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

被引:140
作者
Donadieu, Jean [1 ]
Larabi, Islam Amine [2 ]
Tardieu, Mathilde [3 ]
Visser, Johannes [4 ]
Hutter, Caroline [5 ]
Sieni, Elena [6 ]
Kabbara, Nabil [7 ,8 ]
Barkaoui, Mohamed [1 ]
Miron, Jean [1 ]
Chalard, Francois [1 ]
Milne, Paul [9 ]
Haroche, Julien [10 ]
Cohen, Fleur [10 ]
Helias-Rodzewicz, Zofia [11 ]
Simon, Nicolas [12 ]
Jehanne, Mathilde [13 ]
Kolenova, Alexandra [14 ]
Pagnier, Anne [3 ,18 ]
Aladjidi, Nathalie [15 ]
Schneider, Pascale [16 ]
Plat, Genevieve [17 ]
Lutun, Anne [18 ]
Sonntagbauer, Anne [19 ]
Lehrnbecher, Thomas [19 ]
Ferster, Alina [20 ]
Efremova, Viktoria [21 ]
Ahlmann, Martina [22 ]
Blanc, Laurence [23 ]
Nicholson, James [4 ]
Lambilliote, Anne [24 ]
Boudiaf, Houda [25 ]
Lissat, Andrej [26 ]
Svojgr, Karel [27 ]
Bernard, Fanette [28 ]
Elitzur, Sarah [29 ]
Golan, Michal [30 ]
Evseev, Dmitriy [31 ]
Maschan, Michael [31 ]
Idbaih, Ahmed [32 ]
Slater, Olga [33 ]
Minkov, Milen [5 ]
Taly, Valerie [34 ]
Collin, Matthew [9 ]
Alvarez, Jean-Claude [2 ]
Emile, Jean-Francois [11 ]
Heritier, Sebastien [1 ,11 ]
机构
[1] Trousseau Hosp, Paris, France
[2] Ctr Hosp Univ R Poincare, Garches, France
[3] CHU Grenoble, Grenoble, France
[4] Cambridge Univ Hosp, Cambridge, England
[5] Med Univ Vienna, Vienna, Austria
[6] Azienda Osped Univ A Meyer, Florence, Italy
[7] Ctr Hosp Nord, Zgharta, Lebanon
[8] Rafic Hariri Univ Hosp, Beirut, Lebanon
[9] Newcastle Univ, Newcastle Upon Tyne, Tyne & Wear, England
[10] CHU Pitie Salpetriere, Paris, France
[11] Univ Paris Saclay, Boulogne, France
[12] Hop St Marguerite, Marseille, France
[13] Ctr Hosp Univ Felix Guyon, St Denis, Reunion, France
[14] Comenius Univ Childrens Hosp, Limbova 1, Bratislava, Slovakia
[15] CHU Bordeaux, Bordeaux, France
[16] CHU Rouen, Rouen, France
[17] CHU Toulouse, Toulouse, France
[18] CHU Amiens, Amiens, France
[19] Univ Klinikum Frankfurt, Frankfurt, Germany
[20] Hop Univ Enfants Reine Fabiola, Brussels, Belgium
[21] Univ Hosp, Minsk, BELARUS
[22] Univ Klinikum Munster, Klin Kinder & Jugendmed Padiatr Hamatol & Onkol, Munster, Germany
[23] CHU Poitiers, Poitiers, France
[24] CHU Lille, Lille, France
[25] Hop Mustapha, Mustapha, Algeria
[26] Charite Univ Med Berlin, Berlin, Germany
[27] Univ Hosp Motol, Prague, Czech Republic
[28] Hop Univ Geneve, Geneva, Switzerland
[29] Schneider Childrens Med Ctr, Petah Tiqwa, Israel
[30] Edmond & Lily Safra Childrens Hosp, Tel Hahsomer, Israel
[31] Dmitriy Rogachev Natl Ctr Pediat Hematol Oncol &, Moscow, Russia
[32] Ctr Hosp Univ La Pitie Salpetriere Charles Foix, Paris, France
[33] Great Ormond St Hosp Sick Children, London, England
[34] Univ Paris Sorbonne Cite, Paris, France
关键词
MELANOMA; DISEASE; TRANSPLANTATION; ORIGIN; PLASMA; LIFE;
D O I
10.1200/JCO.19.00456
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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页码:2857 / +
页数:10
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