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长春瑞滨联合卡铂化疗治疗晚期肺癌的临床观察 被引量:1

Effect of Chemotherapy on Tumor Markers Levels in Advanced Lung Cancer Patients
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摘要 目的:探讨长春瑞滨联合卡铂化疗对晚期肺癌的治疗效果和安全性。方法:选取我院肿瘤科收治的晚期肺癌患者60例,根据不同治疗方案分为实验组与对照组,每组各30例患者。比较两组患者治疗前后的CEA、CA50、CYFRA21-1水平、白细胞计数及T淋巴细胞亚群CD4+、CD8+水平的变化。结果:治疗前,两组患者的CEA、CA50、CYFRA21-1水平、白细胞计数及T淋巴细胞亚群CD4+、CD8+水平比较均无统计学差异(P>0.05)。治疗后,实验组的CEA、CA50、CYFRA21-1、CD8+水平均明显低于对照组,而白细胞计数及T淋巴细胞亚群CD4+、CD4+/CD8+水平均显著高于对照组,差异均具有统计学意义(P<0.05)。结论:与放疗相比,长春瑞滨联合卡铂化疗能显著提高晚期肺癌的疗效,且不降低患者的细胞免疫。 Objective: To investigate the clinical efficacy and safety of vinorelbine combined with carboplatin chemotherapy in the treatment of advanced lung cancer. Methods: 60 patients with advanced lung cancer were selected and randomly divided into the experimental group and control group according to different treatments, 30 cases in each group. The CEA, CA50, CYFRA21-1 levels,white blood cells count and T lymphocyte subsets CD4+, CD8+level were compared before and after treatment. Results: No statistically significant difference was found in the CEA, CA50, CYFRA21-1 levels, white blood cell count and T lymphocyte subsets CD4+, CD8+levels before treatment between two groups(P〉0.05). Compared with the control group, the CEA, CA50, CYFRA21-1, CD8+levels of experimental group were significantly lower after treatment(P〈0.05), while the white blood cell count, CD4+, CD4+/CD8+were significantly higher after treatment(P〈0.05). Conclusion: Compared with radiotherapy, vinorelbine combined with carboplatin chemotherapy could significantly improve the clinical efficacy of advanced lung cancer and had no effect on the cellular immunity.
出处 《现代生物医学进展》 CAS 2015年第25期4923-4925,4941,共4页 Progress in Modern Biomedicine
基金 国家自然科学基金面上项目(81173610)
关键词 化疗 晚期肺癌 白细胞计数 细胞免疫 CEA CA50 CYFRA21-1 Chemotherapy Advanced lung cancer White blood cells Tumor markers
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  • 1Gerber DE, Schiller JH. Maintenance Chemotherapy for Advanced Non-Small-Cell Lung Cancer: New Life for an Old Idea[J]. Journal of Clinical Oncology, 2013, 31(8): 1009-1020.
  • 2Lindeman NI, Cagle PT, Beasley MB, et al. Molecular Testing Guideline for Selection of Lung Cancer Patients for EGFR and ALK Tyrosine Kinase Inhibitors: Guideline tiom the College of American Pathologists, Imemational Association for the Study of Lung Cancer, and Association for Molecular Pathology[J]. Archives of pathol & laboratory medicine, 2013, 137(6): 828-860.
  • 3Charles AK, Kathryn W, Adam P, et al. Dicker,Ribonucleotide Reductase Expression in Cervix Cancer: a Radiation Therapy Oncology Group Translational Science Analysis [J]. Int J Gynecol Cancer, 2013, 23(4): 615-621.
  • 4Nishino M, Hatabu H, Johnson BE, et al.State of the Art: Response Assessment in Lung Cancer in the Era of Genomic Medicine [J]. Radiology, 2014, 271(1): 6-27.
  • 5Larsen JE, Cascone T, Gerber DE, et al.Targeted Therapies for Lung Cancer: Clinical Experience and Novel Agents [J]. Cancer Journal, 2011, 17(6): 512-527.
  • 6Shtivelman E, Hensing T, Simon GR, et al. Molecular pathways and therapeutic targets in lung cancer[J]. Oncotarget, 2014, 5(6): 1392-14 33.
  • 7Chert W, Li Z, Bai L, Lin Y. NF-kappaB in mediator for lung carcinogenesis and a target for lung cancer prevention and therapy[J]. Front biosci, 2011, 16(4): 1172-1185.
  • 8Tufman A, Tian F, Huber RM. Can MicroRNAs Improve the Management of Lung Cancer Patients7 A Clinician's Perspective [J]. Theranostics, 2013, 3(12): 953-963.
  • 9Chambers SK, Duma J, Occhipinti S, et al. A systematic review of the impact of stigma and nihilism on lung cancer outcomes [J]. BMC Cancer, 2012, 12(9): 184.
  • 10Hohenforst-Schmidt W, Zarogoulidis P, Darwiche K, et al. Intratumoral chemotherapy for lung cancer: re-challenge current targeted therapies [J]. Drug Design, Development and Therapy, 2013, 7(4): 571-583.

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