Retrospective analysis of combination carboplatin and vinblastine for pediatric low-grade glioma.
Adolescent
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Brain Neoplasms
/ drug therapy
Carboplatin
/ administration & dosage
Child
Child, Preschool
Female
Follow-Up Studies
Glioma
/ drug therapy
Humans
Infant
Infant, Newborn
Male
Neoplasm Grading
Retrospective Studies
Survival Rate
Vinblastine
/ administration & dosage
Brain tumor
Chemotherapy
Low-grade glioma
Pediatrics
Journal
Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
26
03
2020
accepted:
29
05
2020
pubmed:
9
6
2020
medline:
8
6
2021
entrez:
8
6
2020
Statut:
ppublish
Résumé
Low-grade glioma (LGG) represent the most common pediatric central nervous system tumor. When total surgical resection is not feasible, chemotherapy is first-line therapy in children. Multiple pediatric LGG chemotherapy regimens have been investigated with variable 2-year event free survival (EFS) rates of 39-69%. To date, treatment of pediatric LGG with a carboplatin and vinblastine (C/VBL) chemotherapy regimen has only been evaluated in a phase 1 dose-finding study. A retrospective review of pediatric patients with LGG who were treated with C/VBL at Children's Hospital of Colorado or Akron Children's Hospital from 2011 to 2017 was conducted. Data collected included patient demographics, tumor location, disease response, neurofibromatosis 1 (NF1) status, therapy duration and toxicities. Response to therapy was determined by objective findings on imaging and treating physicians' evaluation. Forty-six patients were identified for analysis, all of whom were chemotherapy-naive. Only five patients treated in this cohort had NF1. BRAF fusion was identified in 65% (22/34) of tested tumors. Best therapy response was partial response in nine patients and stable disease in twenty-five patients. Twelve patients had progressive disease. One-year, 3-year, and 5-year EFS probabilities for all patients were 69.6%, 39.4%, and 34.5%, respectively. Nine patients had admissions for febrile neutropenia and seven patients experienced one delay in chemotherapy due to neutropenia. Only two patients had to discontinue this chemotherapy regimen because of treatment-related toxicities [carboplatin allergy (n = 1) and vinblastine neuropathy (n = 1)]. C/VBL achieves similar EFS rates to other single-agent and combination cytotoxic chemotherapy regimens for pediatric LGG with manageable toxicities.
Identifiants
pubmed: 32506370
doi: 10.1007/s11060-020-03549-x
pii: 10.1007/s11060-020-03549-x
doi:
Substances chimiques
Vinblastine
5V9KLZ54CY
Carboplatin
BG3F62OND5
Types de publication
Clinical Trial, Phase I
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
569-575Subventions
Organisme : NCI NIH HHS
ID : P30-CA046934
Pays : United States
Organisme : NCI NIH HHS
ID : P30-CA046934
Pays : United States
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