Imaging expression of prostate-specific membrane antigen and response to PSMA-targeted β-emitting radionuclide therapies in metastatic castration-resistant prostate cancer.


Journal

The Prostate
ISSN: 1097-0045
Titre abrégé: Prostate
Pays: United States
ID NLM: 8101368

Informations de publication

Date de publication:
04 2021
Historique:
received: 17 11 2020
revised: 22 12 2020
accepted: 02 01 2021
pubmed: 20 1 2021
medline: 19 8 2021
entrez: 19 1 2021
Statut: ppublish

Résumé

Prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy (TRT) has demonstrated efficacy and tolerability with a dose-response effect in phase I/II trials in men with metastatic castration-resistant prostate cancer (mCRPC). The need for positive PSMA imaging before PSMA-TRT to select patients is largely practiced, but its utility is not proven. Given target heterogeneity, developing a biomarker to identify the optimal patient population remains an unmet need. The aim of this study was to assess PSMA uptake by imaging and response to PSMA-TRT. We performed an analysis of men with mCRPC enrolled in sequential prospective phase I/II trials of PSMA-TRT. Each patient had baseline PSMA imaging by planar 215 men with progressive mCRPC received PSMA-TRT as follows: Collectively, the data provide evidence in favor of the hypothesis that patients with high PSMA uptake and high administered radionuclide dose correlate with a higher chance of response.

Sections du résumé

BACKGROUND
Prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy (TRT) has demonstrated efficacy and tolerability with a dose-response effect in phase I/II trials in men with metastatic castration-resistant prostate cancer (mCRPC). The need for positive PSMA imaging before PSMA-TRT to select patients is largely practiced, but its utility is not proven. Given target heterogeneity, developing a biomarker to identify the optimal patient population remains an unmet need. The aim of this study was to assess PSMA uptake by imaging and response to PSMA-TRT.
METHODS
We performed an analysis of men with mCRPC enrolled in sequential prospective phase I/II trials of PSMA-TRT. Each patient had baseline PSMA imaging by planar
RESULTS
215 men with progressive mCRPC received PSMA-TRT as follows:
CONCLUSION
Collectively, the data provide evidence in favor of the hypothesis that patients with high PSMA uptake and high administered radionuclide dose correlate with a higher chance of response.

Identifiants

pubmed: 33465252
doi: 10.1002/pros.24104
pmc: PMC7904644
mid: NIHMS1661599
doi:

Substances chimiques

Antigens, Surface 0
Radioisotopes 0
Radiopharmaceuticals 0
Lutetium 5H0DOZ21UJ
FOLH1 protein, human EC 3.4.17.21
Glutamate Carboxypeptidase II EC 3.4.17.21
Prostate-Specific Antigen EC 3.4.21.77

Banques de données

ClinicalTrials.gov
['NCT00003391', 'NCT00195039', 'NCT00538668', 'NCT03545165', 'NCT03042468', 'NCT03276572']

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

279-285

Subventions

Organisme : NCI NIH HHS
ID : R01 CA207645
Pays : United States
Organisme : NIH HHS
ID : 1-KL2-RR024997-01
Pays : United States
Organisme : NIH HHS
ID : 7R01CA207645
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002384
Pays : United States
Organisme : NCI NIH HHS
ID : L30 CA142419
Pays : United States
Organisme : NCRR NIH HHS
ID : KL2 RR024997
Pays : United States
Organisme : NIH HHS
ID : ULI RR024996
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR024996
Pays : United States
Organisme : NIH HHS
ID : PTBF5405
Pays : United States

Informations de copyright

© 2021 Wiley Periodicals LLC.

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Auteurs

Panagiotis J Vlachostergios (PJ)

Department of Medicine, Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, USA.

Muhammad Junaid Niaz (MJ)

Department of Urology, Weill Cornell Medicine, New York, USA.

Myrto Skafida (M)

Department of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, USA.

Seyed Ali Mosallaie (SA)

Department of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, USA.

Charlene Thomas (C)

Department of Healthcare Policy & Research, Division of Biostatistics and Epidemiology, Weill Cornell Medicine, New York, USA.

Paul J Christos (PJ)

Department of Healthcare Policy & Research, Division of Biostatistics and Epidemiology, Weill Cornell Medicine, New York, USA.

Joseph R Osborne (JR)

Department of Radiology, Division of Molecular Imaging and Therapeutics, Weill Cornell Medicine, New York, USA.
Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, USA.

Ana M Molina (AM)

Department of Medicine, Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, USA.
Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, USA.

David M Nanus (DM)

Department of Medicine, Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, USA.
Department of Urology, Weill Cornell Medicine, New York, USA.
Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, USA.

Neil Harrison Bander (NH)

Department of Urology, Weill Cornell Medicine, New York, USA.
Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, USA.

Scott T Tagawa (ST)

Department of Medicine, Division of Hematology and Medical Oncology, Weill Cornell Medicine, New York, USA.
Department of Urology, Weill Cornell Medicine, New York, USA.
Sandra and Edward Meyer Cancer Center, Weill Cornell Medicine, New York, USA.

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Classifications MeSH