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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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. |
format | Online Article Text |
id | pubmed-4021101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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