UCL Discovery Stage
UCL home » Library Services » Electronic resources » UCL Discovery Stage

Outcome of children and adolescents with central nervous system tumors in phase I trials

Carceller, F; Bautista, F; Jiménez, I; Hladun-Álvaro, R; Giraud, C; Bergamaschi, L; Dandapani, M; ... Marshall, LV; + view all (2018) Outcome of children and adolescents with central nervous system tumors in phase I trials. Journal of Neuro-Oncology , 137 (1) pp. 83-92. 10.1007/s11060-017-2698-z. Green open access

[thumbnail of OS Brain Tumours_Manuscript_v3.1_Submitted version including figures and tables.pdf]
Preview
Text
OS Brain Tumours_Manuscript_v3.1_Submitted version including figures and tables.pdf - Accepted Version

Download (359kB) | Preview

Abstract

Central nervous system (CNS) tumors are a leading cause of death in pediatric oncology. New drugs are desperately needed to improve survival. We evaluated the outcome of children and adolescents with CNS tumors participating in phase I trials within the Innovative Therapies for Children with Cancer (ITCC) consortium. Patients with solid tumors aged < 18 years at enrollment in their first dose-finding trial between 2000 and 2014 at eight ITCC centers were included retrospectively. Survival was evaluated using univariate/multivariate analyses. Overall, 114 patients were included (109 evaluable for efficacy). Median age was 10.2 years (range 1.0-17.9). Main diagnoses included: medulloblastoma/primitive neuroectodermal tumors (32.5%) and high-grade gliomas (23.7%). Complete/partial responses (CR/PR) were reported in 7.3% patients and stable disease (SD) in 23.9%. Performance status of 90-100%, school/work attendance, normal ALT/AST and CR/PR/SD correlated with better overall survival (OS) in the univariate analysis. No variables assessable at screening/enrollment were associated with OS in the multivariate analysis. Five patients (4.5%) were discontinued from study due to toxicity. No toxic deaths occurred. Median OS was 11.9 months with CR/PR, 14.5 months with SD and 3.7 months with progressive disease (p < 0.001). The enrollment of children and adolescents with CNS tumors in phase I trials is feasible, safe and offers potential benefit for the patients. Sustained disease stabilization has a promising role as a marker of anti-tumor activity in children with CNS tumors participating in phase I trials.

Type: Article
Title: Outcome of children and adolescents with central nervous system tumors in phase I trials
Open access status: An open access version is available from UCL Discovery
DOI: 10.1007/s11060-017-2698-z
Publisher version: https://doi.org/10.1007/s11060-017-2698-z
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Targeted drugs, Children, Adolescents, Central nervous system, tumor, Brain tumor, Phase I trial
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Biology and Cancer Dept
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10068763
Downloads since deposit
792Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item