首页|替雷利珠单抗一线治疗晚期非小细胞肺癌的快速卫生技术评估

替雷利珠单抗一线治疗晚期非小细胞肺癌的快速卫生技术评估

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目的 评价替雷利珠单抗(TIS)一线治疗晚期非小细胞肺癌(NSCLC)的有效性、安全性和经济性。方法 计算机检索PubMed、Embase、Cochrane LibraryA CNKI、WanFang Data、SinoMed数据库和卫生技术评估(HTA)相关网站,搜集TIS-线治疗晚期NSCLC的HTA报告、系统评价/Meta分析和药物经济学研究,检索时限均从建库至2024年4月30日。由2名研究者独立筛选文献、提取资料和质量评价,并采用定性描述方法进行快速卫生技术评估。结果 共纳入9篇文献,包括系统评价/Meta分析7篇,药物经济学研究2篇。有效性方面,与化疗(CT)相比,TIS+CT可提高晚期NSCLC患者的无进展生存期(PFS)和客观缓解率(ORR),可提高任何程序性细胞死亡受体配体-1(PD-L1)表达情况、伴或不伴肝转移、年龄≥ 65岁或<65岁、有吸烟病史的晚期NSCLC患者的PFS;与CT相比,TIS+CT可提高晚期非鳞状NSCLC患者的PFS,可提高PD-L1≥50%的晚期非鳞状NSCLC患者的PFS;与CT相比,TIS+CT可提高PD-L1为1%~49%、PD-L1≥50%、男性、年龄≥ 65岁、有吸烟史、ECOG评分1分、ⅢB期和Ⅳ期晚期鳞状NSCLC患者的PFS。安全性方面,与卡瑞利珠单抗+CT和阿替利珠单抗+贝伐珠单抗+CT相比,TIS+CT可降低严重不良反应发生率。经济学方面,对于无表皮生长因子受体突变和渐变淋巴瘤激酶重排的非鳞状NSCLC,与CT相比,TIS+CT在中国具有一定的成本-效果优势。亚组分析结果显示,在PD-L1表达≥50%、肝转移和有吸烟史的非鳞状NSCLC患者中,一线TIS+CT方案的生存益处更大。结论 TIS+CT 一线治疗晚期NSCLC具有较好的有效性、安全性和经济性。
First-line treatment with tislelizumab for advanced non-small cell lung cancer:a rapid health technology assessment
Objective To evaluate the efficacy,safety,and economy of tislelizumab(TIS)as a first-line treatment for advanced non-small cell lung cancer(NSCLC).Methods PubMed,Embase,Cochrane Library,CNKI,WanFang Data,SinoMed databases and health technology assessment(HTA)websites were electronically searched to collect the HTA report,systematic review/Meta-analysis and pharmacoeconomic research of TIS as a first-line treatment for advanced NSCLC from the inception to April 30,2024.Two reviewers independently screened literature,extracted data,and evaluated quality,and qualitative descriptive methods were used for rapid health technology assessment(rHTA).Results A total of 9 articles were included,in which 7 systematic review/Meta-analysis and 2 pharmacoeconomic studies.In terms of effectiveness,compared with chemotherapy(CT),TIS+CT could improve the progression free survival(PFS)and objective response rate(ORR)of advanced NSCLC patients.It could also improve PFS in patients with advanced NSCLC who have the any expression of programmed cell death receptor ligand-1(PD-L1),with or without liver metastasis,aged>65 years or<65 years,and with a history of smoking;Compared with CT,TIS+CT could improve the PFS of advanced non squamous NSCLC patients,and could increase the PFS of advanced non squamous NSCLC patients with PD-L1>50%;Compared with CT,TIS+CT could improve the PFS of patients with advanced squamous cell carcinoma NSCLC in stages ⅢB and IV,with PD-L1 being 1%-49%,PD-L1>50%,male,age>65 years old,smoking history,ECOG score of 1 point.In terms of safety,compared with camrelizumab+CT and atezolizumab+bevacizumab+CT,TIS+CT could reduce the incidence of serious adverse reactions.In terms of economics,for non squamous NSCLC without epidermal growth factor receptor(EGFR)mutations and gradual lymphoma kinase(ALK)rearrangements,TIS+CT had certain cost-effectiveness advantages compared to CT in China.The subgroup analysis results showed that the first-line TIS+CT regimen had greater survival benefits in non squamous NSCLC patients with PD-L1 expression>50%,liver metastasis,and a history of smoking.Conclusion TIS+CT first-line treatment for advanced NSCLC has good efficacy,safety,and economy.

TislelizumabNon-small cell lung cancerFirst-line treatmentRapid health technology assessment

李文燕、潘希丁、揭琼、李园园、唐慕菲

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南京医科大学附属南京医院(南京市第一医院)药学部(南京 210006)

替雷利珠单抗 非小细胞肺癌 一线治疗 快速卫生技术评估

南京市药学会-常州四药医院药学科研基金项目

2018YX007

2024

药物流行病学杂志
中国药学会 武汉医药(集团)股份有限公司

药物流行病学杂志

CSTPCD
影响因子:0.746
ISSN:1005-0698
年,卷(期):2024.33(7)