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Influence of Surgical Excision on the Survival of Patients With Stage 4 High-Risk Neuroblastoma: A Report From the HR-NBL1/SIOPEN Study.
Holmes, Keith; Pötschger, Ulrike; Pearson, Andrew D J; Sarnacki, Sabine; Cecchetto, Giovanni; Gomez-Chacon, Javier; Squire, Roly; Freud, Enrique; Bysiek, Adam; Matthyssens, Lucas E; Metzelder, Martin; Monclair, Tom; Stenman, Jakob; Rygl, Michal; Rasmussen, Lars; Joseph, Jean-Marc; Irtan, Sabine; Avanzini, Stefano; Godzinski, Jan; Björnland, Kristin; Elliott, Martin; Luksch, Roberto; Castel, Victoria; Ash, Shifra; Balwierz, Walentyna; Laureys, Geneviève; Ruud, Ellen; Papadakis, Vassilios; Malis, Josef; Owens, Cormac; Schroeder, Henrik; Beck-Popovic, Maja; Trahair, Toby; Forjaz de Lacerda, Ana; Ambros, Peter F; Gaze, Mark N; McHugh, Kieran; Valteau-Couanet, Dominique; Ladenstein, Ruth Lydia.
Afiliación
  • Holmes K; Paediatric Surgery, St George's Hospital London and Royal Marsden Hospital, Sutton, United Kingdom.
  • Pötschger U; Children's Cancer Research Institute, Department of Paediatrics, Medical University of Vienna, Vienna, Austria.
  • Pearson ADJ; Institute of Cancer Research and Royal Marsden Hospital, Sutton, United Kingdom.
  • Sarnacki S; Department of Pediatric Surgery, Necker Enfants-Malades Hospital, Assistance Publique Hôpitaux de Paris, University de Paris, Paris, France.
  • Cecchetto G; Pediatric Surgery, Department of Women's and Children's Health, University of Padua, Padua, Italy.
  • Gomez-Chacon J; Paediatric Oncology, Paediatric Surgical Oncology Unit, Hospital Universitario La FE, Valencia, Spain.
  • Squire R; Paediatric Oncology, Leeds Teaching Hospital, Leeds, United Kingdom.
  • Freud E; Schneider Children's Medical Center of Israel, Petach, Tikvah, Israel.
  • Bysiek A; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Matthyssens LE; Department of Pediatric Surgery, University Children's Hospital, Kraków, Poland.
  • Metzelder M; Department of Gastrointestinal and Paediatric Surgery, Princess Elisabeth Children's Hospital, Ghent University Hospital, Ghent, Belgium.
  • Monclair T; Paediatric Surgery, Medical University of Vienna, Vienna, Austria.
  • Stenman J; Oslo University Hospital Rikshospitalet, Oslo, Norway.
  • Rygl M; Karolinska University Hospital, Stockholm, Sweden.
  • Rasmussen L; University Hospital Motol, Prague, Czech Republic.
  • Joseph JM; Department of Surgical Gastroenterology A, Odense University Hospital, Odense, Denmark.
  • Irtan S; University Hospital Lausanne, Lausanne, Switzerland.
  • Avanzini S; Sorbonne University, Department of Visceral and Neonatal Pediatric Surgery, Armand Trousseau Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Godzinski J; Pediatric Surgery Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Björnland K; Department of Paediatric Surgery, Marciniak Hospital, and Department of Paediatric Traumatology and Emergency Medicine, Wroclaw Medical University, Wroclaw, Poland.
  • Elliott M; Oslo University Hospital Rikshospitalet, Oslo, Norway.
  • Luksch R; University of Oslo, Oslo, Norway.
  • Castel V; Paediatric Oncology, Leeds Teaching Hospital, Leeds, United Kingdom.
  • Ash S; Paediatric Oncology, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.
  • Balwierz W; Paediatric Oncology, Paediatric Surgical Oncology Unit, Hospital Universitario La FE, Valencia, Spain.
  • Laureys G; Schneider Children's Medical Center of Israel, Petach, Tikvah, Israel.
  • Ruud E; Jagiellonian University Medical College, Kraków, Poland.
  • Papadakis V; Department of Paediatric Haematology and Oncology, Princess Elisabeth Children's Hospital, Ghent University Hospital, Ghent, Belgium.
  • Malis J; Oslo University Hospital Rikshospitalet, Oslo, Norway.
  • Owens C; University of Oslo, Oslo, Norway.
  • Schroeder H; Agia Sofia Children's Hospital, Athens, Greece.
  • Beck-Popovic M; University Hospital Motol, Prague, Czech Republic.
  • Trahair T; Paediatric Haematology/Oncology, Our Lady's Children's Hospital, Crumlin, Dublin, Republic of Ireland.
  • Forjaz de Lacerda A; University Hospital of Aarhus, Aarhus, Denmark.
  • Ambros PF; University Hospital Lausanne, Lausanne, Switzerland.
  • Gaze MN; Sydney Children's Hospital, Randwick, New South Wales, Australia.
  • McHugh K; Portuguese Institute of Oncology, Lisbon, Portugal.
  • Valteau-Couanet D; Children's Cancer Research Institute, Department of Paediatrics, Medical University of Vienna, Vienna, Austria.
  • Ladenstein RL; University College Hospital, London, United Kingdom.
J Clin Oncol ; 38(25): 2902-2915, 2020 09 01.
Article en En | MEDLINE | ID: mdl-32639845
PURPOSE: To evaluate the impact of surgeon-assessed extent of primary tumor resection on local progression and survival in patients in the International Society of Pediatric Oncology Europe Neuroblastoma Group High-Risk Neuroblastoma 1 trial. PATIENTS AND METHODS: Patients recruited between 2002 and 2015 with stage 4 disease > 1 year or stage 4/4S with MYCN amplification < 1 year who had completed induction without progression, achieved response criteria for high-dose therapy (HDT), and had no resection before induction were included. Data were collected on the extent of primary tumor excision, severe operative complications, and outcome. RESULTS: A total of 1,531 patients were included (median observation time, 6.1 years). Surgeon-assessed extent of resection included complete macroscopic excision (CME) in 1,172 patients (77%) and incomplete macroscopic resection (IME) in 359 (23%). Surgical mortality was 7 (0.46%) of 1,531. Severe operative complications occurred in 142 patients (9.7%), and nephrectomy was performed in 124 (8.8%). Five-year event-free survival (EFS) ± SE (0.40 ± 0.01) and overall survival (OS; 0.45 ± 0.02) were significantly higher with CME compared with IME (5-year EFS, 0.33 ± 0.03; 5-year OS, 0.37 ± 0.03; P < .001 and P = .004). The cumulative incidence of local progression (CILP) was significantly lower after CME (0.17 ± 0.01) compared with IME (0.30 ± 0.02; P < .001). With immunotherapy, outcomes were still superior with CME versus IME (5-year EFS, 0.47 ± 0.02 v 0.39 ± 0.04; P = .038); CILP was 0.14 ± 0.01 after CME and 0.27 ± 0.03 after IME (P < .002). A hazard ratio of 1.3 for EFS associated with IME compared with CME was observed before and after the introduction of immunotherapy (P = .030 and P = .038). CONCLUSION: In patients with stage 4 high-risk neuroblastoma who have responded to induction therapy, CME of the primary tumor is associated with improved survival and local control after HDT, local radiotherapy (21 Gy), and immunotherapy.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neuroblastoma Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Oncol Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neuroblastoma Tipo de estudio: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: J Clin Oncol Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido