Tanioka Hiroaki, Tsuji Akihito, Morita Sojiro, Horimi Tadashi, Takamatsu Masahiro, Shirasaka Tetsuhiko, Mizushima Takaaki, Ochi Koji, Kiura Katsuyuki, Tanimoto Mitsune
Okayama University Medical School, 2-5-1 Okayamashi, Shikata-cho, Okayama, 700-8558, Japan.
Anticancer Res. 2003 Mar-Apr;23(2C):1891-7.
In this study we evaluated the efficacy and toxicities of combination chemotherapy consisting of continuous 5-fluorouracil (5-FU) infusion and low-dose cisplatin infusion (low-dose FP therapy) in the treatment of advanced hepatocellular carcinoma (HCC).
Thirty-eight patients with advanced HCC in whom local treatment was not indicated were enrolled. The low-dose FP therapy consisted of 5-FU (170 mg/m2/day on days 1 to 7/week, continuous infusion) and cisplatin (3 mg/m2/day in 100 ml normal saline, infusion more than 30 minutes, on days 1 to 5/weeks). The patients were treated for 4 consecutive weeks with a subsequent one-week rest period.
Thirty-seven of the 38 patients (97%) completed this therapy. A partial response was obtained in 18 (47%), no change in 10 and progressive disease in 9. The time to progression was 211 days. The most common toxicity was nausea/vomiting (13.2%).
Low-dose FP therapy has a substantial effect on low-grade toxicity in long-term treatment. Low-dose FP therapy is useful for the treatment of advanced HCC.
在本研究中,我们评估了持续输注5-氟尿嘧啶(5-FU)与低剂量顺铂输注联合化疗(低剂量FP疗法)治疗晚期肝细胞癌(HCC)的疗效和毒性。
纳入38例不适合局部治疗的晚期HCC患者。低剂量FP疗法包括5-FU(每周第1至7天,170mg/m²/天,持续输注)和顺铂(每周第1至5天,3mg/m²/天加入100ml生理盐水中,输注超过30分钟)。患者连续治疗4周,随后休息1周。
38例患者中有37例(97%)完成了该治疗。18例(47%)获得部分缓解,10例病情稳定,9例病情进展。疾病进展时间为211天。最常见的毒性反应是恶心/呕吐(13.2%)。
低剂量FP疗法在长期治疗中对低级别毒性有显著影响。低剂量FP疗法对晚期HCC的治疗有用。