Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/222984
Full metadata record
DC FieldValueLanguage
dc.contributor.authorStupp, Roger-
dc.contributor.authorTaillibert, Sophie-
dc.contributor.authorKanner, Andrew-
dc.contributor.authorRead, William-
dc.contributor.authorM. Steinberg, David-
dc.contributor.authorLhermitte, Benoit-
dc.contributor.authorToms, Steven-
dc.contributor.authorIdbaih, Ahmed-
dc.contributor.authorS. Ahluwalia, Manmeet-
dc.contributor.authorFink, Karen-
dc.contributor.authorDi Meco, Francesco-
dc.contributor.authorLieberman, Frank-
dc.contributor.authorZhu, Jay-jiguang-
dc.contributor.authorStragliotto, Giuseppe-
dc.contributor.authorD. Tran, David-
dc.contributor.authorBrem, Steven-
dc.contributor.authorF. Hottinger, Andreas-
dc.contributor.authorD. Kirson, Eilon-
dc.contributor.authorLavy-shahaf, Gitit-
dc.contributor.authorWeinberg, Uri-
dc.contributor.authorKim, Chae-yong-
dc.contributor.authorPaek, Sun-ha-
dc.contributor.authorNicholas, Garth-
dc.contributor.authorBruna, Jordi-
dc.contributor.authorHirte, Hal-
dc.contributor.authorWeller, Michael-
dc.contributor.authorPalti, Yoram-
dc.contributor.authorE. Hegi, Monika-
dc.contributor.authorRam, Zvi-
dc.date.accessioned2025-09-05T10:05:54Z-
dc.date.available2025-09-05T10:05:54Z-
dc.date.issued2017-12-19-
dc.identifier.urihttps://hdl.handle.net/2445/222984-
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 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.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherAmerican Medical Association (AMA)-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1001/jama.2017.18718-
dc.relation.ispartofJAMA, 2017, vol. 318, issue. 23, p. 2306-
dc.relation.urihttps://doi.org/10.1001/jama.2017.18718-
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))-
dc.titleEffect of Tumor-Treating Fields Plus Maintenance Temozolomide vs Maintenance Temozolomide Alone on Survival in Patients With Glioblastoma-
dc.typeinfo:eu-repo/semantics/article-
dc.date.updated2025-08-29T12:35:34Z-
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccess-
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

Files in This Item:
File Description SizeFormat 
effect of tumor-treating fields plus mai.pdf615.75 kBAdobe PDFView/Open


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