کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2125443 | 1547231 | 2009 | 4 صفحه PDF | دانلود رایگان |

Aim of the studyIn multiple-day chemotherapy (MDC), the combination of a 5-HT3-antagonist plus dexamethasone is still a standard of care. The role of a NK-1-antagonist remains to be defined.Patients and methodsSeventy eight cancer patients undergoing multiple-day chemotherapy of high (HEC) or moderate (MEC) emetic risk received granisetron, dexamethasone plus aprepitant during chemotherapy. After the end of chemotherapy, aprepitant plus dexamethasone was given for another 2 days. Primary end-point was complete response (CR) in the overall phase (day 1 until 5 days after the end of chemotherapy).ResultsThirty eight patients underwent HEC and 40 patients underwent MEC for a median of 3.5 days. CR was seen in 57.9% and 72.5% of patients receiving HEC and MEC, respectively. The tolerability of the aprepitant regimen over 5–7 days was comparable with a 3-day aprepitant regimen.ConclusionsThis is the first report in MDC with a NK-1-antagonist containing antiemetic regimen showing a favourable safety profile with good antiemetic efficacy.
Journal: European Journal of Cancer - Volume 45, Issue 7, May 2009, Pages 1184–1187