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Published in: World Journal of Urology 5/2004

01-10-2004 | Topic Paper

PET and prostate cancer

Authors: G. Sanz, J. Rioja, J. J. Zudaire, J. M. Berián, J. A. Richter

Published in: World Journal of Urology | Issue 5/2004

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Abstract

The diagnosis of prostate cancer leaves some questions without answers. The different diagnostic techniques are limited in three situations: (1) staging of the tumour: identification of node involvement, (2) quantification of the tumour volume and its location inside the gland, (3) premature identification of relapse after radical treatment. These are the three problems that we need to consider in the diagnosis of prostate carcinoma. Imaging techniques can tell us the morphological alterations in the structures and organs. Positron emission tomography (PET) introduces a new way of identifying damage by counting metabolic activity. The tracers are substances that are marked with a radioactive molecule that is picked up more readily by the tumours. The presence of these substances in a set anatomic zone means higher consumption and therefore more metabolic activity. The radiotracer most frequently used in PET is glucose marked with fluoride 18. The first studies with marked glucose and prostate tumours started at the end of the 1990s. There are many contradictions in the results of these studies due to renal elimination, which produces an accumulation in the urinary tract and does not correctly show the prostate zone and iliobturator nodes area, and its capitation by zones with inflammatory process or prostatic hyperplasia. Choline is a substance that is present in cellular membranes. When it is marked with carbon 11, it changes to a new tracer. This radiotracer has affinity with prostate damage and allows the better differentiation of malignant from benign processes. It also has the advantage of the absence of renal elimination. Trials that used choline marked with carbon 11 (11C choline) are beginning to obtain very promising results. This union of a method that identifies metabolic activity with an imaging technique increases the sensitivity in the diagnostic test and can help find the exact location of the 11C choline deposits. The PET-CT combines the PET with computerised tomography. The 11C choline PET-CT is presented as a promising technique for answering the three problems mentioned above.
Literature
1.
go back to reference Mathews D, Orhan K (2002) Oz positron emission tomography in prostate and renal cell carcinoma. Curr Opin Urol 12:381–385CrossRefPubMed Mathews D, Orhan K (2002) Oz positron emission tomography in prostate and renal cell carcinoma. Curr Opin Urol 12:381–385CrossRefPubMed
2.
go back to reference Hara T, Kosaba N, Kishi H (1998) PET imaging of prostate cancer using carbon-11-choline. J Nucl Mec 39:990–995 Hara T, Kosaba N, Kishi H (1998) PET imaging of prostate cancer using carbon-11-choline. J Nucl Mec 39:990–995
3.
go back to reference De Jong IJ, Pruim J et al. (2003) Preoperative staging of pelvic lymph nodes in prostate cancer by 11C-choline PET. J Nucl Med 44:331–335PubMed De Jong IJ, Pruim J et al. (2003) Preoperative staging of pelvic lymph nodes in prostate cancer by 11C-choline PET. J Nucl Med 44:331–335PubMed
4.
go back to reference De Jong IJ, Pruim J, Elsinga PH et al. (2003) 11C-choline positron emission tomography for the evaluation after treatment of localized prostate cancer. Eur Urol 44:32–39CrossRefPubMed De Jong IJ, Pruim J, Elsinga PH et al. (2003) 11C-choline positron emission tomography for the evaluation after treatment of localized prostate cancer. Eur Urol 44:32–39CrossRefPubMed
5.
go back to reference Liu IJ, Zafar MB, Lai YH et al. (2001) Fluorodeoxyglucose positron emission tomography studies in diagnosis and staging of clinically organ-confined prostate cancer. Urology 57:108–111CrossRefPubMed Liu IJ, Zafar MB, Lai YH et al. (2001) Fluorodeoxyglucose positron emission tomography studies in diagnosis and staging of clinically organ-confined prostate cancer. Urology 57:108–111CrossRefPubMed
6.
go back to reference LópezJ, Boan J, Rioja J et al. (2003) Metástasis pulmonar solitaria tras prostatectomía radical. Actas Urol Esp 27:637–639PubMed LópezJ, Boan J, Rioja J et al. (2003) Metástasis pulmonar solitaria tras prostatectomía radical. Actas Urol Esp 27:637–639PubMed
7.
go back to reference Picchio M, Messa C, Landoni C et al. (2003) Value of 11C-choline-positron emission tomography for re-staging prostate cancer: a comparison with 18F fluorodeoxyglucose-positron emission tomography. J Urol 169:1337–1340CrossRefPubMed Picchio M, Messa C, Landoni C et al. (2003) Value of 11C-choline-positron emission tomography for re-staging prostate cancer: a comparison with 18F fluorodeoxyglucose-positron emission tomography. J Urol 169:1337–1340CrossRefPubMed
8.
go back to reference Sanz G, Robles JE, Gimenez M et al. (1999) Positron emission tomography with 18 fluorine labelled deoxyglucose: utility in localized and advanced prostate cancer. BJU Int 84:1028–1031CrossRefPubMed Sanz G, Robles JE, Gimenez M et al. (1999) Positron emission tomography with 18 fluorine labelled deoxyglucose: utility in localized and advanced prostate cancer. BJU Int 84:1028–1031CrossRefPubMed
9.
go back to reference Yeung H, Schoder H, Larson S (2002) Utility of PET/CT for assesing equivocal PET lesions in oncology—initial experience. J Nucl Med :43:32 Yeung H, Schoder H, Larson S (2002) Utility of PET/CT for assesing equivocal PET lesions in oncology—initial experience. J Nucl Med :43:32
Metadata
Title
PET and prostate cancer
Authors
G. Sanz
J. Rioja
J. J. Zudaire
J. M. Berián
J. A. Richter
Publication date
01-10-2004
Publisher
Springer-Verlag
Published in
World Journal of Urology / Issue 5/2004
Print ISSN: 0724-4983
Electronic ISSN: 1433-8726
DOI
https://doi.org/10.1007/s00345-004-0418-8

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