threshold for triggering biopsy might be considered in men on dutasteride undergoing mpMRI for prostate cancer. Key points • Dutasteride increases ADC and reduces conspicuity in small mpMRI - visible prostate cancers . • Knowledge of dutasteride exposure is important in the interpretation of prostate mpMRI . • A lower threshold for triggering biopsy may be appropriate on dutasteride .
doi_str_mv 10.1007/s00330-017-4858-0
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Results from a placebo-controlled, randomised clinical trial</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Giganti, Francesco ; Moore, Caroline M. ; Robertson, Nicola L. ; McCartan, Neil ; Jameson, Charles ; Bott, Simon R. J. ; Winkler, Mathias ; Gambarota, Giulio ; Whitcher, Brandon ; Castro, Ramiro ; Emberton, Mark ; Allen, Clare ; Kirkham, Alex</creator><creatorcontrib>Giganti, Francesco ; Moore, Caroline M. ; Robertson, Nicola L. ; McCartan, Neil ; Jameson, Charles ; Bott, Simon R. J. ; Winkler, Mathias ; Gambarota, Giulio ; Whitcher, Brandon ; Castro, Ramiro ; Emberton, Mark ; Allen, Clare ; Kirkham, Alex</creatorcontrib><description>Objectives To investigate changes in the Apparent Diffusion Coefficient (ADC) using diffusion-weighted imaging (DWI) in men on active surveillance for prostate cancer taking dutasteride 0.5 mg or placebo . Methods We analysed 37 men, randomised to 6 months of daily dutasteride (n = 18) or placebo (n = 19), undergoing 3T multi-parametric Magnetic Resonance Imaging (mpMRI) scans at baseline and 6 months. Images were reviewed blind to treatment allocation and clinical information. Mean ADC of peripheral (PZ) and transition (TZ) zones, and MR-suspicious lesions were compared between groups over 6 months. Conspicuity was defined as the PZ divided by tumour ADC, and its change over 6 months was assessed. Results A decrease in mean conspicuity in the dutasteride group (but not the controls) was seen over 6 months (1.54 vs 1.38; p = 0.025). Absolute changes in ADC and conspicuity were significantly different between placebo and dutasteride groups at 6 months: (-0.03 vs 0.08, p = 0.033) and (0.11 vs –0.16, p = 0.012), as were percentage changes in the same parameters: (-2.27% vs 8.56% p = 0.048) and (9.25% vs -9.89% p = 0.013). Conclusions Dutasteride was associated with increased tumour ADC and reduced conspicuity . A lower threshold for triggering biopsy might be considered in men on dutasteride undergoing mpMRI for prostate cancer. Key points • Dutasteride increases ADC and reduces conspicuity in small mpMRI - visible prostate cancers . • Knowledge of dutasteride exposure is important in the interpretation of prostate mpMRI . • A lower threshold for triggering biopsy may be appropriate on dutasteride .</description><identifier>ISSN: 0938-7994</identifier><identifier>EISSN: 1432-1084</identifier><identifier>DOI: 10.1007/s00330-017-4858-0</identifier><identifier>PMID: 28523355</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>5-alpha Reductase Inhibitors - therapeutic use ; Aged ; Bioengineering ; Biopsy ; Cancer ; Clinical trials ; Conspicuity ; Diagnostic Radiology ; Diffusion coefficient ; Diffusion Magnetic Resonance Imaging ; Dutasteride - therapeutic use ; Human health and pathology ; Humans ; Imaging ; Internal Medicine ; Interventional Radiology ; Lesions ; Life Sciences ; Magnetic resonance imaging ; Male ; Medication ; Medicine ; Medicine &amp; Public Health ; Men ; Middle Aged ; Neuroradiology ; NMR ; Nuclear magnetic resonance ; Pharmaceutical sciences ; Prostate cancer ; Prostatic Hyperplasia - drug therapy ; Prostatic Neoplasms - diagnostic imaging ; Prostatic Neoplasms - pathology ; Radiology ; Randomization ; Reviews ; Surveillance ; Tumors ; Ultrasound ; Urogenital ; Urology and Nephrology</subject><ispartof>European radiology, 2017-11, Vol.27 (11), p.4767-4774</ispartof><rights>The Author(s) 2017</rights><rights>European Radiology is a copyright of Springer, 2017.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c504t-f27a0e73fbea24ddd54c8cc5f0ab0c82da06e1ab42e02c0ad600d596c20c5e153</citedby><cites>FETCH-LOGICAL-c504t-f27a0e73fbea24ddd54c8cc5f0ab0c82da06e1ab42e02c0ad600d596c20c5e153</cites><orcidid>0000-0001-5218-6431</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00330-017-4858-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00330-017-4858-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28523355$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-rennes.hal.science/hal-01624586$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Giganti, Francesco</creatorcontrib><creatorcontrib>Moore, Caroline M.</creatorcontrib><creatorcontrib>Robertson, Nicola L.</creatorcontrib><creatorcontrib>McCartan, Neil</creatorcontrib><creatorcontrib>Jameson, Charles</creatorcontrib><creatorcontrib>Bott, Simon R. J.</creatorcontrib><creatorcontrib>Winkler, Mathias</creatorcontrib><creatorcontrib>Gambarota, Giulio</creatorcontrib><creatorcontrib>Whitcher, Brandon</creatorcontrib><creatorcontrib>Castro, Ramiro</creatorcontrib><creatorcontrib>Emberton, Mark</creatorcontrib><creatorcontrib>Allen, Clare</creatorcontrib><creatorcontrib>Kirkham, Alex</creatorcontrib><title>MRI findings in men on active surveillance for prostate cancer: does dutasteride make MRI visible lesions less conspicuous? Results from a placebo-controlled, randomised clinical trial</title><title>European radiology</title><addtitle>Eur Radiol</addtitle><addtitle>Eur Radiol</addtitle><description>Objectives To investigate changes in the Apparent Diffusion Coefficient (ADC) using diffusion-weighted imaging (DWI) in men on active surveillance for prostate cancer taking dutasteride 0.5 mg or placebo . Methods We analysed 37 men, randomised to 6 months of daily dutasteride (n = 18) or placebo (n = 19), undergoing 3T multi-parametric Magnetic Resonance Imaging (mpMRI) scans at baseline and 6 months. Images were reviewed blind to treatment allocation and clinical information. Mean ADC of peripheral (PZ) and transition (TZ) zones, and MR-suspicious lesions were compared between groups over 6 months. Conspicuity was defined as the PZ divided by tumour ADC, and its change over 6 months was assessed. Results A decrease in mean conspicuity in the dutasteride group (but not the controls) was seen over 6 months (1.54 vs 1.38; p = 0.025). Absolute changes in ADC and conspicuity were significantly different between placebo and dutasteride groups at 6 months: (-0.03 vs 0.08, p = 0.033) and (0.11 vs –0.16, p = 0.012), as were percentage changes in the same parameters: (-2.27% vs 8.56% p = 0.048) and (9.25% vs -9.89% p = 0.013). Conclusions Dutasteride was associated with increased tumour ADC and reduced conspicuity . A lower threshold for triggering biopsy might be considered in men on dutasteride undergoing mpMRI for prostate cancer. Key points • Dutasteride increases ADC and reduces conspicuity in small mpMRI - visible prostate cancers . • Knowledge of dutasteride exposure is important in the interpretation of prostate mpMRI . • A lower threshold for triggering biopsy may be appropriate on dutasteride .</description><subject>5-alpha Reductase Inhibitors - therapeutic use</subject><subject>Aged</subject><subject>Bioengineering</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Clinical trials</subject><subject>Conspicuity</subject><subject>Diagnostic Radiology</subject><subject>Diffusion coefficient</subject><subject>Diffusion Magnetic Resonance Imaging</subject><subject>Dutasteride - therapeutic use</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Imaging</subject><subject>Internal Medicine</subject><subject>Interventional Radiology</subject><subject>Lesions</subject><subject>Life Sciences</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Medication</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Men</subject><subject>Middle Aged</subject><subject>Neuroradiology</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pharmaceutical sciences</subject><subject>Prostate cancer</subject><subject>Prostatic Hyperplasia - drug therapy</subject><subject>Prostatic Neoplasms - diagnostic imaging</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Radiology</subject><subject>Randomization</subject><subject>Reviews</subject><subject>Surveillance</subject><subject>Tumors</subject><subject>Ultrasound</subject><subject>Urogenital</subject><subject>Urology and Nephrology</subject><issn>0938-7994</issn><issn>1432-1084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kt9rFDEQxxdR7Fn9A3yRgC8Krk6SzW7OB6UUtYUToehzyCaz19Rsck12D_zP_PPMcrXUguQhYeYz3_mRqarnFN5SgO5dBuAcaqBd3Ugha3hQrWjDWU1BNg-rFay5rLv1ujmqnuR8BQBr2nSPqyMmBeNciFX1--vFORlcsC5sM3GBjBhIDESbye2R5Dnt0Xmvg0EyxER2KeZJT0jMYkrviY2YiZ0nnSdMziIZ9U8ki-reZdd7JB6ziyEvdyamvHbOzHHOH8kF5tlPmQwpjkSTndcG-1gXZkrRe7RvSNLBxtFltMR4F5zRnkzJaf-0ejRon_HZzX1c_fj86fvpWb359uX89GRTGwHNVA-s04AdH3rUrLHWisZIY8QAugcjmdXQItV9wxCYAW1bACvWrWFgBFLBj6sPB93d3I9oDZbatFe75EadfqmonfrXE9yl2sa9Ei0XIBeB1weBy3thZycbtdiAtqwRst3Twr66SZbi9Yx5UqV1g8v8sUxM0TWA5JJyVtCX99CrOKdQRlGoZjmSd4WiB8qUf8sJh9sKKKhlh9Rhh0oRnVp2SEGJeXG349uIv0tTAHYAcnGFLaY7qf-r-gdp69ZK</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Giganti, Francesco</creator><creator>Moore, Caroline M.</creator><creator>Robertson, Nicola L.</creator><creator>McCartan, Neil</creator><creator>Jameson, Charles</creator><creator>Bott, Simon R. 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Results from a placebo-controlled, randomised clinical trial</title><author>Giganti, Francesco ; Moore, Caroline M. ; Robertson, Nicola L. ; McCartan, Neil ; Jameson, Charles ; Bott, Simon R. J. ; Winkler, Mathias ; Gambarota, Giulio ; Whitcher, Brandon ; Castro, Ramiro ; Emberton, Mark ; Allen, Clare ; Kirkham, Alex</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-f27a0e73fbea24ddd54c8cc5f0ab0c82da06e1ab42e02c0ad600d596c20c5e153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>5-alpha Reductase Inhibitors - therapeutic use</topic><topic>Aged</topic><topic>Bioengineering</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Clinical trials</topic><topic>Conspicuity</topic><topic>Diagnostic Radiology</topic><topic>Diffusion coefficient</topic><topic>Diffusion Magnetic Resonance Imaging</topic><topic>Dutasteride - therapeutic use</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Imaging</topic><topic>Internal Medicine</topic><topic>Interventional Radiology</topic><topic>Lesions</topic><topic>Life Sciences</topic><topic>Magnetic resonance imaging</topic><topic>Male</topic><topic>Medication</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Men</topic><topic>Middle Aged</topic><topic>Neuroradiology</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pharmaceutical sciences</topic><topic>Prostate cancer</topic><topic>Prostatic Hyperplasia - drug therapy</topic><topic>Prostatic Neoplasms - diagnostic imaging</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Radiology</topic><topic>Randomization</topic><topic>Reviews</topic><topic>Surveillance</topic><topic>Tumors</topic><topic>Ultrasound</topic><topic>Urogenital</topic><topic>Urology and Nephrology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giganti, Francesco</creatorcontrib><creatorcontrib>Moore, Caroline M.</creatorcontrib><creatorcontrib>Robertson, Nicola L.</creatorcontrib><creatorcontrib>McCartan, Neil</creatorcontrib><creatorcontrib>Jameson, Charles</creatorcontrib><creatorcontrib>Bott, Simon R. 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J.</au><au>Winkler, Mathias</au><au>Gambarota, Giulio</au><au>Whitcher, Brandon</au><au>Castro, Ramiro</au><au>Emberton, Mark</au><au>Allen, Clare</au><au>Kirkham, Alex</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MRI findings in men on active surveillance for prostate cancer: does dutasteride make MRI visible lesions less conspicuous? Results from a placebo-controlled, randomised clinical trial</atitle><jtitle>European radiology</jtitle><stitle>Eur Radiol</stitle><addtitle>Eur Radiol</addtitle><date>2017-11-01</date><risdate>2017</risdate><volume>27</volume><issue>11</issue><spage>4767</spage><epage>4774</epage><pages>4767-4774</pages><issn>0938-7994</issn><eissn>1432-1084</eissn><abstract>Objectives To investigate changes in the Apparent Diffusion Coefficient (ADC) using diffusion-weighted imaging (DWI) in men on active surveillance for prostate cancer taking dutasteride 0.5 mg or placebo . Methods We analysed 37 men, randomised to 6 months of daily dutasteride (n = 18) or placebo (n = 19), undergoing 3T multi-parametric Magnetic Resonance Imaging (mpMRI) scans at baseline and 6 months. Images were reviewed blind to treatment allocation and clinical information. Mean ADC of peripheral (PZ) and transition (TZ) zones, and MR-suspicious lesions were compared between groups over 6 months. Conspicuity was defined as the PZ divided by tumour ADC, and its change over 6 months was assessed. Results A decrease in mean conspicuity in the dutasteride group (but not the controls) was seen over 6 months (1.54 vs 1.38; p = 0.025). Absolute changes in ADC and conspicuity were significantly different between placebo and dutasteride groups at 6 months: (-0.03 vs 0.08, p = 0.033) and (0.11 vs –0.16, p = 0.012), as were percentage changes in the same parameters: (-2.27% vs 8.56% p = 0.048) and (9.25% vs -9.89% p = 0.013). Conclusions Dutasteride was associated with increased tumour ADC and reduced conspicuity . A lower threshold for triggering biopsy might be considered in men on dutasteride undergoing mpMRI for prostate cancer. Key points • Dutasteride increases ADC and reduces conspicuity in small mpMRI - visible prostate cancers . • Knowledge of dutasteride exposure is important in the interpretation of prostate mpMRI . • A lower threshold for triggering biopsy may be appropriate on dutasteride .</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28523355</pmid><doi>10.1007/s00330-017-4858-0</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5218-6431</orcidid><oa>free_for_read</oa></addata></record>
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subjects 5-alpha Reductase Inhibitors - therapeutic use
Aged
Bioengineering
Biopsy
Cancer
Clinical trials
Conspicuity
Diagnostic Radiology
Diffusion coefficient
Diffusion Magnetic Resonance Imaging
Dutasteride - therapeutic use
Human health and pathology
Humans
Imaging
Internal Medicine
Interventional Radiology
Lesions
Life Sciences
Magnetic resonance imaging
Male
Medication
Medicine
Medicine & Public Health
Men
Middle Aged
Neuroradiology
NMR
Nuclear magnetic resonance
Pharmaceutical sciences
Prostate cancer
Prostatic Hyperplasia - drug therapy
Prostatic Neoplasms - diagnostic imaging
Prostatic Neoplasms - pathology
Radiology
Randomization
Reviews
Surveillance
Tumors
Ultrasound
Urogenital
Urology and Nephrology
title MRI findings in men on active surveillance for prostate cancer: does dutasteride make MRI visible lesions less conspicuous? Results from a placebo-controlled, randomised clinical trial
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