Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/224144
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dc.contributor.authorBruna, Jordi-
dc.contributor.authorVidela, Sebastián-
dc.contributor.authorA. Argyriou, Andreas-
dc.contributor.authorVelasco, Roser-
dc.contributor.authorVilloria, Jesús-
dc.contributor.authorSantos, Cristina-
dc.contributor.authorNadal, Cristina-
dc.contributor.authorCavaletti, Guido-
dc.contributor.authorAlberti, Paola-
dc.contributor.authorBriani, Chiara-
dc.contributor.authorP. Kalofonos, Haralabos-
dc.contributor.authorCortinovis, Diego-
dc.contributor.authorSust, Mariano-
dc.contributor.authorVaqué, Anna-
dc.contributor.authorKlein, Thomas-
dc.contributor.authorPlata-salamán, Carlos-
dc.date.accessioned2025-11-06T09:08:22Z-
dc.date.available2025-11-06T09:08:22Z-
dc.date.issued2017-09-18-
dc.identifier.urihttps://hdl.handle.net/2445/224144-
dc.description.abstractThis 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.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier BV-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1007/s13311-017-0572-5-
dc.relation.ispartofNeurotherapeutics, 2017, vol. 15, issue. 1, p. 178-189-
dc.relation.urihttps://doi.org/10.1007/s13311-017-0572-5-
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.titleEfficacy of a Novel Sigma-1 Receptor Antagonist for Oxaliplatin-Induced Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase IIa Clinical Trial-
dc.typeinfo:eu-repo/semantics/article-
dc.date.updated2025-11-04T11:17:43Z-
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccess-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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