• 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/PDL-1 抑制剂与心脏毒性:分子、病因与管理概述。

PD-1/PDL-1 Inhibitors and Cardiotoxicity; Molecular, Etiological and Management Outlines.

机构信息

Department of Oncology, First Affiliated Hospital of Dalian Medical University, Zhongshan Road No. 222, Dalian 116021, China.

Department of Stomatology, Oral Pathology, Dalian Medical University, Zhongshan Road No. 222, Dalian 116021, China.

出版信息

J Adv Res. 2020 Oct 3;29:45-54. doi: 10.1016/j.jare.2020.09.006. eCollection 2021 Mar.

DOI:10.1016/j.jare.2020.09.006
PMID:33842004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8020146/
Abstract

BACKGROUND

The US Food and Drug Administration (FDA) has approved several immunotherapeutic drugs for cancer since 2010, and many more are still being evaluated in other clinical studies. These inhibitors significantly increase response rates and result in the treatment of patients with advanced cancer. However, cancer immunotherapy leads to essential cardiac toxicity properties that have become distinct from other cancer patients' care and are mostly related to their etiology.

AIM OF REVIEW

As potential implications, the occurrence of cardiovascular adverse events is particularly challenging and needs a comprehensive understanding of overall cancer-related etiology, clinical outcomes with different variable severity, and management.

KEY SCIENTIFIC CONCEPTS OF REVIEW

In terms of improving the overall survival of patients with cancer, clinicians should be careful in selecting either programmed cell death-1 (PD-1) or its programmed cell death ligand (PDL-1) inhibitors by evaluating their risk and clinical benefit for early intervention and decrease the level of morbidity and mortality of their patients. This review focuses on the effectiveness of PD-1/PL-1 antibodies and associated cardiotoxicity adverse events, including etiological mechanisms, diagnosis, and treatment.

摘要

背景

自 2010 年以来,美国食品和药物管理局(FDA)已批准了几种癌症免疫治疗药物,还有许多药物正在其他临床研究中进行评估。这些抑制剂显著提高了反应率,并使晚期癌症患者得到了治疗。然而,癌症免疫疗法导致了严重的心脏毒性,这与其他癌症患者的治疗不同,主要与病因有关。

目的

由于潜在的影响,心血管不良事件的发生尤其具有挑战性,需要全面了解与癌症相关的总体病因、不同严重程度的临床结果以及管理。

审查的关键科学概念

为了提高癌症患者的总体生存率,临床医生应通过评估其风险和临床获益来谨慎选择程序性细胞死亡蛋白-1(PD-1)或其程序性细胞死亡配体(PDL-1)抑制剂,以便进行早期干预,降低患者的发病率和死亡率。本综述重点介绍了 PD-1/PL-1 抗体及其相关的心脏毒性不良事件的有效性,包括病因机制、诊断和治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/691243460b1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/35c7b83eb444/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/62cf4e2348b4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/691243460b1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/35c7b83eb444/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/62cf4e2348b4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c078/8020146/691243460b1e/gr2.jpg

相似文献

1
PD-1/PDL-1 Inhibitors and Cardiotoxicity; Molecular, Etiological and Management Outlines.PD-1/PDL-1 抑制剂与心脏毒性:分子、病因与管理概述。
J Adv Res. 2020 Oct 3;29:45-54. doi: 10.1016/j.jare.2020.09.006. eCollection 2021 Mar.
2
T cell checkpoint regulators in the heart.心脏中的 T 细胞检查点调节剂。
Cardiovasc Res. 2019 Apr 15;115(5):869-877. doi: 10.1093/cvr/cvz025.
3
Immune Checkpoint Inhibitors and Cardiac Toxicity in Patients Treated for Non-Small Lung Cancer: A Review.免疫检查点抑制剂在非小细胞肺癌治疗中的心脏毒性:综述。
Int J Mol Sci. 2020 Sep 29;21(19):7195. doi: 10.3390/ijms21197195.
4
Another side of the association between body mass index (BMI) and clinical outcomes of cancer patients receiving programmed cell death protein-1 (PD-1)/ Programmed cell death-ligand 1 (PD-L1) checkpoint inhibitors: A multicentre analysis of immune-related adverse events.另一角度看待癌症患者 BMI 与程序性死亡蛋白-1(PD-1)/程序性死亡配体 1(PD-L1)检查点抑制剂临床获益的相关性:免疫相关不良事件的多中心分析。
Eur J Cancer. 2020 Mar;128:17-26. doi: 10.1016/j.ejca.2019.12.031. Epub 2020 Mar 5.
5
[Clinical predictive value of PD-1/PD-L1-induced electrocardiogram changes for cardiotoxicity].[PD-1/PD-L1诱导的心电图变化对心脏毒性的临床预测价值]
Zhonghua Zhong Liu Za Zhi. 2024 Oct 23;46(10):979-986. doi: 10.3760/cma.j.cn112152-20231024-00230.
6
Atypical autoimmune adverse effects with checkpoint blockade therapies.检查点阻断疗法的非典型自身免疫不良反应。
Ann Oncol. 2017 Feb 1;28(2):206-207. doi: 10.1093/annonc/mdw658.
7
Immune-related adverse events associated with programmed cell death protein-1 and programmed cell death ligand 1 inhibitors for non-small cell lung cancer: a PRISMA systematic review and meta-analysis.免疫相关不良事件与非小细胞肺癌的程序性细胞死亡蛋白-1 和程序性死亡配体 1 抑制剂相关:PRISMA 系统评价和荟萃分析。
BMC Cancer. 2019 Jun 10;19(1):558. doi: 10.1186/s12885-019-5701-6.
8
How can we manage the cardiac toxicity of immune checkpoint inhibitors?我们如何管理免疫检查点抑制剂的心脏毒性?
Expert Opin Drug Saf. 2021 Jun;20(6):685-694. doi: 10.1080/14740338.2021.1906860. Epub 2021 Apr 1.
9
Could PD-1/PDL1 immune checkpoints be linked to HLA signature?程序性死亡蛋白1/程序性死亡配体1(PD-1/PDL1)免疫检查点与人类白细胞抗原(HLA)特征有关联吗?
Immunotherapy. 2019 Dec;11(18):1523-1526. doi: 10.2217/imt-2019-0160. Epub 2019 Dec 9.
10
Patient reported outcomes in anti-PD-1/PD-L1 inhibitor immunotherapy registration trials: FDA analysis of data submitted and future directions.抗 PD-1/PD-L1 抑制剂免疫治疗注册试验中的患者报告结局:FDA 对提交数据的分析及未来方向
Clin Trials. 2019 Jun;16(3):322-326. doi: 10.1177/1740774519836991. Epub 2019 Mar 18.

引用本文的文献

1
Cardiovascular Toxicity Associated With Immune Checkpoint Inhibitors: Interpreting the Discrepancy Between Clinical Trials and Real-World Data.免疫检查点抑制剂相关的心血管毒性:解读临床试验与真实世界数据之间的差异
Cureus. 2025 Jun 30;17(6):e87049. doi: 10.7759/cureus.87049. eCollection 2025 Jun.
2
Cancer therapy-induced cardiotoxicity: mechanisms and mitigations.癌症治疗引起的心脏毒性:机制与缓解措施
Heart Fail Rev. 2025 Jun 7. doi: 10.1007/s10741-025-10531-0.
3
PD-1 inhibition disrupts collagen homeostasis and aggravates cardiac dysfunction through endothelial-fibroblast crosstalk and EndMT.

本文引用的文献

1
Cardiac dysfunction in cancer patients: beyond direct cardiomyocyte damage of anticancer drugs: novel cardio-oncology insights from the joint 2019 meeting of the ESC Working Groups of Myocardial Function and Cellular Biology of the Heart.癌症患者的心脏功能障碍:超越抗癌药物对心肌细胞的直接损伤:ESC 心肌功能工作组和心脏细胞生物学工作组 2019 年联合会议的心脏肿瘤学新见解。
Cardiovasc Res. 2020 Sep 1;116(11):1820-1834. doi: 10.1093/cvr/cvaa222.
2
PD-1: Its Discovery, Involvement in Cancer Immunotherapy, and Beyond.PD-1:它的发现、在癌症免疫疗法中的作用及其他。
Cells. 2020 Jun 1;9(6):1376. doi: 10.3390/cells9061376.
3
Cardiovascular magnetic resonance in immune checkpoint inhibitor-associated myocarditis.
程序性死亡受体1(PD-1)抑制通过内皮细胞-成纤维细胞相互作用和内皮-间质转化破坏胶原蛋白稳态并加重心脏功能障碍。
Front Pharmacol. 2025 Mar 17;16:1549487. doi: 10.3389/fphar.2025.1549487. eCollection 2025.
4
Formononetin: a review of its source, pharmacology, drug combination, toxicity, derivatives, and drug delivery systems.芒柄花黄素:来源、药理学、药物联用、毒性、衍生物及药物递送系统综述
Front Pharmacol. 2025 Mar 3;16:1534798. doi: 10.3389/fphar.2025.1534798. eCollection 2025.
5
The Role of Immunotherapy in Lung Cancer Treatment: Current Strategies, Future Directions, and Insights into Metastasis and Immune Microenvironment.免疫疗法在肺癌治疗中的作用:当前策略、未来方向以及对转移和免疫微环境的见解
Curr Gene Ther. 2025 Jan 6. doi: 10.2174/0115665232340926241105064739.
6
Pan‑cancer analysis on the role of KMT2C expression in tumor progression and immunotherapy.KMT2C表达在肿瘤进展和免疫治疗中作用的泛癌分析
Oncol Lett. 2024 Jul 19;28(3):444. doi: 10.3892/ol.2024.14577. eCollection 2024 Sep.
7
Aging-related biomarker discovery in the era of immune checkpoint inhibitors for cancer patients.癌症患者免疫检查点抑制剂时代与衰老相关生物标志物的发现。
Front Immunol. 2024 Mar 15;15:1348189. doi: 10.3389/fimmu.2024.1348189. eCollection 2024.
8
Combinatorial immune checkpoint blockade increases myocardial expression of NLRP-3 and secretion of H-FABP, NT-Pro-BNP, interleukin-1β and interleukin-6: biochemical implications in cardio-immuno-oncology.联合免疫检查点阻断增加心肌中NLRP-3的表达以及H-FABP、NT-Pro-BNP、白细胞介素-1β和白细胞介素-6的分泌:心脏免疫肿瘤学中的生化意义
Front Cardiovasc Med. 2024 Jan 23;11:1232269. doi: 10.3389/fcvm.2024.1232269. eCollection 2024.
9
Late Cardiac Toxic Effects Associated With Treatment Protocols for Hodgkin Lymphoma in Children.儿童霍奇金淋巴瘤治疗方案相关的晚期心脏毒性效应。
JAMA Netw Open. 2024 Jan 2;7(1):e2351062. doi: 10.1001/jamanetworkopen.2023.51062.
10
Immune perturbation network identifies an EMT subtype with chromosomal instability and tumor immune-desert microenvironment.免疫扰动网络识别出一种具有染色体不稳定性和肿瘤免疫荒漠微环境的上皮-间质转化亚型。
iScience. 2023 Sep 9;26(10):107871. doi: 10.1016/j.isci.2023.107871. eCollection 2023 Oct 20.
免疫检查点抑制剂相关心肌炎的心血管磁共振成像
Eur Heart J. 2020 May 7;41(18):1733-1743. doi: 10.1093/eurheartj/ehaa051.
4
Global Longitudinal Strain and Cardiac Events in Patients With Immune Checkpoint Inhibitor-Related Myocarditis.全球应变与免疫检查点抑制剂相关心肌炎患者的心脏事件。
J Am Coll Cardiol. 2020 Feb 11;75(5):467-478. doi: 10.1016/j.jacc.2019.11.049.
5
Important distinction between acute coronary syndromes and Takotsubo syndrome.急性冠状动脉综合征与应激性心肌病之间的重要区别。
Nat Rev Cardiol. 2020 Apr;17(4):258. doi: 10.1038/s41569-020-0342-7.
6
Immune Checkpoint Inhibitor Myocarditis: Pathophysiological Characteristics, Diagnosis, and Treatment.免疫检查点抑制剂相关性心肌炎:病理生理特征、诊断与治疗
J Am Heart Assoc. 2020 Jan 21;9(2):e013757. doi: 10.1161/JAHA.119.013757.
7
A review of cancer immunotherapy toxicity.癌症免疫疗法毒性综述。
CA Cancer J Clin. 2020 Mar;70(2):86-104. doi: 10.3322/caac.21596. Epub 2020 Jan 16.
8
Immune Checkpoint Inhibitor-Associated Cardiotoxicity: Current Understanding on Its Mechanism, Diagnosis and Management.免疫检查点抑制剂相关心脏毒性:目前对其机制、诊断和管理的认识
Front Pharmacol. 2019 Nov 29;10:1350. doi: 10.3389/fphar.2019.01350. eCollection 2019.
9
Cardiovascular Toxicities of Immune Checkpoint Inhibitors: JACC Review Topic of the Week.免疫检查点抑制剂的心血管毒性:JACC 每周综述专题。
J Am Coll Cardiol. 2019 Oct 1;74(13):1714-1727. doi: 10.1016/j.jacc.2019.07.079.
10
Cardiotoxicity from immune checkpoint inhibitors.免疫检查点抑制剂引起的心脏毒性。
Int J Cardiol Heart Vasc. 2019 Sep 7;25:100420. doi: 10.1016/j.ijcha.2019.100420. eCollection 2019 Dec.