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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.
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.
Afiliación
  • van der Beek JN; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Hol JA; Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
  • Coulomb-l'Hermine A; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Graf N; Sorbonne Université/Assistance Publique Hôpitaux de Paris-Hôpital Armand Trousseau, Paris, France.
  • van Tinteren H; Department of Pediatric Oncology and Hematology, Saarland University Medical Center and Saarland University Faculty of Medicine, Homburg, Germany.
  • Pritchard-Jones K; Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Houwing ME; UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • de Krijger RR; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Vujanic GM; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Dzhuma K; Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Schenk JP; Department of Pathology, Sidra Medicine, Doha, Qatar.
  • Littooij AS; UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Ramírez-Villar GL; Clinic of Diagnostic and Interventional Radiology, Division of Pediatric Radiology, Heidelberg University Hospital, Heidelberg, Germany.
  • Murphy D; Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
  • Ray S; Department of Radiology and Nuclear Medicine, University Medical Center Utrecht/Wilhelmina Children's Hospital, Utrecht University, Utrecht, The Netherlands.
  • Al-Saadi R; Department of Paediatric Oncology, Hospital Universitario Virgen del Rocío, Seville, Spain.
  • Gessler M; Department of Paediatric Oncology, Royal Hospital for Children, Glasgow, Scotland.
  • Godzinski J; Department of Paediatric Oncology, Royal Hospital for Children, Glasgow, Scotland.
  • Ruebe C; UCL Great Ormond Street Institute of Child Health, University College London, London, UK.
  • Collini P; Department of Histopathology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Verschuur AC; Theodor-Boveri-Institute/Biocenter, University of Wuerzburg, Wuerzburg, Germany.
  • Frisk T; Department of Paediatric Surgery, Marciniak Hospital, Wroclaw, Poland.
  • Vokuhl C; Department of Paediatric Traumatology and Emergency Medicine, Marciniak Hospital, Wroclaw, Poland.
  • Hulsbergen-van de Kaa CA; Department of Radiation Oncology, Saarland University Medical Center and Saarland University Faculty of Medicine, Homburg, Germany.
  • de Camargo B; Department of Pathology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.
  • Sandstedt B; Department of Pediatric Oncology, Hôpital d'Enfants de la Timone, Marseille, France.
  • Selle B; Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
  • Tytgat GAM; Section of Pediatric Pathology, University Hospital Bonn, Bonn, Germany.
  • van den Heuvel-Eibrink MM; Laboratory of Pathology East Netherlands (LABPON), Hengelo, The Netherlands.
Int J Cancer ; 148(11): 2724-2735, 2021 06 01.
Article en En | MEDLINE | ID: mdl-33460450
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Factores de Transcripción Básicos con Cremalleras de Leucinas y Motivos Hélice-Asa-Hélice / Neoplasias Renales Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Factores de Transcripción Básicos con Cremalleras de Leucinas y Motivos Hélice-Asa-Hélice / Neoplasias Renales Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Revista: Int J Cancer Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos