Please use this identifier to cite or link to this item: 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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