Clinically insignificant prostate cancer suitable for active surveillance according to Prostate Cancer Research International: Active surveillance criteria: Utility of PI‐RADS v2

Background Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has been addressed, but few studies have reported the value of PI‐RADS v2 for assessing risk stratification in patients with PCa, especially on se...

Full description

Saved in:
Bibliographic Details
Published inJournal of magnetic resonance imaging Vol. 47; no. 4; pp. 1072 - 1079
Main Authors Yim, Jae Hyun, Kim, Chan Kyo, Kim, Jae‐Hun
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.04.2018
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has been addressed, but few studies have reported the value of PI‐RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS. Purpose To investigate the utility of PI‐RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS. Study Type Retrospective. Subjects In all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy. Field Strength/Sequence 3.0T, including T2‐weighted, diffusion‐weighted, and dynamic contrast‐enhanced imaging. Assessment Insignificant cancer was defined histopathologically as an organ‐confined disease with a tumor volume <0.5 cm3 without Gleason score 4–5. Patients were divided into two groups based on the PI‐RADS v2 and tumor ADC: A, PI‐RADS score ≤3 and ADC ≥1.095 × 10−3mm2/s; and B, PI‐RADS score 4–5 or ADC <1.095 × 10−3mm2/s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer. Results Of the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate‐specific antigen density (PSAD), PI‐RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI‐RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI‐RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786). Data Conclusion The PI‐RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS. Level of Evidence: 4 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018;47:1072–1079.
AbstractList Background Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has been addressed, but few studies have reported the value of PI‐RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS. Purpose To investigate the utility of PI‐RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS. Study Type Retrospective. Subjects In all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy. Field Strength/Sequence 3.0T, including T2‐weighted, diffusion‐weighted, and dynamic contrast‐enhanced imaging. Assessment Insignificant cancer was defined histopathologically as an organ‐confined disease with a tumor volume <0.5 cm3 without Gleason score 4–5. Patients were divided into two groups based on the PI‐RADS v2 and tumor ADC: A, PI‐RADS score ≤3 and ADC ≥1.095 × 10−3mm2/s; and B, PI‐RADS score 4–5 or ADC <1.095 × 10−3mm2/s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer. Results Of the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate‐specific antigen density (PSAD), PI‐RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI‐RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI‐RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786). Data Conclusion The PI‐RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS. Level of Evidence: 4 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018;47:1072–1079.
BackgroundActive surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has been addressed, but few studies have reported the value of PI‐RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS.PurposeTo investigate the utility of PI‐RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS.Study TypeRetrospective.SubjectsIn all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy.Field Strength/Sequence3.0T, including T2‐weighted, diffusion‐weighted, and dynamic contrast‐enhanced imaging.AssessmentInsignificant cancer was defined histopathologically as an organ‐confined disease with a tumor volume <0.5 cm3 without Gleason score 4–5. Patients were divided into two groups based on the PI‐RADS v2 and tumor ADC: A, PI‐RADS score ≤3 and ADC ≥1.095 × 10−3mm2/s; and B, PI‐RADS score 4–5 or ADC <1.095 × 10−3mm2/s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer.ResultsOf the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate‐specific antigen density (PSAD), PI‐RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI‐RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI‐RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786).Data ConclusionThe PI‐RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS.Level of Evidence: 4Technical Efficacy: Stage 2J. Magn. Reson. Imaging 2018;47:1072–1079.
Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging-Reporting and Data System (PI-RADS) v2 has been addressed, but few studies have reported the value of PI-RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS. To investigate the utility of PI-RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS. Retrospective. In all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy. 3.0T, including T -weighted, diffusion-weighted, and dynamic contrast-enhanced imaging. Insignificant cancer was defined histopathologically as an organ-confined disease with a tumor volume <0.5 cm without Gleason score 4-5. Patients were divided into two groups based on the PI-RADS v2 and tumor ADC: A, PI-RADS score ≤3 and ADC ≥1.095 × 10 mm /s; and B, PI-RADS score 4-5 or ADC <1.095 × 10 mm /s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer. Of the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate-specific antigen density (PSAD), PI-RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI-RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI-RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786). The PI-RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS. 4 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018;47:1072-1079.
Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging-Reporting and Data System (PI-RADS) v2 has been addressed, but few studies have reported the value of PI-RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS.BACKGROUNDActive surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging-Reporting and Data System (PI-RADS) v2 has been addressed, but few studies have reported the value of PI-RADS v2 for assessing risk stratification in patients with PCa, especially on selecting potential candidates for AS.To investigate the utility of PI-RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS.PURPOSETo investigate the utility of PI-RADS v2 and apparent diffusion coefficient (ADC) in evaluating patients with insignificant PCa, who are suitable for AS.Retrospective.STUDY TYPERetrospective.In all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy.SUBJECTSIn all, 238 patients with PCa who met the Prostate Cancer Research International: Active Surveillance criteria underwent radical prostatectomy.3.0T, including T2 -weighted, diffusion-weighted, and dynamic contrast-enhanced imaging.FIELD STRENGTH/SEQUENCE3.0T, including T2 -weighted, diffusion-weighted, and dynamic contrast-enhanced imaging.Insignificant cancer was defined histopathologically as an organ-confined disease with a tumor volume <0.5 cm3 without Gleason score 4-5. Patients were divided into two groups based on the PI-RADS v2 and tumor ADC: A, PI-RADS score ≤3 and ADC ≥1.095 × 10-3 mm2 /s; and B, PI-RADS score 4-5 or ADC <1.095 × 10-3 mm2 /s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer.ASSESSMENTInsignificant cancer was defined histopathologically as an organ-confined disease with a tumor volume <0.5 cm3 without Gleason score 4-5. Patients were divided into two groups based on the PI-RADS v2 and tumor ADC: A, PI-RADS score ≤3 and ADC ≥1.095 × 10-3 mm2 /s; and B, PI-RADS score 4-5 or ADC <1.095 × 10-3 mm2 /s. Preoperative clinical and imaging variables were evaluated regarding the associations with insignificant cancer.Of the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate-specific antigen density (PSAD), PI-RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI-RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI-RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786).RESULTSOf the 238 patients, 101 (42.8%) were diagnosed with insignificant cancer on pathological findings. The number of positive cores, prostate-specific antigen density (PSAD), PI-RADS v2 and tumor ADC were significantly associated with insignificant cancer on univariate analysis (P < 0.05). However, multivariate analysis indicated tumor ADC (odds ratio [OR] = 4.57, P < 0.001) and PI-RADS v2 (OR = 3.60, P < 0.001) were independent predictors of insignificant cancer. Area under the receiver operating characteristics curve (AUC) reached 0.803 when PI-RADS v2 (AUC = 0.747) was combined with tumor ADC (AUC = 0.786).The PI-RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS.DATA CONCLUSIONThe PI-RADS v2 together with tumor ADC may be a useful marker for predicting patients with insignificant PCa when considering AS.4 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018;47:1072-1079.LEVEL OF EVIDENCE4 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018;47:1072-1079.
Author Yim, Jae Hyun
Kim, Chan Kyo
Kim, Jae‐Hun
Author_xml – sequence: 1
  givenname: Jae Hyun
  surname: Yim
  fullname: Yim, Jae Hyun
  organization: Samsung Medical Center, Sungkyunkwan University School of Medicine
– sequence: 2
  givenname: Chan Kyo
  orcidid: 0000-0003-0482-1140
  surname: Kim
  fullname: Kim, Chan Kyo
  email: chankyokim@skku.edu
  organization: SAIHST, Sungkyunkwan University
– sequence: 3
  givenname: Jae‐Hun
  surname: Kim
  fullname: Kim, Jae‐Hun
  organization: Samsung Medical Center, Sungkyunkwan University School of Medicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28901655$$D View this record in MEDLINE/PubMed
BookMark eNp9kU1uFDEQhS0URH5gwwGQJTYIqYPtbnfb2Y2Gv0FBRANZW47HDjXyuBPbPWh2HIHDcCJOgpvObKKIje0qfa9Ufu8YHYQ-WISeU3JKCWFv1psIp4wL3j5CR5QzVpWiPShvwuuKCtIdouOU1oQQKRv-BB0yIQltOT9Cv-ceAhjt_Q5DSHAdwJUyZHwT-5R1trhUxkacBsj6ylvs-oi1ybC1pRe3FrwfidIzfVxBuMa5xxd79XxSL22yOprveBGyjUFn6IP2Z3j2wCAToTCgz_BlBg95h3uHLxZ_fv5azt5-xVv2FD122if77O4-QZfv332bf6zOv3xYzGfnlal511Zci1Z0UhLmiBTSObZqnOBUU1kO4ZpOEkf1yo3turVa6Lppddcx03DObX2CXk1zixe3g01ZbSAZO65p-yEpKmvREk64LOjLe-i6H8o_fVKMUCZ4Qxgv1Is7arja2JW6ibDRcaf2eRSATIAp_qVonTLF9dGsHDV4RYkaI1dj5Opf5EXy-p5kP_VBmE7wD_B29x9Sffq8XEyav33_v68
CitedBy_id crossref_primary_10_1016_j_clgc_2019_09_018
crossref_primary_10_1016_j_ejrad_2019_03_010
crossref_primary_10_1002_jmri_26896
crossref_primary_10_1515_med_2024_1039
crossref_primary_10_3348_jksr_2022_0169
crossref_primary_10_1259_bjr_20190757
crossref_primary_10_1590_0100_3984_2020_0069
crossref_primary_10_3390_diagnostics15010106
crossref_primary_10_2214_AJR_20_24495
crossref_primary_10_1007_s00261_025_04871_6
crossref_primary_10_1245_s10434_018_6720_2
crossref_primary_10_1038_s41391_018_0111_4
crossref_primary_10_1245_s10434_018_6746_5
crossref_primary_10_5534_wjmh_200037
crossref_primary_10_3390_curroncol28030169
crossref_primary_10_4111_icu_20200159
crossref_primary_10_1080_21681805_2018_1545799
Cites_doi 10.1016/j.crad.2008.02.001
10.1089/end.2015.0027
10.1002/pros.23062
10.1002/jmri.22598
10.1016/j.eururo.2014.01.027
10.1016/j.eururo.2007.05.011
10.1148/radiol.11091409
10.1007/s00330-015-4077-5
10.1016/j.eururo.2014.10.033
10.2214/AJR.13.11945
10.1200/JCO.2010.32.8112
10.1159/000444197
10.1016/j.eururo.2012.03.011
10.1016/j.eururo.2014.10.026
10.1007/s00330-016-4230-9
10.1148/radiol.13121325
10.1016/j.eururo.2010.08.027
10.1002/jmri.25441
10.1038/bjc.2013.181
10.1016/j.juro.2008.07.051
10.1016/j.eururo.2014.10.050
10.1016/j.eururo.2015.08.038
10.1016/j.eururo.2015.01.013
10.1016/j.eururo.2015.08.052
10.1177/0284185114547900
10.1111/bju.12423
10.1016/j.juro.2009.07.024
10.1007/s00330-014-3566-2
10.1148/radiol.11091822
10.1111/j.1464-410X.2009.08887.x
ContentType Journal Article
Copyright 2017 International Society for Magnetic Resonance in Medicine
2017 International Society for Magnetic Resonance in Medicine.
2018 International Society for Magnetic Resonance in Medicine
Copyright_xml – notice: 2017 International Society for Magnetic Resonance in Medicine
– notice: 2017 International Society for Magnetic Resonance in Medicine.
– notice: 2018 International Society for Magnetic Resonance in Medicine
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7QO
7TK
8FD
FR3
K9.
P64
7X8
DOI 10.1002/jmri.25856
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Biotechnology Research Abstracts
Neurosciences Abstracts
Technology Research Database
Engineering Research Database
ProQuest Health & Medical Complete (Alumni)
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
ProQuest Health & Medical Complete (Alumni)
Engineering Research Database
Biotechnology Research Abstracts
Technology Research Database
Neurosciences Abstracts
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitleList
ProQuest Health & Medical Complete (Alumni)
MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1522-2586
EndPage 1079
ExternalDocumentID 28901655
10_1002_jmri_25856
JMRI25856
Genre article
Journal Article
GroupedDBID ---
-DZ
.3N
.GA
.GJ
.Y3
05W
0R~
10A
1L6
1OB
1OC
1ZS
31~
33P
3O-
3SF
3WU
4.4
4ZD
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5RE
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHQN
AAIPD
AAMMB
AAMNL
AANHP
AANLZ
AAONW
AASGY
AAWTL
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABIJN
ABJNI
ABLJU
ABOCM
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCZN
ACGFO
ACGFS
ACGOF
ACIWK
ACMXC
ACPOU
ACPRK
ACRPL
ACSCC
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
AEFGJ
AEGXH
AEIGN
AEIMD
AENEX
AEUYR
AEYWJ
AFBPY
AFFPM
AFGKR
AFRAH
AFWVQ
AFZJQ
AGHNM
AGQPQ
AGXDD
AGYGG
AHBTC
AHMBA
AIACR
AIAGR
AIDQK
AIDYY
AITYG
AIURR
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ASPBG
ATUGU
AVWKF
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CS3
D-6
D-7
D-E
D-F
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
DU5
EBD
EBS
EJD
EMOBN
F00
F01
F04
F5P
FEDTE
FUBAC
G-S
G.N
GNP
GODZA
H.X
HBH
HDBZQ
HF~
HGLYW
HHY
HHZ
HVGLF
HZ~
IX1
J0M
JPC
KBYEO
KQQ
LATKE
LAW
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
M65
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
NNB
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
PQQKQ
Q.N
Q11
QB0
QRW
R.K
RIWAO
RJQFR
ROL
RX1
RYL
SAMSI
SUPJJ
SV3
TEORI
TWZ
UB1
V2E
V8K
V9Y
W8V
W99
WBKPD
WHWMO
WIB
WIH
WIJ
WIK
WIN
WJL
WOHZO
WQJ
WVDHM
WXI
WXSBR
XG1
XV2
ZXP
ZZTAW
~IA
~WT
AAHHS
AAYXX
ACCFJ
AEEZP
AEQDE
AIWBW
AJBDE
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7QO
7TK
8FD
FR3
K9.
P64
7X8
ID FETCH-LOGICAL-c3576-5a86879902f0989ff2d4f851a1951a8f4790f1adfd4f836ea8a346a772c4555e3
IEDL.DBID DR2
ISSN 1053-1807
1522-2586
IngestDate Fri Jul 11 07:04:13 EDT 2025
Fri Jul 25 12:12:12 EDT 2025
Thu Apr 03 07:05:05 EDT 2025
Tue Jul 01 03:56:38 EDT 2025
Thu Apr 24 23:10:56 EDT 2025
Wed Aug 20 07:26:44 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords prostate cancer
PRIAS
MRI
PI-RADS
active surveillance
Language English
License http://onlinelibrary.wiley.com/termsAndConditions#vor
2017 International Society for Magnetic Resonance in Medicine.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3576-5a86879902f0989ff2d4f851a1951a8f4790f1adfd4f836ea8a346a772c4555e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0003-0482-1140
PMID 28901655
PQID 2012854025
PQPubID 1006400
PageCount 8
ParticipantIDs proquest_miscellaneous_1938605059
proquest_journals_2012854025
pubmed_primary_28901655
crossref_citationtrail_10_1002_jmri_25856
crossref_primary_10_1002_jmri_25856
wiley_primary_10_1002_jmri_25856_JMRI25856
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate April 2018
2018-04-00
20180401
PublicationDateYYYYMMDD 2018-04-01
PublicationDate_xml – month: 04
  year: 2018
  text: April 2018
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: Nashville
PublicationSubtitle JMRI
PublicationTitle Journal of magnetic resonance imaging
PublicationTitleAlternate J Magn Reson Imaging
PublicationYear 2018
Publisher Wiley Subscription Services, Inc
Publisher_xml – name: Wiley Subscription Services, Inc
References 2011; 259
2015; 56
2010; 58
2013; 108
2010; 105
2009; 182
2015; 75
2017; 45
2016; 96
2013; 268
2011; 34
2007; 52
2014; 65
2014; 113
2015; 68
2008; 180
2015; 67
2015; 25
2015; 29
2008; 63
2011; 261
2011; 29
2016; 26
2016; 69
2014; 203
2012; 62
e_1_2_5_27_1
e_1_2_5_28_1
e_1_2_5_25_1
e_1_2_5_26_1
e_1_2_5_23_1
e_1_2_5_24_1
e_1_2_5_21_1
e_1_2_5_22_1
e_1_2_5_29_1
Park JJ (e_1_2_5_16_1)
e_1_2_5_20_1
e_1_2_5_15_1
e_1_2_5_14_1
e_1_2_5_17_1
e_1_2_5_9_1
e_1_2_5_8_1
e_1_2_5_11_1
e_1_2_5_7_1
e_1_2_5_10_1
e_1_2_5_6_1
e_1_2_5_13_1
e_1_2_5_32_1
e_1_2_5_5_1
e_1_2_5_12_1
e_1_2_5_4_1
e_1_2_5_3_1
e_1_2_5_2_1
e_1_2_5_19_1
e_1_2_5_18_1
e_1_2_5_30_1
e_1_2_5_31_1
References_xml – volume: 96
  start-page: 459
  year: 2016
  end-page: 469
  article-title: Role of multi‐parametric magnetic resonance image and PIRADS score in patients with prostate cancer eligible for active surveillance according PRIAS criteria
  publication-title: Urol Int
– volume: 29
  start-page: 1115
  year: 2015
  end-page: 1121
  article-title: Magnetic resonance imaging/transrectal ultrasonography fusion prostate biopsy significantly outperforms systematic 12‐core biopsy for prediction of total magnetic resonance imaging tumor volume in active surveillance patients
  publication-title: J Endourol
– volume: 67
  start-page: 1112
  year: 2015
  end-page: 1121
  article-title: Use of the Prostate Imaging Reporting and Data System (PI‐RADS) for prostate cancer detection with multiparametric magnetic resonance imaging: a diagnostic meta‐analysis
  publication-title: Eur Urol
– volume: 180
  start-page: 1964
  year: 2008
  end-page: 1967
  article-title: Pathological upgrading and up staging with immediate repeat biopsy in patients eligible for active surveillance
  publication-title: J Urol
– volume: 69
  start-page: 16
  year: 2016
  end-page: 40
  article-title: PI‐RADS Prostate Imaging — Reporting and Data System: 2015, Version 2
  publication-title: Eur Urol
– volume: 259
  start-page: 453
  year: 2011
  end-page: 461
  article-title: Relationship between apparent diffusion coefficients at 3.0‐T MR imaging and Gleason grade in peripheral zone prostate cancer
  publication-title: Radiology
– volume: 113
  start-page: 864
  year: 2014
  end-page: 870
  article-title: Role of multiparametric 3.0‐Tesla magnetic resonance imaging in patients with prostate cancer eligible for active surveillance
  publication-title: BJU Int
– volume: 58
  start-page: 831
  year: 2010
  end-page: 835
  article-title: Careful selection and close monitoring of low‐risk prostate cancer patients on active surveillance minimizes the need for treatment
  publication-title: Eur Urol
– volume: 182
  start-page: 2274
  year: 2009
  end-page: 2278
  article-title: Radical prostatectomy findings in patients in whom active surveillance of prostate cancer fails
  publication-title: J Urol
– volume: 45
  start-page: 586
  year: 2017
  end-page: 596
  article-title: MR‐based prognostic nomogram for prostate cancer after radical prostatectomy
  publication-title: J Magn Reson Imaging
– volume: 56
  start-page: 1009
  year: 2015
  end-page: 1015
  article-title: High and ultra‐high b‐value diffusion‐weighted imaging in prostate cancer: a quantitative analysis
  publication-title: Acta Radiol
– volume: 105
  start-page: 956
  year: 2010
  end-page: 962
  article-title: Short‐term outcomes of the prospective multicentre ‘Prostate Cancer Research International: Active Surveillance’ study
  publication-title: BJU Int
– article-title: Role of PI‐RADSv2 with multiparametric MRI in determining who needs active surveillance or definitive treatment according to PRIAS
  publication-title: J Magn Reson Imaging 2016
– volume: 26
  start-page: 2502
  year: 2016
  end-page: 2509
  article-title: Prediction of biochemical recurrence after radical prostatectomy with PI‐RADS version 2 in prostate cancers: initial results
  publication-title: Eur Radiol
– volume: 261
  start-page: 46
  year: 2011
  end-page: 66
  article-title: Prostate cancer: multiparametric MR imaging for detection, localization, and staging
  publication-title: Radiology
– volume: 34
  start-page: 95
  year: 2011
  end-page: 100
  article-title: Prostate cancer: utility of fusion of T2‐weighted and high b‐value diffusion‐weighted images for peripheral zone tumor detection and localization
  publication-title: J Magn Reson Imaging
– volume: 63
  start-page: 774
  year: 2008
  end-page: 782
  article-title: Diffusion‐weighted magnetic resonance imaging: a potential non‐invasive marker of tumour aggressiveness in localized prostate cancer
  publication-title: Clin Radiol
– volume: 67
  start-page: 627
  year: 2015
  end-page: 636
  article-title: Magnetic resonance imaging in active surveillance of prostate cancer: a systematic review
  publication-title: Eur Urol
– volume: 62
  start-page: 462
  year: 2012
  end-page: 468
  article-title: Pathologic prostate cancer characteristics in patients eligible for active surveillance: a head‐to‐head comparison of contemporary protocols
  publication-title: Eur Urol
– volume: 68
  start-page: 1045
  year: 2015
  end-page: 1053
  article-title: Can clinically significant prostate cancer be detected with multiparametric magnetic resonance imaging? A systematic review of the literature
  publication-title: Eur Urol
– volume: 268
  start-page: 144
  year: 2013
  end-page: 152
  article-title: Prostate cancer: can multiparametric MR imaging help identify patients who are candidates for active surveillance?
  publication-title: Radiology
– volume: 26
  start-page: 3580
  year: 2016
  end-page: 3587
  article-title: PI‐RADS version 2 for prediction of pathological downgrading after radical prostatectomy: a preliminary study in patients with biopsy‐proven Gleason Score 7 (3 + 4) prostate cancer
  publication-title: Eur Radiol
– volume: 65
  start-page: 1023
  year: 2014
  end-page: 1031
  article-title: Novel tools to improve patient selection and monitoring on active surveillance for low‐risk prostate cancer: a systematic review
  publication-title: Eur Urol
– volume: 52
  start-page: 1560
  year: 2007
  end-page: 1563
  article-title: Prospective validation of active surveillance in prostate cancer: the PRIAS study
  publication-title: Eur Urol
– volume: 69
  start-page: 41
  year: 2016
  end-page: 49
  article-title: Synopsis of the PI‐RADS v2 guidelines for multiparametric prostate magnetic resonance imaging and recommendations for use
  publication-title: Eur Urol
– volume: 25
  start-page: 1786
  year: 2015
  end-page: 1792
  article-title: Diffusion‐weighted magnetic resonance imaging for prediction of insignificant prostate cancer in potential candidates for active surveillance
  publication-title: Eur Radiol
– volume: 203
  start-page: 341
  year: 2014
  end-page: 346
  article-title: Preoperative assessment of prostate cancer using prebiopsy MRI
  publication-title: AJR Am J Roentgenol
– volume: 29
  start-page: 2185
  year: 2011
  end-page: 2190
  article-title: Active surveillance program for prostate cancer: an update of the Johns Hopkins experience
  publication-title: J Clin Oncol
– volume: 68
  start-page: 8
  year: 2015
  end-page: 19
  article-title: Detection of clinically significant prostate cancer using magnetic resonance imaging‐ultrasound fusion targeted biopsy: a systematic review
  publication-title: Eur Urol
– volume: 108
  start-page: 1784
  year: 2013
  end-page: 1789
  article-title: Quality of life after prostate cancer treatments in patients comparable at baseline
  publication-title: Br J Cancer
– volume: 75
  start-page: 1768
  year: 2015
  end-page: 1773
  article-title: Tumor volume in insignificant prostate cancer: Increasing the threshold is a safe approach to reduce over‐treatment
  publication-title: Prostate
– ident: e_1_2_5_21_1
  doi: 10.1016/j.crad.2008.02.001
– ident: e_1_2_5_23_1
  doi: 10.1089/end.2015.0027
– ident: e_1_2_5_8_1
  doi: 10.1002/pros.23062
– ident: e_1_2_5_10_1
  doi: 10.1002/jmri.22598
– ident: e_1_2_5_12_1
  doi: 10.1016/j.eururo.2014.01.027
– ident: e_1_2_5_18_1
  doi: 10.1016/j.eururo.2007.05.011
– ident: e_1_2_5_30_1
  doi: 10.1148/radiol.11091409
– ident: e_1_2_5_31_1
  doi: 10.1007/s00330-015-4077-5
– ident: e_1_2_5_29_1
  doi: 10.1016/j.eururo.2014.10.033
– ident: e_1_2_5_11_1
  doi: 10.2214/AJR.13.11945
– ident: e_1_2_5_5_1
  doi: 10.1200/JCO.2010.32.8112
– ident: e_1_2_5_17_1
  doi: 10.1159/000444197
– ident: e_1_2_5_7_1
  doi: 10.1016/j.eururo.2012.03.011
– ident: e_1_2_5_26_1
  doi: 10.1016/j.eururo.2014.10.026
– ident: e_1_2_5_28_1
  doi: 10.1007/s00330-016-4230-9
– ident: e_1_2_5_24_1
  doi: 10.1148/radiol.13121325
– ident: e_1_2_5_4_1
  doi: 10.1016/j.eururo.2010.08.027
– ident: e_1_2_5_32_1
  doi: 10.1002/jmri.25441
– ident: e_1_2_5_2_1
  doi: 10.1038/bjc.2013.181
– ident: e_1_2_5_3_1
  doi: 10.1016/j.juro.2008.07.051
– ident: e_1_2_5_13_1
  doi: 10.1016/j.eururo.2014.10.050
– ident: e_1_2_5_20_1
  doi: 10.1016/j.eururo.2015.08.038
– ident: e_1_2_5_14_1
  doi: 10.1016/j.eururo.2015.01.013
– ident: e_1_2_5_15_1
  doi: 10.1016/j.eururo.2015.08.052
– ident: e_1_2_5_19_1
  doi: 10.1177/0284185114547900
– ident: e_1_2_5_25_1
  doi: 10.1111/bju.12423
– ident: e_1_2_5_22_1
  doi: 10.1016/j.juro.2009.07.024
– ident: e_1_2_5_16_1
  article-title: Role of PI‐RADSv2 with multiparametric MRI in determining who needs active surveillance or definitive treatment according to PRIAS
  publication-title: J Magn Reson Imaging 2016
– ident: e_1_2_5_27_1
  doi: 10.1007/s00330-014-3566-2
– ident: e_1_2_5_9_1
  doi: 10.1148/radiol.11091822
– ident: e_1_2_5_6_1
  doi: 10.1111/j.1464-410X.2009.08887.x
SSID ssj0009945
Score 2.3319826
Snippet Background Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has...
Active surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging-Reporting and Data System (PI-RADS) v2 has been...
BackgroundActive surveillance (AS) is an important treatment strategy for prostate cancer (PCa). Prostate Imaging‐Reporting and Data System (PI‐RADS) v2 has...
SourceID proquest
pubmed
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1072
SubjectTerms active surveillance
Aged
Cancer
Cancer research
Cancer surgery
Contrast Media
Cores
Diffusion coefficient
Diffusion Magnetic Resonance Imaging - methods
Field strength
Humans
Image Enhancement - methods
Imaging
Internationality
Magnetic resonance imaging
Magnetic Resonance Imaging - methods
Male
Medical research
Middle Aged
MRI
Multivariate analysis
Patients
PI‐RADS
PRIAS
Prostate - diagnostic imaging
Prostate cancer
Prostatectomy
Prostatic Neoplasms - diagnostic imaging
Radiology Information Systems
Retrospective Studies
Surveillance
Title Clinically insignificant prostate cancer suitable for active surveillance according to Prostate Cancer Research International: Active surveillance criteria: Utility of PI‐RADS v2
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.25856
https://www.ncbi.nlm.nih.gov/pubmed/28901655
https://www.proquest.com/docview/2012854025
https://www.proquest.com/docview/1938605059
Volume 47
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LaxsxEBYhh5JLH0kfbtOg0F5aWGdXL2tDLyYPkkBKcGvIpSxaWQK37jrY60B66k_oj-kv6i_pjPZh3IRCe1u00kqLZjTfSKNvCHktXcqVdC6ylslIgM2ITC7zKBciNzpXltsQIPtenQzF2aW8XCPvmrswFT9Eu-GGmhHWa1Rwk8_3lqShn7_Oxl0GaBf5tjFYCxHRYMkdlaYhQzHgBx4lOu613KRsb9l01RrdgpiriDWYnOMH5FMz2CrS5Et3UeZd--0PHsf__ZuH5H6NRWm_Ep5HZM0Vm-TeeX3avkV-1qShk8kNHRcY6YFxRTAV9ArvigBKpRaFZkbni3GJd7AoQGBqwhIKZbNrhzmNoAaUoZcLZpKWU3rRtD6oWjfRf3Rle3Kf9u_4ECxyyC5t9umwxLDeGzr19OL01_cfg_7hB3rNHpPh8dHHg5OozvIQWQ7OTiSNVroHRpH5ONWp92wkPOBAkwD4M9qLXhr7xIw8FnPljDZcKANegRVSSsefkPViWrhnhGphvFdauIRbYZPExCB3I_C708TGXJoOedPMdmZrCnTMxDHJKvJmluE0ZGEaOuRVW_eqIv64s9Z2IzRZrfzzjKHRByTMZIfstq9BbfEsxhRuuphngJu1wiyCaYc8rYSt7QbPfhMlofXbIDJ_6T87Ox-chqfn_1L5BdmAQeoqAmmbrJezhXsJ4KrMd4IS_Qb8oSRS
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3bbhMxELWgSMAL90uggBG8gLTp7voSb9-iQpWUpqpCI_XN8jq2FAibKtlUKk98Ah_DF_ElzHg3GwUqJHhbecd7kWc8Z-zxGUJeC5cxKZyLrE1FxMFnRCYXeZRznhuVS8tsSJA9kr0RPzgVp3VuDp6FqfghmgU3tIwwX6OB44L0zpo19NOX-aSdAtyVV8k1LOkdIqrhmj0qy0KNYkAQLEpU3GnYSdOddd9Nf_QHyNzErMHp7N-uKqsuAlch5pp8bi_LvG2__sbk-N__c4fcquEo7Vb6c5dcccU9cn1Qb7jfJz9q3tDp9IJOCkz2wNQiGA16hsdFAKhSi3ozp4vlpMRjWBRQMDVhFoW2-bnDskYgAW0Y6IKnpOWMHq9671W9VwmAdGOFcpd2L3kQzHNIMG126ajEzN4LOvP0uP_z2_dh991Hep4-IKP99yd7vagu9BBZBvFOJIySqgN-MfVxpjLv0zH3AAVNAvjPKM87WewTM_bYzKQzyjAuDQQGlgshHHtItopZ4R4TqrjxXiruEma5TRITg-qNIfTOEhszYVrkzWq4ta1Z0LEYx1RX_M2pxmHQYRha5FUje1Zxf1wqtb3SGl3b_0Kn6PcBDKeiRV42t8FycTvGFG62XGiAzkpiIcGsRR5V2ta8Brd_Eymg99ugM395vz4YDPvh6sm_CL8gN3ong0N92D_68JTchA9WVULSNtkq50v3DLBWmT8PFvULGFQobQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3bbhMxEB2VIlW8cL8EChjBC0ib7sV2vBUvUUPUFFpFgUh9QSuvY0tpwyZKNpXKE5_Ax_BFfAkze0kUqJDgbeW11155xnPGHp8BeCVsHElhrWdMKDyONsPTqUi9lPNUq1SayBQBsifycMiPTsXpFryt78KU_BCrDTfSjGK9JgWfjdzemjT07Mt83AwR7cprcJ1LX5FMdwZr8qg4LlIUI4CIvED5rRU5abi3brtpjv7AmJuQtbA53VvwuR5tGWpy3lzmadN8_Y3I8X9_5zbcrMAoa5fScwe2bHYXdo6r4_Z78KNiDZ1MLtk4o1APCizCuWAzuiyCMJUZkpo5WyzHOV3CYoiBmS7WUCybX1hKaoQ1sIzcXLSTLJ-yft36oGxdh_-xjf3Jfda-4kO4yhG9tN5nw5ziei_Z1LF-7-e374N25yO7CO_DsPvu08GhV6V58EyE3o4ntJKqhVYxdH6sYufCEXcIBHWA6E8rx1ux7wI9clQcSauVjrjU6BYYLoSw0QPYzqaZfQRMce2cVNwGkeEmCLSPgjdCxzsOjB8J3YDX9WwnpuJAp1Qck6Rkbw4TmoakmIYGvFzVnZXMH1fW2q2FJqm0f5GEZPURCoeiAS9Wr1Fv6TBGZ3a6XCQInJWkNIJxAx6Wwrbqhg5_Aymw9ZtCZP7Sf3J0POgVT4__pfJz2Ol3usmH3sn7J3ADx6vKaKRd2M7nS_sUgVaePiv06Rer0ycl
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Clinically+insignificant+prostate+cancer+suitable+for+active+surveillance+according+to+Prostate+Cancer+Research+International%3A+Active+surveillance+criteria%3A+Utility+of+PI-RADS+v2&rft.jtitle=Journal+of+magnetic+resonance+imaging&rft.au=Yim%2C+Jae+Hyun&rft.au=Kim%2C+Chan+Kyo&rft.au=Kim%2C+Jae-Hun&rft.date=2018-04-01&rft.eissn=1522-2586&rft.volume=47&rft.issue=4&rft.spage=1072&rft_id=info:doi/10.1002%2Fjmri.25856&rft_id=info%3Apmid%2F28901655&rft.externalDocID=28901655
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1053-1807&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1053-1807&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1053-1807&client=summon