切换至 "中华医学电子期刊资源库"

中华普外科手术学杂志(电子版) ›› 2023, Vol. 17 ›› Issue (01) : 52 -58. doi: 10.3877/cma.j.issn.1674-3946.2023.01.014

论著

紫杉醇/白蛋白紫杉醇为基础的化疗联合PD-1/PD-L1抑制剂治疗三阴性乳腺癌的疗效和安全性:荟萃分析
张彬月1, 贾红燕2,()   
  1. 1. 030001 太原,山西医科大学第一临床医学院
    2. 030001 太原,山西医科大学第一医院乳腺科
  • 收稿日期:2022-03-09 出版日期:2023-02-26
  • 通信作者: 贾红燕

Efficacy and safety of paclitaxel/albumin paclitaxel based chemotherapy combined with PD-1/PD-L1 inhibitors in triple-negative breast cancer:a Meta-analysis

Binyue Zhang1, Hongyan Jia2,()   

  1. 1. First Clinical Medical College,Shaanxi Medical University,Taiyuan Shaaxi Province 030001,China
    2. Department of Mammary Gland,The First hospital of Shaanxi Medical University,Taiyuan Shaaxi Province 030001,China
  • Received:2022-03-09 Published:2023-02-26
  • Corresponding author: Hongyan Jia
  • Supported by:
    Shaanxi Provincial Natural Science Foundation Project(201901D111347); Shaanxi Province Overseas Students’scientific and technological activities funded project(20200036); The research funding project of returned overseas students in Shaanxi province(2021-157)
引用本文:

张彬月, 贾红燕. 紫杉醇/白蛋白紫杉醇为基础的化疗联合PD-1/PD-L1抑制剂治疗三阴性乳腺癌的疗效和安全性:荟萃分析[J]. 中华普外科手术学杂志(电子版), 2023, 17(01): 52-58.

Binyue Zhang, Hongyan Jia. Efficacy and safety of paclitaxel/albumin paclitaxel based chemotherapy combined with PD-1/PD-L1 inhibitors in triple-negative breast cancer:a Meta-analysis[J]. Chinese Journal of Operative Procedures of General Surgery(Electronic Edition), 2023, 17(01): 52-58.

目的

探讨以紫杉醇/白蛋白紫杉醇为主体的化疗方案联合程序性死亡受体-1(PD-1)/程序性死亡受体-配体1(PD-L1)抑制剂在治疗三阴性乳腺癌(TNBC)的疗效及安全性。

方法

检索国内外数据库,检索时限均从数据库建库起至2021年12月9日。根据纳入及排除标准选择接受治疗的TNBC患者,试验组方案为PD-1/PD-L1抑制剂联合以紫杉醇/白蛋白紫杉醇为基础的化疗,对照组方案为安慰剂联合以紫杉醇/白蛋白紫杉醇为基础的化疗。采用RevMan 5.4.1软件分析相关数据。通过异质性检验后,采用固定效应模型或随机效应模型进行Meta分析,通过漏斗图评价发表偏倚性。

结果

PD-1/PD-L1抑制剂联合以紫杉醇/白蛋白紫杉醇为基础的化疗试验组,其总生存率(OS)显著长于安慰剂联合化疗的对照组(P<0.05);在无进展生存期(PFS)及客观缓解率(ORR)方面,试验组也均优于对照组(P<0.05);试验组中出现治疗相关不良反应(TRAE)患者人数高于对照组(P<0.05);PD-L1受体阳性的TNBC患者中,在OS及PFS方面,试验组均优于对照组。

结论

接受PD-1/PD-L1抑制剂治疗联合紫杉醇/白蛋白紫杉醇为基础的TNBC化疗患者OS、PFS、ORR方面均有显著改善。

Objective

To investigate the efficacy and safety of paclitaxel/albumin-paclitaxel chemotherapy combined with programmed death receptor-1(PD-1)/Programmed death receptor-Ligand 1(PD-L1)inhibitors in the treatment of triple-negative breast cancer(TNBC).

Methods

The time limit for searching domestic and foreign databases is from the establishment of the database to December 9,2021. TNBC patients were selected to receive treatment according to inclusion and exclusion criteria. The experimental group was treated with PD-1/PD-L1 inhibitor combined with paclitaxel/albumin-paclitaxel based chemotherapy,and the control group was treated with placebo combined with paclitaxel/albumin-paclitaxel based chemotherapy. RevMan 5.4.1 software was used to analyze relevant data. After the heterogeneity test,the fixed effects model or random effects model was used for Meta-analysis,and the funnel plot was used to evaluate the publication bias.

Results

The overall survival rate(OS)of PD-1/PD-L1 inhibitor combined with paclitaxel/albumin-paclitaxel based chemotherapy group was significantly higher than that of placebo combined with chemotherapy group(P<0.05). In terms of progression-free survival(PFS)and objective response rate(ORR),experimental groups were also better than control groups(P<0.05). The number of patients with treatment-related adverse reactions(TRAE)in experimental group was higher than that in control group(P<0.05). In PD-L1 receptor positive TNBC patients,the experimental group was superior to the control group in terms of OS and PFS.

Conclusion

Patients receiving PD-1/PD-L1 inhibitor therapy combined with paclitaxel/albumin-paclitaxel based TNBC chemotherapy showed significant improvements in OS,PFS and ORR.

表1 6篇纳入研究的国家、平均年龄、干预措施、样本量及结局指标
图1 纳入文献试验方法学质量评估
图2 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的总生存期荟萃分析
图3 剔除导致异质性原因后,紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的总生存期荟萃分析
图4 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的无进展生存期荟萃分析
图5 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的客观缓解率荟萃分析
图6 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的治疗相关不良反应荟萃分析
图7 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的OS荟萃分析(PD-L1受体阳性)
图8 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的PFS荟萃分析(PD-L1受体阳性)
图9 剔除异质性来源文献后,紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的PFS荟萃分析(PD-L1受体阳性)
图10 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的ORR荟萃分析(PD-L1受体阳性)
图11 紫杉醇/白蛋白紫杉醇为主体的化疗方案联合PD-1/PD-L1抑制剂在治疗TNBC的ORR的倒漏斗图
[1]
Yin LDuan JJBian XW,et al. Triple-negative breast cancer molecular subtyping and treatment progress[J]. Breast Cancer Res202022(1):61.
[2]
Hwang SYPark SKwon Y. Recent therapeutic trends and promising targets in triple negative breast cancer[J]. Pharmacol Ther2019199:30-57.
[3]
Manjunath MChoudhary B. Triple-negative breast cancer:A run-through of features,classification and current therapies[J]. Oncol Lett202122(1):512.
[4]
Wu HTLin JLiu YE,et al. Luteolin suppresses androgen receptor-positive triple-negative breast cancer cell proliferation and metastasis by epigenetic regulation of MMP9 expression via the AKT/mTOR signaling pathway[J]. Phytomedicine202181:153437.
[5]
Kwapisz D. Pembrolizumab and atezolizumab in triple-negative breast cancer[J]. Cancer Immunology202170(3):607-617.
[6]
朱荔,王建东. 免疫检查点抑制剂在乳腺癌免疫治疗中应用进展[J]. 中国实用外科杂志202141(11):1297-1303.
[7]
Emens LAAdams SBarrios CH,et al. First-line atezolizumab plus nab-paclitaxel for unresectable,locally advanced,or metastatic triple-negative breast cancer:IMpassion130 final overall survival analysis[J]. Ann Oncol202132(8):983-993.
[8]
Basch EBecker CRogak LJ,et al. Composite grading algorithm for the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events(PRO-CTCAE)[J]. Clin Trials202118(1):104-114.
[9]
Emens LAAdams SBarrios CH,et al. First-line atezolizumab plus nab-paclitaxel for unresectable,locally advanced,or metastatic triple-negative breast cancer:IMpassion130 final overall survival analysis[J]. Ann Oncol202132(8):983-993.
[10]
Basch EBecker CRogak LJ,et al. Composite grading algorithm for the National Cancer Institute's Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events(PRO-CTCAE)[J]. Clin Trials202118(1):104-114.
[11]
Schmid PAdams SRugo HS,et al. Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer[J]. N Engl J Med2018379(22):2108-2121.
[12]
Mittendorf EAZhang HBarrios CH,et al. Neoadjuvant atezolizumab in combination with sequential nab-paclitaxel and anthracycline-based chemotherapy versus placebo and chemotherapy in patients with early-stage triple-negative breast cancer(IMpassion031):a randomised,double-blind,phase 3 trial[J]. Lancet2020396(10257):1090-1100.
[13]
Cortes JCescon DWRugo HS,et al. Pembrolizumab plus chemotherapy versus placebo plus chemotherapy for previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer(KEYNOTE-355):a randomised,placebo-controlled,double-blind,phase 3 clinical trial[J]. Lancet2020396(10265):1817-1828.
[14]
Miles DGligorov JAndré F,et al. Primary results from IMpassion131,a double-blind,placebo-controlled,randomised phase III trial of first-line paclitaxel with or without atezolizumab for unresectable locally advanced/metastatic triple-negative breast cancer[J]. Ann Oncol202132(8):994-1004.
[15]
Iwata HInoue KKaneko K,et al. Subgroup analysis of Japanese patients in a Phase 3 study of atezolizumab in advanced triple-negative breast cancer(IMpassion130)[J]. Jpn J Clin Oncol201949(12):1083-1091.
[16]
虞小亭,刘正人,谢熠,等. 肝细胞生长因子在乳腺癌新辅助化疗前后的变化及其临床意义[J/CD]. 中华普外科手术学杂志(电子版),202115(03):306-309.
[17]
崔志超,马杰,王雅琪,等. HER2阳性乳腺癌患者新辅助化疗后免疫分型变化的研究[J/CD]. 中华普外科手术学杂志(电子版),202014(02):189-192.
[18]
中国抗癌协会乳腺癌专业委员会. 中国抗癌协会乳腺癌诊治指南与规范(2021年版)[J]. 中国癌症杂志202131(10):954-1040.
[19]
Ai LXu AXu J. Roles of PD-1/PD-L1 Pathway:Signaling,Cancer,and Beyond[J]. Adv Exp Med Biol20201248:33-59.
[20]
林少妍,马飞,徐兵河. PD-1/PD-L1抑制剂在三阴性乳腺癌治疗中的研究进展[J]. 临床药物治疗杂志201816(07):7-10.
[21]
Emens LA. Immunotherapy in Triple-Negative Breast Cancer[J]. Cancer J202127(1):59-66.
[22]
Kwapisz D. Pembrolizumab and atezolizumab in triple-negative breast cancer[J]. Cancer Immunol Immunother202170(3):607-617.
[23]
李健斌,江泽飞. 2021年中国临床肿瘤学会乳腺癌诊疗指南更新要点解读[J]. 中华医学杂志2021101(24):1835-1838.
[24]
Andrews LPYano HVignali DAA. Inhibitory receptors and ligands beyond PD-1,PD-L1 and CTLA-4:breakthroughs or backups[J]. Nat Immunol201920(11):1425-1434.
[25]
Hall PESchmid P. Emerging drugs for the treatment of triple-negative breast cancer:a focus on phase II immunotherapy trials[J]. Expert Opin Emerg Drugs202126(2):131-147.
[26]
Keenan TETolaney SM. Role of Immunotherapy in Triple-Negative Breast Cancer[J]. J Nat Compr Canc Netw202018(4):479-489.
[1] 康一坤, 袁芃. 三阴性乳腺癌分子遗传学及临床特征研究进展[J]. 中华乳腺病杂志(电子版), 2023, 17(05): 290-293.
[2] 张思平, 刘伟, 马鹏程. 全膝关节置换术后下肢轻度内翻对线对疗效的影响[J]. 中华关节外科杂志(电子版), 2023, 17(06): 808-817.
[3] 罗旺林, 杨传军, 许国星, 俞建国, 孙伟东, 颜文娟, 冯志. 开放性楔形胫骨高位截骨术不同植入材料的Meta分析[J]. 中华关节外科杂志(电子版), 2023, 17(06): 818-826.
[4] 马鹏程, 刘伟, 张思平. 股骨髋臼撞击综合征关节镜手术中闭合关节囊的疗效影响[J]. 中华关节外科杂志(电子版), 2023, 17(05): 653-662.
[5] 陈宏兴, 张立军, 张勇, 李虎, 周驰, 凡一诺. 膝骨关节炎关节镜清理术后中药外用疗效的Meta分析[J]. 中华关节外科杂志(电子版), 2023, 17(05): 663-672.
[6] 林昌盛, 战军, 肖雪. 上皮性卵巢癌患者诊疗中基因检测及分子靶向药物治疗[J]. 中华妇幼临床医学杂志(电子版), 2023, 19(05): 505-510.
[7] 李雄雄, 周灿, 徐婷, 任予, 尚进. 初诊导管原位癌伴微浸润腋窝淋巴结转移率的Meta分析[J]. 中华普通外科学文献(电子版), 2023, 17(06): 466-474.
[8] 张再博, 王冰雨, 焦志凯, 檀碧波. 胃癌术后下肢深静脉血栓危险因素的Meta分析[J]. 中华普通外科学文献(电子版), 2023, 17(06): 475-480.
[9] 武慧铭, 郭仁凯, 李辉宇. 机器人辅助下经自然腔道取标本手术治疗结直肠癌安全性和有效性的Meta分析[J]. 中华普通外科学文献(电子版), 2023, 17(05): 395-400.
[10] 栗艳松, 冯会敏, 刘明超, 刘泽鹏, 姜秋霞. STIP1在三阴性乳腺癌组织中的表达及临床意义研究[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 52-56.
[11] 马伟强, 马斌林, 吴中语, 张莹. microRNA在三阴性乳腺癌进展中发挥的作用[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 111-114.
[12] 莫闲, 杨闯. 肝硬化患者并发门静脉血栓危险因素的Meta分析[J]. 中华普外科手术学杂志(电子版), 2023, 17(06): 678-683.
[13] 段文忠, 白延霞, 徐文亭, 祁虹霞, 吕志坚. 七氟烷和丙泊酚在肝切除术中麻醉效果比较Meta分析[J]. 中华肝脏外科手术学电子杂志, 2023, 12(06): 640-645.
[14] 杨海龙, 邓满军, 樊羿辰, 徐梦钰, 陈芳德, 吴威浩, 张生元. 腹腔镜胆总管探查术一期缝合术后胆漏危险因素Meta分析[J]. 中华肝脏外科手术学电子杂志, 2023, 12(05): 545-550.
[15] 符梅沙, 周玉华, 李慧, 薛春颜. 淋巴细胞免疫治疗对复发性流产患者外周血T淋巴细胞亚群分布与PD1/PD-L1表达的影响及意义[J]. 中华临床医师杂志(电子版), 2023, 17(06): 726-730.
阅读次数
全文


摘要