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Clinical impact of 68Ga-PSMA-11 PET on patient management and outcome, including all patients referred for an increase in PSA level during the first year after its clinical introduction

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Abstract

Purpose

The fast-increasing use of positron emission tomography (PET) with prostate-specific membrane antigen (PSMA) ligand for the imaging of prostate cancer (PCA) biochemical recurrence has led to a rapid change in treatment concepts. Since the superiority of 68Ga-PSMA-11 PET in detecting recurrent PCA is well established, the aim of our study was to assess its effect on management and outcome in all patients imaged during the first year after its introduction into clinical routine.

Methods

Of 327 patients imaged, 223 were referred for recurrent PCA and gave written informed consent for further analysis of their data for this retrospective consecutive cohort analysis. Twenty patients were lost to further follow-up. The rate of detection of recurrence by 68Ga-PSMA-11 PET was based on the clinical reports. Management before the availability of PET diagnostic information was assessed according to guidelines (therapy option without 68Ga-PSMA-11 PET). In the 203 patients with follow-up 6 months after 68Ga-PSMA-11 PET, the therapies effectively implemented as well as follow-up PSA levels were evaluated, with a PSA value of <0.2 ng/ml representing a complete response and a decrease in PSA value of at least 50% from baseline representing a partial response.

Results

68Ga-PSMA-11 PET was positive and identified recurrence in 166 of the 223 patients (74%), with a detection rate of 50% for recurrent disease at low PSA values of <0.5 ng/ml. 68Ga-PSMA-11 PET led to a change in management in 122 of the 203 patients (60%). A substantial increase in the use of metastasis-targeted treatment and a reduction in the use of systemic treatment were observed, with 59 of the 203 patients (29%) undergoing targeted radiotherapy (RTXa) only, and 20 patients (10%) undergoing RTXa with hormonal therapy as the two most frequently selected therapy options. The proportion of patients in whom systemic therapy was selected decreased from 60% (133 of 223 patients) to 34% (70 of 203 patients) on the basis of the information provided by the 68Ga-PSMA-11 PET scan. PSMA PET-directed metastasis-targeted treatment led to a complete response after 6 months in 45% of patients.

Conclusion

The high rate of recurrence detection by PSMA PET was confirmed and PSMA PET led to a change in management in 60% of patients. Focal therapy for PSMA-positive lesions is a promising approach with complete responses in 45% of patients.

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Acknowledgments

The authors acknowledge the technicians Josephine Trinckauf and Marlena Hofbauer and their team for the excellent work in producing high-quality PET images.

Funding

The Department of Nuclear Medicine holds an institutional Research Contract with GE Healthcare. The authors thank the Sick legat and the Iten-Kohaut Foundation for their financial support.

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Authors and Affiliations

Authors

Contributions

Julian Müller – data collection, manuscript editing.

Daniela A. Ferraro – data collection, manuscript editing.

Urs J. Muehlematter – statistics, data analysis.

Helena I. Garcia Schüler – data analysis, manuscript editing.

Sarah Kedzia - data collection, data analysis, manuscript editing.

Daniel Eberli, Matthias Guckenberger, Stephanie G. C. Kroeze, Tullio Sulser, Daniel M. Schmid, Aurelius Omlin, Alexander Müller, Thomas Zilli, Hubert John, Helmut Kranzbuehler – patient assessment, data analysis.

Philipp A. Kaufmann, Gustav K. von Schulthess, Irene A. Burger – study design and manuscript editing.

All authors reviewed and agreed to the manuscript content.

Corresponding author

Correspondence to Irene A. Burger.

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Conflicts of interest

I.A.B., G.K.v.S. and P.A.K. received research grants and speaker honoraria from GE Healthcare. I.A.B. received research grants from Swiss Life and speaker honoraria from Bayer Health Care and Astellas Pharma AG. M.G. received research grants from Varian. A.O. has an advisory role (compensated, institutional): Astellas, Bayer, Sanofi, Roche, Janssen, MSD, Molecular Partners. Research support (institutional): Teva, Janssen. Travel support: Astellas, Bayer, Sanofi, Janssen. Speaker Bureau (compensated, institutional): Astellas, Janssen, Bayer. All other authors declare no conflicts of interest.

Ethical approval and consent to participate

The local ethics committee approved the study protocol and all patients gave general written informed consent for retrospective use of their data (BASEC Nr. 2018–01284).

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Not applicable.

Availability of data and material

Patient imaging was done in the scope of routine clinical diagnostic studies, and the raw data are stored in the hospital archiving system at the Zurich University Hospital, Zurich, Switzerland.

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Müller, J., Ferraro, D.A., Muehlematter, U.J. et al. Clinical impact of 68Ga-PSMA-11 PET on patient management and outcome, including all patients referred for an increase in PSA level during the first year after its clinical introduction. Eur J Nucl Med Mol Imaging 46, 889–900 (2019). https://doi.org/10.1007/s00259-018-4203-0

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