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首页|期刊导航|中国肿瘤生物治疗杂志|PEG-rhG-CSF联合信迪利单抗和化疗对晚期非鳞非小细胞肺癌的疗效及安全性探索

PEG-rhG-CSF联合信迪利单抗和化疗对晚期非鳞非小细胞肺癌的疗效及安全性探索

赵彤 刘建勇 朱婷婷 陈雷 张伟克

中国肿瘤生物治疗杂志2025,Vol.32Issue(12):1271-1279,9.
中国肿瘤生物治疗杂志2025,Vol.32Issue(12):1271-1279,9.DOI:10.3872/j.issn.1007-385x.2025.12.008

PEG-rhG-CSF联合信迪利单抗和化疗对晚期非鳞非小细胞肺癌的疗效及安全性探索

Efficacy and safety of PEG-rhG-CSF combined with sintilimab and chemotherapy in the treatment of advanced non-squamous non-small cell lung cancer

赵彤 1刘建勇 2朱婷婷 1陈雷 1张伟克1

作者信息

  • 1. 济南市第八人民医院 肿瘤科,山东 济南 271104
  • 2. 济南市人民医院 影像科,山东 济南 271100
  • 折叠

摘要

Abstract

Objective:To evaluate the efficacy and safety of Pegylated Recombinant Human Granulocyte Colony-Stimulating Factor(PEG-rhG-CSF)combined with sintilimab and platinum-based chemotherapy in the treatment of advanced non-squamous non-small cell lung cancer(NSCLC).Methods:A prospective,randomized controlled study was conducted on 187 patients with stage Ⅳ non-squamous NSCLC admitted to the Department of Oncology at Jinan Eighth People's Hospital from January 2020 to December 2021.The patients were randomly divided into an experimental group(PEG-rhG-CSF+sintilimab+pemetrexed+platinum;n=94)or a control group(sintilimab+pemetrexed+platinum,n=93)using a random number table method.All patients were followed for two years.Short-term clinical efficacy,progression-free survival(PFS),overall survival(OS),and treatment-related adverse reactions were compared between the two groups.Results:The objective response rate(ORR)in the experimental group was higher than that in the control group(61.63%[53/86]vs 45.35%[39/86],χ²=4.554,P=0.032 8).The disease control rate(DCR)did not differ significantly between the two groups(87.21%[75/86]vs 81.40%[70/86],χ²=1.092,P=0.079 1).The median progression-free survival(PFS)in the experimental group was significantly longer than that in the control group[10.6 months vs 9.1 months;HR=0.72;χ²=3.899 8,P=0.048 3].The median overall survival(OS)in the experimental group was also significantly longer than that in the control group[not reached vs 22.6 months;HR=0.63;χ²=4.7716,P=0.028 9].Consistent OS benefits(all HR<1)were observed in the predefined subgroup analyses,including age<65 years(yes or no),gender,smoking history(yes or no),PD-L1 TPS≥1%(yes or no),platinum-based drugs(cisplatin or carboplatin),and ECOG PS score(0 or 1).The incidence of neutropenia was significantly lower in the experimental group than that in the control group(P<0.000 1),while the incidence of fever was significantly higher(P=0.045 1).No significant differences were observed between the two groups in nausea,anemia,fatigue,constipation,diarrhea,decreased appetite,vomiting,cough,dyspnea,peripheral edema,muscle pain,rash,thrombocytopenia,hypothyroidism,immune pneumonitis,or immune-related colitis(all P>0.05).Conclusion:The combination of PEG-rhG-CSF with sintilimab,pemetrexed,and platinum-based chemotherapy in advanced non-squamous NSCLC patients may improve short-term clinical efficacy and long-term survival,reduce the incidence of neutropenia,and maintain controllable safety.

关键词

晚期非鳞非小细胞肺癌/PEG-rhG-CSF/中性粒细胞减少/信迪利单抗/免疫疗法

Key words

advanced non-squamous non-small cell lung cancer(nsq-NSCLC)neutrophilopenia/sintilimab/immunotherapy

分类

医药卫生

引用本文复制引用

赵彤,刘建勇,朱婷婷,陈雷,张伟克..PEG-rhG-CSF联合信迪利单抗和化疗对晚期非鳞非小细胞肺癌的疗效及安全性探索[J].中国肿瘤生物治疗杂志,2025,32(12):1271-1279,9.

基金项目

山东省医学会临床科研项目-齐鲁专项课题(No.YXH2022ZX02046) (No.YXH2022ZX02046)

中国肿瘤生物治疗杂志

OA北大核心

1007-385X

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