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

Author:

Donadieu Jean1,Larabi Islam Amine2,Tardieu Mathilde3,Visser Johannes4,Hutter Caroline5,Sieni Elena6,Kabbara Nabil78,Barkaoui Mohamed1,Miron Jean1,Chalard François1,Milne Paul9,Haroche Julien10,Cohen Fleur10,Hélias-Rodzewicz Zofia11,Simon Nicolas12,Jehanne Mathilde13,Kolenova Alexandra14,Pagnier Anne3,Aladjidi Nathalie15,Schneider Pascale16,Plat Geneviève17,Lutun Anne18,Sonntagbauer Anne19,Lehrnbecher Thomas19,Ferster Alina20,Efremova Viktoria21,Ahlmann Martina22,Blanc Laurence23,Nicholson James4,Lambilliote Anne24,Boudiaf Houda25,Lissat Andrej26,Svojgr Karel27,Bernard Fanette28,Elitzur Sarah29,Golan Michal30,Evseev Dmitriy31,Maschan Michael31,Idbaih Ahmed32,Slater Olga33,Minkov Milen5,Taly Valerie34,Collin Matthew9,Alvarez Jean-Claude2,Emile Jean-François11,Héritier Sébastien111

Affiliation:

1. Trousseau Hospital, Paris, France

2. Centre Hospitalier Universitaire R.-Poincaré, Garches, France

3. Centre Hospitalier Universitaire de Grenoble, Grenoble, France

4. Cambridge University Hospitals, Cambridge, United Kingdom

5. Medical University of Vienna, Vienna, Austria

6. Azienda Ospedaliero-Universitaria A. Meyer, Florence, Italy

7. Centre Hospitalier du Nord, Zgharta, Lebanon

8. Rafic Hariri University Hospital, Beirut, Lebanon

9. Newcastle University, Newcastle upon Tyne, United Kingdom

10. Centre Hospitalier Universitaire Pitié-Salpêtrière, Paris, France

11. Université Paris-Saclay, Boulogne-Billancourt, France

12. Hôpital Sainte Marguerite, Marseille, France

13. Centre Hospitalier Universitaire Félix-Guyon (Saint-Denis), La Réunion, France

14. Comenius University Children’s Hospital Limbova 1, Bratislava, Slovakia

15. Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France

16. Centre Hospitalier Universitaire de Rouen, Rouen, France

17. Centre Hospitalier Universitaire de Toulouse, Toulouse, France

18. Centre Hospitalier Universitaire d’Amiens, Amiens, France

19. Universitätsklinikum Frankfurt, Frankfurt am Main, Germany

20. Hôpital Universitaire des Enfants Reine Fabiola, Brussels, Belgium

21. University Hospital, Minsk, Belarus

22. Universitätsklinikum Münster Klinik für Kinder- und Jugendmedizin-Pädiatrische Hämatologie und Onkologie, Münster, Germany

23. Centre Hospitalier Universitaire de Poitiers, Poitiers, France

24. Centre Hospitalier Universitaire de Lille, Lille, France

25. Hôpital Mustapha, Mustapha, Algeria

26. Charité–University Medicine Berlin, Berlin, Germany

27. University Hospital Motol, Prague, Czech Republic

28. Hôpitaux Universitaires de Genève, Geneva, Switzerland

29. Schneider Children’s Medical Center, Petah Tikva, Israel

30. The Edmond and Lily Safra Children’s Hospital, Tel-Hahsomer, Israel

31. Dmitriy Rogachev National Center for Pediatric Hematology, Oncology and Immunology, Moscow, Russia

32. Centre Hospitalier Universitaire La Pitié-Salpêtrière–Charles Foix, Paris, France

33. Great Ormond Street Hospital, London, United Kingdom

34. Université Paris Sorbonne Cité, Paris, France

Abstract

PURPOSE Off-label use of vemurafenib (VMF) to treat BRAFV600E 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 BRAFV600E 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 BRAFV600E clone. CONCLUSION VMF seemed safe and effective in children with refractory BRAFV600E-positive LCH. Additional studies are needed to find effective maintenance therapy approaches.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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