J Clin Oncol. 1998 Sep;16(9):2937-42. doi: 10.1200/JCO.1998.16.9.2937.
A 5-hydroxytryptamine 3 (5-HT3) receptor antagonist plus dexamethasone is the most efficacious antiemetic prophylactic treatment for the prevention of cisplatin-induced acute emesis, but the optimal intravenous (i.v.) dose of dexamethasone is unknown. This prompted us to perform a multicenter, randomized, double-blind, dose-finding study that compared four different doses of dexamethasone.
Patients were randomized to receive dexamethasone, either 4, 8, 12, or 20 mg, administered by 15-minute i.v. infusion 45 minutes before cisplatin. Ondansetron 8 mg was added to dexamethasone and was administered i.v. 30 minutes before cisplatin. From March 1996 to July 1997, 531 patients were enrolled onto the study and 530 were assessable according to the intention-to-treat principle (133 patients received 4 mg; 136 patients, 8 mg; 130 patients, 12 mg; and 131 patients, 20 mg of dexamethasone).
Complete protection from acute vomiting and nausea was achieved by 69.2% and 60.9% of patients, respectively, who received 4 mg of dexamethasone, by 69.1% and 61.0% of those who received 8 mg, by 78.5% and 66.9% of those who received 12 mg, and by 83.2% and 71.0% of those who received 20 mg of dexamethasone. Complete protection from vomiting was significantly superior in patients who received 20 mg compared with those who received 4 and 8 mg of dexamethasone (P < .005) and was superior, but not significantly, compared with those who received 12 mg. Complete protection from nausea was superior, but not significantly, in patients who received 20 mg of dexamethasone. Multifactorial analysis confirmed these results. Antiemetic treatment was well tolerated, and no significant difference was found among the four groups in the incidence of adverse events.
A 20-mg single i.v. dose of dexamethasone should be considered the most efficacious prophylactic dose for the prevention of cisplatin-induced acute emesis.
5-羟色胺3(5-HT3)受体拮抗剂加地塞米松是预防顺铂所致急性呕吐最有效的止吐预防性治疗方法,但地塞米松的最佳静脉注射剂量尚不清楚。这促使我们开展一项多中心、随机、双盲、剂量探索性研究,比较四种不同剂量的地塞米松。
患者被随机分组,在顺铂给药前45分钟通过15分钟静脉输注接受4、8、12或20毫克地塞米松。在顺铂给药前30分钟,将8毫克昂丹司琼添加到地塞米松中并静脉注射。从1996年3月至1997年7月,531例患者纳入本研究,根据意向性分析原则,530例患者可进行评估(133例患者接受4毫克地塞米松;136例患者接受8毫克;130例患者接受12毫克;131例患者接受20毫克地塞米松)。
接受4毫克地塞米松的患者中,分别有69.2%和60.9%完全预防了急性呕吐和恶心;接受8毫克地塞米松的患者中,分别有69.1%和61.0%;接受12毫克地塞米松的患者中,分别有78.5%和66.9%;接受20毫克地塞米松的患者中,分别有83.2%和71.0%。接受20毫克地塞米松的患者在完全预防呕吐方面显著优于接受4毫克和8毫克地塞米松的患者(P<0.005),且优于接受12毫克地塞米松的患者,但差异不显著。接受20毫克地塞米松的患者在完全预防恶心方面优于其他患者,但差异不显著。多因素分析证实了这些结果。止吐治疗耐受性良好,四组不良事件发生率无显著差异。
单次静脉注射20毫克地塞米松应被视为预防顺铂所致急性呕吐最有效的预防剂量。