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[1]张莉莉,许 峰,谢勋鹏,等.贝伐珠单抗辅助化疗非小细胞肺癌的临床应用[J].中华肺部疾病杂志,2025,(02):284-288.[doi:10.3877/cma.j.issn.1674-6902.2025.02.015]
 Zhang Lili,Xu Feng,Xie Xunpeng,et al.Clinical application of bevacizumab as adjuvant chemotherapy for non-small cell lung cancer[J].,2025,(02):284-288.[doi:10.3877/cma.j.issn.1674-6902.2025.02.015]
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贝伐珠单抗辅助化疗非小细胞肺癌的临床应用(PDF)

《中华肺部疾病杂志》[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2025年02期
页码:
284-288
栏目:
论著
出版日期:
2025-04-25

文章信息/Info

Title:
Clinical application of bevacizumab as adjuvant chemotherapy for non-small cell lung cancer
作者:
张莉莉1许 峰2谢勋鹏1张学良3季红华4季雯绯1
226000 南通,南通市第三人民医院 南通大学附属南通第三医院肿瘤科1;226006 南通,南通市肿瘤医院胸外科2;226006 南通,南通市肿瘤医院胃肠外科3;226000 南通,南通市第三人民医院 南通大学附属南通第三医院呼吸科4
Author(s):
Zhang Lili1 Xu Feng2 Xie Xunpeng1 Zhang Xueliang3 Ji Honghua4 Ji Wenfei1.
1Department of Oncology; 4Department of respiratory medicine, Nantong Third Hospital affiliated to Nantong University, Nantong 226000, China; 2Department of Thoracic Surgery; 3Stomach Enterochirurgia, Nantong Cancer Hospital, Nantong 226006, China
关键词:
贝伐珠单抗 规范化疗 非小细胞肺癌 临床疗效
Keywords:
Bevacizumab Standardized chemotherapy Non-small cell lung cancer Clinical efficacy
分类号:
R734.2
DOI:
10.3877/cma.j.issn.1674-6902.2025.02.015
摘要:
目的 分析贝伐珠单抗注射液(安维汀)联合标准化化疗在老年非小细胞肺癌(non small-cell lung cancer, NSCLC)患者中的疗效及安全性。方法 将2017年1月至2022年12月我院收治的老年NSCLC患者74例,根据治疗方法不同分为,接受紫杉醇与顺铂联合化疗(TP)方案34例为对照组,采用TP联合贝伐珠单抗40例为观察组。疗程6个周期(18周)治疗。分析两组的临床疗效、肿瘤标志物水平及免疫功能、总体生存率(overall survival rate, OS)、无进展生存期(progression-free survival, PFS)以及治疗相关的不良事件(adverse events, AEs)。结果 观察组有效31例(77.50%)高于对照组有效20例(58.82%),两组比较无明显差异。观察组治疗后,癌胚抗原(carcinoembryonic antigen, CEA)(16.75±2.45)ng/ml、糖类抗原125(carbohydrate antigen 125, CA125)(35.97±4.46)ng/ml, 细胞角蛋白19片段(cytokeratin, CY211)(15.45±2.43)U/ml低于对照组CEA(20.93±3.16)ng/ml、CA125(50.11±6.58)ng/ml,CY211(20.35±3.26)U/ml; 观察组治疗后,免疫功能CD3+(49.16±4.32),CD4+(30.31±3.41),CD8+(32.56±4.30),自然杀伤细胞(natural killer cell, NK)(21.02±3.06)优于对照组(45.40±4.12),(26.68±3.02),(35.79±4.69),(17.69±2.21)(P<0.05)。观察组随访期间死亡11例,平均OS 20.34个月(18.70,21.96); 对照组随访期间死亡16例,平均OS 15.03个月(12.83,17.37),两组差异具有统计学意义(χ2=4.992,P=0.025)。观察组药物不良反应率20.00%,对照组23.53%,差异没有统计学意义(P>0.05)。 结论 贝伐珠单抗注射液(安维汀)联合标准化化疗可提高NSCLC患者的临床疗效,延长无进展生存期和总体生存期,未增加不良反应发生率,对老年NSCLC治疗中具有临床意义。
Abstract:
Objective To analyze the efficacy and safety of Bevacizumab injection(Avastin)combined with standardized chemotherapy in elderly patients with non-small cell lung cancer(NSCLC). Methods A total of 74 elderly NSCLC patients admitted to our hospital from January 2017 to December 2022 were enrolled, divided into two groups based on treatment methods: 34 patients received a combination of paclitaxel and cisplatin chemotherapy(TP)as the control group, and 40 patients received a combination of TP and bevacizumab as the observation group. The treatment course lasted six cycles(18 weeks). Clinical efficacy, tumor marker levels, immune function, overall survival rate(OS), progression-free survival(progression-free survival, PFS), and treatment-related adverse events(AE)were analyzed between the two groups. Results The total effective rate in the observation group was 31 cases(77.50%), while that in the control group was 20 cases(58.82%). The total effective rate of the observation group was higher than that of the control group there was no significant difference between two groups. After treatment, the carcinoembryonic antigen(carcinoembryonic antigen, CEA)level in the observation group decreased to 16.75±2.45)ng/ml, carbohydrate antigen 125(carbohydrate antigen 125, CA125)(35.97±4.46)ng/ml, cytokeratin 19 fragment(cytokeratin, CY211)(15.45±2.43)U/ml; lower than the control group CEA(20.93±3.16)ng/ml, CA125(50.11±6.58)ng/ml, CY211(20.35±3.26)U/ml; in the observation group after treatment, immune function CD3+(49.16±4.32), CD4+(30.31±3.41), CD8+(32.56±4.30), natural killer cells(NK)(21.02±3.06)were better than the control group(45.40±4.12),(26.68±3.02),(35.79±4.69),(17.69±2.21)(P<0.05). During the follow-up period of the observation group, 11 cases died, and an average OS of 20.34 months(18.70,21.96); 16 deaths in the control group, average OS 15.03 months(12.83,17.37), the difference between the two groups was statistically significant(χ2=4.992, P=0.025). The adverse drug reaction rate in the observation group was 20.00%, in the control group was 23.53%, with no statistical significance(P>0.05). Conclusion Bevacizumab injection(Avastin)combined with standardized chemotherapy can improve clinical efficacy in elderly NSCLC patients, extend progression-free survival and overall survival, without increasing the incidence of adverse reactions, demonstrating good clinical efficacy and safety in the treatment of elderly NSCLC.

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备注/Memo

备注/Memo:
基金项目: 江苏省基础研究计划自然科学基金(BK20230151)
通信作者: 张学良, Email: zhangxueliang2000@126.com
更新日期/Last Update: 2025-04-25