Ellis P A, Norman A, Hill A, O'Brien M E, Nicolson M, Hickish T, Cunningham D
Cancer Research Campaign, Section of Medicine, Institute of Cancer Research, Sutton, Surrey, U.K.
Eur J Cancer. 1995 Sep;31A(10):1594-8. doi: 10.1016/0959-8049(95)00323-b.
Hepatobiliary tumours are rare, often present late and have a poor prognosis, with no current effective systemic therapy available. This study aimed to evaluate the activity and toxicity of epirubicin, cisplatin and continuous infusional 5-fluorouracil (5-FU) (ECF) in patients with these tumours. From March 1991 to November 1993, 25 patients with advanced biliary tumours and 7 with hepatoma were treated with epirubicin 50 mg/m2 and cisplatin 60 mg/m2 intravenously (i.v.) day 1, each given every 21 days and 5-FU 200 mg/m2/day given as a continuous 24 h i.v. infusion throughout the treatment course. 8 of the 20 (40%) evaluable patients with biliary tumours responded. Median duration of response was 10 months. 2 of the 7 (29%) patients with hepatoma responded. The regimen was well tolerated with minimal haematological and non-haematological toxicity. This novel regimen is active in advanced hepatobiliary tumours.
肝胆肿瘤较为罕见,通常发现较晚,预后较差,目前尚无有效的全身治疗方法。本研究旨在评估表柔比星、顺铂和持续输注氟尿嘧啶(5-FU)(ECF方案)对这些肿瘤患者的疗效和毒性。1991年3月至1993年11月,25例晚期胆管肿瘤患者和7例肝癌患者接受了治疗,第1天静脉注射(i.v.)表柔比星50mg/m²和顺铂60mg/m²,每21天给药一次,整个治疗过程中5-FU以200mg/m²/天的剂量持续24小时静脉输注。20例可评估的胆管肿瘤患者中有8例(40%)有反应。中位反应持续时间为10个月。7例肝癌患者中有2例(29%)有反应。该方案耐受性良好,血液学和非血液学毒性极小。这种新方案对晚期肝胆肿瘤有效。