国际肿瘤学杂志 ›› 2020, Vol. 47 ›› Issue (5): 272-277.doi: 10.3760/cma.j.cn371439-20191112-00017

• 论著 • 上一篇    下一篇

β-榄香烯联合吉非替尼治疗一线应用吉非替尼后缓慢进展晚期肺腺癌患者的临床疗效

宋春青, 张颖, 张志国, 郭宏伟, 陆汉红, 韩磊()   

  1. 首都医科大学大兴教学医院肿瘤内科,北京 102600
  • 收稿日期:2019-11-12 修回日期:2020-03-25 出版日期:2020-05-08 发布日期:2020-07-02
  • 通讯作者: 韩磊 E-mail:zhangyh1029@aliyun.com
  • 基金资助:
    吴阶平医学基金会临床科研专项基金(320.6750.17569)

Efficacy of β-elemene combined with gefitinib in the treatment of advanced lung adenocarcinoma patients with slow progression after first-line gefitinib treatment

Song Chunqing, Zhang Ying, Zhang Zhiguo, Guo Hongwei, Lu Hanhong, Han Lei()   

  1. Department of Oncology, Daxing Teaching Hospital of Capital University of Medical Sciences, Beijing 102600, China
  • Received:2019-11-12 Revised:2020-03-25 Online:2020-05-08 Published:2020-07-02
  • Contact: Han Lei E-mail:zhangyh1029@aliyun.com
  • Supported by:
    Wu Jieping Medical Foundation Clinical Research Special Fund(320.6750.17569)

摘要:

目的 探讨β-榄香烯联合吉非替尼治疗一线应用吉非替尼后缓慢进展晚期肺腺癌患者的临床疗效及对生命质量和免疫功能的影响。方法 采用前瞻性队列研究设计,纳入我院2017年6月至2018年12月收治的符合入组标准的晚期肺腺癌患者,采用随机数字表法分为试验组和对照组,试验组给予榄香烯联合吉非替尼治疗,对照组仅给予吉非替尼治疗。治疗2周期后比较两组患者的临床疗效、生命质量及免疫功能。并随访从疾病缓慢进展至疾病出现快速进展的时间(PFS2)。结果 共纳入61例患者,试验组、对照组分别为30例和31例。试验组和对照组的疾病控制率分别为83.3%(25/30)和58.1%(18/31),差异有统计学意义(χ 2=4.680,P=0.031),试验组近期疗效优于对照组,差异有统计学意义(Z=-2.623,P=0.009)。试验组中位PFS2为4.20个月(95%CI为3.94~4.46),对照组中位PFS2为4.00个月(95%CI为2.94~5.07),差异有统计学意义(χ 2=4.948,P=0.026)。两组生命质量比较,在躯体功能、情绪功能、总体生命质量方面,试验组治疗前后评分差值较对照组高,差异均有统计学意义[6.67(-6.66,20.00) vs. 0(-6.66,6.66),Z=-2.429,P=0.015;29.17(2.08,56.26) vs. 12.49(-14.59,39.57),Z=-2.263,P=0.024;16.67(-33.33,56.67) vs. 8.34(-18.74,35.42),Z=-2.249,P=0.025]。免疫功能方面,试验组治疗后CD4 +T细胞水平较治疗前升高(44.27%±6.78% vs. 41.17%±3.73%,t=-2.426,P=0.022),CD8 +T细胞水平较治疗前降低(21.47%±3.18% vs. 23.50%±2.37%,t=2.532,P=0.017)。治疗后试验组CD4 +T细胞水平明显高于对照组(44.27%±6.78% vs. 39.63%±5.80%,t=2.725,P=0.011)。结论 β-榄香烯联合吉非替尼治疗一线吉非替尼治疗后缓慢进展晚期肺腺癌患者有一定的疗效,生命质量和免疫功能均有所改善,值得临床进一步研究。

关键词: 癌,非小细胞肺, 抗药性,肿瘤, 榄香烯, 吉非替尼

Abstract:

Objective To investigate the efficacy of β-elemene combined with gefitinib in the treatment of advanced lung adenocarcinoma patients with slow progression after first-line gefitinib treatment and its effects on quality of life and immune function. Methods A prospective cohort study design was used to enroll patients with advanced lung adenocarcinoma who met the inclusion criteria from June 2017 to December 2018 in our hospital. They were divided into experimental group and control group by random number table method. The experimental group was given elemene combined with gefitinib, and the control group was only given gefitinib. The clinical efficacy, quality of life and immune function of the two groups were compared after 2 cycles of treatment. The PFS2 (time from slow progression of disease to rapid progression of disease) was followed up. Results A total of 61 patients were included. There were 30 cases in the experimental group and 31 cases in the control group. The disease control rates of the experimental group and the control group were 83.3% (25/30) and 58.1% (18/31) respectively, and the difference was statistically significant (χ 2=4.680, P=0.031). The short-term efficacy of the experimental group was better than that of the control group, and the difference was statistically significant (Z=-2.623, P=0.009). The median PFS2 of the experimental group was 4.20 months (95%CI: 3.94-4.46), and the median PFS2 of the control group was 4.00 months (95%CI: 2.94-5.07), with a statistically significant difference (χ 2=4.948, P=0.026). Quality of life was compared between the two groups: in terms of physical function, emotional function and overall quality of life, score differences before and after treatment of the experimental group were higher than those of the control group, with statistically significant differences [6.67(-6.66, 20.00) vs. 0(-6.66, 6.66), Z=-2.429, P=0.015; 29.17(2.08, 56.26) vs. 12.49(-14.59, 39.57), Z=-2.263, P=0.024; 16.67(-33.33, 56.67) vs. 8.34(-18.74, 35.42), Z=-2.249, P=0.025]. In terms of immune function, CD4 +T cells level in the experimental group increased after treatment compared with that before treatment (44.27%±6.78% vs. 41.17%±3.73%, t=-2.426, P=0.022), and CD8 +T cells level decreased compared with that before treatment (21.47%±3.18% vs. 23.50%±2.37%, t=2.532, P=0.017). After treatment, the level of CD4 +T cells in the experimental group was significantly higher than that in the control group (44.27%±6.78% vs. 39.63%±5.80%, t=2.725, P=0.011). Conclusion β-elemene combined with gefitinib has a certain effect in the treatment of advanced lung adenocarcinoma patients with slow progression after first-line gefitinib treatment, and the quality of life and immune function are improved. It is worthy of further clinical research.

Key words: Carcinoma,non-small-cell lung, Drug resistance,neoplasm, Elemene, Gefitinib