期刊文献+

生物化学疗法治疗晚期肝癌的临床研究

The clinical study of biochemotherapy in treatment of advanced liver cancer
下载PDF
导出
摘要 目的 比较生物化学疗法与单用化疗对晚期肝癌的疗效及观察其不良反应。方法 36例晚期肝癌患者随机分组接受生物化学疗法(A组)或单用化疗(B组)。A组:5-FU 375mg/m2 iv第1-5天,HCPT 6mg/m2 iv第1-5天,每3周重复,共2周期。化疗间歇期输注总数2-3×109个的TAK细胞。B组:单用化疗,方案同上。结果 A组有效率23.5%,B组有效率12.5%,(P>0.05)。A、B组主要不良反应分别为:白细胞减少(58.8%和62.5%)、血小板减少(17.6%和12.5%)、血红蛋白减少(35.3%和31.3%)、恶心呕吐(70.6%和68.8%)、脱发(29.4%和25%)、肝功损害(52.9%和43.8%)、肾功损害(5.8%和12.5%)、发热(29.4%和0%)和骨/肌肉酸痛(35.3%和0%)。发热、骨肌肉酸痛A组明显高于B组(P<0.05)。结论 生物化学疗法治疗晚期肝癌有效、安全,不良反应可以耐受。 To compare with the difference between biochemotherapy and chemotherapy in the efficacy and toxicity for treatment of patients with advanced liver cancer. Methods 36 patients with advanced liver cancer were randomized into A group or B group. A group recieved biochemotherapy 5 - FU 375mg/m2 iv d1-5, HCPT 6mg/m iv d1- 5, once every 3 weeks for 2 cycles. Interval time of chemotherapy re - infused TAK cells in tatal [ (2-3)×109]. B group recieved the same chemotherapy only. Results Overall response rate of A group was 23.5% , and B group 12.5% . ( P > 0.05). The main adverse effect A and B group were: leukopenia (58.8% vs62.5%); thrombocytopenia (17.6% vs 12.5%); anemia (35.3% vs31.3%); nausea/vomiting (70.6% vs 68.8%); alopecia (29.4% vs 25%); liver functional lesion (52.9% vs 43.8%); kidney functional lesion (5.8% vs 12.5%); fever (29.4% vs 0%) and bone/ muscle pain (35.3% vs 0%), respectively. But the incidence of fever and bone/ muscle pain was difference between this two group ( P < 0.05) . Conclusions The biochemotherapy in treatment of patients with advanced liver cancer is safety and efficiency. Overall toxicity was acceptable.
出处 《癌症进展》 2003年第4期219-221,共3页 Oncology Progress
基金 福建省科学技术委员会98肝癌攻关课题(98-Z-155)资助。
关键词 生物化学疗法 肝癌 疗效 不良反应 biochemotherapy liver cancer efficacy adverse effect
  • 相关文献

参考文献5

二级参考文献30

  • 1赵跃武,刘政国,孔令非,王宝梅,银平章.32例肝癌组织中多药耐药基因及其产物P-糖蛋白的实验研究[J].中国民康医学,1998,13(3):150-151. 被引量:4
  • 2Chang A E,Cancer Investigation,1992年,10卷,357页
  • 3Sutherland H J;Eaves C J;Lansdorp P M.Kinetics of committed and primitive blood progenitor mobilization after chemotherapy and growth factor treatment and their use in autotransplants,1994.
  • 4Gottesman MM;Hrycyna CA.Genetic analysis of the multidrug transpoteer[J],1995(0).
  • 5Morrow CS.Glutation- s- transferases and drug resistance,1990.
  • 6Larkin A;Moran E;Alexander D.Related Articles Preliminary immunocytochemical studies of MDR- 1 and MDR- 3 Pgp expression in B- cell leukaemias[J],1999(02).
  • 7Rowe PM.Multidrug- resistance gene employed to advantage[J],1997(9055).
  • 8Biedler IL;Riehm H.Cellular resistance to actinomycin D in Chinese hamster cells in vitro: cross- resistance,radioautographic and cytogenetic studies,1970.
  • 9Roninson IB;Abelson HT;Housman DE.Amplification of specific DNA sequences correlates with multidrug ersistance in Chinese hamster cells[J],1984(5969).
  • 10Gros P;Neriah BY;Croop JM.Isolation and expression of a complementary DNA that confers multidrug resistance[J],1986(6090).

共引文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部