Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study

Jean Donadieu, Islam Amine Larabi, M. Tardieu(Centre Hospitalier Universitaire de Grenoble), Johannes Visser(Cambridge University Hospitals NHS Foundation Trust), Caroline Hutter(Medical University of Vienna), Elena Sieni(Meyer Children's Hospital), Nabil Kabbara(Rafik Hariri University Hospital), Mohamed Barkaoui, Jean Miron, François Chalard, Paul Milne(Newcastle University), Julien Haroche(Sorbonne Université), Fleur Cohen(Sorbonne Université), Zofia Hélias‐Rodzewicz(Université Paris-Saclay), Nicolas Simon(Hôpital Sainte-Marguerite), M Jehanne(Centre Hospitalier Universitaire de La Réunion), Alexandra Kolenová(Comenius University Bratislava), Anne Pagnier(Centre Hospitalier Universitaire de Grenoble), Nathalie Aladjidi(Centre Hospitalier Universitaire de Bordeaux), Pascale Schneider(Centre Hospitalier Universitaire de Rouen), Geneviève Plat(Centre Hospitalier Universitaire de Toulouse), Anne Lutun(Centre Hospitalier Universitaire Amiens-Picardie), Anne Sonntagbauer(Goethe University Frankfurt), Thomas Lehrnbecher(Goethe University Frankfurt), Alina Ferster(Queen Fabiola Children's University Hospital), Viktoria Efremova(9th City Clinical Hospital), Martina Ahlmann(Klinik und Poliklinik für Kinder- und Jugendmedizin), Laurence Blanc(Centre Hospitalier Universitaire de Poitiers), James C. Nicholson(Cambridge University Hospitals NHS Foundation Trust), Anne Lambilliote(Centre Hospitalier Universitaire de Lille), Houda Boudiaf(Hôpital Mustapha Pacha), Andrej Lissat(Charité - Universitätsmedizin Berlin), Karel Švojgr(University Hospital in Motol), Fanette Bernard(Hôpital Beau-Séjour), Sarah Elitzur(Schneider Children's Medical Center), Michal Golan(Edmond and Lily Safra Children's Hospital), D. A. Evseev(Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology), Michael Maschan(Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology), Ahmed Idbaïh(Sorbonne Université), Olga Slater(Great Ormond Street Hospital), Milen Minkov(Medical University of Vienna), Valérie Taly(Sorbonne Paris Cité), Matthew Collin(Newcastle University), Jean‐Claude Alvarez, Jean‐François Emile(Université Paris-Saclay), Sébastien Héritier(Université Paris-Saclay)
Journal of Clinical Oncology
September 12, 2019
Cited by 219Open Access
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Abstract

PURPOSE Off-label use of vemurafenib (VMF) to treat BRAF V600E mutation–positive, refractory, childhood Langerhans cell histiocytosis (LCH) was evaluated. PATIENTS AND METHODS Fifty-four patients from 12 countries took VMF 20 mg/kg/d. They were classified according to risk organ involvement: liver, spleen, and/or blood cytopenia. The main evaluation criteria were adverse events (Common Terminology Criteria for Adverse Events [version 4.3]) and therapeutic responses according to Disease Activity Score. RESULTS LCH extent was distributed as follows: 44 with positive and 10 with negative risk organ involvement. Median age at diagnosis was 0.9 years (range, 0.1 to 6.5 years). Median age at VMF initiation was 1.8 years (range, 0.18 to 14 years), with a median follow-up of 22 months (range, 4.3 to 57 months), whereas median treatment duration was 13.9 months (for 855 patient-months). At 8 weeks, 38 complete responses and 16 partial responses had been achieved, with the median Disease Activity Score decreasing from 7 at diagnosis to 0 ( P < .001). Skin rash, the most frequent adverse event, affected 74% of patients. No secondary skin cancer was observed. Therapeutic plasma VMF concentrations (range, 10 to 20 mg/L) seemed to be safe and effective. VMF discontinuation for 30 patients led to 24 LCH reactivations. The blood BRAF V600E allele load, assessed as circulating cell-free DNA, decreased after starting VMF but remained positive (median, 3.6% at diagnosis, and 1.6% during VMF treatment; P < .001) and was associated with a higher risk of reactivation at VMF discontinuation. None of the various empirical therapies (hematopoietic stem-cell transplantation, cladribine and cytarabine, anti-MEK agent, vinblastine, etc) used for maintenance could eradicate the BRAF V600E clone. CONCLUSION VMF seemed safe and effective in children with refractory BRAF V600E -positive LCH. Additional studies are needed to find effective maintenance therapy approaches.


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