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Imaging Efficacy of [18F]CTT1057 PET/CT in Patients with Biochemically Recurrent Prostate Cancer: Results from GuidePath-A Phase 3, Prospective Multicenter Study

dc.contributor.authorFanti, Stefano
dc.contributor.authorRobles Barba, Javier Jesus
dc.contributor.authorBehr, Spencer
dc.contributor.authorMaurer, Tobias
dc.contributor.authorParedes Barranco, Pilar
dc.contributor.authorWalz, Jochen
dc.contributor.authorDuch, Joan
dc.contributor.authorSimo Perdigo, Marc
dc.contributor.authorMainta, Ismini Charis
dc.contributor.authorBonnefoy, Pierre Benoit
dc.contributor.authorCoulanges, Medge
dc.contributor.authorTang, Jun
dc.contributor.authorSeigne, Christelle
dc.contributor.authorWilke, Celine
dc.contributor.authorCatafau, Ana M.
dc.contributor.authorIagaru, Andrei
dc.contributor.authorAggarwal, Rahul
dc.date.accessioned2025-09-25T10:37:12Z
dc.date.issued2025-08-01
dc.date.updated2025-09-25T10:37:12Z
dc.description.abstractImproved diagnostic accuracy in patients with prostate cancer at first biochemical recurrence (BCR) with low prostate-specific antigen (PSA) levels is needed. This prospective study (GuidePath; NCT04838613) aimed to evaluate the imaging performance of the prostate-specific membrane antigen (PSMA)-targeted PET radiotracer [18F]CTT1057 to detect PSMA-positive lesions in patients diagnosed predominantly at first BCR. Methods: Eligible patients had a PSA of 0.2 ng/mL or greater after radical prostatectomy or an increase in PSA level of at least 2 ng/mL above nadir after radiation therapy. Patients received 370 MBq of [18F]CTT1057 and 150 MBq of [68Ga]Ga-PSMA-11 and underwent PET/CT 90 min (±30 min) and 50-100 after injection, respectively. [18F]CTT1057 images were assessed by 3 independent readers blinded to all clinical information. Coprimary endpoints were region-level correct localization rate (CLR) and patient-level positive predictive value (PPV) of [18F]CTT1057 to detect PSMA-positive lesions and were compared with a hierarchical composite truth standard (CTS). The CTS comprised 3 levels of standard-of-truth procedures (in order of priority): histopathology (CTS level 1); imaging, including at least 1 contrast-enhanced CT scan and 1 [68Ga]Ga-PSMA-11 PET/CT scan (CTS level 2); and a decrease in PSA level of 50% or greater 3 mo after radiation therapy (CTS level 3). For study success, the lower-bound 95% CI had to surpass 50% for region-level CLR and 20% for patient-level PPV for at least 2 of the 3 [18F]CTT1057 PET/CT readers. Results: Of 202 patients screened, 161 were evaluable for efficacy. Among these, 93.2% were experiencing their first BCR, 96.3% had received radical prostatectomy as initial definitive therapy, and baseline median PSA level was 0.4 ng/mL (interquartile range, 0.3-0.8 ng/mL). The imaging standard of truth was used for 159-160 patients (99%) across the 3 readers. Both coprimary endpoints were met. Region-level CLR ranged from 65.2% to 75.0% (lower-bound 95% CI, 53.4%-62.1%), and patient-level PPV ranged from 64.6% to 76.5% (lower-bound 95% CI, 51.8%-62.5%). Conclusion: [18F]CTT1057 met the predefined thresholds for region-level CLR and patient-level PPV in a clinically relevant patient cohort predominantly at first BCR with low PSA levels. [18F]CTT1057 is an accurate PSMA-targeted PET radiotracer for BCR detection.
dc.format.extent7 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec760681
dc.identifier.issn0161-5505
dc.identifier.pmid40473464
dc.identifier.urihttps://hdl.handle.net/2445/223386
dc.language.isoeng
dc.publisherThe Society of Nuclear Medicine and Molecular Imaging
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2967/jnumed.124.269266
dc.relation.ispartofJournal of Nuclear Medicine, 2025, vol. 66, num.8, p. 1210-1216
dc.relation.urihttps://doi.org/10.2967/jnumed.124.269266
dc.rightscc-by (c) The Society of Nuclear Medicine and Molecular Imaging, 2025
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.sourceArticles publicats en revistes (Fonaments Clínics)
dc.subject.classificationAssaigs clínics
dc.subject.classificationImatges mèdiques
dc.subject.classificationCàncer de pròstata
dc.subject.otherClinical trials
dc.subject.otherImaging systems in medicine
dc.subject.otherProstate cancer
dc.titleImaging Efficacy of [18F]CTT1057 PET/CT in Patients with Biochemically Recurrent Prostate Cancer: Results from GuidePath-A Phase 3, Prospective Multicenter Study
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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