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Central nervous system relapse in high-risk stage 4 neuroblastoma: The HR-NBL1/SIOPEN trial experience.
Berlanga, P; Pasqualini, C; Pötschger, U; Sangüesa, C; Castellani, M R; Cañete, A; Luksch, R; Elliot, M; Schreier, G; Kropf, M; Morgenstern, D; Papadakis, V; Ash, S; Ruud, E; Brock, P; Wieczorek, A; Kogner, P; Trahair, T; Ambros, P; Boterberg, T; Castel, V; Valteau-Couanet, D; Ladenstein, R.
  • Berlanga P; Department of Pediatric and Adolescent Oncology, Gustave Roussy, Paris-Saclay University, Paris, France. Electronic address: pablo.berlanga@gustaveroussy.fr.
  • Pasqualini C; Department of Pediatric and Adolescent Oncology, Gustave Roussy, Paris-Saclay University, Paris, France.
  • Pötschger U; Department for Studies and Statistics and Integrated Research, Children's Cancer Research Institute, Vienna, Austria.
  • Sangüesa C; Pediatric Radiology Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
  • Castellani MR; Nuclear Medicine Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Cañete A; Pediatric Oncology Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
  • Luksch R; Pediatric Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Elliot M; Pediatric Oncology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
  • Schreier G; Centre for Health and Bioresources, AIT Austrian Institute of Technology GmbH, Graz, Austria.
  • Kropf M; Centre for Health and Bioresources, AIT Austrian Institute of Technology GmbH, Graz, Austria.
  • Morgenstern D; Division of Pediatric Hematology/Oncology, The Hospital for Sick Children, University of Toronto, Toronto, Canada.
  • Papadakis V; Paediatric Hematology/Oncology, Agia Sofia Children's Hospital, Athens, Greece.
  • Ash S; Department of Pediatric Hematology Oncology, Schneider Children's Medical Center of Israel, Sackler Faculty of Medicine Tel Aviv University, Petach Tikvah, Israel.
  • Ruud E; Department of Paediatric Medicine, Rikshospitalet, Oslo, Norway.
  • Brock P; Department of Pediatric Oncology, Great Ormond Street Hospital, London, UK.
  • Wieczorek A; Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
  • Kogner P; Department of Women's and Children's Health, Karolinska Institutet, 17177, Stockholm, Sweden.
  • Trahair T; Kids Cancer Centre, Sydney Children's Hospital, Randwick, NSW, Australia.
  • Ambros P; Department of Tumor Biology, Children's Cancer Research Institute, Vienna, Austria.
  • Boterberg T; Department of Radiation Oncology, Ghent University Hospital, Ghent, Belgium.
  • Castel V; Pediatric Oncology Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
  • Valteau-Couanet D; Department of Pediatric and Adolescent Oncology, Gustave Roussy, Paris-Saclay University, Paris, France.
  • Ladenstein R; St Anna Children's Hospital, Vienna, Austria; Department for Studies and Statistics and Integrated Research, Vienna, Austria; Children's Cancer Research Institute, Vienna, Austria.
Eur J Cancer ; 144: 1-8, 2021 02.
Article en En | MEDLINE | ID: mdl-33316634
ABSTRACT

BACKGROUND:

There is rising concern on the impact of new strategies, such as high-dose chemotherapy (HDC) and immunotherapy, on the pattern of relapse in high-risk neuroblastoma (HR-NBL). Our aim is to evaluate the incidence and identify risk factors for first recurrence in the central nervous system (CNS) in HR-NBL. PATIENTS AND

METHODS:

Data from patients with stage 4V HR-NBL included from February 2002 to June 2015 in the prospective HR-NBL trial of the European International Society of Pediatric Oncology Neuroblastoma Group were analysed. Characteristics at diagnosis, treatment and the pattern of first relapse were studied. CNS imaging at relapse was centrally reviewed.

RESULTS:

The 1977 included patients had a median age of 3 years (1 day-20 years); 1163 were boys. Among the 1161 first relapses, 53 were in the CNS, with an overall incidence of 2.7%, representing 6.2% of all metastatic relapses. One- and three-year post-relapse overall survival was 25 ± 6% and 8 ± 4%, respectively. Higher risk of CNS recurrence was associated with female sex (hazard ratio [HR] = 2.0 [95% confidence interval {CI} 1.1-3.5]; P = 0.016), MYCN-amplification (HR = 2.4 [95% CI 1.2-4.4]; P = 0.008), liver (HR = 2.5 [95% CI 1.2-5.1]; P = 0.01) or >1 metastatic compartment involvement (HR = 7.1 [95% CI 1.0-48.4]; P = 0.047) at diagnosis. Neither HDC nor immunotherapy was associated with higher risk of CNS recurrence. Stable incidence of CNS relapse was reported over time.

CONCLUSIONS:

The risk of CNS recurrence is linked to both patient and disease characteristics, with neither impact of HDC nor immunotherapy. These findings support the current treatment strategy and do not justify a CNS prophylactic treatment.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Primarias Secundarias / Neoplasias del Sistema Nervioso Central / Recurrencia Local de Neoplasia / Neuroblastoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Primarias Secundarias / Neoplasias del Sistema Nervioso Central / Recurrencia Local de Neoplasia / Neuroblastoma Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Año: 2021 Tipo del documento: Article