Efficacy of a Novel Sigma-1 Receptor Antagonist for Oxaliplatin-Induced Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase IIa Clinical Trial

被引:87
作者
Bruna, Jordi [1 ]
Videla, Sebastian [2 ]
Argyriou, Andreas A. [3 ]
Velasco, Roser [1 ]
Villoria, Jesus [4 ]
Santos, Cristina [1 ]
Nadal, Cristina [5 ]
Cavaletti, Guido [6 ]
Alberti, Paola [6 ]
Briani, Chiara [7 ]
Kalofonos, Haralabos P. [3 ]
Cortinovis, Diego [8 ]
Sust, Mariano [2 ]
Vaque, Anna [2 ]
Klein, Thomas [9 ]
Plata-Salaman, Carlos [2 ]
机构
[1] Hosp Univ Bellvitge, ICO LHospitalet, Barcelona, Spain
[2] Labs Dr Esteve, Clin Invest, Barcelona, Spain
[3] Univ Hosp Patras, Patras, Greece
[4] Medicxact, Madrid, Spain
[5] Hosp Clin Barcelona, Barcelona, Spain
[6] Univ Milano Bicocca, Monza, Italy
[7] Azienda Osped Padova, Padua, Italy
[8] San Gerardo Hosp, Monza, Italy
[9] Mundipharma Res GmbH & Co KG, Limburg, Lahn, Germany
关键词
Neurotoxicity; Neuropathic pain; Adverse effects; Chemotherapy; Colorectal cancer; MR309/E-52862; INDUCED PERIPHERAL NEUROTOXICITY; QUALITY-OF-LIFE; COLORECTAL-CANCER; OUTCOME MEASURES; PAIN; RELIABILITY;
D O I
10.1007/s13311-017-0572-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 cycle) was tested in patients with colorectal cancer receiving FOLFOX in a phase II, randomized, double-blind, 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. Sixty-three (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)degrees 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 1 treatment-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 exposure, and showed a potential neuroprotective role for chronic cumulative oxaipn. Furthermore, MR309 showed an acceptable safety profile.
引用
收藏
页码:178 / 189
页数:12
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