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Risk stratification of high-risk metastatic neuroblastoma: A report from the HR-NBL-1/SIOPEN study.
Morgenstern, Daniel A; Pötschger, Ulrike; Moreno, Lucas; Papadakis, Vassilios; Owens, Cormac; Ash, Shifra; Pasqualini, Claudia; Luksch, Roberto; Garaventa, Alberto; Canete, Adela; Elliot, Martin; Wieczorek, Aleksandra; Laureys, Geneviève; Kogner, Per; Malis, Josef; Ruud, Ellen; Beck-Popovic, Maja; Schleiermacher, Gudrun; Valteau-Couanet, Dominique; Ladenstein, Ruth.
Afiliação
  • Morgenstern DA; Paediatric Haematology/Oncology, Hospital for Sick Children and University of Toronto, Toronto, Canada.
  • Pötschger U; Paediatric Haematology/Oncology, Great Ormond Street Hospital and UCL Institute of Child Health, London, UK.
  • Moreno L; Studies and Statistics on Integrated Research and Projects, St Anna Kinderkrebsforschung, Vienna, Austria.
  • Papadakis V; Paediatric Haematology/Oncology, Hospital Nino Jesús, Madrid, Spain.
  • Owens C; Paediatric Haematology/Oncology, Agia Sofia Children's Hospital, Athens, Greece.
  • Ash S; Paediatric Haematology/Oncology, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
  • Pasqualini C; Paediatric Haematology/Oncology, Schneider Children's Medical Center of Israel, Petah Tikva, Israel.
  • Luksch R; Department of Paediatric and Adolescent Oncology, Institut Gustav Roussy, Viellejuif, France.
  • Garaventa A; Dipartimento di Ematologia e Onco-ematologia Pediatrica, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Canete A; Paediatric Oncology, Istituto Giannia Gaslini, Genova, Italy.
  • Elliot M; Pediatric Oncology Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
  • Wieczorek A; Paediatric Oncology, Leeds Teaching Hospital NHS Trust, Leeds, UK.
  • Laureys G; Department of Pediatric Oncology and Hematology, Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.
  • Kogner P; Department of Pediatric Hematology/Oncology and Stem Cell Transplantation University Hospital Ghent, Ghent, Belgium.
  • Malis J; Department of Women's and Children's Health, Karolinska Institutet, Astrid Lindgren Children's Hospital, Karolinska University Hospital, Stockholm, Sweden.
  • Ruud E; Department of Pediatric Hematology and Oncology, University Hospital Motol, Prague, Czech Republic.
  • Beck-Popovic M; Department of Paediatric Medicine, Rikshospitalet, Oslo University Hospital, Oslo, Norway.
  • Schleiermacher G; Department of Pediatrics and Pediatric Surgery, Pediatric Haematology Oncology Unit, University Hospital Lausanne, Lausanne, Switzerland.
  • Valteau-Couanet D; Department of Paediatrics, Institut Curie, Paris, France.
  • Ladenstein R; Department of Paediatric and Adolescent Oncology, Institut Gustav Roussy, Viellejuif, France.
Pediatr Blood Cancer ; 65(11): e27363, 2018 11.
Article em En | MEDLINE | ID: mdl-30015396
ABSTRACT

BACKGROUND:

Risk stratification is crucial to treatment decision-making in neuroblastoma. This study aimed to explore factors present at diagnosis affecting outcome in patients aged ≥18 months with metastatic neuroblastoma and to develop a simple risk score for prognostication. PROCEDURE Data were derived from the European high-risk neuroblastoma 1 (HR-NBL1)/International Society for Paediatric Oncology European Neuroblastoma (SIOPEN) trial with analysis restricted to patients aged ≥18 months with metastatic disease and treated prior to the introduction of immunotherapy. Primary endpoint was 5-year event-free survival (EFS). Prognostic factors assessed were sex, age, tumour MYCN amplification (MNA) status, serum lactate dehydrogenase (LDH)/ferritin, primary tumour and metastatic sites. Factors significant in univariate analysis were incorporated into a multi-variable model and an additive scoring system developed based on estimated log-cumulative hazard ratios.

RESULTS:

The cohort included 1053 patients with median follow-up 5.5 years and EFS 27 ± 1%. In univariate analyses, age; serum LDH and ferritin; involvement of bone marrow, bone, liver or lung; and >1 metastatic system/compartment were associated with worse EFS. Tumour MNA was not associated with worse EFS. A multi-variable model and risk score incorporating age (>5 years, 2 points), serum LDH (>1250 U/L, 1 point) and number of metastatic systems (>1, 2 points) were developed. EFS was significantly correlated with risk score EFS 52 ± 9% for score = 0 versus 6 ± 3% for score = 5 (P < 0.0001).

CONCLUSIONS:

A simple score can identify an "ultra-high risk" (UHR) cohort (score = 5) comprising 8% of patients with 5-year EFS <10%. These patients appear not to benefit from induction therapy and could potentially be directed earlier to alternative experimental therapies in future trials.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Neuroblastoma Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Blood Cancer Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores Tumorais / Neuroblastoma Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Pediatr Blood Cancer Assunto da revista: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá