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PSMA PET/CT and PET/MRI in primary staging of prostate cancer and its effect on patient management

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Abstract

Purpose

In the last decade, prostate specific membrane antigen (PSMA) positron emission tomography (PET) has gained its role as a novel tool in the primary staging of prostate cancer (PCa). This review focuses on the current knowledge on PSMA PET in primary PCa staging, which includes the Tumor-, Node-, Metastasis- (T-, N-, M-) staging, and the impact of PSMA PET on patient management.

Methods

A literature search was performed in all databases of Web of Science for peer-reviewed, original studies published in English until June 2022. The results were screened by abstract in the setting of primary staging of PCa, using PSMA PET tracers for imaging modalities PET/computed tomography (CT) and PET/magnetic resonance imaging (MRI).

Results

The available literature shows that PSMA PET is an accurate test in the primary staging of PCa. For T-staging, the combination of PSMA PET with the current gold standard multi-parametric MRI (mpMRI) may have a synergistic impact for assessment of tumor volume. For N- and M-staging, multiple studies show that PSMA PET clearly outperforms current conventional imaging modalities, which is also confirmed in the proPSMA randomized controlled trial that revealed a 27% higher accuracy of PSMA PET compared to conventional imaging. Several studies show that PSMA PET, due to its high accuracy, can lead to treatment adaption.

Conclusions

Despite the clear superiority of PSMA PET over conventional imaging for primary staging of intermediate- and high-risk PCa, PSMA PET is currently not yet identified as the gold standard imaging modality in this setting in the European Association of Urology (EAU) guidelines, given that no prospective studies demonstrating a clear benefit of treatment adaptation are available at this moment. The results of prospective trials exploring the benefit of PSMA PET-based treatment algorithms are, therefore, strongly awaited.

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References

  1. Rawla P (2019) Epidemiology of prostate Cancer. World J Oncol 10:63–89. https://doi.org/10.14740/wjon1191

  2. Artibani W, Porcaro AB, De Marco V et al (2018) Management of biochemical recurrence after primary curative treatment for prostate cancer: a review. Urol Int 100:251–262. https://doi.org/10.1159/000481438

    Article  CAS  PubMed  Google Scholar 

  3. EAU Guidelines. Edn. presented at the EAU Annual Congress Milan 2023

  4. Hövels AM, Heesakkers RAM, Adang EM et al (2008) The diagnostic accuracy of CT and MRI in the staging of pelvic lymph nodes in patients with prostate cancer: a meta-analysis. Clin Radiol 63:387–395. https://doi.org/10.1016/j.crad.2007.05.022

    Article  PubMed  Google Scholar 

  5. Clinckaert A, Callens K, Cooreman A, et al (2022) The prevalence of lower limb and genital lymphedema after prostate cancer treatment: a systematic review. Cancers (Basel). https://doi.org/10.3390/cancers14225667

  6. Fossati N, Willemse P-PM, van den Broeck T et al (2017) The benefits and harms of different extents of lymph node dissection during radical prostatectomy for prostate cancer: a systematic review. Eur Urol 72:84–109. https://doi.org/10.1016/j.eururo.2016.12.003

    Article  PubMed  Google Scholar 

  7. Hofman MS, Lawrentschuk N, Francis RJ et al (2020) Prostate-specific membrane antigen PET-CT in patients with high-risk prostate cancer before curative-intent surgery or radiotherapy (proPSMA): a prospective, randomised, multicentre study. The Lancet 395:1208–1216. https://doi.org/10.1016/S0140-6736(20)30314-7

    Article  CAS  Google Scholar 

  8. Fendler WP, Calais J, Eiber M et al (2019) Assessment of 68Ga-PSMA-11 PET accuracy in localizing recurrent prostate cancer: a prospective single-arm clinical trial. JAMA Oncol 5:856–863. https://doi.org/10.1001/jamaoncol.2019.0096

    Article  PubMed  PubMed Central  Google Scholar 

  9. Werner RA, Derlin T, Lapa C et al (2020) (18)F-Labeled, PSMA-targeted radiotracers: leveraging the advantages of radiofluorination for prostate cancer molecular imaging. Theranostics 10:1–16. https://doi.org/10.7150/thno.37894

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Sanchez-Crespo A (2013) Comparison of Gallium-68 and Fluorine-18 imaging characteristics in positron emission tomography. Appl Radiat Isot 76:55–62. https://doi.org/10.1016/j.apradiso.2012.06.034

    Article  CAS  PubMed  Google Scholar 

  11. James D. Brierley (2017) TNM classification of malignant tumors, 8th ed. UICC International Union Against Cancer

  12. Johnson DC, Raman SS, Mirak SA et al (2019) Detection of individual prostate cancer foci via multiparametric magnetic resonance imaging. Eur Urol 75:712–720. https://doi.org/10.1016/j.eururo.2018.11.031

    Article  CAS  PubMed  Google Scholar 

  13. Priester A, Natarajan S, Khoshnoodi P et al (2017) Magnetic resonance imaging underestimation of prostate cancer geometry: use of patient specific molds to correlate images with whole mount pathology. J Urol 197:320–326. https://doi.org/10.1016/j.juro.2016.07.084

    Article  PubMed  Google Scholar 

  14. Eiber M, Weirich G, Holzapfel K et al (2016) Simultaneous (68)Ga-PSMA HBED-CC PET/MRI improves the localization of primary prostate cancer. Eur Urol 70:829–836. https://doi.org/10.1016/j.eururo.2015.12.053

    Article  CAS  PubMed  Google Scholar 

  15. Berger I, Annabattula C, Lewis J et al (2018) 68Ga-PSMA PET/CT vs. mpMRI for locoregional prostate cancer staging: correlation with final histopathology. Prostate Cancer Prostatic Dis 21:204–211. https://doi.org/10.1038/s41391-018-0048-7

    Article  CAS  PubMed  Google Scholar 

  16. Muehlematter UJ, Burger IA, Becker AS et al (2019) Diagnostic accuracy of multiparametric MRI versus 68Ga-PSMA-11 PET/MRI for extracapsular extension and seminal vesicle invasion in patients with prostate cancer. Radiology 293:350–358. https://doi.org/10.1148/radiol.2019190687

    Article  PubMed  Google Scholar 

  17. Zamboglou C, Drendel V, Jilg CA et al (2017) Comparison of (68)Ga-HBED-CC PSMA-PET/CT and multiparametric MRI for gross tumour volume detection in patients with primary prostate cancer based on slice by slice comparison with histopathology. Theranostics 7:228–237. https://doi.org/10.7150/thno.16638

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Jansen BHE, Bodar YJL, Zwezerijnen GJC et al (2021) Pelvic lymph-node staging with 18F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer—the SALT trial. Eur J Nucl Med Mol Imaging 48:509–520. https://doi.org/10.1007/s00259-020-04974-w

    Article  CAS  PubMed  Google Scholar 

  19. Chun FK-H, Karakiewicz PI, Briganti A, et al (2006) Prostate cancer nomograms: an update. Eur Urol 50:914–26; discussion 926. https://doi.org/10.1016/j.eururo.2006.07.042

  20. Milonas D, Venclovas Z, Muilwijk T et al (2020) External validation of Memorial Sloan Kettering Cancer Center nomogram and prediction of optimal candidate for lymph node dissection in clinically localized prostate cancer. Cent European J Urol 73:19–25. https://doi.org/10.5173/ceju.2020.0079

    Article  PubMed  PubMed Central  Google Scholar 

  21. Gandaglia G, Martini A, Ploussard G et al (2020) External validation of the 2019 briganti nomogram for the identification of prostate cancer patients who should be considered for an extended pelvic lymph node dissection. Eur Urol 78:138–142. https://doi.org/10.1016/j.eururo.2020.03.023

    Article  PubMed  Google Scholar 

  22. Gandaglia G, Fossati N, Zaffuto E et al (2017) Development and internal validation of a novel model to identify the candidates for extended pelvic lymph node dissection in prostate cancer. Eur Urol 72:632–640. https://doi.org/10.1016/j.eururo.2017.03.049

    Article  PubMed  Google Scholar 

  23. Burkhard FC, Schumacher M, Studer UE (2005) The role of lymphadenectomy in prostate cancer. Nat Clin Pract Urol 2:336–342. https://doi.org/10.1038/ncpuro0245

    Article  PubMed  Google Scholar 

  24. Loeb S, Partin AW, Schaeffer EM (2010) Complications of pelvic lymphadenectomy: do the risks outweigh the benefits? Rev Urol 12:20–24

    PubMed  PubMed Central  Google Scholar 

  25. Briganti A, Larcher A, Abdollah F et al (2012) Updated nomogram predicting lymph node invasion in patients with prostate cancer undergoing extended pelvic lymph node dissection: the essential importance of percentage of positive cores. Eur Urol 61:480–487. https://doi.org/10.1016/j.eururo.2011.10.044

    Article  PubMed  Google Scholar 

  26. Hope TA, Eiber M, Armstrong WR et al (2021) Diagnostic accuracy of 68Ga-PSMA-11 PET for pelvic nodal metastasis detection prior to radical prostatectomy and pelvic lymph node dissection: a multicenter prospective phase 3 imaging trial. JAMA Oncol 7:1635–1642. https://doi.org/10.1001/jamaoncol.2021.3771

    Article  PubMed  PubMed Central  Google Scholar 

  27. Kasivisvanathan V, Murphy DG, Link E, et al (2023) A1237: Baseline PSMA PET-CT is prognostic for treatment failure in men with intermediate-to-high risk prostate cancer: 54 months follow-up of the proPSMA randomised trial. 38th Annual EAU Congress, Milan

  28. Ferraro DA, Muehlematter UJ, Garcia Schüler HI et al (2020) 68Ga-PSMA-11 PET has the potential to improve patient selection for extended pelvic lymph node dissection in intermediate to high-risk prostate cancer. Eur J Nucl Med Mol Imaging 47:147–159. https://doi.org/10.1007/s00259-019-04511-4

    Article  PubMed  Google Scholar 

  29. Wang Y, Tang Y, Gao X et al (2022) Optimization of prostate cancer patient lymph node staging via the integration of neutrophil-lymphocyte ratios, platelet-lymphocyte ratios, and (68)Ga-PSMA-PET-derived SUVmax values. Prostate 82:1415–1421. https://doi.org/10.1002/pros.24415

    Article  CAS  PubMed  Google Scholar 

  30. Hinsenveld FJ, Wit EMK, van Leeuwen PJ et al (2020) Prostate-specific membrane antigen PET/CT combined with sentinel node biopsy for primary lymph node staging in prostate cancer. J Nucl Med 61:540–545. https://doi.org/10.2967/jnumed.119.232199

    Article  CAS  PubMed  Google Scholar 

  31. Muraglia L, Mattana F, Zuccotti G et al (2023) Prostate-specific membrane antigen (PSMA) radioguided surgery in prostate cancer: an overview of current application and future perspectives. Clin Transl Imaging 11:255–261. https://doi.org/10.1007/s40336-023-00558-4

    Article  Google Scholar 

  32. Shen G, Deng H, Hu S, Jia Z (2014) Comparison of choline-PET/CT, MRI, SPECT, and bone scintigraphy in the diagnosis of bone metastases in patients with prostate cancer: a meta-analysis. Skeletal Radiol 43:1503–1513. https://doi.org/10.1007/s00256-014-1903-9

    Article  PubMed  Google Scholar 

  33. McLoughlin LC, O’Kelly F, O’Brien C et al (2016) The improved accuracy of planar bone scintigraphy by adding single photon emission computed tomography (SPECT-CT) to detect skeletal metastases from prostate cancer. Ir J Med Sci 185:101–105. https://doi.org/10.1007/s11845-014-1228-7

    Article  CAS  PubMed  Google Scholar 

  34. Anttinen M, Ettala O, Malaspina S et al (2021) A prospective comparison of 18F-prostate-Specific Membrane Antigen-1007 Positron Emission Tomography Computed Tomography, Whole-body 1.5 T Magnetic Resonance Imaging with Diffusion-weighted Imaging, and Single-photon Emission Computed Tomography/Computed. Eur Urol Oncol 4:635–644. https://doi.org/10.1016/j.euo.2020.06.012

    Article  PubMed  Google Scholar 

  35. de Galiza BF, Queiroz MA, Nunes RF et al (2020) Nonprostatic diseases on PSMA PET imaging: a spectrum of benign and malignant findings. Cancer Imaging 20:23. https://doi.org/10.1186/s40644-020-00300-7

    Article  Google Scholar 

  36. De Coster L, Sciot R, Everaerts W et al (2017) Fibrous dysplasia mimicking bone metastasis on 68GA-PSMA PET/MRI. Eur J Nucl Med Mol Imaging 44:1607–1608. https://doi.org/10.1007/s00259-017-3712-6

    Article  PubMed  Google Scholar 

  37. Rauscher I, Krönke M, König M et al (2020) Matched-pair comparison of (68)Ga-PSMA-11 PET/CT and (18)F-PSMA-1007 PET/CT: frequency of pitfalls and detection efficacy in biochemical recurrence after radical prostatectomy. J Nucl Med 61:51–57. https://doi.org/10.2967/jnumed.119.229187

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Zacho HD, Ravn S, Afshar-Oromieh A, et al (2020) Added value of 68Ga-PSMA PET/CT for the detection of bone metastases in patients with newly diagnosed prostate cancer and a previous 99mTc bone scintigraphy. EJNMMI Res. https://doi.org/10.1186/s13550-020-00618-0

  39. Seifert R, Telli T, Opitz M, et al (2022) Non-specific PSMA-1007 bone uptake evaluated through PSMA-11 PET, bone scan and MRI triple validation in patients with biochemical recurrence of prostate cancer. J Nucl Med. https://doi.org/10.2967/jnumed.118.215434

  40. Cardinale J, Schäfer M, Benešová M et al (2017) Preclinical evaluation of 18F-PSMA-1007, a new prostate-specific membrane antigen ligand for prostate cancer imaging. J Nucl Med 58:425–431. https://doi.org/10.2967/jnumed.116.181768

    Article  CAS  PubMed  Google Scholar 

  41. Roach PJ, Francis R, Emmett L et al (2018) The impact of 68Ga-PSMA PET/CT on management intent in prostate cancer: results of an Australian prospective multicenter study. J Nucl Med 59:82–88. https://doi.org/10.2967/jnumed.117.197160

    Article  CAS  PubMed  Google Scholar 

  42. Koerber SA, Will L, Kratochwil C et al (2019) 68Ga-PSMA-11 PET/CT in primary and recurrent prostate carcinoma: implications for radiotherapeutic management in 121 patients. J Nucl Med 60:234–240. https://doi.org/10.2967/jnumed.118.211086

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Ferraro DA, Garcia Schüler HI, Muehlematter UJ et al (2020) Impact of 68Ga-PSMA-11 PET staging on clinical decision-making in patients with intermediate or high-risk prostate cancer. Eur J Nucl Med Mol Imaging 47:652–664. https://doi.org/10.1007/s00259-019-04568-1

    Article  CAS  PubMed  Google Scholar 

  44. Moradi F, Duan H, Song H, et al (2022) 68Ga-PSMA-11 PET/MRI in patients with newly diagnosed intermediate- or high-risk prostate adenocarcinoma: PET findings correlate with outcomes after definitive treatment. J Nucl Med 63:1822 LP–1828. https://doi.org/10.2967/jnumed.122.263897

  45. Xiang M, Ma TM, Savjani R et al (2021) Performance of a prostate-specific membrane antigen positron emission tomography/computed tomography-derived risk-stratification tool for high-risk and very high-risk prostate cancer. JAMA Netw Open 4:e2138550. https://doi.org/10.1001/jamanetworkopen.2021.38550

    Article  PubMed  PubMed Central  Google Scholar 

  46. Hicks RJ, Murphy DG, Williams SG (2017) Seduction by sensitivity: reality, illusion, or delusion? The challenge of assessing outcomes after psma imaging selection of patients for treatment. J Nucl Med 58:1969–1971. https://doi.org/10.2967/jnumed.117.198812

    Article  CAS  PubMed  Google Scholar 

  47. Szigeti F, Schweighofer-Zwink G, Meissnitzer M et al (2022) Incremental impact of [68Ga]Ga-PSMA-11 PET/CT in primary N and M staging of prostate cancer prior to curative-intent surgery: a prospective clinical trial in comparison with mpMRI. Mol Imaging Biol 24:50–59. https://doi.org/10.1007/s11307-021-01650-9

    Article  CAS  PubMed  Google Scholar 

  48. Buyyounouski MK, Choyke PL, McKenney JK, et al (2017) Prostate cancer—major changes in the American Joint Committee on Cancer eighth edition cancer staging manual. CA Cancer J Clin 67:245–253. https://doi.org/10.3322/caac.21391

  49. Grubmuller B, Baltzer P, Hartenbach S et al (2018) PSMA ligand PET/MRI for primary prostate cancer: staging performance and clinical impact. Clin Cancer Res 24:6300–6307. https://doi.org/10.1158/1078-0432.CCR-18-0768

    Article  PubMed  Google Scholar 

  50. Koseoglu E, Kordan Y, Kilic M et al (2021) Diagnostic ability ofGa-68 PSMA PET to detect dominant and non-dominant tumors, upgrading and adverse pathology in patients with PIRADS 4–5 index lesions undergoing radical prostatectomy. Prostate Cancer Prostatic Dis 24:202–209. https://doi.org/10.1038/s41391-020-00270-8

    Article  CAS  PubMed  Google Scholar 

  51. Skawran SM, Sanchez V, Ghafoor S, et al (2022) Primary staging in patients with intermediate- and high-risk prostate cancer: multiparametric MRI and 68Ga-PSMA-PET/MRI—What is the value of quantitative data from multiparametric MRI alone or in conjunction with clinical information? Eur J Radiol. https://doi.org/10.1016/j.ejrad.2021.110044

  52. Ucar T, Gunduz N, Demirci E, et al (2022) Comparison of 68Ga-PSMA PET/CT and mp-MRI in regard to local staging for prostate cancer with histopathological results: a retrospective study. Prostate 82:1462–1468. https://doi.org/10.1002/pros.24420

  53. Klingenberg S, Jochumsen MR, Ulhøi BP et al (2021) 68Ga-PSMA PET/CT for primary lymph node and distant metastasis NM staging of high-risk prostate cancer. J Nucl Med 62:214–220. https://doi.org/10.2967/jnumed.120.245605

    Article  CAS  PubMed  Google Scholar 

  54. Langbein T, Wang H, Rauscher I et al (2022) Utility of (18)F-rhPSMA-7.3 PET for imaging of primary prostate cancer and preoperative efficacy in N-staging of unfavorable intermediate- to very high-risk patients validated by histopathology. J Nucl Med 63:1334–1342. https://doi.org/10.2967/jnumed.121.263440

    Article  CAS  PubMed  Google Scholar 

  55. Franklin A, Yaxley WJ, Raveenthiran S et al (2021) Histological comparison between predictive value of preoperative 3-T multiparametric MRI and 68Ga-PSMA PET/CT scan for pathological outcomes at radical prostatectomy and pelvic lymph node dissection for prostate cancer. BJU Int 127:71–79. https://doi.org/10.1111/bju.15134

    Article  CAS  PubMed  Google Scholar 

  56. Yaxley JW, Raveenthiran S, Nouhaud FX et al (2019) Outcomes of primary lymph node staging of intermediate and high risk prostate cancer with 68Ga-PSMA positron emission tomography/computerized tomography compared to histological correlation of pelvic lymph node pathology. J Urol 201:815–820. https://doi.org/10.1097/JU.0000000000000053

    Article  PubMed  Google Scholar 

  57. Wang H, Amiel T, Würnschimmel C, et al (2021) PSMA-ligand uptake can serve as a novel biomarker in primary prostate cancer to predict outcome after radical prostatectomy. EJNMMI Res. https://doi.org/10.1186/s13550-021-00818-2

  58. Lenis AT, Pooli A, Lec PM et al (2022) Prostate-specific membrane antigen positron emission tomography/computed tomography compared with conventional imaging for initial staging of treatment-naïve intermediate- and high-risk prostate cancer: a retrospective single-center study. Eur Urol Oncol 5:544–552. https://doi.org/10.1016/j.euo.2020.08.012

    Article  PubMed  Google Scholar 

  59. van Kalmthout LWM, van Melick HHE, Lavalaye J et al (2020) Prospective validation of Gallium-68 prostate specific membrane antigen-positron emission tomography/computerized tomography for primary staging of prostate cancer. J Urol 203:537–544. https://doi.org/10.1097/JU.0000000000000531

    Article  PubMed  Google Scholar 

  60. Hermsen R, Wedick EBC, Vinken MJM et al (2022) Lymph node staging with fluorine-18 prostate specific membrane antigen 1007-positron emission tomography/computed tomography in newly diagnosed intermediate- to high-risk prostate cancer using histopathological evaluation of extended pelvic node dissecti. Eur J Nucl Med Mol Imaging 49:3929–3937. https://doi.org/10.1007/s00259-022-05827-4

    Article  CAS  PubMed  Google Scholar 

  61. Uprimny C, Kroiss AS, Decristoforo C et al (2017) 68Ga-PSMA-11 PET/CT in primary staging of prostate cancer: PSA and Gleason score predict the intensity of tracer accumulation in the primary tumour. Eur J Nucl Med Mol Imaging 44:941–949. https://doi.org/10.1007/s00259-017-3631-6

    Article  CAS  PubMed  Google Scholar 

  62. Kopp J, Kopp D, Bernhardt E et al (2020) 68Ga-PSMA PET/CT based primary staging and histological correlation after extended pelvic lymph node dissection at radical prostatectomy. World J Urol 38:3085–3090. https://doi.org/10.1007/s00345-020-03131-0

    Article  CAS  PubMed  Google Scholar 

  63. Sprute K, Kramer V, Koerber SA et al (2021) Diagnostic accuracy of 18F-PSMA-1007 PET/CT imaging for lymph node staging of prostate carcinoma in primary and biochemical recurrence. J Nucl Med 62:208–213. https://doi.org/10.2967/jnumed.120.246363

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Cytawa W, Seitz AK, Kircher S et al (2020) 68Ga-PSMA I&T PET/CT for primary staging of prostate cancer. Eur J Nucl Med Mol Imaging 47:168–177. https://doi.org/10.1007/s00259-019-04524-z

    Article  CAS  PubMed  Google Scholar 

  65. Van Damme J, Tombal B, Collette L, et al (2021) Comparison of (68)Ga-prostate specific membrane antigen (PSMA) positron emission tomography computed tomography (PET-CT) and whole-body magnetic resonance imaging (WB-MRI) with diffusion sequences (DWI) in the staging of advanced prostate cancer. Cancers (Basel). https://doi.org/10.3390/cancers13215286

  66. Malaspina S, Anttinen M, Taimen P et al (2021) Prospective comparison of 18 F-PSMA-1007 PET/CT, whole-body MRI and CT in primary nodal staging of unfavourable intermediate-and high-risk prostate cancer. Eur J Nucl Med Mol Imaging 48:2951–2959. https://doi.org/10.1007/s00259-021-05296-1/Published

    Article  PubMed  PubMed Central  Google Scholar 

  67. Kroenke M, Wurzer A, Schwamborn K et al (2020) Histologically confirmed diagnostic efficacy of 18F-rhPSMA-7 PET for N-staging of patients with primary high-risk prostate cancer. J Nucl Med 61:710–715. https://doi.org/10.2967/jnumed.119.234906

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Kulkarni SC, Sundaram PS, Padma S (2020) In primary lymph nodal staging of patients with high-risk and intermediate-risk prostate cancer, how critical is the role ofGallium-68 prostate-specific membrane antigen positron emission tomography-computed tomography? Nucl Med Commun 139–146. https://doi.org/10.1097/MNM.0000000000001110

  69. Erdem S, Simsek DH, Degirmenci E et al (2022) How accurate is 68Gallium-prostate specific membrane antigen positron emission tomography/computed tomography (68Ga-PSMA PET/CT) on primary lymph node staging before radical prostatectomy in intermediate and high risk prostate cancer? A study of patient. Urol Oncol Semin Original Investig 40:6.e1-6.e9. https://doi.org/10.1016/j.urolonc.2021.07.006

    Article  CAS  Google Scholar 

  70. Zhang Q, Zang S, Zhang C et al (2017) Comparison of 68Ga-PSMA-11 PET-CT with mpMRI for preoperative lymph node staging in patients with intermediate to high-risk prostate cancer. J Transl Med 15:1–9. https://doi.org/10.1186/s12967-017-1333-2

    Article  Google Scholar 

  71. Pyka T, Okamoto S, Dahlbender M et al (2016) Comparison of bone scintigraphy and 68Ga-PSMA PET for skeletal staging in prostate cancer. Eur J Nucl Med Mol Imaging 43:2114–2121. https://doi.org/10.1007/s00259-016-3435-0

    Article  CAS  PubMed  Google Scholar 

  72. Şimsek DH, Işik EG, Civan C, et al (2021) The impact of 68Ga-Psma PET/CT on therapy management of high risk prostate cancer. Istanbul Tip Fakultesi Dergisi 84:48–56. https://doi.org/10.26650/IUITFD.2020.831103

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Acknowledgements

NAB is a PhD fellow at the Research Foundation-Flanders (FWO), project number 1SB8923N. CMD is a senior clinical investigator at the Research Foundation-Flanders (FWO).

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Claes, P., Ahmadi Bidakhvidi, N., Giesen, A. et al. PSMA PET/CT and PET/MRI in primary staging of prostate cancer and its effect on patient management. Clin Transl Imaging 12, 31–54 (2024). https://doi.org/10.1007/s40336-023-00582-4

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