Minireviews Open Access
Copyright ©2014 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Clin Urol. Mar 24, 2014; 3(1): 44-46
Published online Mar 24, 2014. doi: 10.5410/wjcu.v3.i1.44
Role of magnetic resonance imaging in the diagnostic work up of clinical localized prostate cancer: A review
Martin H Umbehr, Michael Müntener, Department of Urology, City Hospital Triemli of Zurich, 8063 Zurich, Switzerland
Cédric Poyet, Department of Urology, University Hospital of Zurich, 8091 Zurich, Switzerland
Olivio F Donati, Department of Radiology, University Hospital of Zurich, 8091 Zurich, Switzerland
Author contributions: All the authors contributed equally to this work by writing and editing the manuscript.
Correspondence to: Martin H Umbehr, MD, Department of Urology, City Hospital Triemli of Zurich, Birmensdorferstrasse 497, 8063 Zurich, Switzerland. martin.umbehr@triemli.zuerich.ch
Telephone: +41-44-4661111 Fax: +41-44-4662701
Received: November 3, 2013
Revised: December 24, 2013
Accepted: January 14, 2014
Published online: March 24, 2014
Processing time: 141 Days and 15.2 Hours

Abstract

Imaging plays an increasingly important role in the work up of prostate cancer (PCa) and magnetic resonance imaging (MRI) is generally accepted as the most accurate and promising imaging modality in the local staging of PCa due to its high spatial resolution and excellent soft tissue contrast. The quality and performance of MRI of the prostate has improved dramatically during the last decade. Mainly, the combination of morphological information and functional information on cell density, tissue perfusion or metabolism as provided in multi-parametric prostate MRI (mpMRI) has led to a substantial increase in lesion detection and characterization. The correlation between functional parameters as provided by MRI and the aggressiveness of PCa as determined by the Gleason Score may help in differentiating clinically significant from indolent PCa non-invasively. Besides these pros, radiologists are confronted with an immense amount of information and standardized acquisition, interpretation and reporting of mpMRI is not yet a reality. Furthermore, prostate MRI availability is still limited to high volume centers in many countries; hence, it is not yet a routine tool in common daily practice. Hence, development of guidelines for standardized acquisition, interpretation and reporting of prostate MRI exams is urgently needed in order to provide useful information for treating clinicians. Preferably, multi-centric clinical studies comparing MRI findings to step-section histological specimens are mandatory during the coming years. Furthermore, simplification of the acquisition must be achieved in order to make this imaging modality applicable for daily use in common uro-radiological practice.

Key Words: Localized prostate cancer; Magnetic resonance imaging; Local imaging; Staging; Diagnostic work up

Core tip: This review gives an overview about the current strengths and pitfalls of magnetic resonance imaging in the work up of clinical localized prostate cancer as well as suggestions for steps in the future.



INTRODUCTION

Imaging plays an increasingly important role in the work up of prostate cancer (PCa). An important mainstay of magnetic resonance imaging (MRI) is the local staging in patients with clinically localized PCa. In these patients, not only the information whether or not the disease is confined to the capsule is crucial, but also information on the aggressiveness of the PCa is desired. The latter information is especially important in PCa due to its heterogeneity in terms of histopathology and clinical outcome. Exact characterization of PCa is a prerequisite in order to offer personalized treatment options and minimize the evident problem of over-diagnosis and over-treatment of indolent PCa[1]. Furthermore, because of prostate specific antigen (PSA) screening, even in opportunistic forms, most PCa are detected while still in a clinically localized stage[2]. In the end, a combination of tumor characteristics, such as stage and aggressiveness of PCa, and patient characteristics, such as the age, co-morbidities and preferences of the patient, will help decide on the best available (curative) treatment option. For men who suffer from aggressive localized PCa variants, meaning PCa with a Gleason score ≥ 7, traditional whole gland approaches such as radical prostatectomy or irradiation of the prostate gland are still considered the gold standard treatment modalities. However, patients suffering from a less aggressive, so called “indolent”, variants of PCa can nowadays be offered less aggressive treatment options which aim at preserving the prostate and thereby minimizing treatment related adverse events. Of these treatment options active surveillance (AS) should be mentioned first. In AS, patients with low risk PCa are closely observed and followed and curative intervention is only suggested in the case of disease progression during follow up. AS is considered a safe treatment strategy as long as inclusion criteria are strictly set and respected[3]. More recently, focal therapy emerged as another option. However, although short term safety of this approach has been described in the literature[4], long term outcome data are still lacking.

Deciding on the optimal treatment plan for a man suffering from PCa involves knowledge of differentiating limited from extensive tumor burden, organ confined from non-organ confined disease, and indolent from aggressive cancer variants. MRI may help in gathering this crucial information and is therefore an important test for urologists and radio-oncologists in order to offer personalized treatment to patients suffering from PCa.

THE ROLE OF MRI TODAY

Today, MRI is generally accepted as the most accurate and promising imaging modality in the local staging of PCa[5] due to its high spatial resolution and excellent soft tissue contrast. Furthermore, its ability to detect prostate cancer foci in anatomical locations within the prostate gland which are difficult to sample and therefore often missed by TRUS-Biopsy (i.e., the anterior zone) has been shown by Sciarra et al[6]. The quality and performance of MRI of the prostate has improved dramatically during the last decade[5,7-9]. Mainly, the combination of morphological/anatomical information and functional information on cell density, tissue perfusion or metabolism as provided in multi-parametric prostate MRI (mpMRI) has led to a substantial increase in lesion detection and characterization[10,11]. The correlation between functional parameters as provided by MRI and the aggressiveness of PCa as determined by the Gleason score which has recently been discovered[11-15] may help in differentiating clinically significant from indolent PCa non-invasively.

THE ROLE OF MRI IN THE FUTURE

These promising developments have led to great enthusiasm and it is conceivable that the traditional ultrasound guided random prostate biopsy with its well known problem of under-sampling[16] might be completely replaced by MRI guided targeted biopsy procedures. Quite possibly overtreatment could be decreased due to the identification of only significant PCa[17] while indolent PCa remains undiscovered. However, there are several crucial and as yet unsolved problems with MRI in PCa today. As described by Gupta et al[7] and supported by others[18], radiologists are confronted with an immense amount of information in mpMRI and standardized acquisition, interpretation and reporting of mpMRI is not yet a reality. However, standardization is urgently needed in this field should MRI ever play a crucial role in PCa work up, as prospected by Choyke et al[17]. In this respect, there are currently promising developments[19,20] in progress. Furthermore, prostate MRI availability is still limited to high volume centers in many countries; hence, it is not yet a routine tool in common daily practice. As a consequence, reading prostate MRI correctly is not a routine task for most radiologists today but the experience of the radiologist in reading and interpreting prostate MR findings, probably more so than in other exams, is a crucial factor[21,22]. The role and responsibility of the radiologist will change as urologists and radio-oncologists will most likely base their treatment recommendations much more on MRI-findings than they used to. The quality and reproducibility of reading prostate MRI are important and mandatory prerequisites for a high quality care of patients with PCa.

NEXT STEPS

MpMRI has been shown to be an important and highly promising imaging modality in the work up of patients with PCa. As its technical potential seems to be far from fully exploited, mpMRI may truly revolutionize management of patients with PCa and subsequently personalize the treatment of PCa. However, proper interpretation of prostate MRI is still limited to some specialized radiologists and a certain number of prostate MRIs have to be interpreted on a regular basis in order to maintain a high quality of radiological reports. Development of guidelines for standardized acquisition, interpretation and reporting of prostate MRI exams is urgently needed in order to provide useful information for treating clinicians. In this regard, further and preferably multi-centric clinical studies comparing MRI findings to step-section histological specimens are mandatory during the coming years. Furthermore, simplification of the acquisition must be achieved in order to make this imaging modality applicable for daily use in common uroradiological practice.

Footnotes

P- Reviewers: Cai T, Mazaris E S- Editor: Song XX L- Editor: Roemmele A E- Editor: Wu HL

References
1.  Ilic D, Neuberger MM, Djulbegovic M, Dahm P. Screening for prostate cancer. Cochrane Database Syst Rev. 2013;1:CD004720.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 144]  [Cited by in F6Publishing: 242]  [Article Influence: 22.0]  [Reference Citation Analysis (0)]
2.  Schröder FH, Hugosson J, Roobol MJ, Tammela TL, Ciatto S, Nelen V, Kwiatkowski M, Lujan M, Lilja H, Zappa M. Screening and prostate-cancer mortality in a randomized European study. N Engl J Med. 2009;360:1320-1328.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2835]  [Cited by in F6Publishing: 2693]  [Article Influence: 179.5]  [Reference Citation Analysis (1)]
3.  Tosoian JJ, JohnBull E, Trock BJ, Landis P, Epstein JI, Partin AW, Walsh PC, Carter HB. Pathological outcomes in men with low risk and very low risk prostate cancer: implications on the practice of active surveillance. J Urol. 2013;190:1218-1222.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 65]  [Cited by in F6Publishing: 65]  [Article Influence: 5.9]  [Reference Citation Analysis (0)]
4.  Emberton M. Are we ready for the new wave of focal therapy interventions for men with early prostate cancer? BJU Int. 2013;112:423-424.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 1]  [Reference Citation Analysis (0)]
5.  Pinto F, Totaro A, Palermo G, Calarco A, Sacco E, D’Addessi A, Racioppi M, Valentini A, Gui B, Bassi P. Imaging in prostate cancer staging: present role and future perspectives. Urol Int. 2012;88:125-136.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 48]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
6.  Sciarra A, Panebianco V, Ciccariello M, Salciccia S, Cattarino S, Lisi D, Gentilucci A, Alfarone A, Bernardo S, Passariello R. Value of magnetic resonance spectroscopy imaging and dynamic contrast-enhanced imaging for detecting prostate cancer foci in men with prior negative biopsy. Clin Cancer Res. 2010;16:1875-1883.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 123]  [Cited by in F6Publishing: 104]  [Article Influence: 7.4]  [Reference Citation Analysis (0)]
7.  Gupta RT, Kauffman CR, Polascik TJ, Taneja SS, Rosenkrantz AB. The state of prostate MRI in 2013. Oncology (Williston Park). 2013;27:262-270.  [PubMed]  [DOI]  [Cited in This Article: ]
8.  Engelbrecht MR, Jager GJ, Laheij RJ, Verbeek AL, van Lier HJ, Barentsz JO. Local staging of prostate cancer using magnetic resonance imaging: a meta-analysis. Eur Radiol. 2002;12:2294-2302.  [PubMed]  [DOI]  [Cited in This Article: ]
9.  Wu LM, Xu JR, Ye YQ, Lu Q, Hu JN. The clinical value of diffusion-weighted imaging in combination with T2-weighted imaging in diagnosing prostate carcinoma: a systematic review and meta-analysis. AJR Am J Roentgenol. 2012;199:103-110.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 99]  [Cited by in F6Publishing: 112]  [Article Influence: 9.3]  [Reference Citation Analysis (0)]
10.  Jung SI, Donati OF, Vargas HA, Goldman D, Hricak H, Akin O. Transition zone prostate cancer: incremental value of diffusion-weighted endorectal MR imaging in tumor detection and assessment of aggressiveness. Radiology. 2013;269:493-503.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 87]  [Cited by in F6Publishing: 95]  [Article Influence: 8.6]  [Reference Citation Analysis (0)]
11.  Vargas HA, Akin O, Franiel T, Mazaheri Y, Zheng J, Moskowitz C, Udo K, Eastham J, Hricak H. Diffusion-weighted endorectal MR imaging at 3 T for prostate cancer: tumor detection and assessment of aggressiveness. Radiology. 2011;259:775-784.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 328]  [Cited by in F6Publishing: 330]  [Article Influence: 25.4]  [Reference Citation Analysis (0)]
12.  Hambrock T, Hoeks C, Hulsbergen-van de Kaa C, Scheenen T, Fütterer J, Bouwense S, van Oort I, Schröder F, Huisman H, Barentsz J. Prospective assessment of prostate cancer aggressiveness using 3-T diffusion-weighted magnetic resonance imaging-guided biopsies versus a systematic 10-core transrectal ultrasound prostate biopsy cohort. Eur Urol. 2012;61:177-184.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 244]  [Cited by in F6Publishing: 258]  [Article Influence: 19.8]  [Reference Citation Analysis (0)]
13.  Rastinehad AR, Baccala AA, Chung PH, Proano JM, Kruecker J, Xu S, Locklin JK, Turkbey B, Shih J, Bratslavsky G. D’Amico risk stratification correlates with degree of suspicion of prostate cancer on multiparametric magnetic resonance imaging. J Urol. 2011;185:815-820.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 91]  [Cited by in F6Publishing: 95]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
14.  Yerram NK, Volkin D, Turkbey B, Nix J, Hoang AN, Vourganti S, Gupta GN, Linehan WM, Choyke PL, Wood BJ. Low suspicion lesions on multiparametric magnetic resonance imaging predict for the absence of high-risk prostate cancer. BJU Int. 2012;110:E783-E788.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 76]  [Cited by in F6Publishing: 82]  [Article Influence: 6.8]  [Reference Citation Analysis (0)]
15.  Donati OF, Jung SI, Vargas HA, Gultekin DH, Zheng J, Moskowitz CS, Hricak H, Zelefsky MJ, Akin O. Multiparametric prostate MR imaging with T2-weighted, diffusion-weighted, and dynamic contrast-enhanced sequences: are all pulse sequences necessary to detect locally recurrent prostate cancer after radiation therapy? Radiology. 2013;268:440-450.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 94]  [Cited by in F6Publishing: 99]  [Article Influence: 9.0]  [Reference Citation Analysis (0)]
16.  Divrik RT, Eroglu A, Sahin A, Zorlu F, Ozen H. Increasing the number of biopsies increases the concordance of Gleason scores of needle biopsies and prostatectomy specimens. Urol Oncol. 2007;25:376-382.  [PubMed]  [DOI]  [Cited in This Article: ]
17.  Choyke PL, Turkbey B. The state of prostate MRI in 2013: into the breach. Oncology (Williston Park). 2013;27:274, 276.  [PubMed]  [DOI]  [Cited in This Article: ]
18.  Cornfeld D, Sprenkle P. Multiparametric MRi: standardizations needed. Oncology (Williston Park). 2013;27:277,280.  [PubMed]  [DOI]  [Cited in This Article: ]
19.  Barentsz JO, Richenberg J, Clements R, Choyke P, Verma S, Villeirs G, Rouviere O, Logager V, Fütterer JJ. ESUR prostate MR guidelines 2012. Eur Radiol. 2012;22:746-757.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1747]  [Cited by in F6Publishing: 1830]  [Article Influence: 152.5]  [Reference Citation Analysis (0)]
20.  Dickinson L, Ahmed HU, Allen C, Barentsz JO, Carey B, Futterer JJ, Heijmink SW, Hoskin PJ, Kirkham A, Padhani AR. Magnetic resonance imaging for the detection, localisation, and characterisation of prostate cancer: recommendations from a European consensus meeting. Eur Urol. 2011;59:477-494.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 557]  [Cited by in F6Publishing: 548]  [Article Influence: 39.1]  [Reference Citation Analysis (0)]
21.  Scheidler J, Weöres I, Brinkschmidt C, Zeitler H, Panzer S, Scharf M, Heuck A, Siebels M. Diagnosis of prostate cancer in patients with persistently elevated PSA and tumor-negative biopsy in ambulatory care: performance of MR imaging in a multi-reader environment. Rofo. 2012;184:130-135.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 15]  [Cited by in F6Publishing: 10]  [Article Influence: 0.8]  [Reference Citation Analysis (0)]
22.  Akin O, Riedl CC, Ishill NM, Moskowitz CS, Zhang J, Hricak H. Interactive dedicated training curriculum improves accuracy in the interpretation of MR imaging of prostate cancer. Eur Radiol. 2010;20:995-1002.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 80]  [Cited by in F6Publishing: 79]  [Article Influence: 5.6]  [Reference Citation Analysis (0)]