Howell J D, Warren H W, Anderson J H, Kerr D J, McArdle C S
University Department of Surgery, Royal Infirmary, Glasgow, United Kingdom.
Eur J Surg. 1999 Jul;165(7):652-8. doi: 10.1080/11024159950189708.
To compare two regimens of intra-arterial chemotherapy for the treatment of hepatic metastases from colorectal cancer.
Open study.
Teaching hospital, UK SUBJECT: 57 patients with unresectable metastases confined to the liver, and an indwelling catheter in the hepatic artery.
The first 33 patients had a 24-hour intra-arterial infusion of 5-fluorouracil (5-FU) 1500 mg/m2, together with folinic acid 200 mg/m2 intravenously for the first and last two hours of the 5-FU infusion. This was repeated at weekly intervals for six weeks followed by a two-week gap before the next cycle. The remaining 24 patients had a two-weekly regimen in which folinic acid 200 mg/m2 was infused intravenously over 2 hours followed by an intra-arterial loading dose of 5-FU 400 mg/m2 over 15 minutes; 5-FU 1600 mg/m2 was then given by intra-arterial infusion over 22 hours. This was repeated on day 2 and then at two-weekly intervals.
Response rate and toxicity.
Median follow-up was 21 months, and estimated median survival 19 months. 29 patients (51%) have responded, 5 completely. There are no significant differences between the groups. Sites of progression were liver alone 26 (53%), lung alone 9 (18%), liver and lung 3 (6%), and the remainder in local or regional nodes (n = 7) or bone (n = 4). Six patients experienced WHO grade 3 or 4 toxicity.
The two regimens have high response rates and cause little systemic toxicity. Intra-arterial chemotherapy for hepatic metastases from colorectal cancer is currently being compared with conventional systemic chemotherapy in a randomised controlled trial.
比较两种动脉内化疗方案治疗结直肠癌肝转移的疗效。
开放性研究。
英国教学医院
57例肝内不可切除转移瘤患者,且肝动脉内留置导管。
前33例患者接受24小时动脉内输注5-氟尿嘧啶(5-FU)1500mg/m²,在5-FU输注的首末两小时静脉注射亚叶酸200mg/m²。每周重复一次,共六周,然后间隔两周进入下一个周期。其余24例患者接受每两周一次的方案,即先静脉输注亚叶酸200mg/m²,持续2小时,随后在15分钟内动脉内给予5-FU负荷剂量400mg/m²;然后在22小时内动脉内输注5-FU 1600mg/m²。在第2天重复一次,然后每两周重复一次。
缓解率和毒性。
中位随访时间为21个月,估计中位生存期为19个月。29例患者(51%)有反应,5例完全缓解。两组之间无显著差异。进展部位仅为肝脏26例(53%),仅为肺部9例(18%),肝脏和肺部3例(6%),其余为局部或区域淋巴结转移(n = 7)或骨转移(n = 4)。6例患者出现世界卫生组织3级或4级毒性反应。
两种方案缓解率高,全身毒性小。目前正在一项随机对照试验中比较结直肠癌肝转移的动脉内化疗与传统全身化疗。