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Long-term follow-up of surgical intervention pattern in pediatric low-grade gliomas: report from the German SIOP-LGG 2004 cohort.
Thomale, Ulrich-Wilhelm; Gnekow, Astrid K; Kandels, Daniela; Bison, Brigitte; Hernáiz Driever, Pablo; Witt, Olaf; Pietsch, Torsten; Koch, Arend; Capper, David; Kortmann, Rolf-Dieter; Timmermann, Beate; Harrabi, Semi; Simon, Michèle; El Damaty, Ahmed; Krauss, Juergen; Schuhmann, Martin U; Aigner, Annette.
Afiliação
  • Thomale UW; 1Pediatric Neurosurgery, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin.
  • Gnekow AK; 2Pediatric and Adolescent Medicine, Swabian Children's Cancer Research Center, Medical Faculty, University of Augsburg.
  • Kandels D; 2Pediatric and Adolescent Medicine, Swabian Children's Cancer Research Center, Medical Faculty, University of Augsburg.
  • Bison B; 3Institute of Diagnostic and Interventional Neuroradiology, University Hospital Würzburg.
  • Hernáiz Driever P; 4Institute of Diagnostic and Interventional Neuroradiology, Medical Faculty, University of Augsburg.
  • Witt O; 5Department of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin.
  • Pietsch T; 6Hopp Children's Cancer Center Heidelberg (KiTZ), German Cancer Research Center (DKFZ), and Heidelberg University Hospital, Heidelberg.
  • Koch A; 7Department of Neuropathology, DGNN Brain Tumor Reference Centre, University of Bonn Medical Centre, Bonn.
  • Capper D; 8Institute for Neuropathology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin.
  • Kortmann RD; 8Institute for Neuropathology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin.
  • Timmermann B; 9Department of Radiation Oncology, University Hospital Leipzig.
  • Harrabi S; 10Department of Particle Therapy, University Hospital Essen, West German Proton Therapy Centre Essen (WPE), West German Cancer Centre (WTZ), German Cancer Consortium (DKTK), Essen.
  • Simon M; 11Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg.
  • El Damaty A; 5Department of Pediatric Oncology/Hematology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin.
  • Krauss J; 12Division of Pediatric Neurosurgery, Department of Neurosurgery, Heidelberg University Hospital, Heidelberg.
  • Schuhmann MU; 13Department of Pediatric Neurosurgery, University Children's Hospital, University of Würzburg.
  • Aigner A; 14Division of Pediatric Neurosurgery, Department of Neurosurgery, University Hospital of Tuebingen, Eberhard Karls University of Tuebingen; and.
J Neurosurg Pediatr ; : 1-14, 2022 Jul 22.
Article em En | MEDLINE | ID: mdl-35901673
OBJECTIVE: Neurosurgical treatment is an integral part of the treatment algorithms for pediatric low-grade glioma (LGG), yet patterns of surgical procedures are rarely challenged. The objective of this study was to evaluate surgical treatment patterns in pediatric LGG. METHODS: The German Societé Internationale d'Oncologie Pédiatrique (SIOP)-LGG 2004 cohort was analyzed to identify relevant patient and tumor characteristics associated with time to death, next surgery, number of resections, and radiological outcome. RESULTS: A total of 1271 patients underwent 1713 neurosurgical interventions (1 intervention in 947, 2 in 230, 3 in 70, and 4-6 in 24). The median age of the study population was 8.57 years at first surgery, and 46.1% were female. Neurofibromatosis type 1 (NF1) was found in 4.4%, and 5.4% had tumor dissemination. Three hundred fifty-four patients (27.9%) had chemotherapy and/or radiotherapy. The cumulative incidence of second surgery at 10 years was 26%, and was higher for infants, those with spinal and supratentorial midline (SML) tumors, and those with pilomyxoid astrocytomas. The hazard ratio for subsequent surgery was higher given dissemination and noncomplete initial resection, and lower for caudal brainstem and SML tumors. Among 1225 patients with fully documented surgical records and radiological outcome, 613 reached complete remission during the observation period, and 50 patients died. Patients with pilocytic astrocytoma had higher chances for a final complete remission, whereas patients with initial partial or subtotal tumor resection, dissemination, NF1, or primary tumor sites in the spinal cord and SML had lower chances. CONCLUSIONS: Neurosurgery is a key element of pediatric LGG treatment. In almost 50% of the patients, however, at least some tumor burden will remain during long-term follow-up. This study found that most of these patients reached a stable disease status without further surgeries. Multidisciplinary team decisions must balance the goal of complete resection, risk factors, repeated surgeries, and possible treatment alternatives in a wide range of heterogeneous entities. Procedural details and neurological outcome should be recorded to better assess their impact on long-term outcome.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Neurosurg Pediatr Assunto da revista: NEUROCIRURGIA / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Neurosurg Pediatr Assunto da revista: NEUROCIRURGIA / PEDIATRIA Ano de publicação: 2022 Tipo de documento: Article