中国药物警戒 ›› 2021, Vol. 18 ›› Issue (6): 562-565.
DOI: 10.19803/j.1672-8629.2021.06.14

• 基础与临床研究 • 上一篇    下一篇

吉非替尼联合白蛋白结合型紫杉醇对NSCLC患者生活质量和生存期的影响

曹洪丽1, 于盼盼2, 杨静3, 席家宁1,*   

  1. 1首都医科大学附属北京康复医院,北京 100144;
    2河北科技学院护理与健康学院基础医学教研室,河北 保定 071000;
    3山东省立第三医院,山东 济南 250000
  • 收稿日期:2021-03-05 出版日期:2021-06-15 发布日期:2021-07-02
  • 通讯作者: *席家宁,男,主任医师,呼吸内科学。E-mail: baobao914@126.com
  • 作者简介:曹洪丽,女,副主任医师,呼吸内科学。
  • 基金资助:
    山东省自然科学基金资助项目(ZR2019PH107); 2020年山东省医学会治疗药物监测科研基金(YXH2020ZX047); 首都医科大学附属北京康复医院科技发展专项立项(2019-002)

Effect of Gefitinib Combined with Paclitaxel on Quality of Life and Survival in Patients with NSCLC

CAO Hongli1, YU Panpan2, YANG Jing3, XI Jianing1,*   

  1. 1Beijing Rehabilitation Hospital Affiliated to Capital Medical University, Beijing 100144, China;
    2Department of Basic Medicine, College of Nursing and Health, Hebei University of Science and Technology,Baoding Hebei 071000, China;
    3Shandong Provincial Third Hospital, Jinan Shandong 250000, China
  • Received:2021-03-05 Online:2021-06-15 Published:2021-07-02

摘要: 目的 探究吉非替尼联合白蛋白结合型紫杉醇化疗方案对晚期非小细胞肺癌(non small cell lung cancer, NSCLC)患者生活质量、生存期的影响,分析其临床价值。方法 选取90例晚期NSCLC患者,随机分为观察组、对照组,对照组予白蛋白结合型紫杉醇、顺铂治疗,观察组加用吉非替尼。比较2组患者临床疗效、不良反应、生活质量及癌症标志物变化,并对比2组生存期。结果 治疗3个月后,观察组有效率、疾病控制率分别为55.56%、84.44%,均高于对照组的22.22%、60.00%(P<0.05)。2组治疗期间不良反应发生率比较,差异无统计学意义(P>0.05)。治疗6个月后,2组生活质量均较治疗前改善,观察组治疗6个月后简明生活质量调查量表(SF-36)各领域得分均高于对照组同时期水平(P<0.05)。治疗3个月后,2组癌胚抗原(CEA)、糖类抗原50(CA50)、糖类抗原125(CA125)均较治疗前下降,观察组治疗6个月后上述指标均低于对照组同时期水平(P<0.05)。观察组无进展生存期为(5.97±0.88)个月,3年生存率为42.22%,均高于对照组的(3.62±0.74)个月、24.44%(P<0.05)。结论 在白蛋白结合型紫杉醇、顺铂化疗方案的基础上,加用吉非替尼能够明显提高晚期NSCLC患者生活质量,延长生存期,在保证治疗安全性的前提下取得更为理想的临床疗效。

关键词: 吉非替尼, 白蛋白结合型紫杉醇, 非小细胞肺癌, 生活质量

Abstract: Objective To investigate the effect of gefitinib combined with paclitaxel on the quality of life and survival of patients with advanced non-small cell lung cancer (NSCLC), and analyze its clinical value. Methods Ninety patients with advanced NSCLC admitted to our hospital were randomly divided into the observation group and control group. The control group was treated with albumin binding paclitaxel and cisplatin, while the observation group was additionally given gefitinib. The clinical efficacy, adverse reactions, quality of life and changes of cancer markers were compared between the two groups. Results After 3 months of treatment, the effective rate and disease control rate of the observation group were 55.56% and 84.44% respectively, which were higher than 22.22% and 60.00% of the control group (P<0.05). There was no significant difference in the incidence of adverse reactions between the two groups (P<0.05). After 6 months of treatment, the quality of life in the two groups was improved, and the scores of SF-36 in each field in the observation group were higher than those of the control group (P<0.05) in the same period. After 3 months of treatment, levels of CEA, CA50 and CA125 in the two groups decreased. After 6 months of treatment, the above indexes in the observation group were lower than those of the control group (P<0.05). The progression free survival time and 3-year survival rate of the observation group were (5.97±0.88) months and 42.22% respectively, which were higher than (3.62±0.74) months and 24.44% in the control group (P<0.05). Conclusion Combined with albumin binding paclitaxel and cisplatin chemotherapy, gefitinib can significantly improve the quality of life, prolong the survival of patients with advanced NSCLC, and achieve a better clinical effect while ensuring the safety of treatment.

Key words: gefitinib, albumin binding paclitaxel, non-small cell lung cancer, quality of life

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