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作 者:韩贵良[1,2] 刘亮[1,2] 于津浦[2] 曹水[1,2] 任秀宝[1,2]
机构地区:[1]天津医科大学附属肿瘤医院生物治疗科,天津300060 [2]天津市肿瘤防治重点实验室,天津300060
出 处:《中国肿瘤生物治疗杂志》2012年第6期577-581,共5页Chinese Journal of Cancer Biotherapy
基 金:国家自然科学基金资助项目(No.30901376);卫生部公益专项基金资助项目(No.200902002-2)~~
摘 要:目的:初步评价细胞因子诱导的杀伤细胞(cytokine-induced killer cell,CIK)在恶性黑素瘤治疗中的效果。方法:收集天津医科大学附属肿瘤医院2005年1月至2010年12月术后接受CIK治疗的38例恶性黑素瘤患者作为CIK治疗组,按1∶3比例选取同期术后未接受CIK治疗的114例恶性黑素瘤患者作为对照组,两组配对因素包括临床分期、性别、年龄、有无溃疡、乳酸脱氢酶(lactate dehyolrogenase,LDH)活性、病理类型、KPS评分(Karnofsky performance status scale)等均衡一致。随访时间为2005年3月至2012年3月,临床疗效的观察终点为总生存(overall survival,OS)期。结果:CIK治疗组与对照组1年OS率分别为86.8%、74.6%(P=0.097),3年OS率分别为76.3%、46.5%(P=0.001),5年OS率分别为71.1%、43.9%(P=0.004);CIK治疗组中位生存期明显长于对照组(CIK治疗组中位生存期未达到观察终点,对照组中位生存期为20.1个月,P=0.004)。单因素和多因素分析显示,病理类型、LDH水平是影响CIK治疗恶性黑素瘤患者疗效的独立影响因素;CIK免疫治疗的疗程数可能与黑素瘤患者OS相关,CIK疗程>8次具有延长黑素瘤患者OS期的趋势。结论:CIK免疫治疗能改善恶性黑素瘤患者的OS期,增加CIK疗程数可能提高其疗效。Objective: To evaluate the efficacy of cytokine-induced killer cells (CIKs) in the treatment of melanoma. Methods: Thirty-eight post-operated melanoma patients in Tumor Hospital Affiliated to Tianjin Medical University from January 2005 to December 2010 receiving CIK treatment were obtained (CIK group) as a treatment group, and 114 mela- noma patients without treatment were obtained as a control group. Pairing considerations included clinical stage, gender, age, ulceration, lactate dehydrogenase (LDH) activity, pathological type, and the Karnofsky performance status scale (KPS). The follow-up period was from March 2005 to March 2012. The endpoint of clinical efficacy was overall survival (OS). Results: The 1-, 3-, 5-year OS rates in the CIK and control groups were 86.8% vs 74.6% (P =0. 097), 76.3% vs 46.5% (P =0. 001 ) and 71.1% vs 43.9% (P =0. 004) , respectively. The median OS in the CIK group was signifi- cantly longer than that in the control group ( the OS in CIK group did not reach median OS, and was 20.1 months in the control group, P = 0. 004). The frequency of CIK immunotherapy may be related to the OS of melanoma patients ( P = 0. 051 ). It seemed a trend to prolong the OS of patients with melanoma when CIK treatment 〉 8 times. Univariate and multivariate analysis showed that the pathological type and LDH activity were independent factors for the clinical efficacy ofCIK in treatment of patients with melanoma. Conclusion: CIK immunotherapy can prolong OS in melanoma patients, and increasing CIK frequency may enhance the clinical efficacy.
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