Abstract

BackgroundMonosialotetrahexosylganglioside (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.MethodsIn 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.ResultsThere 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.ConclusionPatients 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).

Highlights

  • Several studies have shown that patients with colorectal cancer (CRC) treated with oxaliplatin-based chemotherapy experience a survival benefit.[1,2] neuropathy is the most prominent dose-limiting toxicity of oxaliplatin.[3]

  • Patients receiving GM1 were less troubled by the symptoms of acute neuropathy

  • The secondary end points were chronic cumulative neurotoxicity measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Chemotherapy-Induced Peripheral Neuropathy 20 (EORTC QLQ-CIPN20),[23] time to grade 2 neurotoxicity according to the NCI-CTCAE or an oxaliplatin-specific neuropathy grading scale,[24] acute neurotoxicity, and the rates of dose reduction or withdrawal due to oxaliplatin-induced peripheral neurotoxicity (OIPN) in both arms

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Summary

Conclusion

Patients receiving GM1 were less troubled by the symptoms of acute neuropathy. We do not support the use of GM1 to prevent cumulative neurotoxicity. KEYWORDS colorectal cancer, EORTC QLQ-CIPN20, FOLFOX, GM1, neurotoxicity, OIPN, oxaliplatin

| INTRODUCTION
PARTICIPANTS
| Procedures
| Statistical methodology
| RESULTS
| DISCUSSION
DISCLOSURE OF PRIOR PRESENTATION
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