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https://hdl.handle.net/2445/224144Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Bruna, Jordi | - |
| dc.contributor.author | Videla, Sebastián | - |
| dc.contributor.author | A. Argyriou, Andreas | - |
| dc.contributor.author | Velasco, Roser | - |
| dc.contributor.author | Villoria, Jesús | - |
| dc.contributor.author | Santos, Cristina | - |
| dc.contributor.author | Nadal, Cristina | - |
| dc.contributor.author | Cavaletti, Guido | - |
| dc.contributor.author | Alberti, Paola | - |
| dc.contributor.author | Briani, Chiara | - |
| dc.contributor.author | P. Kalofonos, Haralabos | - |
| dc.contributor.author | Cortinovis, Diego | - |
| dc.contributor.author | Sust, Mariano | - |
| dc.contributor.author | Vaqué, Anna | - |
| dc.contributor.author | Klein, Thomas | - |
| dc.contributor.author | Plata-salamán, Carlos | - |
| dc.date.accessioned | 2025-11-06T09:08:22Z | - |
| dc.date.available | 2025-11-06T09:08:22Z | - |
| dc.date.issued | 2017-09-18 | - |
| dc.identifier.uri | https://hdl.handle.net/2445/224144 | - |
| dc.description.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. | - |
| dc.format.mimetype | application/pdf | - |
| dc.language.iso | eng | - |
| dc.publisher | Elsevier BV | - |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1007/s13311-017-0572-5 | - |
| dc.relation.ispartof | Neurotherapeutics, 2017, vol. 15, issue. 1, p. 178-189 | - |
| dc.relation.uri | https://doi.org/10.1007/s13311-017-0572-5 | - |
| dc.source | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | - |
| dc.title | Efficacy of a Novel Sigma-1 Receptor Antagonist for Oxaliplatin-Induced Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Phase IIa Clinical Trial | - |
| dc.type | info:eu-repo/semantics/article | - |
| dc.date.updated | 2025-11-04T11:17:43Z | - |
| dc.rights.accessRights | info:eu-repo/semantics/embargoedAccess | - |
| Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Efficacy of a Novel Sigma-1 Receptor Ant.pdf | 1.91 MB | Adobe PDF | View/Open |
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