Outcome of extracranial malignant rhabdoid tumours in children registered in the European Paediatric Soft Tissue Sarcoma Study Group Non-Rhabdomyosarcoma Soft Tissue Sarcoma 2005 Study—EpSSG NRSTS 2005

Extracranial malignant rhabdoid tumours (MRT) are rare lethal childhood cancers that often occur in infants and have a characteristic genetic mutation in the SMARCB1 gene. The European Paediatric Soft Tissue Sarcoma Study Group (EpSSG) conducted a multinational prospective study of registered cases...

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Bibliographic Details
Published in:European journal of cancer (1990) 2016-06, Vol.60, p.69-82
Main Authors: Brennan, Bernadette, De Salvo, Gian Luca, Orbach, Daniel, De Paoli, Angela, Kelsey, Anna, Mudry, Peter, Francotte, Nadine, Van Noesel, Max, Bisogno, Gianni, Casanova, Michela, Ferrari, Andrea
Format: Article
Language:English
Subjects:
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Chemoradiotherapy, Adjuvant
Child
Child, Preschool
Cyclophosphamide - administration & dosage
Disease-Free Survival
Doxorubicin - administration & dosage
Female
Hematology, Oncology and Palliative Medicine
Humans
Infant
Infant, Newborn
Male
Malignant rhabdoid tumour
Neoplasm Staging
Paediatric
Prognostic factors
Prospective registry
Prospective Studies
Rhabdoid Tumor - mortality
Rhabdoid Tumor - pathology
Rhabdoid Tumor - therapy
Sarcoma - mortality
Sarcoma - pathology
Sarcoma - therapy
Survival
Vincristine - administration & dosage
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