Development and validation of a clinical decision support system based on PSA, microRNAs, and MRI for the detection of prostate cancer.

Clinical decision support system Detection Magnetic resonance imaging Prostate cancer microRNA

Journal

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

Informations de publication

Date de publication:
04 Jan 2024
Historique:
received: 12 04 2023
accepted: 02 12 2023
revised: 29 11 2023
medline: 5 1 2024
pubmed: 5 1 2024
entrez: 4 1 2024
Statut: aheadofprint

Résumé

The aims of this study are to develop and validate a clinical decision support system based on demographics, prostate-specific antigen (PSA), microRNA (miRNA), and MRI for the detection of prostate cancer (PCa) and clinical significant (cs) PCa, and to assess if this system performs better compared to MRI alone. This retrospective, multicenter, observational study included 222 patients (mean age 66, range 46-75 years) who underwent prostate MRI, miRNA (let-7a-5p and miR-103a-3p) assessment, and biopsy. Monoparametric and multiparametric models including age, PSA, miRNA, and MRI outcome were trained on 65% of the data and then validated on the remaining 35% to predict both PCa (any Gleason grade [GG]) and csPCa (GG ≥ 2 vs GG = 1/negative). Accuracy, sensitivity, specificity, positive and negative predictive value (NPV), and area under the receiver operating characteristic curve were calculated. MRI outcome was the best predictor in the monoparametric model for both detection of PCa, with sensitivity of 90% (95%CI 73-98%) and NPV of 93% (95%CI 82-98%), and for csPCa identification, with sensitivity of 91% (95%CI 72-99%) and NPV of 95% (95%CI 84-99%). Sensitivity and NPV of PSA + miRNA for the detection of csPCa were not statistically different from the other models including MRI alone. MRI stand-alone yielded the best prediction models for both PCa and csPCa detection in biopsy-naïve patients. The use of miRNAs let-7a-5p and miR-103a-3p did not improve classification performances compared to MRI stand-alone results. The use of miRNA (let-7a-5p and miR-103a-3p), PSA, and MRI in a clinical decision support system (CDSS) does not improve MRI stand-alone performance in the detection of PCa and csPCa. • Clinical decision support systems including MRI improve the detection of both prostate cancer and clinically significant prostate cancer with respect to PSA test and/or microRNA. • The use of miRNAs let-7a-5p and miR-103a-3p did not significantly improve MRI stand-alone performance. • Results of this study were in line with previous works on MRI and microRNA.

Identifiants

pubmed: 38177618
doi: 10.1007/s00330-023-10542-1
pii: 10.1007/s00330-023-10542-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : HORIZON EUROPE Framework Programme
ID : 952159
Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : MFAG 11742
Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : 20398

Informations de copyright

© 2024. The Author(s).

Références

Siegel RL, Miller KD, Fuchs HE, Jemal A (2022) Cancer statistics, 2022. CA Cancer J Clin 72:7–33. https://doi.org/10.3322/caac.21708
doi: 10.3322/caac.21708 pubmed: 35020204
Dyba T, Randi G, Bray F et al (2021) The European cancer burden in 2020: incidence and mortality estimates for 40 countries and 25 major cancers. Eur J Cancer 157:308–347. https://doi.org/10.1016/j.ejca.2021.07.039
doi: 10.1016/j.ejca.2021.07.039 pubmed: 34560371 pmcid: 8568058
Mottet N, Cornford P (2022) EAU guidelines. Edn. Presented at the EAU Annual Congress Amsterdam 2022. Arnhem, Netherlands
Eastham JA, Auffenberg GB, Barocas DA et al (2022) Clinically localized prostate cancer: AUA/ASTRO guideline, part I: introduction, risk assessment, staging, and risk-based management. J Urol 208:10–18. https://doi.org/10.1097/JU.0000000000002757
doi: 10.1097/JU.0000000000002757 pubmed: 35536144
Callender T, Emberton M, Morris S et al (2021) Benefit, harm, and cost-effectiveness associated with magnetic resonance imaging before biopsy in age-based and risk-stratified screening for prostate cancer. JAMA Netw Open 4. https://doi.org/10.1001/jamanetworkopen.2020.37657
Ahmed HU, El-Shater Bosaily A, Brown LC et al (2017) Diagnostic accuracy of multi-parametric MRI and TRUS biopsy in prostate cancer (PROMIS): a paired validating confirmatory study. Lancet 389:815–822. https://doi.org/10.1016/S0140-6736(16)32401-1
doi: 10.1016/S0140-6736(16)32401-1 pubmed: 28110982
van der Leest M, Cornel E, Israël B et al (2019) Head-to-head comparison of transrectal ultrasound-guided prostate biopsy versus multiparametric prostate resonance imaging with subsequent magnetic resonance-guided biopsy in biopsy-naïve men with elevated prostate-specific antigen: a large prospective multicenter clinical study(figure presented.). Eur Urol 75:570–578. https://doi.org/10.1016/j.eururo.2018.11.023
doi: 10.1016/j.eururo.2018.11.023 pubmed: 30477981
Rouvière O, Puech P, Renard-Penna R et al (2019) Use of prostate systematic and targeted biopsy on the basis of multiparametric MRI in biopsy-naive patients (MRI-FIRST): a prospective, multicentre, paired diagnostic study. Lancet Oncol 20:100–109. https://doi.org/10.1016/S1470-2045(18)30569-2
doi: 10.1016/S1470-2045(18)30569-2 pubmed: 30470502
Houlahan KE, Salmasi A, Sadun TY et al (2019) Molecular hallmarks of multiparametric magnetic resonance imaging visibility in prostate cancer. Eur Urol 76:18–23. https://doi.org/10.1016/j.eururo.2018.12.036
doi: 10.1016/j.eururo.2018.12.036 pubmed: 30685078 pmcid: 10228592
Bertelli E, Mercatelli L, Marzi C et al (2022) Machine and deep learning prediction of prostate cancer aggressiveness using multiparametric MRI. Front Oncol 11. https://doi.org/10.3389/fonc.2021.802964
Porzycki P, Ciszkowicz E (2020) Modern biomarkers in prostate cancer diagnosis. Cent Eur J Urol 73:300–306. https://doi.org/10.5173/ceju.2020.0067R
doi: 10.5173/ceju.2020.0067R
Keck B, Borkowetz A, Poellmann J et al (2021) Serum miRNAs support the indication for MRI‐ultrasound fusion‐guided biopsy of the prostate in patients with low‐PI‐RADS lesions. Cells 10. https://doi.org/10.3390/cells10061315
Mello-Grand M, Bruno A, Sacchetto L et al (2021) Two novel ceramide-like molecules and miR-5100 levels as biomarkers improve prediction of prostate cancer in gray-zone PSA. Front Oncol 11:1–9. https://doi.org/10.3389/fonc.2021.769158
Mello-Grand M, Gregnanin I, Sacchetto L et al (2019) Circulating microRNAs combined with PSA for accurate and non-invasive prostate cancer detection. Carcinogenesis 40:246–253. https://doi.org/10.1093/carcin/bgy167
doi: 10.1093/carcin/bgy167 pubmed: 30452625
Van Wijk Y, Halilaj I, Van Limbergen E et al (2019) Decision support systems in prostate cancer treatment: an overview. Biomed Res Int. https://doi.org/10.1155/2019/4961768
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. https://doi.org/10.1016/j.eururo.2019.02.033
doi: 10.1016/j.eururo.2019.02.033 pubmed: 30898406
Deng Y, Zhu Y, Wang H et al (2019) Ratio-based method to identify true biomarkers by normalizing circulating ncRNA sequencing and quantitative PCR data HHS public access. Anal Chem 91:6746–6753. https://doi.org/10.1021/acs.anal-chem.9b00821
doi: 10.1021/acs.anal-chem.9b00821 pubmed: 31002238 pmcid: 6884007
Porpiglia F, De Luca S, Passera R et al (2016) Multiparametric-magnetic resonance/ultrasound fusion targeted prostate biopsy improves agreement between biopsy and radical prostatectomy Gleason score. Anticancer Res 36:4833–4839. https://doi.org/10.21873/anticanres.11045
doi: 10.21873/anticanres.11045 pubmed: 27630337
Manfredi M, Bernardo T, Moretti C et al (2015) MRI/TRUS fusion software-based targeted biopsy: the new standard of care? Minerva Urol Nefrol 67(3):233–46
pubmed: 26013952
Rodríguez-Covarrubias F, González-Ramírez A, Aguilar-Davidov B et al (2011) Extended sampling at first biopsy improves cancer detection rate: results of a prospective, randomized trial comparing 12 versus 18-core prostate biopsy. J Urol 185:2132–2136. https://doi.org/10.1016/j.juro.2011.02.010
doi: 10.1016/j.juro.2011.02.010 pubmed: 21496851
Nicoletti G, Barra D, Defeudis A et al (2021) Virtual biopsy in prostate cancer: can machine learning distinguish low and high aggressive tumors on MRI? Annu Int Conf IEEE Eng Med Biol Soc 20213374–3377. https://doi.org/10.1109/EMBC46164.2021.9630988
Defeudis A, Panic J, Nicoletti G et al (2023) Virtual biopsy in abdominal pathology: where do we stand? Br J Radiol BJR Open 1–10. https://doi.org/10.1259/bjro.20220055
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. https://doi.org/10.1016/j.euo.2021.03.007
doi: 10.1016/j.euo.2021.03.007 pubmed: 33893066
Kong D, Heath E, Chen W et al (2012) Loss of let-7 up-regulates EZH2 in prostate cancer consistent with the acquisition of cancer stem cell signatures that are attenuated by BR-DIM. PLoS One 7. https://doi.org/10.1371/journal.pone.0033729
Ge J, Mao L, Xu W et al (2021) miR-103a-3p suppresses cell proliferation and invasion by targeting tumor protein D52 in prostate cancer. J Investig Surg 34:984–992. https://doi.org/10.1080/08941939.2020.1738602
doi: 10.1080/08941939.2020.1738602
Pecoraro M, Catanzaro G, Conte F et al (2023) Prospective validation study of a novel integrated pathway based on clinical features, magnetic resonance imaging biomarkers, and microRNAs for early detection of prostate cancer. Eur Urol Oncol. https://doi.org/10.1016/j.euo.2023.05.008

Auteurs

Simone Mazzetti (S)

Radiology Unit, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Department of Surgical Sciences, University of Turin, Turin, Italy.

Arianna Defeudis (A)

Radiology Unit, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy. arianna.defeudis@unito.it.
Department of Surgical Sciences, University of Turin, Turin, Italy. arianna.defeudis@unito.it.

Giulia Nicoletti (G)

Department of Surgical Sciences, University of Turin, Turin, Italy.
Department of Electronics and Telecommunications, Polytechnic of Turin, Turin, Italy.

Giovanna Chiorino (G)

Cancer Genomics Lab, Fondazione Edo ed Elvo Tempia, Biella, Italy.

Stefano De Luca (S)

Department of Urology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Riccardo Faletti (R)

Radiology Unit, Department of Surgical Sciences, University of Turin, Turin, Italy.

Marco Gatti (M)

Radiology Unit, Department of Surgical Sciences, University of Turin, Turin, Italy.

Paolo Gontero (P)

Division of Urology, Department of Surgical Sciences, University of Turin, Turin, Italy.

Matteo Manfredi (M)

Department of Urology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Maurizia Mello-Grand (M)

Cancer Genomics Lab, Fondazione Edo ed Elvo Tempia, Biella, Italy.

Caterina Peraldo-Neia (C)

Cancer Genomics Lab, Fondazione Edo ed Elvo Tempia, Biella, Italy.

Andrea Zitella (A)

Division of Urology, Department of Surgical Sciences, University of Turin, Turin, Italy.

Francesco Porpiglia (F)

Department of Urology, San Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.

Daniele Regge (D)

Radiology Unit, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.

Valentina Giannini (V)

Radiology Unit, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
Department of Surgical Sciences, University of Turin, Turin, Italy.

Classifications MeSH