PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study

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PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study. / Weber, Manuel; Kurek, Claudia Ewa; Barbato, Francesco; Eiber, Matthias; Maurer, Tobias; Nader, Michael; Hadaschik, Boris; Grünwald, Viktor; Herrmann, Ken; Wetter, Axel; Fendler, Wolfgang Peter.

In: J NUCL MED, Vol. 62, No. 1, 01.2021, p. 88-91.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Weber, M, Kurek, CE, Barbato, F, Eiber, M, Maurer, T, Nader, M, Hadaschik, B, Grünwald, V, Herrmann, K, Wetter, A & Fendler, WP 2021, 'PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study', J NUCL MED, vol. 62, no. 1, pp. 88-91. https://doi.org/10.2967/jnumed.120.245456

APA

Weber, M., Kurek, C. E., Barbato, F., Eiber, M., Maurer, T., Nader, M., Hadaschik, B., Grünwald, V., Herrmann, K., Wetter, A., & Fendler, W. P. (2021). PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study. J NUCL MED, 62(1), 88-91. https://doi.org/10.2967/jnumed.120.245456

Vancouver

Bibtex

@article{5f3c011b9eb54d0c8fbdaa8d9529164c,
title = "PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study",
abstract = "The low detection rate of conventional imaging and unspecific fluctuations in prostate-specific antigen can hamper early diagnosis of castration-resistant prostate cancer (CRPC). We thus assessed the value of prostate-specific membrane antigen (PSMA) PET/CT in the detection of early CRPC (prostate-specific antigen ≤ 3 ng/mL). Methods: We identified 55 patients with early CRPC from our institutional database. PSMA PET/CT and its CT component were interpreted independently by 3 masked readers. The primary endpoint was the per-patient detection rate; secondary endpoints were interobserver agreement and predictors of PET positivity. Results: PSMA PET/CT was positive in 41 of 55 (75%) patients. Sixteen of 55 (29%) patients had local disease only, and 25 of 55 (45%) had M1 disease. Overall, PSMA PET/CT interobserver agreement was substantial by Landis and Koch criteria (Fleiss κ = 0.77). Conclusion: PSMA PET/CT localized prostate cancer lesions in 75% of patients and M1 disease in 45%. Detection of early CRPC facilitates disease-delaying therapies for local or oligometastatic disease. PSMA PET/CT is of value in early CRPC and should be included in the CRPC entry criteria of the European Association of Urology and Prostate Cancer Working Group 3.",
author = "Manuel Weber and Kurek, {Claudia Ewa} and Francesco Barbato and Matthias Eiber and Tobias Maurer and Michael Nader and Boris Hadaschik and Viktor Gr{\"u}nwald and Ken Herrmann and Axel Wetter and Fendler, {Wolfgang Peter}",
note = "{\textcopyright} 2021 by the Society of Nuclear Medicine and Molecular Imaging.",
year = "2021",
month = jan,
doi = "10.2967/jnumed.120.245456",
language = "English",
volume = "62",
pages = "88--91",
journal = "J NUCL MED",
issn = "0161-5505",
publisher = "Society of Nuclear Medicine Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - PSMA-ligand PET for early castration-resistant prostate cancer: a retrospective single-center study

AU - Weber, Manuel

AU - Kurek, Claudia Ewa

AU - Barbato, Francesco

AU - Eiber, Matthias

AU - Maurer, Tobias

AU - Nader, Michael

AU - Hadaschik, Boris

AU - Grünwald, Viktor

AU - Herrmann, Ken

AU - Wetter, Axel

AU - Fendler, Wolfgang Peter

N1 - © 2021 by the Society of Nuclear Medicine and Molecular Imaging.

PY - 2021/1

Y1 - 2021/1

N2 - The low detection rate of conventional imaging and unspecific fluctuations in prostate-specific antigen can hamper early diagnosis of castration-resistant prostate cancer (CRPC). We thus assessed the value of prostate-specific membrane antigen (PSMA) PET/CT in the detection of early CRPC (prostate-specific antigen ≤ 3 ng/mL). Methods: We identified 55 patients with early CRPC from our institutional database. PSMA PET/CT and its CT component were interpreted independently by 3 masked readers. The primary endpoint was the per-patient detection rate; secondary endpoints were interobserver agreement and predictors of PET positivity. Results: PSMA PET/CT was positive in 41 of 55 (75%) patients. Sixteen of 55 (29%) patients had local disease only, and 25 of 55 (45%) had M1 disease. Overall, PSMA PET/CT interobserver agreement was substantial by Landis and Koch criteria (Fleiss κ = 0.77). Conclusion: PSMA PET/CT localized prostate cancer lesions in 75% of patients and M1 disease in 45%. Detection of early CRPC facilitates disease-delaying therapies for local or oligometastatic disease. PSMA PET/CT is of value in early CRPC and should be included in the CRPC entry criteria of the European Association of Urology and Prostate Cancer Working Group 3.

AB - The low detection rate of conventional imaging and unspecific fluctuations in prostate-specific antigen can hamper early diagnosis of castration-resistant prostate cancer (CRPC). We thus assessed the value of prostate-specific membrane antigen (PSMA) PET/CT in the detection of early CRPC (prostate-specific antigen ≤ 3 ng/mL). Methods: We identified 55 patients with early CRPC from our institutional database. PSMA PET/CT and its CT component were interpreted independently by 3 masked readers. The primary endpoint was the per-patient detection rate; secondary endpoints were interobserver agreement and predictors of PET positivity. Results: PSMA PET/CT was positive in 41 of 55 (75%) patients. Sixteen of 55 (29%) patients had local disease only, and 25 of 55 (45%) had M1 disease. Overall, PSMA PET/CT interobserver agreement was substantial by Landis and Koch criteria (Fleiss κ = 0.77). Conclusion: PSMA PET/CT localized prostate cancer lesions in 75% of patients and M1 disease in 45%. Detection of early CRPC facilitates disease-delaying therapies for local or oligometastatic disease. PSMA PET/CT is of value in early CRPC and should be included in the CRPC entry criteria of the European Association of Urology and Prostate Cancer Working Group 3.

U2 - 10.2967/jnumed.120.245456

DO - 10.2967/jnumed.120.245456

M3 - SCORING: Journal article

C2 - 32444377

VL - 62

SP - 88

EP - 91

JO - J NUCL MED

JF - J NUCL MED

SN - 0161-5505

IS - 1

ER -