Efficacy and safety of ondansetron orally soluble pellicle for preventing moderate- to high-emetic risk chemotherapy-induced nausea and vomiting.

IF 3.4 2区 医学 Q2 ONCOLOGY BMC Cancer Pub Date : 2025-01-06 DOI:10.1186/s12885-024-13406-z
Lu Sun, Jia Ma, Yajuan Zhou, Xiaofang Ying, Gai Liang, Guoliang Pi, Ying Li, Yan Luo, Jianping Bi, Hanping He, Yi Peng
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Abstract

Objective: Ondansetron orally soluble pellicle can serve as an alternative option for preventing nausea and vomiting in patients who receive chemotherapy. However, there is a lack of clinical evidence regarding ondansetron. This study aimed to explore the efficacy and safety of ondansetron in patients with malignant tumours who received chemotherapy drugs with a moderate-to-high emetic risk.

Methods: In total, 163 patients with malignant tumours received 24 mg of ondansetron via orally soluble pellicles at 30 min before chemotherapy (8 mg each time for three consecutive administrations). The incidence rates of nausea and vomiting in the three days after chemotherapy were recorded.

Results: Regarding the effect of ondansetron on vomiting, the complete response (zero episodes of vomiting), major response (1-2 episodes of vomiting), minor response (3-5 episodes of vomiting), and failure (> 5 episodes of vomiting) rates were 96.9%, 1.2%, 1.2%, and 0%, respectively. The major efficacy rate for vomiting (complete response + major response rates) was 98.1%. Moreover, 96.3% of patients did not experience nausea, 2.5% of patients experienced mild nausea, 1.2% of patients experienced moderate nausea, and 0.0% of patients experienced severe nausea. The major efficacy rate for nausea (no nausea) was 96.3%. Age > 65 years was negatively associated with major efficacy for vomiting, and a chemotherapy regimen involving cisplatin was negatively associated with major efficacy for nausea. A total of 42 (25.8%) patients experienced adverse events. The most common adverse events were elevated levels of alanine transaminase (6.7%), elevated levels of aspartate transaminase (3.7%), fatigue (3.7%), and cough (2.5%).

Conclusion: Ondansetron orally soluble pellicle shows good antiemetic efficacy and high safety in patients with malignant tumours who receive chemotherapy drugs with a moderate-to-high emetic risk.

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口服可溶昂丹司琼膜预防化疗引起的中度至高度呕吐风险的恶心和呕吐的有效性和安全性。
目的:口服昂丹司琼可溶性膜可作为化疗患者预防恶心和呕吐的替代选择。然而,缺乏关于昂丹司琼的临床证据。本研究旨在探讨昂丹司琼在接受化疗药物的恶性肿瘤患者中有中高呕吐风险的疗效和安全性。方法:163例恶性肿瘤患者化疗前30分钟口服溶膜昂丹司琼24 mg(每次8 mg,连续3次)。记录化疗后3天恶心、呕吐的发生率。结果:在昂丹司琼对呕吐的影响方面,完全缓解(0次呕吐)、严重缓解(1-2次呕吐)、轻微缓解(3-5次呕吐)和失败(0 -5次呕吐)率分别为96.9%、1.2%、1.2%和0%。呕吐主要有效率(完全缓解+主要缓解率)为98.1%。此外,96.3%的患者没有出现恶心,2.5%的患者出现轻度恶心,1.2%的患者出现中度恶心,0.0%的患者出现严重恶心。对恶心(无恶心)的主要有效率为96.3%。年龄0 ~ 65岁与呕吐的主要疗效负相关,含顺铂的化疗方案与恶心的主要疗效负相关。共有42例(25.8%)患者出现不良事件。最常见的不良事件是丙氨酸转氨酶水平升高(6.7%)、天冬氨酸转氨酶水平升高(3.7%)、疲劳(3.7%)和咳嗽(2.5%)。结论:昂丹司琼口服可溶性膜在恶性肿瘤患者接受中高催吐风险化疗药物时具有良好的止吐效果和较高的安全性。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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