Shuxian Qu,Zhaozhe Liu,Zhendong Zheng,Zhenyu Ding,Tao Han,Fang Guo,Jianing Qiu,Xiaodong Xie,Dongchu Ma. The influence of autologous cytokine-induced killer cell treatment on the objective efficacy and safety of gefitinib in advanced non-small cell lung cancer. Oncol Transl Med, 2015, 1: 69-72.
The influence of autologous cytokine-induced killer cell treatment on the objective efficacy and safety of gefitinib in advanced non-small cell lung cancer
Received:January 12, 2015  Revised:April 07, 2015
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KeyWord:non-small cell lung cancer (NSCLC); gefitinib; cytokine-induced killer (CIK) cell
Author NameAffiliationE-mail
Shuxian Qu Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China qushuxian2010@163.com 
Zhaozhe Liu Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Zhendong Zheng Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Zhenyu Ding Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Tao Han Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Fang Guo Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Jianing Qiu Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Xiaodong Xie Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China doctor_xxd@163.com 
Dongchu Ma Department of Oncology, General Hospital of Shenyang Military Region, Shenyang, Liaoning 110840, China mdc580819@sina.com 
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Abstract:
      Objective: The aim of the study was to observe the influence of autologous cytokine-induced killer cell (CIK) treatment on the objective efficacy and safety of gefitinib in advanced non-small cell lung cancer (NSCLC). Methods: Sixty-six patients with NSCLC received gefitinib as second-line treatment. They were randomly divided into 2 groups, and informed consent forms were signed before grouping. Gefitinib was administrated to the control group, and autologous CIK treatment was added to the observation group. The objective treatment and adverse reactions were evaluated in both groups. Results: The objective response rate (ORR) and the disease control rate (DCR) of the observation group were slightly higher than those of the control group, although no statistical differences were found between the 2 groups (P > 0.05). The incidences of diarrhea, fatigue, anorexia, oral ulcers, and myelosuppression in the observation group were much lower than those in the control group (P < 0.05). However, there were no statistical differences between the incidences of skin rash, and liver and kidney toxicities (P > 0.05). Conclusion: Autologous CIK in combination with gefitinib is effective as second-line treatment for advanced NSCLC, and can significantly reduce adverse reactions and improve the objective efficacy.
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