Phase II study of combination doxorubicin, interferon-α, and high-dose tamoxifen treatment for advanced hepatocellular carcinoma

被引:0
作者
Lu, YS
Hsu, CU
Li, CC
Kuo, SH
Yeh, KH
Yang, CH
Hsu, CH
Wu, CY
Cheng, AL
机构
[1] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 100, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[3] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
[4] Buddist Tzu Chi Gen Hosp, Dept Hematooncol, Hualien, Taiwan
[5] Natl Taiwan Univ, Coll Med, Canc Res Ctr, Taipei, Taiwan
[6] Far Eastern Mem Hosp, Dept Internal Med, Taipei, Taiwan
[7] Far Eastern Mem Hosp, Dept Med Res, Taipei, Taiwan
关键词
interferon-alpha; tamoxifen; doxorubicin; hepatocellular carcinoma;
D O I
暂无
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Our previous studies showed that high-dose tamoxifen may improve the therapeutic efficacy of doxorubicin (HTD regimen) in hepatocellular carcinoma. Interferon-alpha, either as a single-agent treatment or as a biochemical modulator, has also been reported to be effective in the treatment of hepatocellular carcinoma. In this study, we sought to clarify if the addition of Interferon-alpha2b to HTD regimen could further improve the control of advanced hepatocellular carcinoma. Methodology: Eligible patients had unresectable and non-embolizable hepatocellular carcinoma, objectively measurable tumors, adequate hemogram. and major organ function, age greater than or equal to75 year, and a Karnofsky performance status greater than or equal to60%. The treatment included oral tamoxifen 40mg/m(2), q.i.d., Day 1-7; interferon-alpha2b subcutaneous injection, 5MU/m(2), q.d. (Day 3-5) and 3MU/m(2), q.o.d. (Day 6-21); and intravenous doxorubicin 60mg/m(2), Day 4, repeated every 4 weeks. Results: From May 1997 through July 2002, a total of 30 patients were enrolled, 25 of whom were eligible for assessment of response and toxicity. These included 20 men and 5 women, with a median age of 45 years. They received an average of 3.5 (range: 1-8) courses of chemotherapy. Grade 3-4 leukopenia and Grade 3-4 thrombocytopenia developed in 46.7% and 51.0% of treatment courses, respectively. Gastrointestinal toxicity was generally mild. One patient achieved a complete remission and remained disease-free at this report, with a progression-free survival of 49 months at last follow-up in September 2002. Five patients achieved a partial remission, with a median progression-free survival of 7 months. The total response rate was 24% (95% confidence interval 9.4-45.1%). Median survival for all 25 patients was 6.0 months and the 1-year survival rate was 16%. Conclusions: Combination of interferon-alpha2b, high-dose tamoxifen, and doxorubicin is an effective treatment for advanced hepatocellular carcinoma. However, the data does not support that addition of interferon-a2b is superior to HTD regimen alone.
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页码:815 / 819
页数:5
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