Radiation Oncology Journal
- 제17권2호
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- Pages.141-145
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- 1999
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- 2234-1900(pISSN)
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- 2234-3156(eISSN)
방사선치료 중 오심 및 구토에 대한 그라니세트론의 효과
Granisetron in the Treatment of Radiotherapy-Induced Nausea and Vomiting
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Hong, Seong-Eon
(Department of Radiation Oncology. College of Medicine, Kyung Hee University) ;
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Kang, Jin-O
(Department of Radiation Oncology. College of Medicine, Kyung Hee University)
- 발행 : 1999.06.01
초록
목적: 방사선 치료시 유발되는 오심과 구토에 대하여 5-hydroxytriptamine 길항제인 그라니세트론을 투여하여 그 효과에 대한 임상적 효능과 방법, 사용기간, 부작용 등에 대한 기본적인 자료를 얻고자 본 연구를 시행하였다. 대상 및 방법 : 병리학적으로 암으로 확진된 18세 이상의 성인 남녀 10명(직장암 4명, 자궁경부암 2명, 자궁내막암 1명, 정상피종 1명, 폐암 1명, 백혈병 1명)을 대상으로 그라니세트론 치료의 효과를 조사하였다. 그라니세트론은 경구 투여로 2mg을 하루 1회 사용하였으며, 방사선치료 후 오심이나 구토 증상이 나타나기 시작하면 사용하여 2주간 계속적으로 투여하였다 환자의 오심의 정도, 구토 회수, 부작용 등의 증세는 방사선치료 시작일로부터 하루 한번씩 기록하여 24시간 후와 제7일 째의 결과를 분석하였다. 오심은 무증상, 경증, 증등도, 중증 등 4단계로 분류하였으며 무증상과 경증을 치료효과가 있는 것으로 판정하였다. 구토 억제에 대한 효과는 완전효과, 주효효과, 경미효과, 치료실패 등으로 구분하였고 완전효과와 주효효과를 구토가 조절된 것으로 정의하였다. 결과 : 오심에 대한 효과는 그라니세트론 투여후 제7일에 전체 10명중 9명(90
Purpose : Granisetron is a potent, the most selective 5-HT3 receptor antagonist and is reported to b effective in treatment of radiation-induced emesis. The antiemetic efficacy and safety of oral granisteron was evaluated in patients with receiving highly emetogenic treatment by conventional fractionated irradiation. Materials and Methods : Patients with various cancers who were being treated with irradiation were accrued into the present study. The intensity of nausea was evaluated on first 24 hours and on day-7 by patients according to the degree of interference with normal daily life as followings; a) none; b) present but no interference with normal daily life (mild): c) interference with normal daily life (moderate): and d) bedridden because of nausea (severe). Non or mild state was considered to indicate successful treatment. The efficacy of antiemetic treatment was graded as follows; a) complete response; no vomiting, no worse than mild nausea and receive no rescue antiemetic therapy over the 24h period, b) major response; either one episode of vomiting or moderate/severe nausea or had received rescue medication over 24h period, or any combination of these, c) minor response; two to four episodes of vomiting over the 24h period, regardless of nausea and rescue medication, d) failure; more than four medication. The score of the most symptom was recorded and the total score over 24 hours was summarized. The complete or major response was considered to indicate successful treatment. Results : A total of 10 patients were enrolled into this study, and all were assessable for efficacy analysis. Total nausea control was achieved in 90