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Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases

SIMPLE SUMMARY: Pediatric COG stage II and III adrenocortical carcinoma (ACC) is one of the most unpredictable and challenging tumors in terms of prognosis and management. The EXPeRT/PARTNER recommendation suggested inclusion of the five-item microscopic score to guide management in these patients....

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Autores principales: Kuhlen, Michaela, Mier, Pascal, Kunstreich, Marina, Lessel, Lienhard, Slavetinsky, Christoph, Fuchs, Jörg, Seitz, Guido, Holterhus, Paul-Martin, Wudy, Stefan A., Vokuhl, Christian, Frühwald, Michael C., Vorwerk, Peter, Redlich, Antje
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486626/
https://www.ncbi.nlm.nih.gov/pubmed/37686571
http://dx.doi.org/10.3390/cancers15174296
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author Kuhlen, Michaela
Mier, Pascal
Kunstreich, Marina
Lessel, Lienhard
Slavetinsky, Christoph
Fuchs, Jörg
Seitz, Guido
Holterhus, Paul-Martin
Wudy, Stefan A.
Vokuhl, Christian
Frühwald, Michael C.
Vorwerk, Peter
Redlich, Antje
author_facet Kuhlen, Michaela
Mier, Pascal
Kunstreich, Marina
Lessel, Lienhard
Slavetinsky, Christoph
Fuchs, Jörg
Seitz, Guido
Holterhus, Paul-Martin
Wudy, Stefan A.
Vokuhl, Christian
Frühwald, Michael C.
Vorwerk, Peter
Redlich, Antje
author_sort Kuhlen, Michaela
collection PubMed
description SIMPLE SUMMARY: Pediatric COG stage II and III adrenocortical carcinoma (ACC) is one of the most unpredictable and challenging tumors in terms of prognosis and management. The EXPeRT/PARTNER recommendation suggested inclusion of the five-item microscopic score to guide management in these patients. In this study, we report on 18 pediatric ACC stage II and 37 stage III patients registered with the German MET studies. We explored the five-item microscopic and the pS-GRAS score to predict outcome. Three-year event-free survival estimates were 76.5% in stage II and 49.8% in stage III patients. In COG stage III patients, EFS was impaired for patients with unfavorable histology according to the five-item score. No differences were observed in stage II patients and in the pS-GRAS groups. Further research including molecular studies is needed to identify high-risk features in locally advanced pediatric ACC tumors. ABSTRACT: Background: Locally advanced tumors account for approximately 50% of children and adolescents with adrenocortical carcinoma (ACC), and of these, up to 50% relapse. We explored the five-item microscopic score and the pS-GRAS score for guiding management. Methods: Data from children and adolescents with COG stage II and III ACC registered in the MET studies were included. The five-item and pS-GRAS score were retrospectively calculated. Results: By December 2021, 55 patients with stage II and III (stage II n = 18, stage III n = 37) had been reported. Median age was 4.3 years [0.1–17.8], median duration of follow-up 6.0 years [0–16.7]. 3-year event-free survival (EFS) rate was 76.5% and 49.8% (p = 0.088), respectively. In stage II tumors, neither the five-item score (p = 0.872) nor pS-GRAS grouping (p = 0.218) had any effect as prognostic factors. In stage III patients, EFS was impaired in tumors with unfavorable histology according to the five-item score (100% vs. 30.8%, p = 0.018). No difference was observed for pS-GRAS groups (p = 0.798). Conclusions: In patients with COG stage III, but not stage II, the five-item score affected EFS. Further studies are needed to identify patients at risk in COG stage II.
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spelling pubmed-104866262023-09-09 Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases Kuhlen, Michaela Mier, Pascal Kunstreich, Marina Lessel, Lienhard Slavetinsky, Christoph Fuchs, Jörg Seitz, Guido Holterhus, Paul-Martin Wudy, Stefan A. Vokuhl, Christian Frühwald, Michael C. Vorwerk, Peter Redlich, Antje Cancers (Basel) Article SIMPLE SUMMARY: Pediatric COG stage II and III adrenocortical carcinoma (ACC) is one of the most unpredictable and challenging tumors in terms of prognosis and management. The EXPeRT/PARTNER recommendation suggested inclusion of the five-item microscopic score to guide management in these patients. In this study, we report on 18 pediatric ACC stage II and 37 stage III patients registered with the German MET studies. We explored the five-item microscopic and the pS-GRAS score to predict outcome. Three-year event-free survival estimates were 76.5% in stage II and 49.8% in stage III patients. In COG stage III patients, EFS was impaired for patients with unfavorable histology according to the five-item score. No differences were observed in stage II patients and in the pS-GRAS groups. Further research including molecular studies is needed to identify high-risk features in locally advanced pediatric ACC tumors. ABSTRACT: Background: Locally advanced tumors account for approximately 50% of children and adolescents with adrenocortical carcinoma (ACC), and of these, up to 50% relapse. We explored the five-item microscopic score and the pS-GRAS score for guiding management. Methods: Data from children and adolescents with COG stage II and III ACC registered in the MET studies were included. The five-item and pS-GRAS score were retrospectively calculated. Results: By December 2021, 55 patients with stage II and III (stage II n = 18, stage III n = 37) had been reported. Median age was 4.3 years [0.1–17.8], median duration of follow-up 6.0 years [0–16.7]. 3-year event-free survival (EFS) rate was 76.5% and 49.8% (p = 0.088), respectively. In stage II tumors, neither the five-item score (p = 0.872) nor pS-GRAS grouping (p = 0.218) had any effect as prognostic factors. In stage III patients, EFS was impaired in tumors with unfavorable histology according to the five-item score (100% vs. 30.8%, p = 0.018). No difference was observed for pS-GRAS groups (p = 0.798). Conclusions: In patients with COG stage III, but not stage II, the five-item score affected EFS. Further studies are needed to identify patients at risk in COG stage II. MDPI 2023-08-28 /pmc/articles/PMC10486626/ /pubmed/37686571 http://dx.doi.org/10.3390/cancers15174296 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kuhlen, Michaela
Mier, Pascal
Kunstreich, Marina
Lessel, Lienhard
Slavetinsky, Christoph
Fuchs, Jörg
Seitz, Guido
Holterhus, Paul-Martin
Wudy, Stefan A.
Vokuhl, Christian
Frühwald, Michael C.
Vorwerk, Peter
Redlich, Antje
Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title_full Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title_fullStr Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title_full_unstemmed Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title_short Locally Advanced Adrenocortical Carcinoma in Children and Adolescents—Enigmatic and Challenging Cases
title_sort locally advanced adrenocortical carcinoma in children and adolescents—enigmatic and challenging cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486626/
https://www.ncbi.nlm.nih.gov/pubmed/37686571
http://dx.doi.org/10.3390/cancers15174296
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