Sorbe B, Berglind A M
Department of Gynecologic Oncology, Orebro Medical Center Hospital, Sweden.
Drugs. 1992;43 Suppl 3:33-9. doi: 10.2165/00003495-199200433-00008.
Oral tropisetron, a 5-hydroxytryptamine type 3 (serotonin3) [5-HT3]-receptor antagonist, at a dose of 5mg daily was evaluated as antiemetic prophylaxis during postoperative abdominal irradiation. 20 women with International Federation of Gynecology and Obstetrics (FIGO) stage I to III ovarian carcinoma were included. 12 women received irradiation of whole abdominal fields and 8 of lower abdominal/pelvic fields. Efficacy and adverse events were recorded by the patients in diary-form booklets. The cumulative weekly incidence of patients with nausea, which was generally mild and of short duration, increased from 30% at the start of radiotherapy to 54% at the end of treatment. Episodes of vomiting occurred in less than 10% of the patients. Diarrhoea was common towards the end of the radiotherapy courses, and the proportion of patients needing extra antidiarrhoeal medication (loperamide) increased from 38% during the first week to 100% at the end of the radiotherapy course. Mean weight loss was 1.2kg during the 5- to 6-week course. Overall ratings for quality of life were excellent or good in 75 to 85% of patients. Tropisetron seems to be a promising and well tolerated drug in conjunction with extended radiotherapy of abdominal fields. This was an open study, establishing the methodology for long term follow-up of patients during fractionated radiotherapy.
口服托烷司琼是一种5-羟色胺3型(血清素3)[5-HT3]受体拮抗剂,每日剂量为5毫克,在术后腹部放疗期间被评估用于预防恶心呕吐。纳入了20名国际妇产科联盟(FIGO)I至III期卵巢癌女性患者。12名女性接受全腹野照射,8名接受下腹/盆腔野照射。患者以日记形式记录疗效和不良事件。恶心患者的累积周发生率通常较轻且持续时间短,从放疗开始时的30%增加到治疗结束时的54%。不到10%的患者出现呕吐发作。腹泻在放疗疗程接近尾声时较为常见,需要额外使用止泻药物(洛哌丁胺)的患者比例从第一周的38%增加到放疗疗程结束时的100%。在5至6周的疗程中,平均体重减轻1.2千克。75%至85%的患者对生活质量的总体评价为优秀或良好。托烷司琼与腹部野的延长放疗联合使用时似乎是一种有前景且耐受性良好的药物。这是一项开放性研究,确立了在分次放疗期间对患者进行长期随访的方法。