| Literature DB >> 28727518 |
Alvaro Lassaletta1, Michal Zapotocky1, Matthew Mistry1, Vijay Ramaswamy1, Marion Honnorat1, Rahul Krishnatry1, Ana Guerreiro Stucklin1, Nataliya Zhukova1, Anthony Arnoldo1, Scott Ryall1, Catriona Ling1, Tara McKeown1, Jim Loukides1, Ofelia Cruz1, Carmen de Torres1, Cheng-Ying Ho1, Roger J Packer1, Ruth Tatevossian1, Ibrahim Qaddoumi1, Julie H Harreld1, James D Dalton1, Jean Mulcahy-Levy1, Nicholas Foreman1, Matthias A Karajannis1, Shiyang Wang1, Matija Snuderl1, Amulya Nageswara Rao1, Caterina Giannini1, Mark Kieran1, Keith L Ligon1, Maria Luisa Garre1, Paolo Nozza1, Samantha Mascelli1, Alessandro Raso1, Sabine Mueller1, Theodore Nicolaides1, Karen Silva1, Romain Perbet1, Alexandre Vasiljevic1, Cécile Faure Conter1, Didier Frappaz1, Sarah Leary1, Courtney Crane1, Aden Chan1, Ho-Keung Ng1, Zhi-Feng Shi1, Ying Mao1, Elizabeth Finch1, David Eisenstat1, Bev Wilson1, Anne Sophie Carret1, Peter Hauser1, David Sumerauer1, Lenka Krskova1, Valerie Larouche1, Adam Fleming1, Shayna Zelcer1, Nada Jabado1, James T Rutka1, Peter Dirks1, Michael D Taylor1, Shiyi Chen1, Ute Bartels1, Annie Huang1, David W Ellison1, Eric Bouffet1, Cynthia Hawkins1, Uri Tabori1.
Abstract
Purpose BRAF V600E is a potentially highly targetable mutation detected in a subset of pediatric low-grade gliomas (PLGGs). Its biologic and clinical effect within this diverse group of tumors remains unknown. Patients and Methods A combined clinical and genetic institutional study of patients with PLGGs with long-term follow-up was performed (N = 510). Clinical and treatment data of patients with BRAF V600E mutated PLGG (n = 99) were compared with a large international independent cohort of patients with BRAF V600E mutated-PLGG (n = 180). Results BRAF V600E mutation was detected in 69 of 405 patients (17%) with PLGG across a broad spectrum of histologies and sites, including midline locations, which are not often routinely biopsied in clinical practice. Patients with BRAF V600E PLGG exhibited poor outcomes after chemotherapy and radiation therapies that resulted in a 10-year progression-free survival of 27% (95% CI, 12.1% to 41.9%) and 60.2% (95% CI, 53.3% to 67.1%) for BRAF V600E and wild-type PLGG, respectively ( P < .001). Additional multivariable clinical and molecular stratification revealed that the extent of resection and CDKN2A deletion contributed independently to poor outcome in BRAF V600E PLGG. A similar independent role for CDKN2A and resection on outcome were observed in the independent cohort. Quantitative imaging analysis revealed progressive disease and a lack of response to conventional chemotherapy in most patients with BRAF V600E PLGG. Conclusion BRAF V600E PLGG constitutes a distinct entity with poor prognosis when treated with current adjuvant therapy.Entities:
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Year: 2017 PMID: 28727518 PMCID: PMC5791837 DOI: 10.1200/JCO.2016.71.8726
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544