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The role of irinotecan-bevacizumab as rescue regimen in children with low-grade gliomas: a retrospective nationwide study in 72 patients.
de Marcellus, Charles; Tauziède-Espariat, Arnault; Cuinet, Aurélie; Pasqualini, Claudia; Robert, Matthieu P; Beccaria, Kevin; Puget, Stéphanie; Boddaert, Nathalie; Figarella-Branger, Dominique; De Carli, Emilie; Bourdeaut, Franck; Leblond, Pierre; Fouyssac, Fanny; Andre, Nicolas; Bertozzi, Anne I; Butel, Thibaut; Dufour, Christelle; Valteau-Couanet, Dominique; Varlet, Pascale; Grill, Jacques.
Afiliación
  • de Marcellus C; Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, University Paris-Saclay, Villejuif, France. charles.de-marcellus@aphp.fr.
  • Tauziède-Espariat A; Pediatric Intensive Care Unit, Necker-Enfants Malades University Hospital Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France. charles.de-marcellus@aphp.fr.
  • Cuinet A; Department of Neuropathology, GHU Psychiatrie et Neurosciences, site Sainte-Anne, Paris, France.
  • Pasqualini C; Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, University Paris-Saclay, Villejuif, France.
  • Robert MP; Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, University Paris-Saclay, Villejuif, France.
  • Beccaria K; Department of Ophthalmology, Necker-Enfants Malades University Hospital, Assistance Publique-Hôpitaux de Paris, University Paris Descarte, Paris, France.
  • Puget S; Borelli Centre UMR 9010, CNRS-SSA-ENS Paris Saclay-Paris University, Paris, France.
  • Boddaert N; Department of Pediatric Neurosurgery, Necker-Enfants Malades University Hospital, Assistance Publique- Hôpitaux de Paris, Paris, France.
  • Figarella-Branger D; Department of Pediatric Neurosurgery, Necker-Enfants Malades University Hospital, Assistance Publique- Hôpitaux de Paris, Paris, France.
  • De Carli E; Paediatric Radiology Department, AP-HP, Hôpital Necker Enfants Malades, Université de Paris, 75015, Paris, France.
  • Bourdeaut F; Université de Paris, Institut Imagine INSERM U1163, 75015, Paris, France.
  • Leblond P; APHM, CHU Timone, Department of Pathology and Neuropathology and Aix-Marseille Univ, CNRS, INP Inst Neurophysiopathol, Marseille, France.
  • Fouyssac F; Department of Pediatric Oncology, Angers University Hospital, Angers, France.
  • Andre N; SIREDO Center (Pediatric, Adolescent and Young Adults Oncology), Institut Curie, University of Paris, Paris, France.
  • Bertozzi AI; Pediatric Oncology Unit, Oscar Lambret Comprehensive Cancer Center, Lille, France.
  • Butel T; Department of Pediatric Hematology, Nancy University Hospital, Vandoeuvre-les-Nancy, France.
  • Dufour C; Department of Pediatric Hematology and Oncology, Aix Marseille Universityy, Assistance Publique-Hôpitaux de Marseille, Marseille, France.
  • Valteau-Couanet D; Department of Hematology-Oncology, Children University Hospital, Toulouse, France.
  • Varlet P; Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, University Paris-Saclay, Villejuif, France.
  • Grill J; Department of Pediatric and Adolescent Oncology, Institut Gustave Roussy, University Paris-Saclay, Villejuif, France.
J Neurooncol ; 157(2): 355-364, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35239111
ABSTRACT

INTRODUCTION:

At least half of children with low-grade glioma (LGG) treated with first line chemotherapy experience a relapse/progression and may therefore need a second-line chemotherapy. Irinotecan-bevacizumab has been recommended in this setting in France after encouraging results of pilot studies. We performed a retrospective analysis to define the efficacy, toxicity and predictors for response to the combination on a larger cohort.

METHODS:

We reviewed the files from children < 19 years of age with progressive or refractory LGG treated between 2009 and 2016 in 7 French centers with this combination.

RESULTS:

72 patients (median age 7.8 years [range 1-19]) received a median of 16 courses (range 3-30). The median duration of treatment was 9 months (range 1.4-16.2). 96% of patients experienced at least disease stabilization. The 6-month and 2-year progression-free survivals (PFS) were 91.7% [IC 95% 85.5-98.3] and 38.2% [IC 95% 28.2-51.8] respectively. No progression occurred after treatment in 18 patients with a median follow-up of 35.6 months (range 7.6-75.9 months). Younger patients had a worse PFS (p = 0.005). Prior chemoresistance, NF1 status, duration of treatment, histopathology or radiologic response did not predict response. The most frequent toxicities related to bevacizumab included grades 1-2 proteinuria in 21, epistaxis in 10, fatigue in 12 and hypertension in 8 while gastro-intestinal toxicity was the most frequent side effect related to irinotecan.

CONCLUSIONS:

Bevacizumab-irinotecan has the potential of disease control clinically and radiographically in children with recurrent LGG whatever their previous characteristics; in many cases however these responses are not sustained, especially in younger children.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Neurooncol Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Child / Child, preschool / Humans / Infant Idioma: En Revista: J Neurooncol Año: 2022 Tipo del documento: Article País de afiliación: Francia