Please use this identifier to cite or link to this item: doi:10.22028/D291-40614
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
Author(s): 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.
Language: English
Title: International Journal of Cancer
Volume: 148
Issue: 11
Pages: 2724-2735
Publisher/Platform: Wiley
Year of Publication: 2021
Free key words: pediatric
renal cell carcinoma
survival
treatment
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: 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.
DOI of the first publication: 10.1002/ijc.33476
URL of the first publication: https://doi.org/10.1002/ijc.33476
Link to this record: urn:nbn:de:bsz:291--ds-406141
hdl:20.500.11880/36492
http://dx.doi.org/10.22028/D291-40614
ISSN: 1097-0215
0020-7136
Date of registration: 27-Sep-2023
Description of the related object: Supporting Information
Related object: https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fijc.33476&file=ijc33476-sup-0001-supinfo.pdf
Faculty: M - Medizinische Fakultät
Department: M - Pädiatrie
M - Radiologie
Professorship: M - Prof. Dr. Norbert Graf
M - Prof. Dr. Christian Rübe
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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