Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/224144
Title: Efficacy of a Novel Sigma-1 Receptor Antagonist for Oxaliplatin-Induced Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase IIa Clinical Trial
Author: Bruna, Jordi
Videla, Sebastián
A. Argyriou, Andreas
Velasco, Roser
Villoria, Jesús
Santos, Cristina
Nadal, Cristina
Cavaletti, Guido
Alberti, Paola
Briani, Chiara
P. Kalofonos, Haralabos
Cortinovis, Diego
Sust, Mariano
Vaqué, Anna
Klein, Thomas
Plata-salamán, Carlos
Issue Date: 18-Sep-2017
Publisher: Elsevier BV
Abstract: This trial assessed the efficacy of MR309 (a novel selective sigma-1 receptor ligand previously developed as E-52862) in ameliorating oxaliplatin-induced peripheral neuropathy (oxaipn). A discontinuous regimen of MR309 (400 mg/day, 5 days per ycle) was tested in patients with colorectal cancer receiving FOLFOX in a phase II, randomized, doubleblind, placebo-controlled, multicenter clinical trial. Outcome measures included changes in 24-week quantitative measures of thermal sensitivity and total neuropathy score. In total, 124 patients were randomized (1:1) to MR309 or placebo. Sixtythree (50.8%) patients withdrew prematurely before completing 12 planned oxaliplatin cycles. Premature withdrawal because of cancer progression was less frequent in the MR309 group (7.4% vs 25.0% with placebo; p = 0.054). MR309 significantly reduced cold pain threshold temperature [mean treatment effect difference (SE) vs placebo: 5.29 (1.60)°C; p = 0.001] and suprathreshold cold stimulus-evoked pain intensity [mean treatment effect difference: 1.24 (0.57) points; p = 0.032]. Total neuropathy score, health-related quality-of-life measures, and nerve-conduction parameters changed similarly in both arms, whereas the proportion of patients with severe chronic neuropathy (National Cancer Institute Common Terminology Criteria for Adverse Events ≥ 3) was significantly lower in the MR309 group (3.0% vs 18.2% with placebo; p = 0.046). The total amount of oxaliplatin delivered was greater in the active arm (1618.9 mg vs 1453.8 mg with placebo; p = 0.049). Overall, 19.0% of patients experienced at least 1treatment-related adverse event (25.8% and 11.9% with MR309 and placebo, respectively). Intermittent treatment with MR309 was associated with reduced acute oxaipn and higher oxaliplatin posure, and showed a potential neuroprotective role for chronic cumulative oxaipn. Furthermore,MR309 showed an acceptable safety rofile.
Note: Reproducció del document publicat a: https://doi.org/10.1007/s13311-017-0572-5
It is part of: Neurotherapeutics, 2017, vol. 15, issue. 1, p. 178-189
URI: https://hdl.handle.net/2445/224144
Related resource: https://doi.org/10.1007/s13311-017-0572-5
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

Files in This Item:
File Description SizeFormat 
Efficacy of a Novel Sigma-1 Receptor Ant.pdf1.91 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.