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Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology

BACKGROUND: Medullary thyroid cancer (MTC) is rare, with poorer outcomes than differentiated thyroid cancer. We aimed to identify areas for improvement in the pre‐operative evaluation of patients with possible MTC in a high‐volume endocrine surgery unit in accordance with current practice guidelines...

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Autores principales: Jassal, Karishma, Ravintharan, Nandhini, Prabhakaran, Swetha, Grodski, Simon, Serpell, Jonathan W., Lee, James C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321997/
https://www.ncbi.nlm.nih.gov/pubmed/35412008
http://dx.doi.org/10.1111/ans.17690
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author Jassal, Karishma
Ravintharan, Nandhini
Prabhakaran, Swetha
Grodski, Simon
Serpell, Jonathan W.
Lee, James C.
author_facet Jassal, Karishma
Ravintharan, Nandhini
Prabhakaran, Swetha
Grodski, Simon
Serpell, Jonathan W.
Lee, James C.
author_sort Jassal, Karishma
collection PubMed
description BACKGROUND: Medullary thyroid cancer (MTC) is rare, with poorer outcomes than differentiated thyroid cancer. We aimed to identify areas for improvement in the pre‐operative evaluation of patients with possible MTC in a high‐volume endocrine surgery unit in accordance with current practice guidelines. We hypothesised that the selective use of serum calcitonin (sCT) as a biomarker for possible MTC could guide the extent of initial surgical management. METHODS: We recruited MTC patients between 2000 and 2020 from the Monash University Endocrine Surgery Unit database. Demographics, tumour characteristics, pre‐operative evaluation, operative management, and outcomes were analysed. RESULTS: Of 1454 thyroid cancer patients, 43 (3%) had MTC. Pre‐operatively, 36 (84%) patients with MTC confirmed on cytology (28, 65%), elevated sCT (6, 14%) or RET mutation (2, 4%). Of these 36 patients, 31 (86%) had optimal extent of thyroidectomy and lymph node dissection (LND). Five (14%) had less than total thyroidectomy due to nerve injury. Thirty‐four patients had compartmental LND. In the 12 (27%) patients with indeterminate or non‐diagnostic cytology, 5 had elevated sCT and were managed as above. None of the remaining seven had LND, thus potentially suboptimal surgery. CONCLUSION: Our findings reflect the rarity of MTC, and the challenges of pre‐operative diagnosis. The addition of sCT may improve surgical planning in patients with indeterminate cytology.
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spelling pubmed-93219972022-07-30 Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology Jassal, Karishma Ravintharan, Nandhini Prabhakaran, Swetha Grodski, Simon Serpell, Jonathan W. Lee, James C. ANZ J Surg Endocrine Surgery BACKGROUND: Medullary thyroid cancer (MTC) is rare, with poorer outcomes than differentiated thyroid cancer. We aimed to identify areas for improvement in the pre‐operative evaluation of patients with possible MTC in a high‐volume endocrine surgery unit in accordance with current practice guidelines. We hypothesised that the selective use of serum calcitonin (sCT) as a biomarker for possible MTC could guide the extent of initial surgical management. METHODS: We recruited MTC patients between 2000 and 2020 from the Monash University Endocrine Surgery Unit database. Demographics, tumour characteristics, pre‐operative evaluation, operative management, and outcomes were analysed. RESULTS: Of 1454 thyroid cancer patients, 43 (3%) had MTC. Pre‐operatively, 36 (84%) patients with MTC confirmed on cytology (28, 65%), elevated sCT (6, 14%) or RET mutation (2, 4%). Of these 36 patients, 31 (86%) had optimal extent of thyroidectomy and lymph node dissection (LND). Five (14%) had less than total thyroidectomy due to nerve injury. Thirty‐four patients had compartmental LND. In the 12 (27%) patients with indeterminate or non‐diagnostic cytology, 5 had elevated sCT and were managed as above. None of the remaining seven had LND, thus potentially suboptimal surgery. CONCLUSION: Our findings reflect the rarity of MTC, and the challenges of pre‐operative diagnosis. The addition of sCT may improve surgical planning in patients with indeterminate cytology. John Wiley & Sons Australia, Ltd 2022-04-12 2022-06 /pmc/articles/PMC9321997/ /pubmed/35412008 http://dx.doi.org/10.1111/ans.17690 Text en © 2022 The Authors. ANZ Journal of Surgery published by John Wiley & Sons Australia, Ltd on behalf of Royal Australasian College of Surgeons. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Endocrine Surgery
Jassal, Karishma
Ravintharan, Nandhini
Prabhakaran, Swetha
Grodski, Simon
Serpell, Jonathan W.
Lee, James C.
Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title_full Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title_fullStr Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title_full_unstemmed Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title_short Preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
title_sort preoperative serum calcitonin may improve initial surgery for medullary thyroid cancer in patients with indeterminate cytology
topic Endocrine Surgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9321997/
https://www.ncbi.nlm.nih.gov/pubmed/35412008
http://dx.doi.org/10.1111/ans.17690
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