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Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer

BACKGROUND: Monosialotetrahexosylganglioside (GM1) is a neuroprotective glycosphingolipid that repairs nerves. Oxaliplatin‐based chemotherapy is neurotoxic. This study assessed the efficacy of GM1 for preventing oxaliplatin‐induced peripheral neurotoxicity (OIPN) in colorectal cancer (CRC) patients...

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Autores principales: Wang, De‐shen, Wang, Zhi‐qiang, Chen, Gong, Peng, Jie‐wen, Wang, Wei, Deng, Yan‐hong, Wang, Feng‐hua, Zhang, Jian‐wei, Liang, Han‐lin, Feng, Fen, Xie, Chuan‐bo, Ren, Chao, Jin, Ying, Shi, Si‐mei, Fan, Wen‐hua, Lu, Zhen‐hai, Ding, Pei‐rong, Wang, Feng, Xu, Rui‐hua, Li, Yu‐hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943144/
https://www.ncbi.nlm.nih.gov/pubmed/31724334
http://dx.doi.org/10.1002/cam4.2693
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author Wang, De‐shen
Wang, Zhi‐qiang
Chen, Gong
Peng, Jie‐wen
Wang, Wei
Deng, Yan‐hong
Wang, Feng‐hua
Zhang, Jian‐wei
Liang, Han‐lin
Feng, Fen
Xie, Chuan‐bo
Ren, Chao
Jin, Ying
Shi, Si‐mei
Fan, Wen‐hua
Lu, Zhen‐hai
Ding, Pei‐rong
Wang, Feng
Xu, Rui‐hua
Li, Yu‐hong
author_facet Wang, De‐shen
Wang, Zhi‐qiang
Chen, Gong
Peng, Jie‐wen
Wang, Wei
Deng, Yan‐hong
Wang, Feng‐hua
Zhang, Jian‐wei
Liang, Han‐lin
Feng, Fen
Xie, Chuan‐bo
Ren, Chao
Jin, Ying
Shi, Si‐mei
Fan, Wen‐hua
Lu, Zhen‐hai
Ding, Pei‐rong
Wang, Feng
Xu, Rui‐hua
Li, Yu‐hong
author_sort Wang, De‐shen
collection PubMed
description BACKGROUND: Monosialotetrahexosylganglioside (GM1) is a neuroprotective glycosphingolipid that repairs nerves. Oxaliplatin‐based chemotherapy is neurotoxic. This study assessed the efficacy of GM1 for preventing oxaliplatin‐induced peripheral neurotoxicity (OIPN) in colorectal cancer (CRC) patients receiving oxaliplatin‐based chemotherapy. METHODS: In total, 196 patients with stage II/III CRC undergoing adjuvant chemotherapy with mFOLFOX6 were randomly assigned to intravenous GM1 or a placebo. The primary endpoint was the rate of grade 2 or worse cumulative neurotoxicity (NCI‐CTCAE). The secondary endpoints were chronic cumulative neurotoxicity (EORTC QLQ‐CIPN20), time to grade 2 neurotoxicity (NCI‐CTCAE or the oxaliplatin‐specific neuropathy scale), acute neurotoxicity (analog scale), rates of dose reduction or withdrawal due to OIPN, 3‐year disease‐free survival (DFS) and adverse events. RESULTS: There were no significant differences between the arms in the rate of NCI‐CTCAE grade 2 or worse neurotoxicity (GM1: 33.7% vs placebo: 31.6%; P = .76) or neuropathy measured by the EORTC QLQ‐CIPN20 or time to grade 2 neurotoxicity using NCI‐CTCAE and the oxaliplatin‐specific neuropathy scale. GM1 substantially decreased participant‐reported acute neurotoxicity (sensitivity to cold items [P < .01], discomfort swallowing cold liquids [P < .01], throat discomfort [P < .01], muscle cramps [P < .01]). The rates of dose reduction or withdrawal were not significantly different between the arms (P = .08). The 3‐year DFS rates were 85% and 83% in the GM1 and placebo arms, respectively (P = .19). There were no differences in toxicity between the arms. CONCLUSION: Patients receiving GM1 were less troubled by the symptoms of acute neuropathy. However, we do not support the use of GM1 to prevent cumulative neurotoxicity. (http://ClinicalTrials.gov number, NCT02251977).
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spelling pubmed-69431442020-01-07 Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer Wang, De‐shen Wang, Zhi‐qiang Chen, Gong Peng, Jie‐wen Wang, Wei Deng, Yan‐hong Wang, Feng‐hua Zhang, Jian‐wei Liang, Han‐lin Feng, Fen Xie, Chuan‐bo Ren, Chao Jin, Ying Shi, Si‐mei Fan, Wen‐hua Lu, Zhen‐hai Ding, Pei‐rong Wang, Feng Xu, Rui‐hua Li, Yu‐hong Cancer Med Clinical Cancer Research BACKGROUND: Monosialotetrahexosylganglioside (GM1) is a neuroprotective glycosphingolipid that repairs nerves. Oxaliplatin‐based chemotherapy is neurotoxic. This study assessed the efficacy of GM1 for preventing oxaliplatin‐induced peripheral neurotoxicity (OIPN) in colorectal cancer (CRC) patients receiving oxaliplatin‐based chemotherapy. METHODS: In total, 196 patients with stage II/III CRC undergoing adjuvant chemotherapy with mFOLFOX6 were randomly assigned to intravenous GM1 or a placebo. The primary endpoint was the rate of grade 2 or worse cumulative neurotoxicity (NCI‐CTCAE). The secondary endpoints were chronic cumulative neurotoxicity (EORTC QLQ‐CIPN20), time to grade 2 neurotoxicity (NCI‐CTCAE or the oxaliplatin‐specific neuropathy scale), acute neurotoxicity (analog scale), rates of dose reduction or withdrawal due to OIPN, 3‐year disease‐free survival (DFS) and adverse events. RESULTS: There were no significant differences between the arms in the rate of NCI‐CTCAE grade 2 or worse neurotoxicity (GM1: 33.7% vs placebo: 31.6%; P = .76) or neuropathy measured by the EORTC QLQ‐CIPN20 or time to grade 2 neurotoxicity using NCI‐CTCAE and the oxaliplatin‐specific neuropathy scale. GM1 substantially decreased participant‐reported acute neurotoxicity (sensitivity to cold items [P < .01], discomfort swallowing cold liquids [P < .01], throat discomfort [P < .01], muscle cramps [P < .01]). The rates of dose reduction or withdrawal were not significantly different between the arms (P = .08). The 3‐year DFS rates were 85% and 83% in the GM1 and placebo arms, respectively (P = .19). There were no differences in toxicity between the arms. CONCLUSION: Patients receiving GM1 were less troubled by the symptoms of acute neuropathy. However, we do not support the use of GM1 to prevent cumulative neurotoxicity. (http://ClinicalTrials.gov number, NCT02251977). John Wiley and Sons Inc. 2019-11-13 /pmc/articles/PMC6943144/ /pubmed/31724334 http://dx.doi.org/10.1002/cam4.2693 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Wang, De‐shen
Wang, Zhi‐qiang
Chen, Gong
Peng, Jie‐wen
Wang, Wei
Deng, Yan‐hong
Wang, Feng‐hua
Zhang, Jian‐wei
Liang, Han‐lin
Feng, Fen
Xie, Chuan‐bo
Ren, Chao
Jin, Ying
Shi, Si‐mei
Fan, Wen‐hua
Lu, Zhen‐hai
Ding, Pei‐rong
Wang, Feng
Xu, Rui‐hua
Li, Yu‐hong
Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title_full Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title_fullStr Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title_full_unstemmed Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title_short Phase III randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage II/III colorectal cancer
title_sort phase iii randomized, placebo‐controlled, double‐blind study of monosialotetrahexosylganglioside for the prevention of oxaliplatin‐induced peripheral neurotoxicity in stage ii/iii colorectal cancer
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6943144/
https://www.ncbi.nlm.nih.gov/pubmed/31724334
http://dx.doi.org/10.1002/cam4.2693
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