Roberts J T, Priestman T J
Regional Radiotherapy Centre, Newcastle General Hospital, Newcastle upon Tyne, UK.
Oncology. 1993 May-Jun;50(3):173-9. doi: 10.1159/000227173.
This paper reviews experience with ondansetron in radiotherapy-induced emesis. The efficacy of ondansetron is assessed following a number of different radiotherapy regimens: single-dose radiotherapy, fractionated radiotherapy, total body irradiation (TBI) and hemi-body irradiation. In single-dose radiation-induced emesis, ondansetron (8 mg orally 3 times daily) provided superior anti-emetic control compared with metoclopramide (10 mg orally 3 times daily): 92 and 46% of patients, respectively, experienced complete control of emesis (0 emetic episodes) in the first 24 h following treatment (p < 0.001). Similarly, ondansetron (8 mg orally 3 times daily) was significantly (p < 0.001) more effective than prochlorperazine (10 mg orally 3 times daily) with 59 and 35% of patients, respectively, achieving complete control of emesis on the 'worst day' of a fractionated radiotherapy regimen (up to 20 fractions). Two studies evaluating the efficacy of ondansetron in TBI-induced emesis have demonstrated that ondansetron is effective in paediatric and adult patients receiving chemotherapy and TBI prior to bone marrow transplantation. In these studies, 57-81% of patients experienced 2 or fewer emetic episodes during TBI. For hemi-body irradiation, ondansetron (8 mg) and dexamethasone (8 mg) given orally produced complete control of emesis in 12 out of 14 patients. The effectiveness of this regimen now enables patients receiving hemi-body irradiation to be treated as outpatients in many cases. Anecdotal data also shows that ondansetron is effective when given as intervention treatment in patients with established emesis. In none of the studies were there any serious adverse events following ondansetron treatment. It can therefore be concluded that ondansetron is an effective and well tolerated antiemetic for the prophylaxis and treatment of radiation-induced emesis and nausea. The use of effective anti-emetic treatments may have resource implications such as reducing bed occupancy and enabling the use of fewer, larger fractions of radiotherapy.
本文回顾了昂丹司琼治疗放疗引起的呕吐的经验。在多种不同的放疗方案后评估了昂丹司琼的疗效:单次剂量放疗、分次放疗、全身照射(TBI)和半身照射。在单次剂量放疗引起的呕吐中,与甲氧氯普胺(每日口服3次,每次10 mg)相比,昂丹司琼(每日口服3次,每次8 mg)提供了更好的止吐控制:分别有92%和46%的患者在治疗后的前24小时内呕吐得到完全控制(呕吐发作0次)(p<0.001)。同样,昂丹司琼(每日口服3次,每次8 mg)比丙氯拉嗪(每日口服3次,每次10 mg)显著更有效(p<0.001),在分次放疗方案(最多20次分割)的“最严重日”,分别有59%和35%的患者呕吐得到完全控制。两项评估昂丹司琼在TBI引起的呕吐中的疗效的研究表明,昂丹司琼对接受化疗和骨髓移植前TBI的儿科和成年患者有效。在这些研究中,57%至81%的患者在TBI期间呕吐发作2次或更少。对于半身照射,口服昂丹司琼(8 mg)和地塞米松(8 mg)使14例患者中的12例呕吐得到完全控制。这种方案的有效性现在使许多接受半身照射的患者能够作为门诊患者治疗。轶事数据还表明,昂丹司琼作为已发生呕吐患者的干预治疗有效。在所有研究中,接受昂丹司琼治疗后均未出现任何严重不良事件。因此可以得出结论,昂丹司琼是一种有效且耐受性良好的止吐药,用于预防和治疗放疗引起的呕吐和恶心。使用有效的止吐治疗可能会产生资源影响,例如减少床位占用,并允许使用更少、更大剂量的放疗分割。