Do contemporary imaging and biopsy techniques reliably identify unilateral prostate cancer? Implications for hemiablation patient selection.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 09 2019
Historique:
received: 31 10 2018
revised: 24 01 2019
accepted: 14 03 2019
pubmed: 2 5 2019
medline: 13 5 2020
entrez: 2 5 2019
Statut: ppublish

Résumé

Hemiablation is a less morbid treatment alternative for appropriately selected patients with unilateral prostate cancer (PCa). However, to the authors' knowledge, traditional diagnostic techniques inadequately identify appropriate candidates. In the current study, the authors quantified the accuracy for identifying hemiablation candidates using contemporary diagnostic techniques, including multiparametric magnetic resonance imaging (mpMRI) and MRI-fusion with complete systematic template biopsy. A retrospective analysis of patients undergoing MRI and MRI-fusion prostate biopsy, including full systematic template biopsy, prior to radical prostatectomy in a single tertiary academic institution between June 2010 and February 2018 was performed. Hemiablation candidates had unilateral intermediate-risk PCa (Gleason score [GS] of 3+4 or 4+3, clinical T classification ≤T2, and prostate-specific antigen level <20 ng/dL) on MRI-fusion biopsy and 2) no contralateral highly or very highly suspicious Prostate Imaging Reporting and Data System version 2 (PI-RADSv2) MRI lesions. Hemiablation candidates were inappropriately selected if pathologists identified contralateral GS ≥3+4 or high-risk ipsilateral PCa on prostatectomy. The authors tested a range of hemiablation inclusion criteria and performed multivariable analysis of preoperative predictors of undetected contralateral disease. Of 665 patients, 92 met primary hemiablation criteria. Of these 92 patients, 44 (48%) were incorrectly identified due to ipsilateral GS ≥3+4 tumors crossing the midline (21 patients), undetected distinct contralateral GS ≥3+4 tumors (20 patients), and/or ipsilateral high-risk PCa (3 patients) on prostatectomy. The rate of undetected contralateral disease ranged from 41% to 48% depending on inclusion criteria. On multivariable analysis, men with anterior index tumors were found to be 2.4 times more likely to harbor undetected contralateral GS ≥3+4 PCa compared with men with posterior lesions (P < .05). Clinicians and patients must weigh the risk of inadequate oncologic treatment against the functional benefits of hemiablation. Further investigation into methods for improving patient selection for hemiablation is necessary.

Sections du résumé

BACKGROUND
Hemiablation is a less morbid treatment alternative for appropriately selected patients with unilateral prostate cancer (PCa). However, to the authors' knowledge, traditional diagnostic techniques inadequately identify appropriate candidates. In the current study, the authors quantified the accuracy for identifying hemiablation candidates using contemporary diagnostic techniques, including multiparametric magnetic resonance imaging (mpMRI) and MRI-fusion with complete systematic template biopsy.
METHODS
A retrospective analysis of patients undergoing MRI and MRI-fusion prostate biopsy, including full systematic template biopsy, prior to radical prostatectomy in a single tertiary academic institution between June 2010 and February 2018 was performed. Hemiablation candidates had unilateral intermediate-risk PCa (Gleason score [GS] of 3+4 or 4+3, clinical T classification ≤T2, and prostate-specific antigen level <20 ng/dL) on MRI-fusion biopsy and 2) no contralateral highly or very highly suspicious Prostate Imaging Reporting and Data System version 2 (PI-RADSv2) MRI lesions. Hemiablation candidates were inappropriately selected if pathologists identified contralateral GS ≥3+4 or high-risk ipsilateral PCa on prostatectomy. The authors tested a range of hemiablation inclusion criteria and performed multivariable analysis of preoperative predictors of undetected contralateral disease.
RESULTS
Of 665 patients, 92 met primary hemiablation criteria. Of these 92 patients, 44 (48%) were incorrectly identified due to ipsilateral GS ≥3+4 tumors crossing the midline (21 patients), undetected distinct contralateral GS ≥3+4 tumors (20 patients), and/or ipsilateral high-risk PCa (3 patients) on prostatectomy. The rate of undetected contralateral disease ranged from 41% to 48% depending on inclusion criteria. On multivariable analysis, men with anterior index tumors were found to be 2.4 times more likely to harbor undetected contralateral GS ≥3+4 PCa compared with men with posterior lesions (P < .05).
CONCLUSIONS
Clinicians and patients must weigh the risk of inadequate oncologic treatment against the functional benefits of hemiablation. Further investigation into methods for improving patient selection for hemiablation is necessary.

Identifiants

pubmed: 31042322
doi: 10.1002/cncr.32170
pmc: PMC7368458
mid: NIHMS1598894
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

2955-2964

Subventions

Organisme : NCI NIH HHS
ID : P50 CA092131
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA218547
Pays : United States

Informations de copyright

© 2019 American Cancer Society.

Références

J Urol. 2007 Oct;178(4 Pt 1):1249-52
pubmed: 17698131
Prostate Int. 2014 Mar;2(1):37-42
pubmed: 24693533
Lancet. 2017 Feb 25;389(10071):815-822
pubmed: 28110982
Eur Urol. 2015 Mar;67(3):569-76
pubmed: 25257029
Cancer. 2009 May 15;115(10):2104-10
pubmed: 19288576
Eur Urol. 2017 Feb;71(2):267-273
pubmed: 27720531
Eur Urol. 2019 May;75(5):712-720
pubmed: 30509763
Eur Urol. 2014 Jan;65(1):124-37
pubmed: 24207135
Urol Oncol. 2011 Mar-Apr;29(2):166-70
pubmed: 19451000
Curr Opin Urol. 2017 May;27(3):191-197
pubmed: 28376512
Eur Urol. 2016 Mar;69(3):419-25
pubmed: 26033153
J Natl Compr Canc Netw. 2016 Jan;14(1):19-30
pubmed: 26733552
Prostate Cancer Prostatic Dis. 2017 Sep;20(3):294-299
pubmed: 28349978
Can Urol Assoc J. 2013 Jan-Feb;7(1-2):E82-7
pubmed: 23671513
J Endourol. 2017 Jan;31(1):14-19
pubmed: 27799004
World J Urol. 2019 Mar;37(3):397-407
pubmed: 29948045
Urology. 2018 Feb;112:121-125
pubmed: 29061480
Eur Urol. 2001 Apr;39 Suppl 4:22-3
pubmed: 11340281
Eur Urol. 2012 Jul;62(1):55-63
pubmed: 22445223
J Urol. 2017 Feb;197(2):320-326
pubmed: 27484386
JAMA. 2017 Mar 21;317(11):1126-1140
pubmed: 28324093
Eur Urol. 2015 Jul;68(1):8-19
pubmed: 25454618
BJU Int. 2009 Jul;104(2):195-9
pubmed: 19191784
BJU Int. 2012 Jul;110(2 Pt 2):E64-8
pubmed: 22093108
Eur Urol. 2017 Aug;72(2):238-249
pubmed: 28318726
N Engl J Med. 2009 Oct 22;361(17):1704-6
pubmed: 19846858
Eur Urol. 2014 Apr;65(4):809-15
pubmed: 23523537
Eur Urol. 2017 Jan;71(1):17-34
pubmed: 27595377
Eur Urol. 2012 Dec;62(6):976-83
pubmed: 22698574
Urol Int. 2015;95(2):197-202
pubmed: 25896142
Eur Urol. 2016 Feb;69(2):214-20
pubmed: 26164416
Nat Med. 2009 May;15(5):559-65
pubmed: 19363497
Eur Urol. 2014 May;65(5):907-14
pubmed: 23669165
N Engl J Med. 2018 Aug 09;379(6):589-590
pubmed: 30089067
Urol Oncol. 2014 Aug;32(6):903-11
pubmed: 24239473
Eur Urol. 2013 Apr;63(4):618-22
pubmed: 23265382
J Clin Oncol. 2015 Jan 20;33(3):272-7
pubmed: 25512465
Cancer. 2007 Aug 15;110(4):906-10
pubmed: 17587207

Auteurs

David C Johnson (DC)

National Clinician Scholars Program, Department of Veterans Affairs, Los Angeles, California.
Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Jason J Yang (JJ)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Lorna Kwan (L)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Danielle E Barsa (DE)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Sohrab A Mirak (SA)

Department of Radiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Aydin Pooli (A)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Taylor Sadun (T)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Rajiv Jayadevan (R)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Steve Zhou (S)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Alan M Priester (AM)

Department of Bioengineering, University of California at Los Angeles, Los Angeles, California.

Shyam Natarajan (S)

Department of Bioengineering, University of California at Los Angeles, Los Angeles, California.

Amirhossein M Bajgiran (AM)

Department of Radiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Sepideh Shakeri (S)

Department of Radiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Anthony Sisk (A)

Department of Pathology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Ely R Felker (ER)

Department of Radiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Steven S Raman (SS)

Department of Radiology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Leonard S Marks (LS)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Robert E Reiter (RE)

Department of Urology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH