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DOI 10.1002/cam4.2693

Медицинская библиотека · Cancer medicine · 2019

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

Клиническое исследование III фазыСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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. (ClinicalTrials.gov number, NCT02251977).

Для цитирования: 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.. Cancer medicine. 2019. DOI: 10.1002/cam4.2693.

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