Features of the physiological distribution of 68Ga-PSMA and its importance in the differential diagnosis of metastatic lesions of lymph nodes in patients with prostate cancer
https://doi.org/10.22328/2079-5343-2021-12-3-80-86
Abstract
Introduction. The appearance of new radiopharmaceuticals based on prostate-specific membrane antigen has significantly increased the accuracy of prostate cancer diagnosis. The physiological accumulation of 68Ga-PSMA in the sympathetic ganglia is important in the diagnosis of metastatic lesions of the lymph nodes. Erroneous interpretation of images can lead to an incorrect choice of tactics for the treatment of prostate cancer.
Purpose: improving the diagnosis of prostate cancer with the help of updated data on the physiological accumulation of 68GaPSMA. Identify the sources of potential errors in the interpretation of PET/CT with 68Ga-PSMA.
Materials and methods. In order to stage the verified prostate cancer, PET was performed in our center/CT with 68Ga-PSMA in 109 men. All patients were divided into groups by the level of prostate-specific antigen, Gleason sum, and d’Amico.
Results. In all patients, we observed the accumulation of RFP in the cervical, abdominal and presacral ganglia. The capture level of the radiotracer was in the range of SUV=1,6–2,3 (median SUV=1,9). In the control PET/CT study after treatment, the accumulation of RFP in the cervical, abdominal and presacral ganglia remained at the same values, which made it possible to identify the detected changes as a variant of the physiological norm.
Conclusions. It is necessary to take into account the peculiarities of the physiological distribution and accumulation of radiotracer in organs and tissues, in particular, the capture of 68Ga-PSMA by sympathetic ganglia. This will avoid false-positive cases when describing PET-CT images and will make it possible to increase the informative value of the method.
About the Authors
A. L. DolbovRussian Federation
St. Petersburg
A. A. Stanjevskiy
Russian Federation
St. Petersburg
E. V. Rozengauz
Russian Federation
St. Petersburg
References
1. Rider J.R. et al. Ejaculation Frequency and Risk of Prostate Cancer: Updated Results with an Additional Decade of Follow-up // Eur. Urol. 2016. Vol. 70. Р. 974.
2. Kaprin A.D., Starinsky V.V., Shakhzadova A.O. Malignant neoplasms in Russia in 2019 (morbidity and mortality) / P.A.Herzen — branch of the Federal State Budgetary Institution «NMIRC» of the Ministry of Health of Russia Moscow. 2020 (In Russ.).
3. Bouchelouche K., Turkbey B., Choyke P.L. PSMA PET and Radionuclide Therapy in Prostate Cancer // Semin. Nucl. Med. 2016. Vol. 46, Nо. 6. Р. 522–535. doi: 10.1053/j.semnuclmed.2016.07.006. Epub 2016 Sep 3. PMID: 27825432; PMCID: PMC5123597.
4. Birtle A.J., Freeman A., Masters J.R. et al. BAUS Section of Oncology Cancer Registry. Tumour markers for managing men who present with metastatic prostate cancer and serum prostate-specific antigen levels of <10 ng/mL // BJU Int. 2005. Vol. 96, No. 3. Р. 303–307. doi: 10.1111/j.1464-410X.2005.05619.x. PMID: 16042718
5. Silver D.A., Pellicer I., Fair W.R. et al. Prostate-specific membrane antigen expression in normal and malignant human tissues // Clin. Cancer Res. 1997. Vol. 3. Р. 81–85.
6. Morigi J.J., Fanti S., Murphy D. et al. Rapidly changing landscape of PET/CT imaging in prostate cancer // Curr. Opin Urol. 2016. Vol. 26, No. 5. Р. 493–500. doi: 10.1097/MOU.0000000000000309. PMID: 27467137.
7. Afshar-Oromieh A., Malcher A., Eder M. et al. PET imaging with a [68Ga]gallium-labelled PSMA ligand for the diagnosis of prostate cancer: biodistribution in humans and first evaluation of tumor lesions // Eur. J. Nucl. Med. Mol. Imaging. 2013. Vol. 40, No. 4. Р. 486–495. doi: 10.1007/s00259-012-2298-2. Epub 2012 Nov 24. Erratum in: Eur. J. Nucl. Med. Mol. Imaging. 2013. Vol. 40, No. 5. Р. 797–798. PMID: 23179945.
8. Krohn T., Verburg F.A., Pufe T. et al. [68Ga]PSMA-HBED uptake mimicking lymph node metastasis in coeliac ganglia: an important pitfall in clinical practice // Eur. J. Nucl. Med. Mol. Imaging. 2015. Vol. 42, No. 2. Р. 210–214.
9. Wang Z.J., Webb E.M., Westphalen A.C. et al. Multi-detector row computed tomographic appearance of celiac ganglia // J. Comput. Assist Tomogr. 2010. Vol. 34, No. 3. Р. 343–347. doi: 10.1097/RCT.0b013e3181d26ddd. PMID: 20498533.
10. Rischpler C., Beck T.I., Okamoto S. et al. 68Ga-PSMA-HBED-CC Uptake in Cervical, Celiac, and Sacral Ganglia as an Important Pitfall in Prostate Cancer PET Imaging // J. Nucl. Med. 2018. Vol. 59, No. 9. Р. 1406–1411. doi: 10.2967/jnumed.117.204677. Epub 2018 Jan 25. PMID: 29371407.
11. Berger U.V., Carter R.E., McKee M. et al. N-acetylated alpha-linked acidic dipeptidase is expressed by non-myelinating Schwann cells in the peripheral nervous system // J. Neurocytol. 1995. Vol. 24, No. 2. Р. 99–109. doi: 10.1007/BF01181553. PMID: 7745446.
12. Hofman M.S., Hicks R.J., Maurer T., Eiber M. Prostate-specific Membrane Antigen PET: Clinical Utility in Prostate Cancer, Normal Patterns, Pearls, and Pitfalls // Radiographics. 2018. Vol. 38, No. 1. Р. 200–217. doi: 10.1148/rg.2018170108. PMID: 29320333.
13.
Review
For citations:
Dolbov A.L., Stanjevskiy A.A., Rozengauz E.V. Features of the physiological distribution of 68Ga-PSMA and its importance in the differential diagnosis of metastatic lesions of lymph nodes in patients with prostate cancer. Diagnostic radiology and radiotherapy. 2021;12(3):80-86. (In Russ.) https://doi.org/10.22328/2079-5343-2021-12-3-80-86