• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

PD-1或PD-L1抑制剂治疗不同PD-L1表达水平宫颈癌的疗效:一项单臂荟萃分析。

Efficacy of PD-1 or PD-L1 inhibitors for the therapy of cervical cancer with varying PD-L1 expression levels: a single-arm meta-analysis.

作者信息

Yang Jie, Yu Haizan, Zhang Yilei, Zhu Mingli, Zhang Mengyu, Wang Qiming

机构信息

Department of Gynaecology, III, Women's and Children's Hospital of Ningbo University, Ningbo, Zhejiang, China.

出版信息

Front Oncol. 2024 Aug 20;14:1454372. doi: 10.3389/fonc.2024.1454372. eCollection 2024.

DOI:10.3389/fonc.2024.1454372
PMID:39228980
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11368785/
Abstract

OBJECTIVE

To assess the effectiveness and tolerability of both PD-1 and PD-L1 inhibitors in advanced cervical cancer (CC), focusing on varying PD-L1 levels.

METHODS

A comprehensive exploration was carried out on EMBASE, PubMed, Cochrane Library databases as well as Web of Science up to May 25, 2024, for studies involving advanced CC patients receiving PD-1/PD-L1 inhibitors. Inclusion criteria were studies reporting objective response rate (ORR), disease control rate (DCR), median progression-free survival (PFS), as well as median overall survival (OS). Data extraction and quality assessment were performed by two reviewers using the JBI Case Series Critical Appraisal Checklist, followed by a meta-analysis via STATA/MP 16.0.

RESULTS

Five eligible studies comprising 223 patients were chosen. ORR and DCR were 42% (95% CI: 17%-66%, P = 0.00) and 70% (95% CI: 22%-117%, P = 0.00), respectively, in the PD-L1 positive patients and were 36% (95% CI: 17%-54%, P = 0.00) and 47% (95% CI: 30%-63%, P = 0.00), respectively, in patients with PD-L1 negativity. For patients exhibiting PD-L1 positivity, median PFS and median OS were 3.98 months (95% CI: 0.80-7.16, P = 0.01) and 11.26 months (95% CI: 3.01-12.58, P = 0.00), respectively.

CONCLUSION

With PD-1/PD-L1 inhibitors, PD-L1 positive CC patients demonstrate superior ORR, DCR, median PFS, and median OS, underscoring PD-L1 as one biomarker for immunotherapy response.

摘要

目的

评估程序性死亡受体1(PD-1)抑制剂和程序性死亡配体1(PD-L1)抑制剂在晚期宫颈癌(CC)中的有效性和耐受性,重点关注不同的PD-L1水平。

方法

截至2024年5月25日,对EMBASE、PubMed、Cochrane图书馆数据库以及Web of Science进行了全面检索,以查找涉及接受PD-1/PD-L1抑制剂治疗的晚期CC患者的研究。纳入标准为报告客观缓解率(ORR)、疾病控制率(DCR)、中位无进展生存期(PFS)以及中位总生存期(OS)的研究。由两名审阅者使用JBI病例系列关键评估清单进行数据提取和质量评估,随后通过STATA/MP 16.0进行荟萃分析。

结果

选择了五项符合条件的研究,共223例患者。PD-L1阳性患者的ORR和DCR分别为42%(95%置信区间:17%-66%,P = 0.00)和70%(95%置信区间:22%-117%,P = 0.00),而PD-L1阴性患者的ORR和DCR分别为36%(95%置信区间:17%-54%,P = 0.00)和47%(95%置信区间:30%-63%,P = 0.00)。对于表现出PD-L1阳性的患者,中位PFS和中位OS分别为3.98个月(95%置信区间:0.80-7.16,P = 0.01)和11.26个月(95%置信区间:3.01-12.58,P = 0.00)。

结论

对于接受PD-1/PD-L1抑制剂治疗的患者,PD-L1阳性的CC患者表现出更高的ORR、DCR、中位PFS和中位OS,这突出了PD-L1作为免疫治疗反应的一个生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/2827d19bb049/fonc-14-1454372-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/74838e465657/fonc-14-1454372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/85a5cf9c1d53/fonc-14-1454372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/e999e3ac2ab2/fonc-14-1454372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/c960a37c893e/fonc-14-1454372-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/8fdfd5d4b636/fonc-14-1454372-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/0a704e695856/fonc-14-1454372-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/2827d19bb049/fonc-14-1454372-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/74838e465657/fonc-14-1454372-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/85a5cf9c1d53/fonc-14-1454372-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/e999e3ac2ab2/fonc-14-1454372-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/c960a37c893e/fonc-14-1454372-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/8fdfd5d4b636/fonc-14-1454372-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/0a704e695856/fonc-14-1454372-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/591a/11368785/2827d19bb049/fonc-14-1454372-g007.jpg

相似文献

1
Efficacy of PD-1 or PD-L1 inhibitors for the therapy of cervical cancer with varying PD-L1 expression levels: a single-arm meta-analysis.PD-1或PD-L1抑制剂治疗不同PD-L1表达水平宫颈癌的疗效:一项单臂荟萃分析。
Front Oncol. 2024 Aug 20;14:1454372. doi: 10.3389/fonc.2024.1454372. eCollection 2024.
2
Efficacy and Safety of PD-1/PD-L1 Inhibitors in Advanced Hepatocellular Carcinoma: A Systematic Review and Meta-analysis.PD-1/PD-L1抑制剂在晚期肝细胞癌中的疗效与安全性:一项系统评价和Meta分析
Adv Ther. 2023 Feb;40(2):521-549. doi: 10.1007/s12325-022-02371-3. Epub 2022 Nov 18.
3
Effectiveness and safety of PD-1/PD-L1 or CTLA4 inhibitors combined with chemotherapy as a first-line treatment for lung cancer: A meta-analysis.PD-1/PD-L1或CTLA4抑制剂联合化疗作为肺癌一线治疗的有效性和安全性:一项荟萃分析。
J Thorac Dis. 2018 Dec;10(12):6636-6652. doi: 10.21037/jtd.2018.11.72.
4
The benefit and risk of PD-1/PD-L1 inhibitors plus anti-angiogenic agents as second or later-line treatment for patients with advanced non-small-cell lung cancer: a systematic review and single-arm meta-analysis of prospective clinical trials.PD-1/PD-L1 抑制剂联合抗血管生成药物作为晚期非小细胞肺癌二线或后线治疗的获益与风险:一项针对前瞻性临床试验的系统评价和单臂荟萃分析。
Front Immunol. 2023 Aug 8;14:1218258. doi: 10.3389/fimmu.2023.1218258. eCollection 2023.
5
Clinical benefits of PD-1/PD-L1 inhibitors in advanced hepatocellular carcinoma: a systematic review and meta-analysis.PD-1/PD-L1 抑制剂治疗晚期肝细胞癌的临床获益:系统评价和荟萃分析。
Hepatol Int. 2020 Sep;14(5):765-775. doi: 10.1007/s12072-020-10064-8. Epub 2020 Jun 22.
6
Clinical outcomes of PD-1/PD-L1 inhibitors in patients with advanced hepatocellular carcinoma: a systematic review and meta-analysis.PD-1/PD-L1抑制剂治疗晚期肝细胞癌患者的临床结局:一项系统评价和荟萃分析。
J Cancer Res Clin Oncol. 2023 Mar;149(3):969-978. doi: 10.1007/s00432-022-04057-3. Epub 2022 Jun 30.
7
Efficacy and safety of anti-PD-1/anti-PD-L1 antibody therapy in treatment of advanced gastric cancer or gastroesophageal junction cancer: A meta-analysis.抗PD-1/抗PD-L1抗体疗法治疗晚期胃癌或胃食管交界癌的疗效与安全性:一项荟萃分析。
World J Gastrointest Oncol. 2020 Nov 15;12(11):1346-1363. doi: 10.4251/wjgo.v12.i11.1346.
8
Efficacy and safety evaluation of frontline immunotherapy combinations in advanced esophageal squamous cell carcinoma: a network meta-analysis highlighting the value of PD-L1 expression positivity scores.一线免疫治疗联合方案在晚期食管鳞癌中的疗效和安全性评价:基于 PD-L1 阳性表达评分的价值的网络荟萃分析
Front Immunol. 2024 Jul 10;15:1414753. doi: 10.3389/fimmu.2024.1414753. eCollection 2024.
9
Single or combined immune checkpoint inhibitors compared to first-line platinum-based chemotherapy with or without bevacizumab for people with advanced non-small cell lung cancer.比较单药或联合免疫检查点抑制剂与含或不含贝伐珠单抗的一线含铂化疗方案用于晚期非小细胞肺癌患者。
Cochrane Database Syst Rev. 2020 Dec 14;12(12):CD013257. doi: 10.1002/14651858.CD013257.pub2.
10
Efficacy and safety of PD-1/L1 inhibitors as first-line therapy for metastatic colorectal cancer: a meta-analysis.PD-1/L1 抑制剂作为转移性结直肠癌一线治疗的疗效和安全性:一项荟萃分析。
Front Immunol. 2024 Jul 19;15:1425596. doi: 10.3389/fimmu.2024.1425596. eCollection 2024.

引用本文的文献

1
The benefit and risk of addition of PD-1/PD-L1 inhibitors to chemotherapy for advanced cervical cancer: a phase 3 randomized controlled trials based meta-analysis.晚期宫颈癌患者化疗联合PD-1/PD-L1抑制剂的获益与风险:一项基于3期随机对照试验的荟萃分析。
BMC Cancer. 2025 Mar 12;25(1):450. doi: 10.1186/s12885-025-13843-4.

本文引用的文献

1
Long-term survival outcomes and immune checkpoint inhibitor retreatment in patients with advanced cervical cancer treated with camrelizumab plus apatinib in the phase II CLAP study.CLAP 研究中卡瑞利珠单抗联合阿帕替尼治疗晚期宫颈癌患者的长期生存结局和免疫检查点抑制剂的再治疗。
Cancer Commun (Lond). 2024 Jun;44(6):654-669. doi: 10.1002/cac2.12547. Epub 2024 May 13.
2
Cancer statistics, 2024.2024年癌症统计数据。
CA Cancer J Clin. 2024 Jan-Feb;74(1):12-49. doi: 10.3322/caac.21820. Epub 2024 Jan 17.
3
Efficacy and safety of sintilimab plus albumin-bound-paclitaxel in recurrent or metastatic cervical cancer: a multicenter, open-label, single-arm, phase II trial.
信迪利单抗联合白蛋白结合型紫杉醇治疗复发或转移性宫颈癌的疗效和安全性:一项多中心、开放标签、单臂、II期试验。
EClinicalMedicine. 2023 Oct 24;65:102274. doi: 10.1016/j.eclinm.2023.102274. eCollection 2023 Nov.
4
Global estimates of incidence and mortality of cervical cancer in 2020: a baseline analysis of the WHO Global Cervical Cancer Elimination Initiative.2020 年全球宫颈癌发病率和死亡率估计:世卫组织全球消除宫颈癌倡议的基线分析。
Lancet Glob Health. 2023 Feb;11(2):e197-e206. doi: 10.1016/S2214-109X(22)00501-0. Epub 2022 Dec 14.
5
A multicenter phase 2 trial of camrelizumab plus famitinib for women with recurrent or metastatic cervical squamous cell carcinoma.卡瑞利珠单抗联合法米替尼治疗复发性或转移性宫颈鳞癌的多中心 2 期临床试验。
Nat Commun. 2022 Dec 8;13(1):7581. doi: 10.1038/s41467-022-35133-4.
6
Methodological quality of case series studies: an introduction to the JBI critical appraisal tool.病例系列研究的方法学质量:JBI 批判性评价工具介绍。
JBI Evid Synth. 2020 Oct;18(10):2127-2133. doi: 10.11124/JBISRIR-D-19-00099.
7
PD-1 blockade in recurrent or metastatic cervical cancer: Data from cemiplimab phase I expansion cohorts and characterization of PD-L1 expression in cervical cancer.PD-1 阻断在复发性或转移性宫颈癌中的应用:来自 cemiplimab Ⅰ期扩展队列的数据以及宫颈癌中 PD-L1 表达的特征。
Gynecol Oncol. 2020 Nov;159(2):322-328. doi: 10.1016/j.ygyno.2020.08.026. Epub 2020 Sep 9.
8
Estimates of incidence and mortality of cervical cancer in 2018: a worldwide analysis.2018 年宫颈癌发病率和死亡率的估计:全球分析。
Lancet Glob Health. 2020 Feb;8(2):e191-e203. doi: 10.1016/S2214-109X(19)30482-6. Epub 2019 Dec 4.
9
Efficacy and safety of nivolumab in Japanese patients with uterine cervical cancer, uterine corpus cancer, or soft tissue sarcoma: Multicenter, open-label phase 2 trial.尼伏鲁单抗在日本宫颈癌、子宫体癌或软组织肉瘤患者中的疗效和安全性:多中心、开放标签 2 期试验。
Cancer Sci. 2019 Sep;110(9):2894-2904. doi: 10.1111/cas.14148. Epub 2019 Sep 3.
10
Efficacy and Safety of Pembrolizumab in Previously Treated Advanced Cervical Cancer: Results From the Phase II KEYNOTE-158 Study.帕博利珠单抗治疗既往治疗的晚期宫颈癌的疗效和安全性:来自 II 期 KEYNOTE-158 研究的结果。
J Clin Oncol. 2019 Jun 10;37(17):1470-1478. doi: 10.1200/JCO.18.01265. Epub 2019 Apr 3.