Titre :

Phase II study of oral JAK1/JAK2 inhibitor ruxolitinib in advanced relapsed/refractory Hodgkin lymphoma.

Auteur(s) :

Van Den Neste, Eric [Auteur]
Cliniques Universitaires Saint-Luc [Bruxelles]
Andre, Marc [Auteur]
CHU UCL Namur
Gastinne, Thomas [Auteur]
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital [CHU Nantes]
Stamatoullas-Bastard, Aspasia [Auteur]
Centre de Lutte Contre le Cancer Henri Becquerel Normandie Rouen [CLCC Henri Becquerel]
Haioun, Corinne [Auteur]
CHU Henri Mondor [Créteil]
Belhabri, Amine [Auteur]
Université Claude Bernard Lyon 1 [UCBL]
Reman, Oumedaly [Auteur]
CHU Caen
Casasnovas, Olivier [Auteur]
CHU Dijon
Ghesquieres, Herve [Auteur]
Université Claude Bernard Lyon 1 [UCBL]
Verhoef, Gregor [Auteur]
University Hospitals Leuven [Leuven]
Claessen, Marie-Jose [Auteur]
Erasmus University Rotterdam
Poirel Helene, A [Auteur]
Catholic University of Leuven = Katholieke Universiteit Leuven [KU Leuven]
Copin, Marie-Christine [Auteur]
Mécanismes de la Tumorigénèse et Thérapies Ciblées - UMR 8161 [M3T]
Dubois, Romain [Auteur]
Mouvement, Équilibre, Performance, Santé [MEPS]
Vandenberghe, Peter [Auteur]
University Hospitals Leuven [Leuven]
Stoian, Ioanna-Andrea [Auteur]
Cliniques Universitaires Saint-Luc [Bruxelles]
Cottereau Anne, S [Auteur]
CHU Tenon [AP-HP]
Bailly, Sarah [Auteur]
Cliniques Universitaires Saint-Luc [Bruxelles]
Knoops, Laurent [Auteur]
Université Catholique de Louvain = Catholic University of Louvain [UCL]
Morschhauser, Franck [Auteur]
Groupe de Recherche sur les formes Injectables et les Technologies Associées - ULR 7365 [GRITA]

Titre de la revue :

Haematologica

Nom court de la revue :

Haematologica

Numéro :

108

Date de publication :

2018-05

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

JAK2 constitutive activation/overexpression is common in classical Hodgkin lymphoma, and several cytokines stimulate Hodgkin lymphoma cells by recognizing JAK1-/JAK2-bound receptors. JAK blockade may thus be therapeutically ...
Lire la suite >JAK2 constitutive activation/overexpression is common in classical Hodgkin lymphoma, and several cytokines stimulate Hodgkin lymphoma cells by recognizing JAK1-/JAK2-bound receptors. JAK blockade may thus be therapeutically beneficial in Hodgkin lymphoma. In this phase II study we assessed the safety and efficacy of ruxolitinib, an oral JAK1/2 inhibitor, in patients with relapsed/refractory Hodgkin lymphoma. The primary objective was overall response rate according to the International Harmonization Project 2007 criteria. Thirty-three patients with advanced disease (median number of prior lines of treatment: 5; refractory: 82%) were included; nine (27.3%) received at least six cycles of ruxolitinib and six (18.2%) received more than six cycles. The overall response rate after six cycles was 9.4% (3/32 patients). All three responders had partial responses; another 11 patients had transient stable disease. Best overall response rate was 18.8% (6/32 patients). Rapid alleviation of B-symptoms was common. The median duration of response was 7.7 months, median progression-free survival 3.5 months (95% CI: 1.9-4.6), and the median overall survival 27.1 months (95% CI: 14.4-27.1). Forty adverse events were reported in 14/33 patients (42.4%). One event led to treatment discontinuation, while 87.5% of patients recovered without sequelae. Twenty-five adverse events were grade 3 or higher. These events were mostly anemia (n=11), all considered related to ruxolitinib. Other main causes of grade 3 or higher adverse events included lymphopenia and infections. Of note, no cases of grade 4 neutropenia or thrombocytopenia were observed. Ruxolitinib shows signs of activity, albeit short-lived, beyond a simple anti-inflammatory effect. Its limited toxicity suggests that it has the potential to be combined with other therapeutic modalities. ClinicalTrials.gov: NCT01877005.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Université de Lille
CHU Lille
CNRS

Collections :

• Groupe de Recherche sur les formes Injectables et les Technologies Associées (GRITA) - ULR 7365
• Mécanismes de la Tumorigénèse et Thérapies Ciblées (M3T) - UMR 8161

Équipe(s) de recherche :

Innovation/évaluation des médicaments injectables

Date de dépôt :

2019-02-26T17:06:59Z
2021-03-15T14:31:15Z