Sorbe B, Berglind A M, De Bruijn K
Department of Gynecologic Oncology, Orebro Medical Center Hospital, Sweden.
Eur J Gynaecol Oncol. 1992;13(5):382-9.
Tropisetron, a 5-HT3 receptor antagonist, was evaluated as antiemetic prophylaxis during postoperative abdominal irradiation of ovarian carcinoma patients. Twenty consecutive women with Stages I-III (FIGO) epithelial ovarian carcinomas were included. At the start of radiotherapy all patients were clinically tumor-free. Twelve women received irradiation on whole-abdominal fields, 1.0 Gy per fraction, during 6 weeks. Eight women were irradiated on the lower abdomino-pelvic fields, 1.7 Gy per fraction, during 5 weeks. Efficacy and adverse events were recorded by the patients in diary-form booklets using visual analog scales (VAS). All patients completed the treatment series and none was lost to follow-up. Nausea, generally mild (mean 20 mm VAS) and of short duration, increased from start (30%) to end of radiotherapy (54%). Episodes of vomiting were few in number and occurred in less than 10% of the cases. Diarrhoea was common towards the end of the radiotherapy courses, especially when the dose per fraction was 1.7 Gy and the need for extra antidiarrhoeal medication (loperamide) increased from 38% at the start to 100% at the end. The mean weight loss was only 1.2 kg during 5-6 weeks. The overall ratings for quality of life were excellent or good in 75-85% of the cases. The efficacy of tropisetron was rated excellent or good in 80% of the cases and the tolerability likewise in 85% in the overall evaluation of the drug made by the investigator. Tropisetron therefore seems to be a promising and well-tolerated drug in conjunction with extended radiotherapy on the whole- or lower-abdominal fields.(ABSTRACT TRUNCATED AT 250 WORDS)
托烷司琼是一种5-羟色胺3(5-HT3)受体拮抗剂,在卵巢癌患者术后腹部放疗期间被用作预防性止吐药进行评估。纳入了20名FIGO分期为I-III期的连续上皮性卵巢癌女性患者。放疗开始时,所有患者临床上均无肿瘤。12名女性接受全腹野照射,每次分割剂量为1.0 Gy,持续6周。8名女性接受下腹盆腔野照射,每次分割剂量为1.7 Gy,持续5周。患者使用视觉模拟量表(VAS)以日记形式记录疗效和不良事件。所有患者均完成了治疗疗程,且无一例失访。恶心一般较轻(VAS平均为20 mm)且持续时间短,从放疗开始时的30%增加至放疗结束时的54%。呕吐发作次数较少,不到10%的病例出现。腹泻在放疗疗程接近结束时较为常见,尤其是当每次分割剂量为1.7 Gy时,额外使用止泻药物(洛哌丁胺)的需求从开始时的38%增加至结束时的100%。在5至6周内平均体重减轻仅1.2 kg。75%-85%的病例生活质量总体评分优秀或良好。在研究者对该药物的总体评估中,80%的病例托烷司琼疗效评为优秀或良好,85%的病例耐受性同样良好。因此,在全腹或下腹野延长放疗时,托烷司琼似乎是一种有前景且耐受性良好的药物。(摘要截取自250字)