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程序性死亡受体-1/程序性死亡配体-1抑制剂心脏毒性研究进展

Research progress on cardiac toxicity of programmed death-1/programmed death ligand-1 inhibitors
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摘要 近年来,肿瘤免疫疗法席卷全球,相关研究及应用领域激增。程序性死亡受体-1(PD-1)/程序性死亡配体-1(PD-L1)抑制剂在肺癌、黑色素瘤、乳腺癌和淋巴瘤等适应证上的广泛使用,掀起了免疫抑制剂相关领域的研究热点。PD-1/PD-L1抑制剂通过增强自身免疫系统的活性而引起免疫系统相关的副作用,包括引起相关心脏毒性,通常表现为心肌炎、心包疾病、心律失常、心源性休克或猝死等,因其表现多样、致死率高,所以引起学者的关注。本文就PD-1/PD-L1抑制剂相关心脏毒性的机制、流行病学、作用特点、监测及管理进行综述。 Recently,tumor immunotherapy has swept the world and the related research and application fields have surged.The widespread use of programmed death-1(PD-1)/programmed death ligand-1(PD-L1)inhibitors in the indications such as lung cancer,melanoma,breast cancer and lymphoma has raised much research hotspots.PD-1/PD-L1 blockers cause immune system related side effects(including related cardiotoxicity)by boosting the activity of your own immune system,usually manifested as myocarditis,pericardial disease,arrhythmia,cardiogenic shock or sudden death.Because of its diverse manifestations and high mortality,many scholars have payed attention to this problem.This paper reviews the mechanism,epidemiology,clinical feature,monitoring and management of PD-1/PDL1 inhibitor related cardiotoxicity.
作者 沈珈谊 吕玲春 韦铁民 Shen Jiayi;Lv Lingchun;Wei Tiemin(Department of Cardiology,Lishui Hospital,Zhejiang University School of Medicine,Lishui 323000,China)
出处 《心脑血管病防治》 2023年第1期49-51,共3页 CARDIO-CEREBROVASCULAR DISEASE PREVENTION AND TREATMENT
基金 浙江省基础公益研究计划(LGF19H020008) 丽水市公益技术应用研究(2019GYX28)
关键词 免疫检查点抑制剂 程序性死亡受体-1/程序性死亡配体-1 心脏毒性 研究进展 Immune checkpoint inhibitors Programmed death-1/Programmed death ligand-1 Cardiotoxicity Research progress
作者简介 通信作者:韦铁民,Email:lswtm@sina.com
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  • 1Galluzzi L, Vacchelli E, Bravo-San PJ, et al. Classi- fication of current anticancer immunotherapies [ J ]. Oncotarget, 2014, 5 (24) : 12472-12508.
  • 2Vesely MD, Kershaw MH, Schreiber RD, et al. Natu- ral innate and adaptive immunity to cancer[ J]. Annu Rev Immunol, 2011, 29: 235-271.
  • 3QureshiO S, Zheng Y, Nakamura K, et al. Trans-en- docytosis of CD80 and CD86 : a molecular basis for the cell-extrinsic function of CTLA4 [ J ]. Science, 2011, 332(6029) : 600-603.
  • 4ho A, Kondo S, Tada K, et al. Clinical development of immune checkpoint inhibitors[J]. Biomed Res Int, 2015, 2015: 605478.
  • 5Phan GQ, Yang JC, Sherry RM, et al. Cancer regres- sion and autoimmunity induced by cytotoxic T lympho- cyte-associated antigen 4 blockade in patients with me- tastatic melanoma [ J ]. Proc Natl Acad Sci U S A, 2003, 100(14): 8372-8377.
  • 6Hodi FS, O'Day SJ, McDermott DF, et al. Improved survival with ipilimumab in patients with metastatic melanoma[J]. N Engl J Med, 2010, 363(8) : 711- 723.
  • 7Robert C, Thomas L, Bondarenko I, et al. Ipilimum- ab plus dacarbazine for previously untreated metastatic melanoma[J]. N Engl J Med, 2011, 364(26): 2517-2526.
  • 8Maio M, Grob JJ, Aamdal S, et al. Five-year survival rates for treatment-naive patients with advanced mela- noma who received ipilimumab plus daearbazine in a phase III trial [ J ]. J Clin Oncol, 2015, 33 (10) : 1191-1196.
  • 9Schadendorf D, Hodi FS, Robert C, et al. Pooled A- nalysis of Long-Term Survival Data From Phase II and Phase III Trials of Ipilimumab in Unresectable or Meta- static Melanoma [ J ]. J Clin Oncol, 2015, 33 (17) : 1889-1894.
  • 10Topalian SL, Hodi FS, Brahmer JR, et al. Safety, ac-tivity, and immune correlates of anti-PD-1 antibody in cancer[J]. N Engl J Med, 2012, 366(26): 2443- 2454.

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