首页|复方苦参注射液辅助程序性死亡受体1抑制剂联合多西他赛+顺铂方案化疗治疗非小细胞肺癌的疗效观察

复方苦参注射液辅助程序性死亡受体1抑制剂联合多西他赛+顺铂方案化疗治疗非小细胞肺癌的疗效观察

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目的:探讨复方苦参注射液辅助程序性死亡受体1(PD-1)抑制剂联合多西他赛+顺铂方案化疗治疗非小细胞肺癌的临床疗效.方法:回顾性选取2020年10月~2023年5月某院收治的84例非小细胞肺癌患者为研究对象,根据不同的治疗方案分为对照组和观察组,每组42例.对照组给予PD-1抑制剂联合多西他赛+顺铂方案,观察组在对照组基础上加用复方苦参注射液.评估两组患者临床疗效;应用流式细胞仪测定治疗前后患者血清肿瘤标记物[癌胚抗原(CEA)、异常糖链糖蛋白(TAP)]水平;评估两组患者治疗后的生活能力[卡诺夫斯凯计分(KPS)];比较治疗期间两组患者的不良反应发生情况以评估药物安全性.结果:治疗后,观察组的客观缓解率和疾病控制率分别为69.05%和95.23%,高于对照组的47.62%和76.19%,组间存在统计学差异(P<0.05).治疗前,患者的血清CEA和TAP水平组间比较无统计学差异(P>0.05);治疗后,观察组CEA和TAP水平均低于对照组(P<0.05);治疗后,观察组患者的KPS评分高于对照组(P<0.05).此外,在不良反应发生情况方面,观察组的骨髓抑制率(30.95%)低于对照组(80.95%,P<0.05),且观察组总不良反应发生率(33.33%)也低于对照组(92.86%,P<0.05).结论:与PD-1抑制剂联合多西他赛+顺铂方案相比,采用复方苦参注射液辅助PD-1抑制剂联合多西他赛+顺铂方案化疗治疗非小细胞肺癌的临床疗效较佳,患者生活质量提升更明显,安全性更高,推荐临床广泛应用.
Efficacy of Compound Kushen Injection-Assisted Programmed Death-1 Inhibitor Combined with Docetaxel plus Cisplatin Chemotherapy in the Treatment of Non-Small Cell Lung Carcinoma
Objective:To investigate the clinical efficacy of compound Kushen injection-assisted programmed death-1(PD-1)inhibitor combined with docetaxel plus cisplatin(DP)regimen in the treatment of non-small cell lung carcinoma(NSCLC).Methods:Eighty-four patients with NSCLC treated in a hospital from October 2020 to May 2023 were retrospectively selected and divided into the control group and observation group according to the treatment regimen,with 42 patients in each group.The control group was treated with the PD-1 inhibitor combined with the DP chemotherapy,and the observation group was treated with compound Kushen injection in addition to the treatment given in the control group.The patients'clinical response in the two groups was evaluated.The levels of serum tumor markers[carcinoembryonic antigen(CEA)and tumor abnormal protein(TAP)]before and after treatment were determined in the two groups by flow cytometry.The living ability was evaluated in the two groups based on the Karnofsky performance score(KPS);The safety of the medication was evaluated based on the comparison of adverse reactions during the treatment between the two groups.Results:After treatment,the objective response rate and disease control rate were 69.05%and 95.23%in the observation group,respectively,which were higher than the figures 47.62%and 76.19%in the control group,respectively,with statistically significant difference between the two groups(P<0.05).Before treatment,there was no statistically significant difference in serum CEA and TAP levels between the two groups(P>0.05).After treatment,both CEA and TAP levels in the observation group were lower than those in the control group(P<0.05).After treatment,the KPS in the observation group was higher than that in the control group(P<0.05).In addition,in terms of adverse reactions,the incidence of myelosuppression in the observation group(30.95%)was lower than that in the control group(80.95%,P<0.05),and the total incidence of adverse reactions in the observation group(33.33%)was also lower than that in the control group(92.86%,P<0.05).Conclusion:Compared with the regimen of PD-1 inhibitor combined with DP chemotherapy,compound Kushen injection-assisted PD-1 inhibitor combined with DP chemotherapy demonstrated better clinical efficacy in the treatment of NSCLC,with significantly improved quality of life and higher safety,and thereby is recommended to be widely used in clinical practice.

compound Kushen injectionnon-small cell lung carcinomamalignant tumorchemotherapyapoptosis

康议心、张殿宝

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河南科技大学第一附属医院肿瘤科,洛阳 471000

复方苦参注射液 非小细胞肺癌 恶性肿瘤 化疗 细胞凋亡

河南省医学科技攻关计划联合共建项目

LHGJ20220687

2024

中国合理用药探索
中国执业药师协会

中国合理用药探索

影响因子:0.62
ISSN:2096-3327
年,卷(期):2024.21(5)