Abstract

PurposeTo determine the impact on clinical management of patients with high-risk (HR) prostate cancer at diagnosis and patients with biochemical recurrence (BCR) using a new kit form of 68Ga-prostate-specific membrane antigen (PSMA), namely tris(hydroxypyridinone) (THP)-PSMA, with positron emission tomography-computed tomography (PET-CT).MethodsOne hundred eighteen consecutive patients (50 HR, 68 BCR) had management plans documented at a multidisciplinary meeting before 68Ga-THP-PSMA PET-CT. Patients underwent PET-CT scans 60-min post-injection of 68Ga-THP-PSMA (mean 159 ± 21.2 MBq). Post-scan management plans, Gleason score, prostate-specific antigen (PSA) and PSA doubling time (PSAdt) were recorded.ResultsHR group: 12/50 (24%) patients had management changed (9 inter-modality, 3 intra-modality). Patients with PSA < 20 μg/L had more frequent management changes (9/26, 34.6%) compared with PSA > 20 μg/L (3/24, 12.5%). Gleason scores > 8 were associated with detection of more nodal (4/16, 25% vs 5/31, 16.1%) and bone (2/16, 12.5% vs 2/31, 6.5%) metastases. BCR group: Clinical management changed in 23/68 (34%) patients (17 inter-modality, 6 intra-modality). Forty out of 68 (59%) scans were positive. Positivity rate increased with PSA level (PSA < 0.5 μg/L, 0%; PSA 0.5–1.0 μg/L, 35%; PSA 1.0–5.0 μg/L, 69%; PSA 5.0–10.0 μg/L, 91%), PSAdt of < 6 months (56% vs 45.7%) and Gleason score > 8 (78.9% vs 51.2%).Conclusions68Ga-THP-PSMA PET-CT influences clinical management in significant numbers of patient with HR prostate cancer pre-radical treatment and is associated with PSA. Management change also occurs in patients with BCR and is associated with PSA and Gleason score, despite lower scan positivity rates at low PSA levels < 0.5 μg/L.

Highlights

  • Prostate cancer is the most commonly diagnosed malignancy in men and is a leading cause of cancer-related death [1, 2]

  • This has conventionally been dependent upon digital rectal examination, prostate-specific antigen (PSA) testing and prostate biopsy, complemented with imaging, including multiparametric MRI, computed tomography (CT) and bone scintigraphy [4]

  • A questionnaire was adapted from Roach et al to record management plans before and after 68Ga-THP-prostate-specific membrane antigen (PSMA) positron emission tomography-computed tomography (PET-CT) [17] (Appendix 1)

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Summary

Introduction

Prostate cancer is the most commonly diagnosed malignancy in men and is a leading cause of cancer-related death [1, 2]. Accurate staging of prostate cancer before radical treatment and for the detection of recurrence is vital for directing treatment and predicting prognosis [3]. This has conventionally been dependent upon digital rectal examination, prostate-specific antigen (PSA) testing and prostate biopsy, complemented with imaging, including multiparametric MRI (mpMRI), computed tomography (CT) and bone scintigraphy [4]. Eur J Nucl Med Mol Imaging (2020) 47:674–686 detecting nodal metastases [5] or in those with low PSA levels at biochemical recurrence (BCR) [7] This has led to the investigation of more prostate-specific tracers with greater diagnostic accuracy

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