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第三军医大学西南医院:呼吸内科,生物治疗中心,检验科
纸质出版日期:2013,
网络出版日期:2013-03-30,
移动端阅览
罗虎, 宫亮, 陈永峰, 等. CIK维持治疗中晚期肺癌的临床观察及影响因素分析[J]. 陆军军医大学学报, 2013,35(6):569-572.
LUO HU, GONG LIANG, CHEN YONGFENG, et al. Clinical observation and influencing factors of CIKs in treatment of patients with advanced lung cancer. [J]. Journal of army medical university, 2013, 35(6): 569-572.
目的 分析细胞因子诱导的杀伤细胞(cytokine-induced killer cells
CIK)作为维持治疗手段治疗晚期肺癌患者前后免疫系统变化情况,评估CIK细胞治疗晚期肺癌的有效性并分析其影响因素,对其安全性做初步评估。 方法 选取42例中晚期肺癌患者,并根据性别、年龄、病理类型选择同期行最佳支持治疗的38例患者作为对照组。统计分析应用CIK细胞治疗前后免疫学指标(T细胞亚群、免疫球蛋白等)变化特点,评估其治疗的近期疗效(有效率、控制率),并分析影响CIK治疗效果的因素,比较患者在治疗前后的生活质量变化(KPS评分),观察细胞治疗的安全性。 结果 相比非肺癌患者而言,肺癌患者CD3
+
、CD4
+
及CD8
+
T细胞比例均显著降低(
P
<
0.05);CIK细胞治疗后,CD3
+
、CD4
+
T细胞及CD4
+
/CD8
+
比例较治疗前显著提高(P
<
0.05),而血液中的免疫球蛋白(IgA、IgG、IgM)及肿瘤标志物CEA均无明显改变(
P
>0.05)。CIK治疗组有效率及疾病控制率分别为42.9%和83.3%,均显著高于对照组的7.9%及55.3% (
P
<
0.05) ;肿瘤分期、是否合并重要脏器转移及KPS评分都是影响CIK治疗效果的因素(
P
<
0.05),而性别、年龄、病理类型则对CIK治疗效果无明显影响(
P
>0.05);CIK治疗前后KPS评分改善差异有统计学意义(
P
=0.001),而对照组KPS评分无明显改善(
P
=0.191);CIK治疗组中4例患者出现一过性的发热或寒战外,未见明显毒副作用。 结论 CIK细胞作为维持治疗手段,可改善肺癌患者免疫失衡,提高有效率和疾病控制率,并在一定程度上改善患者的生活质量且无明显毒副作用。
Objective To analyze the changes of immune system after cytokine-induced killer cells (CIKs) as maintenance therapy in treatment of patien
ts with advanced lung cancer
to assess the effectiveness and safety of CIKs treatment
and to find out the factors that may influence the efficacy. Methods Forty-two patients with advanced lung cancer (stage Ⅲ to Ⅳ) admitted to the First Affiliated Hospital of Third Military Medical University in Chongqing from July 2011 to July 2012 and treated with CIKs were enrolled as a CIKs group
and another 38 advanced lung cancer patients treated with optimal supportive care during the same period were enrolled as a control group. The changes of immune system (including subsets of T cells
immunoglobulin A
immunoglobulin G and immunoglobulin M)
therapeutic effects (response rate and disease control rate)
quality of life (KPS score)
and side effects were compared between the two groups. Furthermore
the factors that might influence the efficacy of CIKs therapy were evaluated. Results Compared with people without lung cancer
the ratios of CD3
+
CD4
+
and CD8
+
T cells significantly decreased (
P
<
0.05) in lung cancer patients. After CIKs treatment
the ratios of CD3
+
and CD4
+
T cells and CD4
+
/CD8
+
significantly increased (
P
<
0.05)
while there was no significant change in CD8
+
T cells
immunoglobulin A
immunoglobulin G
immunoglobulin M and cancer embryo antigen (CEA) (
P
>0.05). The response rate (RR) and disease control rate (DCR) were 42.9% and 83.3% in the CIKs group
which were significantly higher than those in the control group (7.9% and 55.3%). Tumor staging
metastasis in vital organs and KPS score were influencing factors for the effectiveness of CIKs treatment (P
<
0.05)
while sex
age and pathological type had no significant effect (
P
>0.05). KPS score significantly increased in the CIKs group (
P
=0.001)
while no obvious change was observed in the control group (
P
=0.191). Four patients suffered from transient fever or chills in the proce
ss of CIKs transfusion
and no other side effect was observed. Conclusion CIKs treatment
as a maintenance therapy
is safe and effective for advanced lung cancer patients
and can also improve the immune imbalance
RR
DCR and quality of life of the patients.
CIK肺癌免疫系统疗效影响因素安全性
CIKlung cancerimmune systemeffectivenessinfluencing factorsafety
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