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https://hdl.handle.net/2445/222984Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Stupp, Roger | - |
| dc.contributor.author | Taillibert, Sophie | - |
| dc.contributor.author | Kanner, Andrew | - |
| dc.contributor.author | Read, William | - |
| dc.contributor.author | Steinberg, David M. | - |
| dc.contributor.author | Lhermitte, Benoit | - |
| dc.contributor.author | Toms, Steven | - |
| dc.contributor.author | Idbaih, Ahmed | - |
| dc.contributor.author | Ahluwalia, Manmeet S. | - |
| dc.contributor.author | Fink, Karen | - |
| dc.contributor.author | Meco, Francesco di | - |
| dc.contributor.author | Lieberman, Frank | - |
| dc.contributor.author | Zhu, Jay Jiguang | - |
| dc.contributor.author | Stragliotto, Giuseppe | - |
| dc.contributor.author | Tran, David D. | - |
| dc.contributor.author | Brem, Steven | - |
| dc.contributor.author | Hottinger, Andreas F. | - |
| dc.contributor.author | Kirson, Eilon D. | - |
| dc.contributor.author | Lavy Shahaf, Gitit | - |
| dc.contributor.author | Weinberg, Uri | - |
| dc.contributor.author | Kim, Chae Yong | - |
| dc.contributor.author | Paek, Sun Ha | - |
| dc.contributor.author | Nicholas, Garth | - |
| dc.contributor.author | Bruna, Jordi | - |
| dc.contributor.author | Hirte, Hal | - |
| dc.contributor.author | Weller, Michael | - |
| dc.contributor.author | Palti, Yoram | - |
| dc.contributor.author | Hegi, Monika E. | - |
| dc.contributor.author | Ram, Zvi | - |
| dc.date.accessioned | 2025-09-05T10:05:54Z | - |
| dc.date.available | 2025-09-05T10:05:54Z | - |
| dc.date.issued | 2017-12-19 | - |
| dc.identifier.issn | 1538-3598 | - |
| dc.identifier.uri | https://hdl.handle.net/2445/222984 | - |
| 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 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.extent | 11 p. | - |
| dc.format.mimetype | application/pdf | - |
| dc.language.iso | eng | - |
| dc.publisher | American Medical Association (AMA) | - |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1001/jama.2017.18718 | - |
| dc.relation.ispartof | JAMA, 2017, vol. 318, num. 23, p. 2306-2316 | - |
| dc.relation.uri | https://doi.org/10.1001/jama.2017.18718 | - |
| dc.rights | (c) American Medical Association, 2017 | - |
| dc.source | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | - |
| dc.subject.classification | Glioma | - |
| dc.subject.classification | Medicaments antineoplàstics | - |
| dc.subject.classification | Tumors cerebrals | - |
| dc.subject.other | Gliomas | - |
| dc.subject.other | Antineoplastic agents | - |
| dc.subject.other | Brain tumors | - |
| dc.title | Effect of tumor-treating fields plus maintenance Temozolomide vs maintenance Temozolomide alone on survival in patients with glioblastoma | - |
| dc.type | info:eu-repo/semantics/article | - |
| dc.type | info:eu-repo/semantics/publishedVersion | - |
| dc.date.updated | 2025-08-29T12:35:34Z | - |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
| dc.identifier.pmid | 29260225 | - |
| Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| effect of tumor-treating fields plus mai.pdf | 615.75 kB | Adobe PDF | View/Open |
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