Palonosetron (AloxiA®) and dexamethasone for the prevention of acute and delayed nausea and vomiting in patients receiving multiple-day chemotherapy

被引:31
作者
Musso, Maurizio [1 ]
Scalone, Renato [1 ]
Bonanno, Vincenza [1 ]
Crescimanno, Alessandra [1 ]
Polizzi, Vita [1 ]
Porretto, Ferdinando [1 ]
Bianchini, Carlo [2 ]
Perrone, Tania [2 ]
机构
[1] La Maddalena Oncol Dept, Oncohaematol & BMT Unit, I-90146 Palermo, Italy
[2] Italfarmaco SpA, Dept Sci, I-20092 Milan, Italy
关键词
Palonosetron; 5-HT3; antagonist; Multiple-day chemotherapy; Antiemetics; Chemotherapy-induced nausea and vomiting (CINV); MODERATELY EMETOGENIC CHEMOTHERAPY; HIGH-DOSE CHEMOTHERAPY; GRANISETRON PLUS DEXAMETHASONE; DAY CISPLATIN CHEMOTHERAPY; STEM-CELL TRANSPLANT; DOUBLE-BLIND; PHASE-III; ANTIEMETIC THERAPY; POSTCHEMOTHERAPY NAUSEA; RANDOMIZED-TRIAL;
D O I
10.1007/s00520-008-0510-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of this study was to determine the efficacy of palonosetron combined with dexamethasone in prevention of acute and delayed chemotherapy-induced nausea and vomiting (CINV) in patients receiving multiple-day chemotherapy and the efficacy of a second dose of palonosetron in treating breakthrough emesis. Forty-six patients treated with multiple-day chemotherapy for hematologic malignancies received palonosetron as prophylaxis for CINV on the first day of chemotherapy and dexamethasone throughout the entire period of chemotherapy. If breakthrough emesis occurred, a second dose of palonosetron was administered after 72 h following the first administration. The results were retrospectively compared to group of patients with similar clinical characteristics undergoing similar multiple-day chemotherapy. This group had received single-dose ondansetron as CINV prophylaxis on the first day of chemotherapy plus dexamethasone throughout the entire period of chemotherapy and metoclopramide for breakthrough emesis. One hundred eighty and 173 chemotherapy cycles were administered in the palonosetron and ondansetron groups, respectively. Nausea and vomiting were absent in 80% of patients of the palonosetron group and 60% of the control group (p < 0.05). In the palonosetron group, 67% of patients who experienced CINV were successfully rescued by a second dose of palonosetron, while in the ondansetron group, only 22% showed a no CINV after metoclopramide treatment (p = 0.04). The present results appear to be encouraging in terms of complete prophylaxis of CINV and treatment of breakthrough emesis in the setting of multiple-day chemotherapy.
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页码:205 / 209
页数:5
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