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Prostate-specific membrane antigen positron emission tomography in addition to multiparametric magnetic resonance imaging and biopsies to select prostate cancer patients for focal therapy.
Geboers, Bart; Meijer, Dennie; Counter, William; Blazevski, Alexandar; Thompson, James; Doan, Paul; Gondoputro, William; Katelaris, Athos; Haynes, Anne-Maree; Delprado, Warick; O'Neill, Gordon; Yuen, Carlo; Vis, Andre N; van Leeuwen, Pim J; Ho, Bao; Liu, Victor; Lee, Jonathan; Donswijk, Maarten L; Oprea-Lager, Daniela; Scheltema, Matthijs J; Emmett, Louise; Stricker, Phillip D.
Afiliação
  • Geboers B; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Meijer D; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Counter W; Department of Radiology and Nuclear Medicine, Amsterdam UMC (location VUmc), Amsterdam, The Netherlands.
  • Blazevski A; Department of Urology, Amsterdam UMC (location VUmc), Amsterdam, The Netherlands.
  • Thompson J; Department of Theranostics and Nuclear Medicine, St. Vincent's Hospital, Sydney, NSW, Australia.
  • Doan P; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Gondoputro W; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Katelaris A; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Haynes AM; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Delprado W; Department of Urology, St. George Hospital, Sydney, NSW, Australia.
  • O'Neill G; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Yuen C; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Vis AN; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • van Leeuwen PJ; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Ho B; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Liu V; St. Vincent's Prostate Cancer Research Centre, Sydney, NSW, Australia.
  • Lee J; Garvan Institute of Medical Research & The Kinghorn Cancer Centre, Sydney, NSW, Australia.
  • Donswijk ML; Douglas Hanly Moir Pathology, Sydney, NSW, Australia.
  • Oprea-Lager D; Department of Urology, St. Vincent's Hospital and Private Clinic, Sydney, NSW, Australia.
  • Scheltema MJ; Department of Urology, St. Vincent's Hospital and Private Clinic, Sydney, NSW, Australia.
  • Emmett L; Department of Urology, Amsterdam UMC (location VUmc), Amsterdam, The Netherlands.
  • Stricker PD; Department of Urology, Antoni van Leeuwenhoek - Netherlands Cancer Institute, Amsterdam, The Netherlands.
BJU Int ; 133 Suppl 4: 14-22, 2024 Apr.
Article em En | MEDLINE | ID: mdl-37858931
ABSTRACT

OBJECTIVE:

To evaluate the additional value of prostate-specific membrane antigen positron emission tomography (PSMA-PET) to conventional diagnostic tools to select patients for hemi-ablative focal therapy (FT). PATIENTS AND

METHODS:

We performed a retrospective analysis on a multicentre cohort (private and institutional) of 138 patients who underwent multiparametric magnetic resonance imaging (mpMRI), PSMA-PET, and systematic biopsies prior to radical prostatectomy between January 2011 and July 2021. Patients were eligible when they met the consensus criteria for FT PSA <15 ng/mL, clinical/radiological T stage ≤T2b, and International Society of Urological Pathology (ISUP) grade 2-3. Clinically significant prostate cancer (csPCa) was defined as ISUP grade ≥2, extracapsular extension >0.5 mm or seminal vesicle involvement at final histopathology. The diagnostic accuracy of mpMRI, systematic biopsies and PSMA-PET for csPCa (separate and combined) was calculated within a four-quadrant prostate model by receiver-operating characteristic and 2 × 2 contingency analysis. Additionally, we assessed whether the diagnostic tools correctly identified patients suitable for hemi-ablative FT.

RESULTS:

In total 552 prostate quadrants were analysed and 272 (49%) contained csPCa on final histopathology. The area under the curve, sensitivity, specificity, positive predictive value and negative predictive value for csPCa were 0.79, 75%, 83%, 81% and 77%, respectively, for combined mpMRI and systematic biopsies, and improved after addition of PSMA-PET to 0.84, 87%, 80%, 81% and 86%, respectively (P < 0.001). On final histopathology 46/138 patients (33%) were not suitable for hemi-ablative FT. Addition of PSMA-PET correctly identified 26/46 (57%) non-suitable patients and resulted in 4/138 (3%) false-positive exclusions.

CONCLUSIONS:

Addition of PSMA-PET to the conventional work-up by mpMRI and systematic biopsies could improve selection for hemi-ablative FT and guide exclusion of patients for whom whole-gland treatments might be a more suitable treatment option.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Imageamento por Ressonância Magnética Multiparamétrica Limite: Humans / Male Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Imageamento por Ressonância Magnética Multiparamétrica Limite: Humans / Male Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália