99mTcPSMA androgen deprivation therapy oligorecurrent prostate cancer prostate specific membrane antigen radioguided surgery

Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
12 Feb 2024
Historique:
medline: 13 2 2024
pubmed: 13 2 2024
entrez: 12 2 2024
Statut: aheadofprint

Résumé

To investigate whether combination treatment of prostate-specific membrane antigen (PSMA)-based radioguided surgery (RGS) with short-term androgen deprivation therapy (ADT) improves oncological outcomes in men with oligorecurrent prostate cancer (PCa) as compared to treatment with short-term ADT only. The TRACE-II study is an investigator-initiated, prospective, randomised controlled clinical trial. Patients (aged >18 years) with hormone-sensitive recurrent PCa after radical prostatectomy or radiotherapy (brachytherapy or external beam radiotherapy), with involvement of ≤2 lymph nodes or local oligorecurrent disease within the pelvis as determined by PSMA positron emission tomography (PET)/computed tomography (CT) are randomly assigned in a 1:1 ratio between 6-month ADT (Arm A) or 6-month ADT plus RGS (Arm B). The primary objective is to determine clinical progression-free survival (CPFS) at 24 months. After PSMA-RGS, CPFS is defined as the time between the start of treatment and the appearance of a re-recurrence (any N1 or M1) as suggested by PSMA-PET/CT or symptoms related to progressive PCa, or death from any cause. The secondary objectives include metastasis-free survival at 2, 5 and 10 years, biochemical progression-free survival at 2 years, and patient-reported quality of life at 2, 5 and 10 years. A total of 60 patients, 30 per arm, will be included. The trial is powered (80%) to detect at least a 30% absolute difference in CPFS between the two study arms in the period 2 years after randomisation. We expect to enrol the required participants in 3 years. The study has an expected duration of 5 years in total. Combining RGS with short-term ADT might be oncologically beneficial for patients with oligorecurrent PCa. In this first randomised controlled trial, we are investigating the potential oncological benefits of this combined treatment, while also focusing on maintaining quality of life.

Identifiants

pubmed: 38346924
doi: 10.1111/bju.16297
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Netherlands Cancer Institute

Informations de copyright

© 2024 BJU International.

Références

Han M, Partin AW, Pound CR, Epstein JI, Walsh PC. Long-term biochemical disease-free and cancer-specific survival following anatomic radical retropubic prostatectomy: the 15-year Johns Hopkins experience. Urol. Clin. North Am. 2001; 28: 555-565
Murphy GP, Tino WT, Holmes EH et al. Measurement of prostate-specific membrane antigen in the serum with a new antibody. Prostate 1996; 28: 266-271
van Leeuwen PJ, Emmett L, Ho B et al. Prospective evaluation of 68Gallium-prostate-specific membrane antigen positron emission tomography/computed tomography for preoperative lymph node staging in prostate cancer. BJU Int. 2017; 119: 209-215
Maurer T, Robu S, Schottelius M et al. 99mTechnetium-based prostate-specific membrane antigen-radioguided surgery in recurrent prostate cancer. Eur. Urol. 2019; 75: 659-666
Van Leeuwen PJ, Stricker P, Hruby G et al. 68Ga-PSMA has a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiation treatment. BJU Int. 2016; 117: 732-739
Emmett L, Van Leeuwen PJ, Nandurkar R et al. Treatment outcomes from 68Ga-PSMA PET/CT-informed salvage radiation treatment in men with rising PSA after radical prostatectomy: prognostic value of a negative PSMA PET. J. Nucl. Med. 2017; 58: 1972-1976
de Barros HA, van Oosterom MN, Donswijk ML et al. Robot-assisted prostate-specific membrane antigen-radioguided salvage surgery in recurrent prostate cancer using a DROP-IN gamma probe: the first prospective feasibility study. Eur. Urol. 2022; 82: 97-105
Robu S, Schottelius M, Eiber M et al. Preclinical evaluation and first patient application of 99mTc-PSMA-I&S for SPECT imaging and radioguided surgery in prostate cancer. J. Nucl. Med. 2017; 58: 235-242
Aalbersberg EA, van Andel L, Geluk-Jonker MM, Beijnen JH, Stokkel MPM, Hendrikx JJMA. Automated synthesis and quality control of [99mTc]Tc-PSMA for radioguided surgery (in a [68Ga]Ga-PSMA workflow). EJNMMI Radiopharm Chem 2020; 5: 10
Knipper S, Tilki D, Mansholt J et al. Metastases-yield and prostate-specific antigen kinetics following salvage lymph node dissection for prostate cancer: a comparison between conventional surgical approach and prostate-specific membrane antigen-radioguided surgery. Eur. Urol. Focus 2019; 5: 50-53
Knipper S, Mehdi Irai M, Simon R et al. Cohort study of oligorecurrent prostate cancer patients: oncological outcomes of patients treated with salvage lymph node dissection via prostate-specific membrane antigen-radioguided surgery. Eur. Urol. 2023; 83: 62-69
Katipally RR, Pitroda SP, Juloori A, Chmura SJ, Weichselbaum RR. The oligometastatic spectrum in the era of improved detection and modern systemic therapy. Nat. Rev. Clin. Oncol. 2022; 19: 585-599
Hellman S, Weichselbaum RR. Oligometastases. J. Clin. Oncol. 1995; 13: 8-10
Brooks ED, Chang JY. Time to abandon single-site irradiation for inducing abscopal effects. Nat. Rev. Clin. Oncol. 2019; 16: 123-135
Bravi CA, Fossati N, Gandaglia G et al. Long-term outcomes of salvage lymph node dissection for nodal recurrence of prostate cancer after radical prostatectomy: not as good as previously thought. Eur. Urol. 2020; 78: 661-669
Scher HI, Halabi S, Tannock I et al. Design and end points of clinical trials for patients with progressive prostate cancer and castrate levels of testosterone: recommendations of the prostate cancer clinical trials working group. J. Clin. Oncol. 2008; 26: 1148-1159
Vallabhajosula S, Nikolopoulou A, Babich JW et al. 99mTc-labeled small-molecule inhibitors of prostate-specific membrane antigen: pharmacokinetics and biodistribution studies in healthy subjects and patients with metastatic prostate cancer. J. Nucl. Med. 2014; 55: 1791-1798
Mottet N, Bellmunt J, Bolla M. EAU-ESTRO-SIOG guidelines on prostate cancer. Eur. Urol. 2017; 71: 618-629
Schaeffer EMC, An Y, Barocas DMPH et al. NCCN guidelines version 1.2023 prostate cancer. 2022
Suardi N, Gandaglia G, Gallina A et al. Long-term outcomes of salvage lymph node dissection for clinically recurrent prostate cancer: results of a single-institution series with a minimum follow-up of 5 years. Eur. Urol. 2015; 67: 299-309
Karnes RJ, Murphy CR, Bergstralh EJ et al. Salvage lymph node dissection for prostate cancer nodal recurrence detected by 11C-choline positron emission tomography/computerized tomography. J. Urol. 2015; 193: 111-116
Steuber T, Jilg C, Tennstedt P et al. Standard of care versus metastases-directed therapy for PET-detected nodal oligorecurrent prostate cancer following multimodality treatment: a multi-institutional case-control study. Eur. Urol. Focus 2019; 5: 1007-1013
Fossati N, Trinh QD, Sammon J et al. Identifying optimal candidates for local treatment of the primary tumor among patients diagnosed with metastatic prostate cancer: a SEER-based study. Eur. Urol. 2015; 67: 3-6
Ploussard G, Gandaglia G, Borgmann H et al. Salvage lymph node dissection for nodal recurrent prostate cancer: a systematic review. Eur. Urol. 2019; 76: 493-504
Horn T, Krönke M, Rauscher I et al. Single lesion on prostate-specific membrane antigen-ligand positron emission tomography and low prostate-specific antigen are prognostic factors for a favorable biochemical response to prostate-specific membrane antigen-targeted radioguided surgery in recurrent prostate cancer. Eur. Urol. 2019; 76: 517-523
Maurer T, Weirich G, Schottelius M et al. Prostate-specific membrane antigen-radioguided surgery for metastatic lymph nodes in prostate cancer. Eur. Urol. 2015; 68: 530-534
Phillips R, Shi WY, Deek M et al. Outcomes of observation vs stereotactic ablative radiation for oligometastatic prostate cancer: the ORIOLE phase 2 randomized clinical trial. JAMA Oncol. 2020; 6: 650-659
Deek MP, Van der Eecken K, Sutera P et al. Long-term outcomes and genetic predictors of response to metastasis-directed therapy versus observation in oligometastatic prostate cancer: analysis of STOMP and ORIOLE trials. J. Clin. Oncol. 2022; 40: 3377-3382
Ost P, Reynders D, Decaestecker K et al. Surveillance or metastasis-directed therapy for oligometastatic prostate cancer recurrence: a prospective, randomized, multicenter phase II trial. J. Clin. Oncol. 2018; 36: 446-453
Tang C, Sherry AD, Haymaker C et al. Addition of metastasis-directed therapy to intermittent hormone therapy for oligometastatic prostate cancer. JAMA Oncol. 2023; 9: 825

Auteurs

Lotte G Zuur (LG)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.

Hilda A de Barros (HA)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.

Matthias N van Oosterom (MN)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Department of Radiology, Interventional Molecular Imaging Laboratory, Leiden University Medical Centre, Leiden, The Netherlands.

Anne-Claire Berrens (AC)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.
Department of Radiology, Interventional Molecular Imaging Laboratory, Leiden University Medical Centre, Leiden, The Netherlands.

Maarten L Donswijk (ML)

Department of Nuclear Medicine, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Jeroen J M A Hendrikx (JJMA)

Department of Nuclear Medicine, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Department of Clinical Pharmacy & Pharmacology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

Elise M Bekers (EM)

Department of Pathology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

André N Vis (AN)

Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.
Department of Urology, Amsterdam University Medical Centres, Amsterdam, The Netherlands.

Esther M Wit (EM)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.

Fijs B van Leeuwen (FB)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Department of Radiology, Interventional Molecular Imaging Laboratory, Leiden University Medical Centre, Leiden, The Netherlands.

Henk G van der Poel (HG)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.
Department of Urology, Amsterdam University Medical Centres, Amsterdam, The Netherlands.

Pim J van Leeuwen (PJ)

Department of Urology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
Netherlands Prostate Cancer Network, Amsterdam, The Netherlands.

Classifications MeSH