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作 者:袁志平[1] 罗峰[1] 姜愚[1] 彭枫[1] 邹立群[1] 姚文秀[1]
出 处:《四川医学》2006年第3期261-263,共3页Sichuan Medical Journal
摘 要:目的 观察生物化疗加沙利度胺对晚期肾癌的治疗作用。方法 选取病理证实均为肾细胞癌的晚期肾癌后患者61例。分两组:①对照组23例行生物化疗;②实验组38例行生物化疗加沙利度胺治疗。所有病人均行病肾姑息切除术或肾动脉栓塞术,术后1—2周开始生物化疗。生物化疗方法:IL-2200万U/次,3次/周皮下注射;IFN-2a300万u/次,3次/周皮下注射;IL-2和IFN-2a均用42周。5-FU500mg加入5%葡萄糖液500ml缓慢静脉滴注(4—6h),第1-5天。21d为1周期,共4-6周期。沙利度胺用法为400mg/d,分2次口服,服用1年或至病情进展。结果 近期疗效两组均无CR病例。对照组PR5例,有效率(CR+PR)21.7%;实验组PR18例,有效率(CR+PR)47.4%,两组差异有显著性(P〈0.05)。两组未见严重不良反应发生。疾病进展期对照组4.7个月,平均5.2个月,实验组6-9个月,平均7个月。随访12个月对照组成活11例,1年生存率为43.4%;实验组成活19例,1年生存率为50%。随访24个月,对照组5例生存。生存率17.4%;实验组7例生存,生存率18.4%,两组差异无显著性(P〉0.05)。结论 生物化疗加沙利度胺对晚期肾癌的治疗与生物化疗相比,能提高近期疗效和延长疾病进展时间,对1年和2年生存率无差别。Objective To evaluate the effect of biochmothetapy (recombinant interferon-2α,recombinant interleukin-2 plus 5- fluovouracil) plus thalidomide in the advanced renal cell canclnoma (RCC) ;Methods Overall 61 patients with advanced RCC underwent pallative nephrectomy or renal arterial embollzation. These cases were assigned to 2 groups, ① biochemotherapy group included 23 case, they were treated with subcutaneous interferon-2α ( IFN-2a), interleukin-2 ( IL-21,5-fluourouracil ( 5-FU) ; ② biochemotherapy plus thalidomide group included 38 cases. The biochemotherapic courses consisted of IFN-2a (3×10^6U3times/w). IL-2 (2×10^6U 3 times/ w) and 5-FU (500mg per day, continuous infusion for 5 days tin a 21-day cycle, total 4 to 6 cycles), the IFN-2a and the IL-2 wcre totally used fo 42 weeks. Thalidomide was continuously administered at a dose of 400 mg twice daffy orally for one year or advantage of disease. The main outcome measure was the response rate and toxin responas;secondary outcomes were disease progressed time and overall survival rate. Results The overall response rate was 21.7 percent (no case complete response and 5 case partial response) in the biochemotherapy group and 47.4 percent (no case complete response and 18 ease partial response) in the biochemothcrapy plus thalidomide group ( P 〈 0.05) .There were not severely slde-effect in both groups.The median time to disease progression was 5.2 months in the biocbcmotherapy group and 7 months in the biocbcmotherapy plus thalidomide group. There was no significant difference in one-year and two-year survival rate in both groups (43.4 percent versus 50 percent for one-year survival rate, 17.4 percent versus 18.4 percent for two-year survival rate).Conclusion Both groups did not show significant effect on one-year and two-year survival rate in those patients, but the biochemotherapy and thalidomide group lengthened disease progressed time and advanced the overall response rate.
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