口服格拉司琼加地塞米松与静脉注射昂丹司琼加地塞米松控制中/重度致吐性化疗引起的恶心呕吐的疗效和安全性比较

T J Chiou, W F Tzeng, W S Wang, C C Yen, F S Fan, J H Liu, P M Chen
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引用次数: 0

摘要

背景:化疗引起的恶心和呕吐会影响肿瘤患者对细胞毒性化疗的依从性。目前,有一些新的止吐疗法用于治疗化疗引起的呕吐。一项单机构、随机、开放、平行试验比较口服格拉司琼加静脉注射地塞米松与静脉注射昂丹司琼预防中度或重度致吐性化疗引起的急性和延迟性呕吐的效果。方法:51例肿瘤患者接受中/重度致吐性化疗,随机分为格拉司琼1 mg口服2次/ d或昂丹司琼8 mg / 8 h静脉注射,化疗当日联合地塞米松10 mg静脉注射。比较两种止吐方案的疗效和安全性。结果:口服格拉司琼加静脉注射地塞米松与静脉注射昂丹司琼加静脉注射地塞米松相比,在化疗开始后24小时内预防恶心的止吐效果相当。格拉司琼和昂丹司琼在开始止吐治疗后第一个24小时内止吐的完全缓解率分别为84.0% (95% CI, 62.9% ~ 95.6%)和84.6% (95% CI, 64.0% ~ 97.5%)。格拉司琼和昂丹司琼开始止吐治疗后迟发性呕吐的完全缓解率分别为16.0% (95% CI, 4.5%-36.1%)和19.2% (95% CI, 6.8%-40.7%)。格拉司琼组12%的患者出现腹泻,昂丹司琼组23.1%的患者出现便秘。结论:口服格拉司琼加静脉注射地塞米松和口服昂丹司琼加静脉注射地塞米松在预防中、重度致吐性化疗引起的急性或延迟性呕吐方面具有潜在的同等效果。口服格拉司琼联合地塞米松似乎是接受中度或重度致吐性化疗的癌症患者的一种合适的替代止吐剂。
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Comparison of the efficacy and safety of oral granisetron plus dexamethasone with intravenous ondansetron plus dexamethasone to control nausea and vomiting induced by moderate/severe emetogenic chemotherapy.

Background: Chemotherapy-induced nausea and vomiting can affect cancer patients' compliance with cytotoxic chemotherapy. Currently, there are some new antiemetic therapies for the treatment of chemotherapy-induced emesis. A single institution, randomized, open, parallel trial was done to compare oral granisetron plus intravenous (i.v.) dexamethasone with intravenous ondansetron for the prevention of moderate or severe emetogenic chemotherapy-induced acute and delayed emesis.

Methods: Fifty-one cancer patients were treated with moderate/severe emetogenic chemotherapy and randomized to receive either oral granisetron 1 mg twice daily or i.v. ondansetron 8 mg every 8 hours combined with i.v. dexamethasone 10 mg on the day of chemotherapy. The efficacy and safety of the two antiemetic regimens were compared.

Results: Oral granisetron plus i.v. dexamethasone had comparable antiemetic efficacy for the prevention of nausea in the first 24-hour period after initiation of chemotherapy compared with intravenous ondansetron plus i.v. dexamethasone. The complete response of antiemesis in the first 24-hour period after initiation of antiemetic therapy between granisetron and ondansetron were 84.0% (95% CI, 62.9%-95.6%) and 84.6 (95% CI, 64.0%-97.5%). The complete response for delayed emesis after initiation of antiemetic therapy between granisetron and ondansetron were 16.0% (95% CI, 4.5%-36.1%) and 19.2% (95% CI, 6.8%-40.7%0. There was diarrhea in 12% of patients receiving granisetron therapy and constipation in 23.1% of the ondansetron group.

Conclusions: Oral granisetron plus i.v. dexamethasone and i.v. ondansetron plus i.v. dexamethasone are potentially equally effective antiemetic agents in the prevention of moderate or severe emetogenic chemotherapy-induced acute or delayed emesis. Oral granisetron with dexamethasone appears to be a suitable alternative antiemetic agent in cancer patients who receive moderately or severely emetogenic chemotherapy.

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