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https://hdl.handle.net/2445/222984
Title: | Effect of Tumor-Treating Fields Plus Maintenance Temozolomide vs Maintenance Temozolomide Alone on Survival in Patients With Glioblastoma |
Author: | Stupp, Roger Taillibert, Sophie Kanner, Andrew Read, William M. Steinberg, David Lhermitte, Benoit Toms, Steven Idbaih, Ahmed S. Ahluwalia, Manmeet Fink, Karen Di Meco, Francesco Lieberman, Frank Zhu, Jay-jiguang Stragliotto, Giuseppe D. Tran, David Brem, Steven F. Hottinger, Andreas D. Kirson, Eilon Lavy-shahaf, Gitit Weinberg, Uri Kim, Chae-yong Paek, Sun-ha Nicholas, Garth Bruna, Jordi Hirte, Hal Weller, Michael Palti, Yoram E. Hegi, Monika Ram, Zvi |
Issue Date: | 19-Dec-2017 |
Publisher: | American Medical Association (AMA) |
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. |
Note: | Reproducció del document publicat a: https://doi.org/10.1001/jama.2017.18718 |
It is part of: | JAMA, 2017, vol. 318, issue. 23, p. 2306 |
URI: | https://hdl.handle.net/2445/222984 |
Related resource: | https://doi.org/10.1001/jama.2017.18718 |
Appears in Collections: | Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) |
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File | Description | Size | Format | |
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effect of tumor-treating fields plus mai.pdf | 615.75 kB | Adobe PDF | View/Open |
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