Falkson H C, Falkson C I, Falkson G
Department of Medical Oncology, University of Pretoria, South Africa.
Invest New Drugs. 1990 Nov;8(4):407-9. doi: 10.1007/BF00198602.
Fifty six patients, with histologically confirmed cancer, who received highly emetogenic chemotherapy, were entered on a randomized double blind, low versus high dose, study of granisetron, a 5HT3 receptor antagonist. A single dose of intravenous granisetron protected the majority of patients from nausea and vomiting, 160 micrograms/kg was more effective than 40 micrograms/kg with no more side effects. Additional doses of granisetron conferred added benefit to patients who experienced breakthrough symptoms. Granisetron at a dose range of 40-240 micrograms/kg over a 24 hour period was well tolerated with the only side effect being mild headache.
56例经组织学确诊为癌症且接受高致吐性化疗的患者,参与了一项关于5-羟色胺3(5HT3)受体拮抗剂格拉司琼的随机双盲、低剂量与高剂量对比研究。单剂量静脉注射格拉司琼可使大多数患者免受恶心和呕吐困扰,160微克/千克的剂量比40微克/千克更有效,且副作用并未增加。额外剂量的格拉司琼对出现突破性症状的患者有额外益处。格拉司琼在24小时内剂量范围为40 - 240微克/千克时耐受性良好,唯一的副作用是轻度头痛。