1.华北理工大学药学院,唐山 063210
2.应急总医院药学部,北京 100028
3.应急总医院东院区综合门诊,北京 100016
Received:12 January 2026,
Revised:2026-05-09,
Accepted:09 May 2026,
Published:30 May 2026
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王晓函,陈威,杨芳,等.抗体偶联药物治疗乳腺癌后致肺炎和间质性肺病的网状Meta分析 Δ[J].中国药房,2026,37(10):1370-1375. DOI: 10.6039/j.issn.1001-0408.2026.10.23.
WANG Xiaohan,CHEN Wei,YANG Fang,et al.Network meta-analysis of pneumonitis and interstitial lung disease associated with antibody-drug conjugates in the treatment of breast cancer[J].ZHONGGUO YAOFANG,2026,37(10):1370-1375.
王晓函,陈威,杨芳,等.抗体偶联药物治疗乳腺癌后致肺炎和间质性肺病的网状Meta分析 Δ[J].中国药房,2026,37(10):1370-1375. DOI: 10.6039/j.issn.1001-0408.2026.10.23. DOI:
WANG Xiaohan,CHEN Wei,YANG Fang,et al.Network meta-analysis of pneumonitis and interstitial lung disease associated with antibody-drug conjugates in the treatment of breast cancer[J].ZHONGGUO YAOFANG,2026,37(10):1370-1375. DOI: 10.6039/j.issn.1001-0408.2026.10.23.
目的
2
比较不同抗体偶联药物(ADC)治疗乳腺癌后致肺炎和间质性肺病(ILD)的发生风险。
方法
2
检索中国知网、维普网、PubMed、Embase等中英文数据库和ClinicalTrials.gov,收集ADC[恩美曲妥珠单抗(T-DM1)、德曲妥珠单抗(T-DXd)、戈沙妥珠单抗(SG)、德达博妥单抗(Dato-DXd)、瑞康曲妥珠单抗(SHR-A1811)、ARX788、T-Duo]治疗乳腺癌后发生肺炎和ILD的随机对照试验(RCT),检索时间为建库至2025年6月15日。筛选文献、提取数据、评价文献质量后,采用Stata 17.0软件进行网状Meta分析,并对各干预措施的累积排序曲线下面积(SUCRA)进行排序。
结果
2
共纳入19项RCT,共计10 556例患者。ARX788、T-DXd的总体肺炎发生率显著高于T-DM1、T-DM1 plus TPC(T-DM1联合帕妥珠单抗或阿替利珠单抗)、TPC(常规治疗)和SG(
P
<0.05),ARX788、T-DXd的1~2级肺炎发生率显著高于T-DM1、T-DM1 plus TPC和TPC(
P
<0.05),上述2个指标SUCRA排序前2位的均为ARX788、T-Duo。T-DXd、T-DM1的≥3级肺炎发生率显著高于SG(
P
<0.05),SUCRA排序前2位的为T-Duo、Dato-DXd。ARX788的总体ILD发生率显著高于T-DM1、SHR-A1811、TPC和SG(
P
<0.05),1~2级ILD发生率显著高于T-DM1、SHR-A1811和TPC(
P
<0.05),≥3级ILD发生率显著高于TPC(
P
<0.05),上述3个指标SUCRA排序前2位的均为ARX788、T-DXd联合帕妥珠单抗。
结论
2
相比于其他ADC,ARX788和T-Duo治疗乳腺癌后患者的肺炎和ILD发生风险较高。
OBJECTIVE
2
To compare the risk of pneumonitis and interstitial lung disease (ILD) associated with different antibody-drug conjugates (ADC) in the treatment of breast cancer.
METHODS
2
CNKI, VIP, PubMed, Embase and other Chinese and English databases, and ClinicalTrials.gov were searched from the inception to June 15, 2025. Randomized controlled trials (RCT) about pneumonitis and ILD associated with ADC (T-DM1, T-DXd, SG, Dato-DXd, SHR-A1811,ARX788, and T-Duo) in the treatment of breast cancer were included. After literature screening, data extraction, and quality assessment, a network meta-analysis was conducted using Stata 17.0 software, and the surface under the cumulative ranking curve(SUCRA) of all interventions were ranked.
RESULTS
2
A total of 19 RCTs involving 10 556 patients were included. The overall incidence of
pneumonitis with ARX788 and T-DXd was significantly higher than that with T-DM1, T-DM1 plus TPC(T-DM1combined with pertuzumab or atezolizumab), TPC(treatment of primary care), and SG (
P
<0.05), for grade 1-2 pneumonitis, ARX788 and T-DXd showed significantly higher incidence than T-DM1, T-DM1 plus TPC, and TPC (
P
<0.05). For both indicators, ARX788 and T-Duo were ranked as the top two by SUCRA. For the incidence of grade ≥3 pneumonitis, T-DXd and T-DM1 were significantly higher than SG (
P
<0.05), T-Duo and Dato-DXd were ranked as the top two by SUCRA. For overall incidence of ILD, ARX788 was significantly higher than T-DM1, SHR-A1811, TPC, and SG (
P
<0.05), for the incidence of grade 1-2 ILD, ARX788 was significantly higher than T-DM1, SHR-A1811, and TPC (
P
<0.05), for the incidence of grade ≥3 ILD, ARX788 was significantly higher than TPC (
P
<0.05). For three indicators above, ARX788 and T-DXd combined with pertuzumab were ranked as the top two by SUCRA.
CONCLUSIONS
2
Compared with other ADCs, ARX788 and T-Duo are associated with a higher risk of pneumonitis and ILD in patients with breast cancer.
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