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Metastatic adult-type non-rhabdomyosarcoma soft tissue sarcomas in children and adolescents: A cohort study from the European paediatric Soft tissue sarcoma Study Group.
Ferrari, Andrea; Orbach, Daniel; Casanova, Michela; van Noesel, Max M; Berlanga, Pablo; Brennan, Bernadette; Corradini, Nadege; Schoot, Reineke A; Ramirez-Villar, Gema L; Hjalgrim, Lisa Lyngsie; Alaggio, Rita; Guillen Burrieza, Gabriela; Safwat, Akmal; Cameron, Alison L; van Rijn, Rick R; Minard-Colin, Veronique; Zanetti, Ilaria; Bisogno, Gianni; Chisholm, Julia C; Merks, Johannes H M.
Afiliación
  • Ferrari A; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
  • Orbach D; SIREDO Oncology Center, Institut Curie, PSL University, Paris, France.
  • Casanova M; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale Tumori, Milano, Italy.
  • van Noesel MM; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
  • Berlanga P; Department of Pediatric and Adolescent Oncology, Gustave-Roussy, Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Brennan B; Pediatric Oncology, Royal Manchester Children's Hospital, Manchester, UK.
  • Corradini N; Department of Pediatric Oncology, Institut d'Hematologie et d'Oncologie Pédiatrique,/Centre Léon Bérard, Lyon, France.
  • Schoot RA; Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
  • Ramirez-Villar GL; Pediatric Oncology Unit, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
  • Hjalgrim LL; Department of Pediatrics and Adolescent Medicine, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Alaggio R; Pathology Department, Ospedale Pediatrico Bambino Gesù IRCCS, Rome, Italy.
  • Guillen Burrieza G; Surgical Oncology and Neonatal Surgery, Pediatric Surgery Department, Hospital Infantil Universitari Vall d'Hebron, Barcelona, Spain.
  • Safwat A; Oncology Department and Danish Center for Particle Therapy, Aarhus University Hospital, Aarhus, Denmark.
  • Cameron AL; Bristol Haematology and Oncology Centre, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, UK.
  • van Rijn RR; Department of Radiology and Nuclear Medicine, UMC University of Amsterdam, Amsterdam, Netherlands.
  • Minard-Colin V; Department of Pediatric and Adolescent Oncology, Gustave-Roussy, Cancer Campus, Université Paris-Saclay, Villejuif, France.
  • Zanetti I; Pediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy.
  • Bisogno G; Pediatric Hematology Oncology Division, University Hospital of Padua, Padua, Italy.
  • Chisholm JC; Department of Women's and Children's Health, University of Padua, Padua, Italy.
  • Merks JHM; Children and Young People's Unit, The Royal Marsden Hospital and Institute of Cancer Research, Sutton, UK.
Cancer ; 129(16): 2542-2552, 2023 08 15.
Article en En | MEDLINE | ID: mdl-37084075
BACKGROUND: Limited data exist on the clinical behavior of pediatric non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) with distant metastases at onset, and a clear standard of care has not yet been defined. METHODS: This cohort study reports on pediatric adult-type metastatic NRSTS enrolled in two concurrent prospective European studies, i.e., the randomized BERNIE study and the single-arm MTS 2008 study developed by the European paediatric Soft tissue sarcoma Study Group. Treatment programs were originally designed for patients with metastatic rhabdomyosarcoma, i.e., nine courses of multidrug chemotherapy (with or without bevacizumab in the BERNIE study), followed by 12 cycles of maintenance therapy, whereas radiotherapy and/or surgery (on primary tumor and/or metastases) were delayed until after seven courses of chemotherapy had been administered. RESULTS: The study included 61 patients <21 years old treated from July 2008 to December 2016. The lung was the site of metastases in 75% of the cases. All patients received multi-agent chemotherapy, 44% had local therapy to primary tumor, and 18% had treatment of metastases. Median time to progression/relapse was 6 months. A high rate of tumor progression was observed during the initial part of the chemotherapy program. With a median follow-up of 41.5 months (range, 2-111 months), 3-year event-free survival and overall survival were 15.4% (95% confidence interval [CI], 7.6-25.7) and 34.9% (95% CI, 22.7-47.5), respectively. There were no statistically significant differences in outcome depending on the type of treatment administered. CONCLUSIONS: The study confirmed the overall poor outcome for patients with metastatic NRSTS, whose treatment remains a challenge. PLAIN LANGUAGE SUMMARY: Pediatric non-rhabdomyosarcoma soft tissue sarcomas form a heterogeneous group of rare tumors. Although recent international studies have defined the standard of care for patients with localized disease, limited data are available on the clinical behavior of patients with distant metastases. This study on 61 metastatic cases treated on two prospective European protocols confirms that the chances of survival of such patients are often dismal and a standard treatment is still lacking.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Sarcoma / Neoplasias de los Tejidos Blandos Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rabdomiosarcoma / Sarcoma / Neoplasias de los Tejidos Blandos Tipo de estudio: Clinical_trials / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos