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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Clinical Oncology
2019
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Donadieu, Jean |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6823889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society of Clinical Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-68238892020-11-01 Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study 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 J Clin Oncol ORIGINAL REPORTS 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. American Society of Clinical Oncology 2019-11-01 2019-09-12 /pmc/articles/PMC6823889/ /pubmed/31513482 http://dx.doi.org/10.1200/JCO.19.00456 Text en © 2019 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | ORIGINAL REPORTS 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 Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title_full | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title_fullStr | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title_full_unstemmed | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title_short | Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study |
title_sort | vemurafenib for refractory multisystem langerhans cell histiocytosis in children: an international observational study |
topic | ORIGINAL REPORTS |
url | 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 |
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