Department of Clinical Pharmacology and Therapeutics, Institute of Biomedical Sciences, Tokushima University Graduate School.
Department of Pharmacy, Tokushima University Hospital.
Biol Pharm Bull. 2021;44(4):478-484. doi: 10.1248/bpb.b20-00609.
Patients who undergo multiple-day chemotherapy sessions experience hard-to-treat nausea and vomiting. Currently, there is no effective standard treatment for this condition. This study compared the preventive effect of first-generation 5-hydroxytryptamine 3 receptor antagonists (5-HT RAs) and second-generation 5-HT RAs palonosetron in multiple-day chemotherapy-induced nausea and vomiting. The design of this study was a retrospective case-control study of patients who received a five-day cisplatin-based chemotherapy and were treated with aprepitant, dexamethasone, granisetron, and ramosetron or palonosetron. The patients were divided into two groups: patients given granisetron and ramosetron (the first-generation group), and those given palonosetron (palonosetron group). The percentage of patients with a complete response or total control was assessed. They were divided into three phases: 0-216 h (overall phase), 0-120 h (remedial phase), and 120-216 h (after phase). The remedial phase was further divided into 0-24 h (early phase) and 24-120 h (later phase). Moreover, the nutritional status of each patient was assessed by noting the patients' total calorie-intake per day and total parenteral nutrition. First-generation 5-HT RAs and palonosetron were used for treatment in 18 and 28 patients, respectively. The complete response rate and caloric oral intake of the later phase were higher in the palonosetron group than in the first-generation group. We conclude that palonosetron treatment was more effective than first-generation 5-HT RAs in controlling multiple-day chemotherapy-induced nausea and vomiting.
接受多日化疗的患者会经历难以治疗的恶心和呕吐。目前,这种情况没有有效的标准治疗方法。本研究比较了第一代 5-羟色胺 3 受体拮抗剂(5-HT3RA)和第二代 5-HT3RA 帕洛诺司琼在多日化疗引起的恶心和呕吐中的预防作用。本研究的设计是一项回顾性病例对照研究,纳入了接受五天顺铂为基础的化疗并接受阿瑞匹坦、地塞米松、格拉司琼和雷莫司琼或帕洛诺司琼治疗的患者。患者分为两组:接受格拉司琼和雷莫司琼(第一代组)和接受帕洛诺司琼(帕洛诺司琼组)的患者。评估完全缓解或总控制的患者比例。他们被分为三个阶段:0-216 小时(总体阶段)、0-120 小时(补救阶段)和 120-216 小时(后阶段)。补救阶段进一步分为 0-24 小时(早期阶段)和 24-120 小时(后期阶段)。此外,通过记录患者每天的总热量摄入和全胃肠外营养来评估每位患者的营养状况。第一代 5-HT3RA 和帕洛诺司琼分别用于治疗 18 例和 28 例患者。帕洛诺司琼组的完全缓解率和后期阶段的热量口服摄入均高于第一代组。我们得出结论,帕洛诺司琼治疗在控制多日化疗引起的恶心和呕吐方面比第一代 5-HT3RA 更有效。