Hochster H S, Green M D, Speyer J, Fazzini E, Blum R, Muggia F M
J Clin Oncol. 1985 Nov;3(11):1535-40. doi: 10.1200/JCO.1985.3.11.1535.
Doxorubicin provides the most consistent response rate in hepatocellular carcinoma. We therefore initiated a trial with its analog 4'epidoxorubicin. Eighteen patients, all without prior treatment, were given the drug as a single agent every 3 weeks with dose escalation whenever possible. Five patients were treated by six-hour infusion and 13 by intravenous (IV) bolus injection, with the median dose being 90 mg/m2. The patients were of diverse ethnic background and included some with underlying cirrhosis and hepatitis B surface antigenemia. Three patients had partial remissions (6, 12, 48 weeks) for a response rate of 17%. Four patients also had prolonged stable disease (14, 26, 27, 38 weeks). Toxicity was mild, although cardiac toxicity developed in three patients at 685, 825, and 1,460 mg/m2 cumulative dose. The response to 4'epidoxorubicin in this study appears to be equivalent to the reported response rates for doxorubicin, with decreased toxicity.
阿霉素在肝细胞癌中具有最稳定的缓解率。因此,我们开展了一项使用其类似物表阿霉素的试验。18例患者均未接受过先前治疗,每3周给予该药单药治疗,尽可能提高剂量。5例患者采用6小时输注治疗,13例采用静脉推注治疗,中位剂量为90mg/m²。患者种族背景各异,包括一些患有潜在肝硬化和乙肝表面抗原血症的患者。3例患者部分缓解(缓解期为6周、12周、48周),缓解率为17%。4例患者疾病稳定期也延长(分别为14周、26周、27周、38周)。毒性较轻,不过3例患者在累积剂量达到685mg/m²、825mg/m²和1460mg/m²时出现了心脏毒性。本研究中表阿霉素的疗效似乎与报道的阿霉素缓解率相当,且毒性有所降低。