Consecutive Prostate-Specific Membrane Antigen (PSMA) and Antigen Receptor (AR) PET Imaging Shows Positive Correlation with AR and PSMA Protein Expression in Primary Hormone-Naïve Prostate Cancer
The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. Th...
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          | Published in | Journal of Nuclear Medicine Vol. 64; no. 6; pp. 863 - 868 | 
|---|---|
| Main Authors | , , , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        United States
          Society of Nuclear Medicine
    
        01.06.2023
     | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 0161-5505 1535-5667 2159-662X 2159-662X 1535-5667  | 
| DOI | 10.2967/jnumed.122.264981 | 
Cover
| Abstract | The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [
Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (
,
'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-
,
'-diacetic acid) [
Ga]Ga-PSMA
([
Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[
F]fluoro-5α-dihydrotestosterone (16β-[
F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care.
This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [
Ga]PSMA PET/MRI and [
F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed.
For [
F]FDHT, the SUV
/SUV
ratio showed a significant, strong correlation (
= 0.72;
= 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [
Ga]PSMA SUV
/SUV
ratio was not significant (
= 0.061), yet a positive correlation trend could be observed (
= 0.61). SUV
/SUV
ratios were higher for [
Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [
F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [
Ga]PSMA PET scan but only 40% for the [
F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%).
[
F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [
F]FDHT PET is inferior to [
Ga]PSMA PET for primary PC diagnosis, but the correlation between [
Ga]PSMA SUVs and PSMA expression is weaker than that between [
F]FDHT and the AR. | 
    
|---|---|
| AbstractList | The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [
Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (
,
'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-
,
'-diacetic acid) [
Ga]Ga-PSMA
([
Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[
F]fluoro-5α-dihydrotestosterone (16β-[
F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care.
This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [
Ga]PSMA PET/MRI and [
F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed.
For [
F]FDHT, the SUV
/SUV
ratio showed a significant, strong correlation (
= 0.72;
= 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [
Ga]PSMA SUV
/SUV
ratio was not significant (
= 0.061), yet a positive correlation trend could be observed (
= 0.61). SUV
/SUV
ratios were higher for [
Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [
F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [
Ga]PSMA PET scan but only 40% for the [
F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%).
[
F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [
F]FDHT PET is inferior to [
Ga]PSMA PET for primary PC diagnosis, but the correlation between [
Ga]PSMA SUVs and PSMA expression is weaker than that between [
F]FDHT and the AR. The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [68Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (N,N′-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N′-diacetic acid) [68Ga]Ga-PSMAHBED-CC ([68Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[18F]fluoro-5α-dihydrotestosterone (16β-[18F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care. Methods: This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [68Ga]PSMA PET/MRI and [18F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed. Results: For [18F]FDHT, the SUVmax/SUVbackground ratio showed a significant, strong correlation (r = 0.72; P = 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [68Ga]PSMA SUVmax/SUVbackground ratio was not significant (P = 0.061), yet a positive correlation trend could be observed (r = 0.61). SUVmax/SUVbackground ratios were higher for [68Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [18F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [68Ga]PSMA PET scan but only 40% for the [18F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%). Conclusion: [18F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [18F]FDHT PET is inferior to [68Ga]PSMA PET for primary PC diagnosis, but the correlation between [68Ga]PSMA SUVs and PSMA expression is weaker than that between [18F]FDHT and the AR. The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [68Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (N,N'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diacetic acid) [68Ga]Ga-PSMAHBED-CC ([68Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[18F]fluoro-5α-dihydrotestosterone (16β-[18F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care. Methods: This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [68Ga]PSMA PET/MRI and [18F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed. Results: For [18F]FDHT, the SUVmax/SUVbackground ratio showed a significant, strong correlation (r = 0.72; P = 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [68Ga]PSMA SUVmax/SUVbackground ratio was not significant (P = 0.061), yet a positive correlation trend could be observed (r = 0.61). SUVmax/SUVbackground ratios were higher for [68Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [18F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [68Ga]PSMA PET scan but only 40% for the [18F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%). Conclusion: [18F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [18F]FDHT PET is inferior to [68Ga]PSMA PET for primary PC diagnosis, but the correlation between [68Ga]PSMA SUVs and PSMA expression is weaker than that between [18F]FDHT and the AR.The present study was carried out to investigate whether PET imaging can be used as a potential substitute for immunohistochemical analysis of tumor samples in prostate cancer (PC) patients. Correlation between imaging signals of 2 PET tracers and the corresponding target structures was assessed. The first tracer was [68Ga]Ga-PSMA (prostate-specific membrane antigen)-HBED-CC (N,N'-bis [2-hydroxy-5-(carboxyethyl)benzyl]ethylenediamine-N,N'-diacetic acid) [68Ga]Ga-PSMAHBED-CC ([68Ga]PSMA), which is already implemented in clinical routines. The second tracer was 16β-[18F]fluoro-5α-dihydrotestosterone (16β-[18F]FDHT), which binds to the androgen receptor (AR). The AR is particularly interesting in PC, because AR expression status and its shift during therapy might directly influence patient care. Methods: This prospective, explorative clinical study included 10 newly diagnosed PC patients. Each patient underwent [68Ga]PSMA PET/MRI and [18F]FDHT PET/MRI scans before prostatectomy. Cancer SUVs were determined and related to background SUVs. After prostatectomy, tumor tissue was sampled, and AR and prostate-specific membrane antigen (PSMA) expression was determined. AR and PSMA expression was evaluated quantitatively with the open-source bioimage analysis software QuPath and with a 4-tier rating system. Correlation between imaging signals and marker expression was statistically assessed. Results: For [18F]FDHT, the SUVmax/SUVbackground ratio showed a significant, strong correlation (r = 0.72; P = 0.019) with the AR optical density of the correlating tissue sample. The correlation between PSMA optical density and the [68Ga]PSMA SUVmax/SUVbackground ratio was not significant (P = 0.061), yet a positive correlation trend could be observed (r = 0.61). SUVmax/SUVbackground ratios were higher for [68Ga]PSMA (mean ± SD, 34.9 ± 24.8) than for [18F]FDHT (4.8 ± 1.2). In line with these findings, the tumor detection rates were 90% for the [68Ga]PSMA PET scan but only 40% for the [18F]FDHT PET scan. The 4-tier rating of PSMA staining intensity yielded very homogeneous results, with values of 3+ for most subjects (90%). AR staining was rated as 1+ in 2 patients (20%), 2+ in 4 patients (40%), and 3+ in 4 patients (40%). Conclusion: [18F]FDHT PET may be useful for monitoring AR expression and alterations in AR expression during treatment of PC patients. This approach may facilitate early detection of treatment resistance and allows for adaptation of therapy to prevent cancer progression. [18F]FDHT PET is inferior to [68Ga]PSMA PET for primary PC diagnosis, but the correlation between [68Ga]PSMA SUVs and PSMA expression is weaker than that between [18F]FDHT and the AR.  | 
    
| Author | Rasul, Sazan Simon, Judit Shariat, Shahrokh Egger, Gerda al Jalali, Valentin Grubmüller, Bernhard Hacker, Marcus Wasinger, Gabriel Mitterhauser, Markus Zeitlinger, Markus Wulkersdorfer, Beatrix Balber, Theresa  | 
    
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| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36657982$$D View this record in MEDLINE/PubMed | 
    
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| CitedBy_id | crossref_primary_10_3390_ijms24098235 crossref_primary_10_1007_s10967_024_09673_6 crossref_primary_10_1016_j_eururo_2024_09_036 crossref_primary_10_1016_j_mednuc_2023_07_008 crossref_primary_10_3390_diagnostics13152613  | 
    
| Cites_doi | 10.1016/S0140-6736(20)30314-7 10.1038/ng0495-401 10.1158/1078-0432.CCR-18-0768 10.1023/A:1006141806801 10.1016/j.eururo.2019.01.049 10.1001/jamaoncol.2020.6973 10.1001/jamaoncol.2017.3588 10.2967/jnumed.117.206490 10.1007/s00259-021-05501-1 10.21037/tau.2019.03.13 10.1002/cncr.32733 10.2967/jnumed.117.195172 10.3322/caac.21492 10.1200/JCO.2013.50.1684  | 
    
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| Keywords | [18F]FDHT PET primary hormone-naïve prostate cancer [68Ga]PSMA PET AR protein expression PSMA protein expression  | 
    
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| SubjectTerms | Androgen receptors Antigens Dihydrotestosterone Edetic Acid - metabolism Ethylenediamine Fluorine isotopes Gallium Radioisotopes Humans Magnetic resonance imaging Male Medical imaging Membranes Optical density Patients Positron emission Positron emission tomography Positron Emission Tomography Computed Tomography - methods Positron-Emission Tomography - methods Prospective Studies Prostate - pathology Prostate cancer Prostate-Specific Antigen Prostatectomy Prostatic Neoplasms - pathology Receptors Staining Treatment resistance Tumors  | 
    
| Title | Consecutive Prostate-Specific Membrane Antigen (PSMA) and Antigen Receptor (AR) PET Imaging Shows Positive Correlation with AR and PSMA Protein Expression in Primary Hormone-Naïve Prostate Cancer | 
    
| URI | https://www.ncbi.nlm.nih.gov/pubmed/36657982 https://www.proquest.com/docview/2821691033 https://www.proquest.com/docview/2768240837 https://jnm.snmjournals.org/content/jnumed/64/6/863.full.pdf  | 
    
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