| Literature DB >> 27573663 |
Alvaro Lassaletta1, Katrin Scheinemann1, Shayna M Zelcer1, Juliette Hukin1, Beverley A Wilson1, Nada Jabado1, Anne Sophie Carret1, Lucie Lafay-Cousin1, Valerie Larouche1, Cynthia E Hawkins1, Gregory Russell Pond1, Ken Poskitt1, Daniel Keene1, Donna L Johnston1, David D Eisenstat1, Rahul Krishnatry1, Matthew Mistry1, Anthony Arnoldo1, Vijay Ramaswamy1, Annie Huang1, Ute Bartels1, Uri Tabori1, Eric Bouffet1.
Abstract
Purpose Vinblastine monotherapy has shown promising activity and a low-toxicity profile in patients with pediatric low-grade glioma (PLGG) who experienced treatment failure after initial treatment with chemotherapy and/or radiation. The aim of this study was to assess the activity of vinblastine in therapy-naïve children. Patients and Methods Patients < 18 years old with unresectable and/or progressive therapy-naïve PLGG were eligible. Vinblastine was administered once per week at a dose of 6 mg/m2 intravenously over a period of 70 weeks. Vision, quality of life, neurofibromatosis type 1 (NF1) status, and BRAF mutation/fusion status were also determined and correlated with outcome. Results Fifty-four patients were enrolled onto the study, with a median age of 8 years (range, 0.7 to 17.2 years). Most patients had chiasmatic/hypothalamic tumors (55.5%), and 13 patients (24.1%) had NF1. The most common histology was pilocytic astrocytoma (46.3%). Seventeen patients were diagnosed using radiologic criteria alone. Best response to chemotherapy was centrally reviewed with a response rate (complete, partial, or minor response) of 25.9%. Disease stabilization (complete, partial, or minor response or stable disease) was achieved in 47 patients (87.0%). Visual improvement was observed in 20% of patients with optic pathway glioma. Five-year overall survival and progression-free survival (PFS) rates were 94.4% (95% CI, 88.5% to 100%) and 53.2% (95% CI, 41.3% to 68.5%), respectively, for the entire cohort. Patients with NF1 had a significantly better PFS (85.1%; 95% CI, 68.0% to 100%) when compared with patients without NF1 (42.0%; 95% CI, 29.1% to 60.7%; P = .012). Age< 3 years or > 10 years was not associated with poor outcome. Treatment was well tolerated, and quality of life was not affected during treatment. In this trial, there was no correlation between BRAF alterations and outcome. Conclusion Vinblastine administered once per week is well tolerated in children with treatment naïve PLGG. Overall survival and PFS are comparable to current therapies, with a favorable toxicity profile and a maintained quality of life.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27573663 DOI: 10.1200/JCO.2016.68.1585
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544