Al-Saleh E, Hoskins P J, Pike J A, Swenerton K D
Division of Gynecologic Oncology, Vancouver Cancer Centre, British Columbia Cancer Agency, Canada.
Gynecol Oncol. 1997 Mar;64(3):468-72. doi: 10.1006/gyno.1996.4567.
Thirty-eight women with primarily advanced (n = 10) or recurrent (n = 28) cervical carcinoma were treated with cisplatin (30 mg/m2/day intravenously) and etoposide (60 mg/m2/day intravenously) for 3 days followed by oral etoposide, 50 mg daily for 7 days, repeated at 28-day intervals. The response rate was 39% (95% confidence limits 24-55%) with response duration of 5 to 36 months. The main toxicities were neutropenia (21% developing neutropenic fever), alopecia, stomatitis, and nausea and vomiting. Despite this all responders had maintained or improved quality of life as defined by symptoms and performance status.
38例主要为晚期(n = 10)或复发性(n = 28)宫颈癌的女性患者接受了顺铂(30mg/m²/天,静脉注射)和依托泊苷(60mg/m²/天,静脉注射)治疗3天,随后口服依托泊苷,每天50mg,共7天,每28天重复一次。缓解率为39%(95%置信区间24 - 55%),缓解持续时间为5至36个月。主要毒性反应为中性粒细胞减少(21%发生中性粒细胞减少性发热)、脱发、口腔炎以及恶心和呕吐。尽管如此,所有缓解者的生活质量根据症状和体能状态定义均得以维持或改善。