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

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: live...

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Detalles Bibliográficos
Autores principales: Donadieu, Jean, Larabi, Islam Amine, Tardieu, Mathilde, Visser, Johannes, Hutter, Caroline, Sieni, Elena, Kabbara, Nabil, Barkaoui, Mohamed, Miron, Jean, Chalard, François, Milne, Paul, Haroche, Julien, Cohen, Fleur, Hélias-Rodzewicz, Zofia, Simon, Nicolas, Jehanne, Mathilde, Kolenova, Alexandra, Pagnier, Anne, Aladjidi, Nathalie, Schneider, Pascale, Plat, Geneviève, Lutun, Anne, Sonntagbauer, Anne, Lehrnbecher, Thomas, Ferster, Alina, Efremova, Viktoria, Ahlmann, Martina, Blanc, Laurence, Nicholson, James, Lambilliote, Anne, Boudiaf, Houda, Lissat, Andrej, Svojgr, Karel, Bernard, Fanette, Elitzur, Sarah, Golan, Michal, Evseev, Dmitriy, Maschan, Michael, Idbaih, Ahmed, Slater, Olga, Minkov, Milen, Taly, Valerie, Collin, Matthew, Alvarez, Jean-Claude, Emile, Jean-François, Héritier, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Clinical Oncology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823889/
https://www.ncbi.nlm.nih.gov/pubmed/31513482
http://dx.doi.org/10.1200/JCO.19.00456
Descripción
Sumario: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.