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S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients
BACKGROUND AND OBJECTIVES: This current study assessed the value of S‐100B measurement to guide fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) scanning for detecting recurrent disease in stage III melanoma patients. METHODS: This study included 100 stage III melan...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851671/ https://www.ncbi.nlm.nih.gov/pubmed/31468535 http://dx.doi.org/10.1002/jso.25682 |
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author | Deckers, Eric A. Wevers, Kevin P. Muller Kobold, Anneke C. Damude, Samantha Vrielink, Otis M. van Ginkel, Robert J. Been, Lukas B. van Leeuwen, Barbara L. Hoekstra, Harald J. Kruijff, Schelto |
author_facet | Deckers, Eric A. Wevers, Kevin P. Muller Kobold, Anneke C. Damude, Samantha Vrielink, Otis M. van Ginkel, Robert J. Been, Lukas B. van Leeuwen, Barbara L. Hoekstra, Harald J. Kruijff, Schelto |
author_sort | Deckers, Eric A. |
collection | PubMed |
description | BACKGROUND AND OBJECTIVES: This current study assessed the value of S‐100B measurement to guide fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) scanning for detecting recurrent disease in stage III melanoma patients. METHODS: This study included 100 stage III melanoma patients in follow‐up after curative lymph node dissection. Follow‐up visits included physical examination and S‐100B monitoring. FDG PET/CT scanning was indicated by clinical symptoms and/or elevated S‐100B. RESULTS: Of 100 patients, 13 (13%) had elevated S‐100B without clinical symptoms, of whom 7 (54%) showed disease evidence upon FDG PET/CT scanning. Twenty‐six patients (26%) had clinical symptoms with normal S‐100B and FDG PET/CT revealed metastasis in 20 (77%). Three patients had clinical symptoms and elevated S‐100B, and FDG PET/CT revealed metastasis in all three (100%). Overall, FDG PET/CT scanning revealed metastasis in 30 of the 42 patients (71.4%). For seven recurrences, elevated S‐100B prompted early detection of asymptomatic disease; 10% of all asymptomatic patients in follow‐up, 23% of all patients with recurrent disease. CONCLUSION: S‐100B cannot exclude recurrent disease during follow‐up of stage III melanoma. However, adding S‐100B measurement to standard clinical assessment can guide FDG PET/CT scanning for detecting recurrent melanoma. |
format | Online Article Text |
id | pubmed-6851671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68516712019-11-18 S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients Deckers, Eric A. Wevers, Kevin P. Muller Kobold, Anneke C. Damude, Samantha Vrielink, Otis M. van Ginkel, Robert J. Been, Lukas B. van Leeuwen, Barbara L. Hoekstra, Harald J. Kruijff, Schelto J Surg Oncol Research Articles BACKGROUND AND OBJECTIVES: This current study assessed the value of S‐100B measurement to guide fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) scanning for detecting recurrent disease in stage III melanoma patients. METHODS: This study included 100 stage III melanoma patients in follow‐up after curative lymph node dissection. Follow‐up visits included physical examination and S‐100B monitoring. FDG PET/CT scanning was indicated by clinical symptoms and/or elevated S‐100B. RESULTS: Of 100 patients, 13 (13%) had elevated S‐100B without clinical symptoms, of whom 7 (54%) showed disease evidence upon FDG PET/CT scanning. Twenty‐six patients (26%) had clinical symptoms with normal S‐100B and FDG PET/CT revealed metastasis in 20 (77%). Three patients had clinical symptoms and elevated S‐100B, and FDG PET/CT revealed metastasis in all three (100%). Overall, FDG PET/CT scanning revealed metastasis in 30 of the 42 patients (71.4%). For seven recurrences, elevated S‐100B prompted early detection of asymptomatic disease; 10% of all asymptomatic patients in follow‐up, 23% of all patients with recurrent disease. CONCLUSION: S‐100B cannot exclude recurrent disease during follow‐up of stage III melanoma. However, adding S‐100B measurement to standard clinical assessment can guide FDG PET/CT scanning for detecting recurrent melanoma. John Wiley and Sons Inc. 2019-08-29 2019-11-01 /pmc/articles/PMC6851671/ /pubmed/31468535 http://dx.doi.org/10.1002/jso.25682 Text en © 2019 The Authors. Journal of Surgical Oncology published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Deckers, Eric A. Wevers, Kevin P. Muller Kobold, Anneke C. Damude, Samantha Vrielink, Otis M. van Ginkel, Robert J. Been, Lukas B. van Leeuwen, Barbara L. Hoekstra, Harald J. Kruijff, Schelto S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title | S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title_full | S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title_fullStr | S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title_full_unstemmed | S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title_short | S‐100B as an extra selection tool for FDG PET/CT scanning in follow‐up of AJCC stage III melanoma patients |
title_sort | s‐100b as an extra selection tool for fdg pet/ct scanning in follow‐up of ajcc stage iii melanoma patients |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851671/ https://www.ncbi.nlm.nih.gov/pubmed/31468535 http://dx.doi.org/10.1002/jso.25682 |
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