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RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma

BACKGROUND: Within a spectrum of cancers implicated by VHL germline pathogenic variants, one rare cancer which may present in patients are pheochromocytomas (PHEOs). These tumors occur in the adrenal glands and predispose patients to a variety of morbid clinical symptoms due to the excess secretion...

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Autores principales: Patel, Mayank, Jha, Abhisek, Ling, Alexander, Chen, Clara C, Millo, Corina, Talvacchio, Sara, Ezemobi, Josephine, Kailah, Charles, David, Taïeb, Carrasquillo, Jorge A, Pacak, Karel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624600/
http://dx.doi.org/10.1210/jendso/bvac150.284
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author Patel, Mayank
Jha, Abhisek
Ling, Alexander
Chen, Clara C
Millo, Corina
Talvacchio, Sara
Ezemobi, Josephine
Kailah, Charles
David, Taïeb
Carrasquillo, Jorge A
Pacak, Karel
author_facet Patel, Mayank
Jha, Abhisek
Ling, Alexander
Chen, Clara C
Millo, Corina
Talvacchio, Sara
Ezemobi, Josephine
Kailah, Charles
David, Taïeb
Carrasquillo, Jorge A
Pacak, Karel
author_sort Patel, Mayank
collection PubMed
description BACKGROUND: Within a spectrum of cancers implicated by VHL germline pathogenic variants, one rare cancer which may present in patients are pheochromocytomas (PHEOs). These tumors occur in the adrenal glands and predispose patients to a variety of morbid clinical symptoms due to the excess secretion of catecholamines. As a part of these patients’ management, imaging is important to localize the tumors of which there are both morphologic (CT and MRI) and molecular (PET/CT with (18)F-FDG, 68Ga-DOTATATE, (18)F-DOPA, and (18)F-DA) imaging modalities. PURPOSE: To determine which imaging modalities provided the optimal detection of VHL-related PHEO. METHODS: The study compared detection of 19 PHEOs (18 histologically proven and 1 is a contralateral tumor awaiting resection) in 12 patients. The CT and MRI were evaluated by a body radiologist and the PET/CT of(18)F-FDG, 68Ga-DOTATATE, (18)F-DOPA, and (18)F-DA were evaluated by a nuclear medicine physician in a blinded fashion. Both experts graded using a five-point Likert scale (1 – not PHEO and 5 – PHEO). For analysis, the Likert scale was dichotomized with 1-3 designating negative for PHEO and 4-5 positive for PHEO. The findings were reported as detection rates of positive PHEOs found on imaging to the gold standard of pathologically (aside from one contralateral PHEO awaiting surgery) proven PHEOs. The McNemar test was performed to compare the statistical relevance of detection rates between histology and the imaging modalities. Two-sided p values <0.05 were considered significant. RESULTS: The detection rates were CT 17/19 [89.5%, 95% CI = 66.9%-98.7%], MRI 17/17 [100%, 95% CI = 80.5%-100%], (18)F-FDG PET/CT 16/17 [94.1%, 95% CI = 80.5%-100%], 68Ga-DOTATATE 5/9 [55.6%, 95% CI = 21.2%-86.3%], (18)F-DOPA 12/14 [85.7%, 95% CI = 57.2%-98.2%], and (18)F-DA 4/6 [66.7%, 95% CI = 22.3%–95.7%]. All McNemar tests showed p-values greater than 0.05, which were not statistically significant. CONCLUSION: The study was performed in a small patient set with VHL-related PHEO showed MRI, with the highest detection percent followed by (18)F-FDG PET/CT. More trials with a larger patient set are needed to support the statistical relevance as it was not seen in this study. Furthermore, performing a study on a patient cohort with additional VHL associated cancers could prove clinically beneficial for patients. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m., Sunday, June 12, 2022 1:18 p.m. - 1:23 p.m.
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spelling pubmed-96246002022-11-14 RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma Patel, Mayank Jha, Abhisek Ling, Alexander Chen, Clara C Millo, Corina Talvacchio, Sara Ezemobi, Josephine Kailah, Charles David, Taïeb Carrasquillo, Jorge A Pacak, Karel J Endocr Soc Adrenal BACKGROUND: Within a spectrum of cancers implicated by VHL germline pathogenic variants, one rare cancer which may present in patients are pheochromocytomas (PHEOs). These tumors occur in the adrenal glands and predispose patients to a variety of morbid clinical symptoms due to the excess secretion of catecholamines. As a part of these patients’ management, imaging is important to localize the tumors of which there are both morphologic (CT and MRI) and molecular (PET/CT with (18)F-FDG, 68Ga-DOTATATE, (18)F-DOPA, and (18)F-DA) imaging modalities. PURPOSE: To determine which imaging modalities provided the optimal detection of VHL-related PHEO. METHODS: The study compared detection of 19 PHEOs (18 histologically proven and 1 is a contralateral tumor awaiting resection) in 12 patients. The CT and MRI were evaluated by a body radiologist and the PET/CT of(18)F-FDG, 68Ga-DOTATATE, (18)F-DOPA, and (18)F-DA were evaluated by a nuclear medicine physician in a blinded fashion. Both experts graded using a five-point Likert scale (1 – not PHEO and 5 – PHEO). For analysis, the Likert scale was dichotomized with 1-3 designating negative for PHEO and 4-5 positive for PHEO. The findings were reported as detection rates of positive PHEOs found on imaging to the gold standard of pathologically (aside from one contralateral PHEO awaiting surgery) proven PHEOs. The McNemar test was performed to compare the statistical relevance of detection rates between histology and the imaging modalities. Two-sided p values <0.05 were considered significant. RESULTS: The detection rates were CT 17/19 [89.5%, 95% CI = 66.9%-98.7%], MRI 17/17 [100%, 95% CI = 80.5%-100%], (18)F-FDG PET/CT 16/17 [94.1%, 95% CI = 80.5%-100%], 68Ga-DOTATATE 5/9 [55.6%, 95% CI = 21.2%-86.3%], (18)F-DOPA 12/14 [85.7%, 95% CI = 57.2%-98.2%], and (18)F-DA 4/6 [66.7%, 95% CI = 22.3%–95.7%]. All McNemar tests showed p-values greater than 0.05, which were not statistically significant. CONCLUSION: The study was performed in a small patient set with VHL-related PHEO showed MRI, with the highest detection percent followed by (18)F-FDG PET/CT. More trials with a larger patient set are needed to support the statistical relevance as it was not seen in this study. Furthermore, performing a study on a patient cohort with additional VHL associated cancers could prove clinically beneficial for patients. Presentation: Sunday, June 12, 2022 12:30 p.m. - 2:30 p.m., Sunday, June 12, 2022 1:18 p.m. - 1:23 p.m. Oxford University Press 2022-11-01 /pmc/articles/PMC9624600/ http://dx.doi.org/10.1210/jendso/bvac150.284 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Adrenal
Patel, Mayank
Jha, Abhisek
Ling, Alexander
Chen, Clara C
Millo, Corina
Talvacchio, Sara
Ezemobi, Josephine
Kailah, Charles
David, Taïeb
Carrasquillo, Jorge A
Pacak, Karel
RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title_full RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title_fullStr RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title_full_unstemmed RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title_short RF21 | PSUN08 Morphologic or Molecular Imaging - Diagnostic Capabilities in von Hippel-Lindau related pheochromocytoma
title_sort rf21 | psun08 morphologic or molecular imaging - diagnostic capabilities in von hippel-lindau related pheochromocytoma
topic Adrenal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624600/
http://dx.doi.org/10.1210/jendso/bvac150.284
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