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Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging

BACKGROUND: Merkel cell carcinoma (MCC) is a rare cutaneous neoplasm with increasing incidence, aggressive behavior and poor prognosis. Somatostatin receptors (SSTR) are expressed in MCC and represent a potential target for both imaging and treatment. METHODS: To non-invasively assess SSTR expressio...

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Autores principales: Buder, Kristina, Lapa, Constantin, Kreissl, Michael C, Schirbel, Andreas, Herrmann, Ken, Schnack, Alexander, Bröcker, Eva-Bettina, Goebeler, Matthias, Buck, Andreas K, Becker, Jürgen C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021101/
https://www.ncbi.nlm.nih.gov/pubmed/24742330
http://dx.doi.org/10.1186/1471-2407-14-268
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author Buder, Kristina
Lapa, Constantin
Kreissl, Michael C
Schirbel, Andreas
Herrmann, Ken
Schnack, Alexander
Bröcker, Eva-Bettina
Goebeler, Matthias
Buck, Andreas K
Becker, Jürgen C
author_facet Buder, Kristina
Lapa, Constantin
Kreissl, Michael C
Schirbel, Andreas
Herrmann, Ken
Schnack, Alexander
Bröcker, Eva-Bettina
Goebeler, Matthias
Buck, Andreas K
Becker, Jürgen C
author_sort Buder, Kristina
collection PubMed
description BACKGROUND: Merkel cell carcinoma (MCC) is a rare cutaneous neoplasm with increasing incidence, aggressive behavior and poor prognosis. Somatostatin receptors (SSTR) are expressed in MCC and represent a potential target for both imaging and treatment. METHODS: To non-invasively assess SSTR expression in MCC using PET and the radiotracers [(68)Ga]DOTA-D-Phe(1)-Tyr(3)-octreotide (DOTATOC) or -octreotate (DOTATATE) as surrogate for tumor burden. In 24 patients with histologically proven MCC SSTR-PET was performed and compared to results of computed tomography (CT). RESULTS: SSTR-PET detected primary and metastatic MCC lesions. On a patient-based analysis, sensitivity of SSTR-PET was 73% for nodal metastases, 100% for bone, and 67% for soft-tissue metastases, respectively. Notably, brain metastases were initially detected by SSTR-PET in 2 patients, whereas liver and lung metastases were diagnosed exclusively by CT. SSTR-PET showed concordance to CT results in 20 out of 24 patients. Four patients (17%) were up-staged due to SSTR-PET and patient management was changed in 3 patients (13%). CONCLUSION: SSTR-PET showed high sensitivity for imaging bone, soft tissue and brain metastases, and particularly in combination with CT had a significant impact on clinical stage and patient management.
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spelling pubmed-40211012014-05-16 Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging Buder, Kristina Lapa, Constantin Kreissl, Michael C Schirbel, Andreas Herrmann, Ken Schnack, Alexander Bröcker, Eva-Bettina Goebeler, Matthias Buck, Andreas K Becker, Jürgen C BMC Cancer Research Article BACKGROUND: Merkel cell carcinoma (MCC) is a rare cutaneous neoplasm with increasing incidence, aggressive behavior and poor prognosis. Somatostatin receptors (SSTR) are expressed in MCC and represent a potential target for both imaging and treatment. METHODS: To non-invasively assess SSTR expression in MCC using PET and the radiotracers [(68)Ga]DOTA-D-Phe(1)-Tyr(3)-octreotide (DOTATOC) or -octreotate (DOTATATE) as surrogate for tumor burden. In 24 patients with histologically proven MCC SSTR-PET was performed and compared to results of computed tomography (CT). RESULTS: SSTR-PET detected primary and metastatic MCC lesions. On a patient-based analysis, sensitivity of SSTR-PET was 73% for nodal metastases, 100% for bone, and 67% for soft-tissue metastases, respectively. Notably, brain metastases were initially detected by SSTR-PET in 2 patients, whereas liver and lung metastases were diagnosed exclusively by CT. SSTR-PET showed concordance to CT results in 20 out of 24 patients. Four patients (17%) were up-staged due to SSTR-PET and patient management was changed in 3 patients (13%). CONCLUSION: SSTR-PET showed high sensitivity for imaging bone, soft tissue and brain metastases, and particularly in combination with CT had a significant impact on clinical stage and patient management. BioMed Central 2014-04-17 /pmc/articles/PMC4021101/ /pubmed/24742330 http://dx.doi.org/10.1186/1471-2407-14-268 Text en Copyright © 2014 Buder et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Buder, Kristina
Lapa, Constantin
Kreissl, Michael C
Schirbel, Andreas
Herrmann, Ken
Schnack, Alexander
Bröcker, Eva-Bettina
Goebeler, Matthias
Buck, Andreas K
Becker, Jürgen C
Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title_full Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title_fullStr Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title_full_unstemmed Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title_short Somatostatin receptor expression in Merkel cell carcinoma as target for molecular imaging
title_sort somatostatin receptor expression in merkel cell carcinoma as target for molecular imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021101/
https://www.ncbi.nlm.nih.gov/pubmed/24742330
http://dx.doi.org/10.1186/1471-2407-14-268
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