The Effects of Ganglioside-Monosialic Acid in Taxane-Induced Peripheral Neurotoxicity in Patients with Breast Cancer: A Randomized Trial

Author:

Su Yanhong1,Huang Jiajia1,Wang Shusen1,Unger Joseph M2,Arias-Fuenzalida Jonathan3,Shi Yanxia1,Li Jibin4,Gao Yongxiang5,Shi Wei1,Wang Xinyue1,Peng Roujun1,Xu Fei1ORCID,An Xin1,Xue Cong1,Xia Wen1,Hong Ruoxi1,Zhong Yongyi1,Lin Ying6,Huang Heng7,Zhang Anqin8,Zhang Lehong9,Cai Li10,Zhang Jinxin5,Yuan Zhongyu1,

Affiliation:

1. Department of Medical Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, Guangdong, China

2. Department of Health Services Research, Fred Hutchinson Cancer Research Center, Seattle, WA

3. Department of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden

4. Department of Clinical Research, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China

5. Department of Medical Statistics and Epidemiology, Sun Yat-sen University, Guangzhou, Guangdong, China

6. Department of Breast Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, China

7. Department of Breast Surgery, Lianjiang People's Hospital, Lianjiang, Guangdong, China

8. Breast Disease Center, Guangdong Women and Children's Hospital, Guangzhou, Guangdong, China

9. Department of Breast Surgery, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China

10. The Fourth Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang, China

Abstract

Abstract Background Taxane-induced peripheral neuropathy (TIPN) is a dose-limiting adverse effect. Ganglioside-monosialic acid (GM1) functions as a neuroprotective factor. We assessed the effects of GM1 on the prevention of TIPN in breast cancer patients. Methods We conducted a randomized, double-blind, placebo-controlled trial including 206 patients with early-stage breast cancer planning to receive taxane-based adjuvant chemotherapy with a follow-up of more than 1 year. Subjects were randomly assigned to receive GM1 (80 mg, day −1 to day 2) or placebo. The primary endpoint was the Functional Assessment of Cancer Treatment Neurotoxicity subscale score after four cycles of chemotherapy. Secondary endpoints included neurotoxicity evaluated by National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.0 and the Eastern Cooperative Oncology Group neuropathy scale. All statistical tests were two-sided. Results In 183 evaluable patients, the GM1 group reported better mean Functional Assessment of Cancer Treatment Neurotoxicity subscale scores than patients in the placebo group after four cycles of chemotherapy (43.27, 95% confidence interval [CI] = 43.05 to 43.49 vs 34.34, 95% CI = 33.78 to 34.89; mean difference = 8.96, 95% CI = 8.38 to 9.54, P < .001). Grade 1 or higher peripheral neurotoxicity in Common Terminology Criteria for Adverse Events v4.0 scale was statistically significantly lower in the GM1 group (14.3% vs 100.0%, P < .001). Additionally, the GM1 group had a statistically significantly lower incidence of grade 1 or higher neurotoxicity assessed by Eastern Cooperative Oncology Group neuropathy scale sensory neuropathy (26.4% vs 97.8%, P < .001) and motor neuropathy subscales (20.9% vs 81.5%, P < .001). Conclusions The treatment with GM1 resulted in a reduction in the severity and incidence of TIPN after four cycles of taxane-containing chemotherapy in patients with breast cancer.

Funder

Qilu Pharmaceutical and Sun Yat-sen University Cancer Center

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference42 articles.

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4. Mitotic block induced in HeLa cells by low concentrations of paclitaxel (Taxol) results in abnormal mitotic exit and apoptotic cell death;Jordan;Cancer Res,1996

5. Peripheral neuropathy induced by microtubule-stabilizing agents;Lee;J Clin Oncol,2006

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