Similar effects of recombinant interferon-α-2b and natural interferon-α when combined with intra-arterial 5-fluorouracil for the treatment of advanced hepatocellular carcinoma

被引:34
作者
Uka, Kiminori
Aikata, Hiroshi
Takaki, Shintaro
Miki, Daiki
Jeong, Soo Cheol
Hiramatsu, Akira
Kodama, Hideaki
Shirakawa, Hiroo
Kawakami, Yoshiiku
Takahashi, Shoichi
Toyota, Naoyuki
Ito, Katsuhide
Chayama, Kazuaki
机构
[1] Hiroshima Univ, Grad Sch Biomed Res, Div Frontier Med Sci,Programs Biomed Res, Dept Med & Mol Sci,Minami Ku, Hiroshima 7348551, Japan
[2] Hiroshima Univ Hosp, Dept Radiol, Hiroshima, Japan
关键词
advanced hepatocellular carcinoma; 5-fluorouracil; natural interferon-alpha; recombinant interferon-alpha-2b;
D O I
10.1111/j.1478-3231.2007.01554.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: Intra-arterial 5-fluorouracil (5-FU) plus interferon (IFN) combination therapy is effective against advanced hepatocellular carcinoma (HCC) with portal vein tumour thrombosis. In this study, we compared the efficiency and safety of recombinant IFN-alpha-2 beta with natural IFN-alpha as components of the combination therapy. Methods: Consecutive HCC patients (n = 31) with portal vein tumour thrombosis were enrolled in this prospective study. They received combination therapy of 5-FU and either recombinant IFN-alpha-2b (R group, n = 15) or natural IFN-alpha ( N group, n = 16). We compared the two groups for the early response rate, adverse reactions, time to progression (TTP) and survival rates. In addition, we assessed the cost-effectiveness of each protocol. Results: The early response rate ( R: 26.7%, N: 31.2%), median TTP ( R: 5.8 months, N: 5.6 months) and median survival time ( R: 7.5 months, N: 6.5 months) were not significantly different between the R and N groups. There were no differences in adverse reactions between the two groups. The estimated cost-effectiveness ratio of recombinant IFN-alpha-2b was better than natural IFN-alpha. Conclusions: In our protocol of combination therapy, there were no significant differences between recombinant IFN-alpha-2b and natural IFN-alpha with regard to early response to therapy, adverse effects, TTP and survival rates. 5-FU could be combined with either recombinant IFN-alpha-2b or natural IFN-alpha, although the cost-effectiveness of the former warrants its use clinically.
引用
收藏
页码:1209 / 1216
页数:8
相关论文
共 45 条
[1]   NOMENCLATURE OF THE HUMAN INTERFERON PROTEINS [J].
ALLEN, G ;
DIAZ, MO ;
FINTER, NB ;
ADOLF, GR ;
DOLY, J ;
LUNDGREN, E ;
PESTKA, S ;
ROBERTS, RM ;
TESTA, D ;
WIETZERBIN, J .
JOURNAL OF INTERFERON RESEARCH, 1994, 14 (04) :223-226
[2]   INTERFERON-ALPHA INCREASES THE FREQUENCY OF INTERFERON-GAMMA-PRODUCING HUMAN CD4+ T-CELLS [J].
BRINKMANN, V ;
GEIGER, T ;
ALKAN, S ;
HEUSSER, CH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) :1655-1663
[3]   INTERFERON EFFECTS UPON FLUOROURACIL METABOLISM BY HL-60 CELLS [J].
ELIAS, L ;
SANDOVAL, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :867-874
[4]   Different relative activities of human cell-derived interferon-alpha subtypes: IFN-alpha 8 has very high antiviral potency [J].
Foster, GR ;
Rodrigues, O ;
Ghouze, F ;
SchulteFrohlinde, E ;
Testa, D ;
Liao, MJ ;
Stark, GR ;
Leadbeater, L ;
Thomas, HC .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1996, 16 (12) :1027-1033
[5]   PRIMARY HEPATOCELLULAR CANCER - PRESENT RESULTS AND FUTURE-PROSPECTS [J].
FRIEDMAN, MA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1983, 9 (12) :1841-1850
[6]   CYTOTOXIC EFFECT OF INTERFERON ON PRIMARY MALIGNANT-TUMOR CELLS - STUDIES IN VARIOUS MALIGNANCIES [J].
GRANDER, D ;
XU, B ;
EINHORN, S .
EUROPEAN JOURNAL OF CANCER, 1993, 29A (14) :1940-1943
[7]  
Health Welfare Statistics Association, 2000, J HLTH WELFARE STAT, V47, P421
[8]  
Horowitz RW, 1997, CLIN CANCER RES, V3, P1317
[9]   Combination of transcatheter arterial chemoembolization using cisplatin-lipiodol suspension and percutaneous ethanol injection for treatment of advanced small hepatocellular carcinoma [J].
Kamada, K ;
Kitamoto, M ;
Aikata, H ;
Kawakami, Y ;
Kono, H ;
Imamura, M ;
Nakanishi, T ;
Chayama, K .
AMERICAN JOURNAL OF SURGERY, 2002, 184 (03) :284-290
[10]   CYTOKINE TRIGGERED MOLECULAR PATHWAYS THAT CONTROL CELL-CYCLE ARREST [J].
KIMCHI, A .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1992, 50 (01) :1-9