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Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group

In children, renal cell carcinoma (RCC) is rare. This study is the first report of pediatric patients with RCC registered by the International Society of Pediatric Oncology‐Renal Tumor Study Group (SIOP‐RTSG). Pediatric patients with histologically confirmed RCC, registered in SIOP 93‐01, 2001 and U...

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Autores principales: van der Beek, Justine N., Hol, Janna A., Coulomb‐l'Hermine, Aurore, Graf, Norbert, van Tinteren, Harm, Pritchard‐Jones, Kathy, Houwing, Maite E., de Krijger, Ronald R., Vujanic, Gordan M., Dzhuma, Kristina, Schenk, Jens‐Peter, Littooij, Annemieke S., Ramírez‐Villar, Gema L., Murphy, Dermot, Ray, Satyajit, Al‐Saadi, Reem, Gessler, Manfred, Godzinski, Jan, Ruebe, Christian, Collini, Paola, Verschuur, Arnaud C., Frisk, Tony, Vokuhl, Christian, Hulsbergen‐van de Kaa, Christina A., de Camargo, Beatriz, Sandstedt, Bengt, Selle, Barbara, Tytgat, Godelieve A. M., van den Heuvel‐Eibrink, Marry M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048605/
https://www.ncbi.nlm.nih.gov/pubmed/33460450
http://dx.doi.org/10.1002/ijc.33476
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author van der Beek, Justine N.
Hol, Janna A.
Coulomb‐l'Hermine, Aurore
Graf, Norbert
van Tinteren, Harm
Pritchard‐Jones, Kathy
Houwing, Maite E.
de Krijger, Ronald R.
Vujanic, Gordan M.
Dzhuma, Kristina
Schenk, Jens‐Peter
Littooij, Annemieke S.
Ramírez‐Villar, Gema L.
Murphy, Dermot
Ray, Satyajit
Al‐Saadi, Reem
Gessler, Manfred
Godzinski, Jan
Ruebe, Christian
Collini, Paola
Verschuur, Arnaud C.
Frisk, Tony
Vokuhl, Christian
Hulsbergen‐van de Kaa, Christina A.
de Camargo, Beatriz
Sandstedt, Bengt
Selle, Barbara
Tytgat, Godelieve A. M.
van den Heuvel‐Eibrink, Marry M.
author_facet van der Beek, Justine N.
Hol, Janna A.
Coulomb‐l'Hermine, Aurore
Graf, Norbert
van Tinteren, Harm
Pritchard‐Jones, Kathy
Houwing, Maite E.
de Krijger, Ronald R.
Vujanic, Gordan M.
Dzhuma, Kristina
Schenk, Jens‐Peter
Littooij, Annemieke S.
Ramírez‐Villar, Gema L.
Murphy, Dermot
Ray, Satyajit
Al‐Saadi, Reem
Gessler, Manfred
Godzinski, Jan
Ruebe, Christian
Collini, Paola
Verschuur, Arnaud C.
Frisk, Tony
Vokuhl, Christian
Hulsbergen‐van de Kaa, Christina A.
de Camargo, Beatriz
Sandstedt, Bengt
Selle, Barbara
Tytgat, Godelieve A. M.
van den Heuvel‐Eibrink, Marry M.
author_sort van der Beek, Justine N.
collection PubMed
description In children, renal cell carcinoma (RCC) is rare. This study is the first report of pediatric patients with RCC registered by the International Society of Pediatric Oncology‐Renal Tumor Study Group (SIOP‐RTSG). Pediatric patients with histologically confirmed RCC, registered in SIOP 93‐01, 2001 and UK‐IMPORT databases, were included. Event‐free survival (EFS) and overall survival (OS) were analyzed using the Kaplan‐Meier method. Between 1993 and 2019, 122 pediatric patients with RCC were registered. Available detailed data (n = 111) revealed 56 localized, 30 regionally advanced, 25 metastatic and no bilateral cases. Histological classification according to World Health Organization 2004, including immunohistochemical and molecular testing for transcription factor E3 (TFE3) and/or EB (TFEB) translocation, was available for 65/122 patients. In this group, the most common histological subtypes were translocation type RCC (MiT‐RCC) (36/64, 56.3%), papillary type (19/64, 29.7%) and clear cell type (4/64, 6.3%). One histological subtype was not reported. In the remaining 57 patients, translocation testing could not be performed, or TFE‐cytogenetics and/or immunohistochemistry results were missing. In this group, the most common RCC histological subtypes were papillary type (21/47, 44.7%) and clear cell type (11/47, 23.4%). Ten histological subtypes were not reported. Estimated 5‐year (5y) EFS and 5y OS of the total group was 70.5% (95% CI = 61.7%‐80.6%) and 84.5% (95% CI = 77.5%‐92.2%), respectively. Estimated 5y OS for localized, regionally advanced, and metastatic disease was 96.8%, 92.3%, and 45.6%, respectively. In conclusion, the registered pediatric patients with RCC showed a reasonable outcome. Survival was substantially lower for patients with metastatic disease. This descriptive study stresses the importance of full, prospective registration including TFE‐testing.
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spelling pubmed-80486052021-04-19 Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group van der Beek, Justine N. Hol, Janna A. Coulomb‐l'Hermine, Aurore Graf, Norbert van Tinteren, Harm Pritchard‐Jones, Kathy Houwing, Maite E. de Krijger, Ronald R. Vujanic, Gordan M. Dzhuma, Kristina Schenk, Jens‐Peter Littooij, Annemieke S. Ramírez‐Villar, Gema L. Murphy, Dermot Ray, Satyajit Al‐Saadi, Reem Gessler, Manfred Godzinski, Jan Ruebe, Christian Collini, Paola Verschuur, Arnaud C. Frisk, Tony Vokuhl, Christian Hulsbergen‐van de Kaa, Christina A. de Camargo, Beatriz Sandstedt, Bengt Selle, Barbara Tytgat, Godelieve A. M. van den Heuvel‐Eibrink, Marry M. Int J Cancer Cancer Epidemiology In children, renal cell carcinoma (RCC) is rare. This study is the first report of pediatric patients with RCC registered by the International Society of Pediatric Oncology‐Renal Tumor Study Group (SIOP‐RTSG). Pediatric patients with histologically confirmed RCC, registered in SIOP 93‐01, 2001 and UK‐IMPORT databases, were included. Event‐free survival (EFS) and overall survival (OS) were analyzed using the Kaplan‐Meier method. Between 1993 and 2019, 122 pediatric patients with RCC were registered. Available detailed data (n = 111) revealed 56 localized, 30 regionally advanced, 25 metastatic and no bilateral cases. Histological classification according to World Health Organization 2004, including immunohistochemical and molecular testing for transcription factor E3 (TFE3) and/or EB (TFEB) translocation, was available for 65/122 patients. In this group, the most common histological subtypes were translocation type RCC (MiT‐RCC) (36/64, 56.3%), papillary type (19/64, 29.7%) and clear cell type (4/64, 6.3%). One histological subtype was not reported. In the remaining 57 patients, translocation testing could not be performed, or TFE‐cytogenetics and/or immunohistochemistry results were missing. In this group, the most common RCC histological subtypes were papillary type (21/47, 44.7%) and clear cell type (11/47, 23.4%). Ten histological subtypes were not reported. Estimated 5‐year (5y) EFS and 5y OS of the total group was 70.5% (95% CI = 61.7%‐80.6%) and 84.5% (95% CI = 77.5%‐92.2%), respectively. Estimated 5y OS for localized, regionally advanced, and metastatic disease was 96.8%, 92.3%, and 45.6%, respectively. In conclusion, the registered pediatric patients with RCC showed a reasonable outcome. Survival was substantially lower for patients with metastatic disease. This descriptive study stresses the importance of full, prospective registration including TFE‐testing. John Wiley & Sons, Inc. 2021-02-03 2021-06-01 /pmc/articles/PMC8048605/ /pubmed/33460450 http://dx.doi.org/10.1002/ijc.33476 Text en © 2021 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Epidemiology
van der Beek, Justine N.
Hol, Janna A.
Coulomb‐l'Hermine, Aurore
Graf, Norbert
van Tinteren, Harm
Pritchard‐Jones, Kathy
Houwing, Maite E.
de Krijger, Ronald R.
Vujanic, Gordan M.
Dzhuma, Kristina
Schenk, Jens‐Peter
Littooij, Annemieke S.
Ramírez‐Villar, Gema L.
Murphy, Dermot
Ray, Satyajit
Al‐Saadi, Reem
Gessler, Manfred
Godzinski, Jan
Ruebe, Christian
Collini, Paola
Verschuur, Arnaud C.
Frisk, Tony
Vokuhl, Christian
Hulsbergen‐van de Kaa, Christina A.
de Camargo, Beatriz
Sandstedt, Bengt
Selle, Barbara
Tytgat, Godelieve A. M.
van den Heuvel‐Eibrink, Marry M.
Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title_full Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title_fullStr Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title_full_unstemmed Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title_short Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A report of the SIOP‐Renal Tumor Study Group
title_sort characteristics and outcome of pediatric renal cell carcinoma patients registered in the international society of pediatric oncology (siop) 93‐01, 2001 and uk‐import database: a report of the siop‐renal tumor study group
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048605/
https://www.ncbi.nlm.nih.gov/pubmed/33460450
http://dx.doi.org/10.1002/ijc.33476
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