Biparametric MRI in prostate cancer during active surveillance: is it safe?

Active surveillance Biparametric MRI Prostate cancer

Journal

European radiology
ISSN: 1432-1084
Titre abrégé: Eur Radiol
Pays: Germany
ID NLM: 9114774

Informations de publication

Date de publication:
24 Apr 2024
Historique:
received: 02 02 2024
accepted: 22 03 2024
revised: 13 03 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 24 4 2024
Statut: aheadofprint

Résumé

Active surveillance (AS) is the preferred option for patients presenting with low-intermediate-risk prostate cancer. MRI now plays a crucial role for baseline assessment and ongoing monitoring of AS. The Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations aid radiological assessment of progression; however, current guidelines do not advise on MRI protocols nor on frequency. Biparametric (bp) imaging without contrast administration offers advantages such as reduced costs and increased throughput, with similar outcomes to multiparametric (mp) MRI shown in the biopsy naïve setting. In AS follow-up, the paradigm shifts from MRI lesion detection to assessment of progression, and patients have the further safety net of continuing clinical surveillance. As such, bpMRI may be appropriate in clinically stable patients on routine AS follow-up pathways; however, there is currently limited published evidence for this approach. It should be noted that mpMRI may be mandated in certain patients and potentially offers additional advantages, including improving image quality, new lesion detection, and staging accuracy. Recently developed AI solutions have enabled higher quality and faster scanning protocols, which may help mitigate against disadvantages of bpMRI. In this article, we explore the current role of MRI in AS and address the need for contrast-enhanced sequences. CLINICAL RELEVANCE STATEMENT: Active surveillance is the preferred plan for patients with lower-risk prostate cancer, and MRI plays a crucial role in patient selection and monitoring; however, current guidelines do not currently recommend how or when to perform MRI in follow-up. KEY POINTS: Noncontrast biparametric MRI has reduced costs and increased throughput and may be appropriate for monitoring stable patients. Multiparametric MRI may be mandated in certain patients, and contrast potentially offers additional advantages. AI solutions enable higher quality, faster scanning protocols, and could mitigate the disadvantages of biparametric imaging.

Identifiants

pubmed: 38656709
doi: 10.1007/s00330-024-10770-z
pii: 10.1007/s00330-024-10770-z
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

Références

Mottet N, van den Bergh RCN, Briers E et al (2021) EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer—2020 update. Part 1: screening, diagnosis, and local treatment with urative intent. Eur Urol 79:243–262
pubmed: 33172724 doi: 10.1016/j.eururo.2020.09.042
Wilt TJ, Jones KM, Barry MJ et al (2017) Follow-up of prostatectomy versus observation for early prostate cancer. N Engl J Med 377:132–142
pubmed: 28700844 doi: 10.1056/NEJMoa1615869
Hamdy FC, Donovan JL, Lane JA et al (2023) Fifteen-year outcomes after monitoring, surgery, or radiotherapy for prostate cancer. N Engl J Med 388:1547–1558
Rajwa P, Sprenkle PC, Leapman MS (2021) When and how should active surveillance for prostate cancer be de-escalated? Eur Urol Focus 7:297–300
pubmed: 32019719 doi: 10.1016/j.euf.2020.01.001
Prostate cancer diagnosis and management: NICE guideline (NG131). 2019
Clinically Localized Prostate Cancer: AUA/ASTRO Guideline. 2022
Moore CM, King LE, Withington J et al (2023) Best current practice and research priorities in active surveillance for prostate cancer-a report of a Movember International Consensus Meeting. Eur Urol Oncol 6:160–182
pubmed: 36710133 doi: 10.1016/j.euo.2023.01.003
Klotz L, Pond G, Loblaw A et al (2020) Randomized study of systematic biopsy versus magnetic resonance imaging and targeted and systematic biopsy in men on active surveillance (ASIST): 2-year postbiopsy follow-up. Eur Urol 77:311–317
pubmed: 31708295 doi: 10.1016/j.eururo.2019.10.007
Gallagher KM, Christopher E, Cameron AJ et al (2019) Four-year outcomes from a multiparametric magnetic resonance imaging (MRI)-based active surveillance programme: PSA dynamics and serial MRI scans allow omission of protocol biopsies. BJU Int 123:429–438
pubmed: 30113755 doi: 10.1111/bju.14513
Westphalen AC, McCulloch CE, Anaokar JM et al (2020) Variability of the positive predictive value of PI-RADS for prostate MRI across 26 centers: experience of the society of abdominal radiology prostate cancer disease-focused panel. Radiology 296:76–84
pubmed: 32315265 doi: 10.1148/radiol.2020190646
Rajwa P, Pradere B, Quhal F et al (2021) Reliability of serial prostate magnetic resonance imaging to detect prostate cancer progression during active surveillance: a systematic review and meta-analysis. Eur Urol 80:549–563
pubmed: 34020828 doi: 10.1016/j.eururo.2021.05.001
Hettiarachchi D, Geraghty R, Rice P et al (2021) Can the use of serial multiparametric magnetic resonance imaging during active surveillance of prostate cancer avoid the need for prostate biopsies?-A systematic diagnostic test accuracy review. Eur Urol Oncol 4:426–436
pubmed: 32972894 doi: 10.1016/j.euo.2020.09.002
Sushentsev N, Abrego L, Colarieti A et al (2023) Using a recurrent neural network to inform the use of prostate-specific antigen (PSA) and PSA density for dynamic monitoring of the risk of prostate cancer progression on active surveillance. Eur Urol Open Sci 52:36–39
pubmed: 37182116 pmcid: 10172696 doi: 10.1016/j.euros.2023.04.002
Turkbey B, Rosenkrantz AB, Haider MA et al(2019) Prostate imaging reporting and data system version 2.1: 2019 update of prostate imaging reporting and data system version 2. Eur Urol 76:340–351
pubmed: 30898406 doi: 10.1016/j.eururo.2019.02.033
McDonald JS, Hunt CH, Kolbe AB et al (2019) Acute adverse events following gadolinium-based contrast agent administration: a single-center retrospective study of 281 945 injections. Radiology 292:620–627
pubmed: 31264948 doi: 10.1148/radiol.2019182834
McDonald RJ, McDonald JS, Kallmes DF et al (2015) Intracranial gadolinium deposition after contrast-enhanced MR imaging. Radiology 275:772–782
pubmed: 25742194 doi: 10.1148/radiol.15150025
Kanda T, Fukusato T, Matsuda M et al (2015) Gadolinium-based contrast agent accumulates in the brain even in subjects without severe renal dysfunction: evaluation of autopsy brain specimens with inductively coupled plasma mass spectroscopy. Radiology 276:228–232
pubmed: 25942417 doi: 10.1148/radiol.2015142690
Gulani V, Calamante F, Shellock FG, Kanal E, Reeder SB (2017) Gadolinium deposition in the brain: summary of evidence and recommendations. Lancet Neurol 16:564–570
pubmed: 28653648 doi: 10.1016/S1474-4422(17)30158-8
Murata N, Gonzalez-Cuyar LF, Murata K et al (2016) Macrocyclic and other non-group 1 gadolinium contrast agents deposit low levels of gadolinium in brain and bone tissue: preliminary results from 9 patients with normal renal function. Invest Radiol 51:447–453
pubmed: 26863577 doi: 10.1097/RLI.0000000000000252
Ponrartana S, Moore MM, Chan SS, Victoria T, Dillman JR, Chavhan GB (2021) Safety issues related to intravenous contrast agent use in magnetic resonance imaging. Pediatr Radiol 51:736–747
pubmed: 33871726 doi: 10.1007/s00247-020-04896-7
Asbach P (2023) Contrast-medium administration for prostate MRI: yes! Contrast-medium administration can be abandoned. Eur Radiol 33:8413–8414
pubmed: 37420101 pmcid: 10667371 doi: 10.1007/s00330-023-09766-y
Rouvière O (2023) Contrast-medium administration for prostate MRI can be abandoned: no(t so simple)! Eur Radiol 33:8415–8416
pubmed: 37436510 doi: 10.1007/s00330-023-09767-x
Schoots IG, Barentsz JO, Bittencourt LK et al (2020) PI-RADS committee position on MRI without contrast medium in biopsy-naive men with suspected prostate cancer: narrative review. AJR Am J Roentgenol 216:3–19
pubmed: 32812795 doi: 10.2214/AJR.20.24268
Porter KK, King A, Galgano SJ, Sherrer RL, Gordetsky JB, Rais-Bahrami S (2020) Financial implications of biparametric prostate MRI. Prostate Cancer Prostatic Dis 23:88–93
pubmed: 31239513 doi: 10.1038/s41391-019-0158-x
Barrett T, Ghafoor S, Gupta RT et al (2022) Prostate MRI qualification: AJR expert panel narrative review. AJR Am J Roentgenol 219:691–702
pubmed: 35544372 doi: 10.2214/AJR.22.27615
Davies C, Castle JT, Stalbow K, Haslam PJ (2019) Prostate mpMRI in the UK: the state of the nation. Clin Radiol 74:894.e11–894.e18
pubmed: 31627803 doi: 10.1016/j.crad.2019.09.129
Bass EJ, Pantovic A, Connor M et al (2021) A systematic review and meta-analysis of the diagnostic accuracy of biparametric prostate MRI for prostate cancer in men at risk. Prostate Cancer Prostatic Dis 24:596–611
pubmed: 33219368 doi: 10.1038/s41391-020-00298-w
Belue MJ, Yilmaz EC, Daryanani A, Turkbey B (2022) Current status of biparametric MRI in prostate cancer diagnosis: literature analysis. Life (Basel) 12:804
pubmed: 35743835
Russo F, Mazzetti S, Regge D et al (2021) Diagnostic accuracy of single-plane biparametric and multiparametric magnetic resonance imaging in prostate cancer: a randomized noninferiority trial in biopsy-naïve men. Eur Urol Oncol 4:855–862
pubmed: 33893066 doi: 10.1016/j.euo.2021.03.007
Asif A, Nathan A, Ng A et al (2023) Comparing biparametric to multiparametric MRI in the diagnosis of clinically significant prostate cancer in biopsy-naive men (PRIME): a prospective, international, multicentre, non-inferiority within-patient, diagnostic yield trial protocol. BMJ Open 13:e070280
pubmed: 37019486 pmcid: 10083803 doi: 10.1136/bmjopen-2022-070280
Imperial Prostate 7 - Prostate Assessment Using Comparative Interventions - Fast Mri and Image-fusion for Cancer (IP7-PACIFIC). 2022. Available from: https://classic.clinicaltrials.gov/ct2/show/NCT05574647
Thurtle D, Barrett T, Thankappan-Nair V et al (2018) Progression and treatment rates using an active surveillance protocol incorporating image-guided baseline biopsies and multiparametric magnetic resonance imaging monitoring for men with favourable-risk prostate cancer. BJU Int 122:59–65
pubmed: 29438586 doi: 10.1111/bju.14166
Stavrinides V, Giganti F, Trock B et al (2020) Five-ryear outcomes of magnetic resonance imaging-based Active Surveillance for prostate cancer: large cohort study. Eur Urol 78:443–451
pubmed: 32360049 pmcid: 7443696 doi: 10.1016/j.eururo.2020.03.035
Light A, Lophatananon A, Keates A et al (2022) Development and external validation of the STRATified CANcer surveillance (STRATCANS) multivariable model for predicting progression in men with newly diagnosed prostate cancer starting active surveillance. J Clin Med 12:216
pubmed: 36615017 pmcid: 9821695 doi: 10.3390/jcm12010216
Moore CM, Giganti F, Albertsen P et al (2017) Reporting magnetic resonance imaging in men on active surveillance for prostate cancer: the PRECISE recommendations—a report of a European School of Oncology Task Force. Eur Urol 71:648–655
pubmed: 27349615 doi: 10.1016/j.eururo.2016.06.011
Sanmugalingam N, Sushentsev N, Lee KL et al (2023) The PRECISE recommendations for prostate MRI in patients on active surveillance for prostate cancer: a critical review. AJR Am J Roentgenol 221:649–660
pubmed: 37341180 doi: 10.2214/AJR.23.29518
Sushentsev N, Caglic I, Sala E et al (2020) The effect of capped biparametric magnetic resonance imaging slots on weekly prostate cancer imaging workload. Br J Radiol 93:20190929
pubmed: 31971823 pmcid: 7362922 doi: 10.1259/bjr.20190929
Cooperberg MR, Meeks W, Fang R, Gaylis FD, Catalona WJ, Makarov DV (2023) Time trends and variation in the use of active surveillance for management of low-risk prostate cancer in the US. JAMA Netw Open 6:E231439
pubmed: 36862409 pmcid: 9982696 doi: 10.1001/jamanetworkopen.2023.1439
de Vos II, Luiting HB, Roobol MJ (2023) Active Surveillance for Prostate Cancer: Past, Current, and Future Trends. J Pers Med 13:629
Biparametric vs multiparametric MRI in men on active surveillance for prostate cancer: a preliminary collaboration between the UK and France Part of the Cities partnership Programme
Kortenbach KC, Boesen L, Løgager V, Thomsen HS (2021) For men enrolled in active surveillance, pre-biopsy biparametric magnetic resonance imaging significantly reduces the risk of reclassification and disease progression after 1 year. Scand J Urol 55:215–220
pubmed: 33749511 doi: 10.1080/21681805.2021.1897158
Thestrup KCD, Løgager V, Boesen L, Thomsen HS (2019) Comparison of bi- and multiparametric magnetic resonance imaging to select men for active surveillance. Acta Radiol Open 8:2058460119866352
pubmed: 31392035 pmcid: 6669856
Caglic I, Sushentsev N, Gnanapragasam VJ et al (2021) MRI-derived PRECISE scores for predicting pathologically-confirmed radiological progression in prostate cancer patients on active surveillance. Eur Radiol 31:2696–2705
pubmed: 33196886 doi: 10.1007/s00330-020-07336-0
Gatti M, Faletti R, Calleris G et al (2019) Prostate cancer detection with biparametric magnetic resonance imaging (bpMRI) by readers with different experience: performance and comparison with multiparametric (mpMRI). Abdom Radiol (NY) 44:1883–1893
pubmed: 30788558 doi: 10.1007/s00261-019-01934-3
Di Campli E, Delli Pizzi A, Seccia B et al (2018) Diagnostic accuracy of biparametric vs multiparametric MRI in clinically significant prostate cancer: Comparison between readers with different experience. Eur J Radiol 101:17–23
pubmed: 29571792 doi: 10.1016/j.ejrad.2018.01.028
Zawaideh JP, Sala E, Shaida N et al (2020) Diagnostic accuracy of biparametric versus multiparametric prostate MRI: assessment of contrast benefit in clinical practice. Eur Radiol 30:4039–4049
pubmed: 32166495 doi: 10.1007/s00330-020-06782-0
Van Hemelrijck M, Ji X, Helleman J et al (2019) Reasons for discontinuing active surveillance: assessment of 21 centres in 12 countries in the Movember GAP3 Consortium. Eur Urol 75:523–531
pubmed: 30385049 doi: 10.1016/j.eururo.2018.10.025
Kinsella N, Helleman J, Bruinsma S et al (2018) Active surveillance for prostate cancer: a systematic review of contemporary worldwide practices. Transl Androl Urol 7:83–97
pubmed: 29594023 pmcid: 5861285 doi: 10.21037/tau.2017.12.24
Kinsella N, Stattin P, Cahill D et al (2018) Factors influencing men’s choice of and adherence to active surveillance for low-risk prostate cancer: a mixed-method systematic review. Eur Urol 74:261–280
pubmed: 29598981 pmcid: 6198662 doi: 10.1016/j.eururo.2018.02.026
Eldred-Evans D, Tam H, Sokhi H, Padhani AR, Winkler M, Ahmed HU (2020) Rethinking prostate cancer screening: could MRI be an alternative screening test? Nat Rev Urol 17:526–539
pubmed: 32694594 doi: 10.1038/s41585-020-0356-2
Ghavimi S, Abdi H, Waterhouse J et al (2018) Natural history of prostatic lesions on serial multiparametric magnetic resonance imaging. Can Urol Assoc J 12:270–275
pubmed: 30139428 pmcid: 6114162 doi: 10.5489/cuaj.4859
Barrett T, de Rooij M, Giganti F, Allen C, Barentsz JO, Padhani AR (2023) Quality checkpoints in the MRI-directed prostate cancer diagnostic pathway. Nat Rev Urol 20:9–22
pubmed: 36168056 doi: 10.1038/s41585-022-00648-4
Wassberg C, Akin O, Vargas HA, Shukla-Dave A, Zhang J, Hricak H (2012) The incremental value of contrast-enhanced MRI in the detection of biopsy-proven local recurrence of prostate cancer after radical prostatectomy: effect of reader experience. AJR. Am J Roentgenol 199:360–366
doi: 10.2214/AJR.11.6923
Caglic I, Sushentsev N, Shah N, Warren AY, Lamb BW, Barrett T (2021) Comparison of biparametric versus multiparametric prostate MRI for the detection of extracapsular extension and seminal vesicle invasion in biopsy naïve patients. Eur J Radiol 141:109804
pubmed: 34062473 doi: 10.1016/j.ejrad.2021.109804
Junker D, Steinkohl F, Fritz V et al (2019) Comparison of multiparametric and biparametric MRI of the prostate: are gadolinium-based contrast agents needed for routine examinations? World J Urol 37:691–699
pubmed: 30078170 doi: 10.1007/s00345-018-2428-y
Bao J, Zhi R, Hou Y et al (2021) Optimized MRI assessment for clinically significant prostate cancer: a STARD-compliant two-center study. J Magn Reson Imaging 53:1210–1219
pubmed: 33075177 doi: 10.1002/jmri.27394
Giganti F, Pecoraro M, Stavrinides V et al (2020) Interobserver reproducibility of the PRECISE scoring system for prostate MRI on active surveillance: results from a two-centre pilot study. Eur Radiol 30:2082–2090
pubmed: 31844959 doi: 10.1007/s00330-019-06557-2
Lee KL, Kessler DA, Dezonie S, et al (2023). Assessment of deep learning-based reconstruction on T2-weighted and diffusion-weighted prostate MRI image quality. Eur J Radiol 166:111017
Giganti F, Allen C, Emberton M, Moore CM, Kasivisvanathan V, PRECISION study group (2020) Prostate imaging quality (PI-QUAL): a new quality control scoring system for multiparametric magnetic resonance imaging of the prostate from the PRECISION trial. Eur Urol Oncol 3:615–619
pubmed: 32646850 doi: 10.1016/j.euo.2020.06.007
Karanasios E, Caglic I, Zawaideh JP, Barrett T (2022) Prostate MRI quality: clinical impact of the PI-QUAL score in prostate cancer diagnostic work-up. Br J Radiol 95:20211372
pubmed: 35179971 pmcid: 10993954 doi: 10.1259/bjr.20211372
Englman C, Maffei D, Allen C, et al (2024) PRECISE Version 2: Updated recommendations for reporting prostate magnetic resonance imaging in patients on active surveillance for prostate cancer. Eur Urol 30:S0302–2838
Sushentsev N, Rundo L, Blyuss O, Gnanapragasam VJ, Sala E, Barrett T(2021) MRI-derived radiomics model for baseline prediction of prostate cancer progression on active surveillance Sci Rep 11:12917
pubmed: 34155265 pmcid: 8217549 doi: 10.1038/s41598-021-92341-6
Sushentsev N, Rundo L, Blyuss O et al (2021) Comparative performance of MRI-derived PRECISE scores and delta-radiomics models for the prediction of prostate cancer progression in patients on active surveillance Eur Radiol 32:680–689
Sushentsev N, Rundo L, Abrego L et al (2023) Time series radiomics for the prediction of prostate cancer progression in patients on active surveillance. Eur Radiol 33:3792–3800
Roest C, Kwee TC, Saha A, Fütterer JJ, Yakar D, Huisman H (2023) AI-assisted biparametric MRI surveillance of prostate cancer: feasibility study. Eur Radiol 33:89–96
pubmed: 35960339 doi: 10.1007/s00330-022-09032-7
Rajwa P, Pradere B, Quhal F et al (2021) Reliability of serial prostate magnetic resonance imaging to detect prostate cancer progression during active surveillance: a systematic review and meta-analysis. Eur Urol 80:549–563
Sushentsev N, Caglic I, Rundo L et al (2022) Serial changes in tumour measurements and apparent diffusion coefficients in prostate cancer patients on active surveillance with and without histopathological progression. Br J Radiol 95:20210842
pubmed: 34538077 doi: 10.1259/bjr.20210842
Giganti F, Allen C, Stavrinides V et al (2021) Tumour growth rates of prostate cancer during active surveillance: is there a difference between MRI-visible low and intermediate-risk disease? Br J Radiol 95:20210321

Auteurs

Iztok Caglic (I)

Department of Radiology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom.

Nikita Sushentsev (N)

Department of Radiology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom.
Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Tom Syer (T)

Department of Radiology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom.
Department of Radiology, University of Cambridge, Cambridge, United Kingdom.

Kang-Lung Lee (KL)

Department of Radiology, University of Cambridge, Cambridge, United Kingdom.
Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan.
School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Tristan Barrett (T)

Department of Radiology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge, United Kingdom. tb507@medschl.cam.ac.uk.
Department of Radiology, University of Cambridge, Cambridge, United Kingdom. tb507@medschl.cam.ac.uk.

Classifications MeSH