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本文引用的文献

1
Efficacy and Toxicity of Immune -Checkpoint Inhibitors in Patients With Preexisting Autoimmune Disorders.免疫检查点抑制剂在已有自身免疫性疾病患者中的疗效与毒性
Front Med (Lausanne). 2020 May 7;7:137. doi: 10.3389/fmed.2020.00137. eCollection 2020.
2
Nivolumab plus Ipilimumab in Advanced Non-Small-Cell Lung Cancer.纳武利尤单抗联合伊匹单抗治疗晚期非小细胞肺癌。
N Engl J Med. 2019 Nov 21;381(21):2020-2031. doi: 10.1056/NEJMoa1910231. Epub 2019 Sep 28.
3
Nivolumab for Newly Diagnosed Advanced-Stage Classic Hodgkin Lymphoma: Safety and Efficacy in the Phase II CheckMate 205 Study.纳武利尤单抗治疗新诊断的晚期经典型霍奇金淋巴瘤:CheckMate 205 研究的 II 期安全性和疗效。
J Clin Oncol. 2019 Aug 10;37(23):1997-2007. doi: 10.1200/JCO.19.00315. Epub 2019 May 21.
4
Safety of Programmed Death-1 Pathway Inhibitors Among Patients With Non-Small-Cell Lung Cancer and Preexisting Autoimmune Disorders.程序性死亡-1 通路抑制剂在患有非小细胞肺癌和既往自身免疫性疾病患者中的安全性。
J Clin Oncol. 2018 Jul 1;36(19):1905-1912. doi: 10.1200/JCO.2017.77.0305. Epub 2018 May 10.
5
Delayed Autoimmune Toxicity Occurring Several Months After Cessation of Anti-PD-1 Therapy.抗 PD-1 治疗停止数月后发生的延迟性自身免疫毒性。
Oncologist. 2018 Jul;23(7):849-851. doi: 10.1634/theoncologist.2017-0531. Epub 2018 Apr 17.
6
Safety and efficacy of anti-programmed death 1 antibodies in patients with cancer and pre-existing autoimmune or inflammatory disease.抗程序性死亡 1 抗体在患有癌症和既往自身免疫或炎症性疾病的患者中的安全性和疗效。
Eur J Cancer. 2018 Mar;91:21-29. doi: 10.1016/j.ejca.2017.12.008. Epub 2018 Jan 10.
7
Atezolizumab versus chemotherapy in patients with platinum-treated locally advanced or metastatic urothelial carcinoma (IMvigor211): a multicentre, open-label, phase 3 randomised controlled trial.阿特珠单抗与化疗用于铂类治疗后局部晚期或转移性尿路上皮癌患者(IMvigor211):一项多中心、开放标签、III 期随机对照临床试验。
Lancet. 2018 Feb 24;391(10122):748-757. doi: 10.1016/S0140-6736(17)33297-X. Epub 2017 Dec 18.
8
Nivolumab in patients with advanced gastric or gastro-oesophageal junction cancer refractory to, or intolerant of, at least two previous chemotherapy regimens (ONO-4538-12, ATTRACTION-2): a randomised, double-blind, placebo-controlled, phase 3 trial.纳武利尤单抗治疗既往至少两种化疗方案治疗失败或不耐受的晚期胃或胃食管结合部腺癌患者(ONO-4538-12,ATTRACTION-2):一项随机、双盲、安慰剂对照、III 期临床试验。
Lancet. 2017 Dec 2;390(10111):2461-2471. doi: 10.1016/S0140-6736(17)31827-5. Epub 2017 Oct 6.
9
Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma.纳武利尤单抗联合伊匹木单抗治疗晚期黑色素瘤的总生存期
N Engl J Med. 2017 Oct 5;377(14):1345-1356. doi: 10.1056/NEJMoa1709684. Epub 2017 Sep 11.
10
Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.免疫疗法毒性管理:ESMO诊断、治疗及随访临床实践指南
Ann Oncol. 2017 Jul 1;28(suppl_4):iv119-iv142. doi: 10.1093/annonc/mdx225.

免疫检查点抑制剂在实体瘤合并自身免疫性疾病或炎症性疾病患者中的应用:真实世界数据。

Use of immune checkpoint inhibitors in patients with solid tumors and pre-existing autoimmune or inflammatory disease: real-world data.

作者信息

Calvo Virginia, Fernández Marta Andrés, Collazo-Lorduy Ana, Franco Fernando, Núñez Beatriz, Provencio Mariano

机构信息

Servicio de Oncología Médica, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, 28222, Spain.

Estudiante de Medicina, Universidad Autónoma de Madrid, Calle Francisco Tomás y Valiente 1, Cantoblanco, Madrid, 28049, Spain.

出版信息

Lung Cancer Manag. 2021 Jul 2;10(4):LMT51. doi: 10.2217/lmt-2021-0003. eCollection 2021 Dec.

DOI:10.2217/lmt-2021-0003
PMID:34899991
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8656306/
Abstract

AIM

Immune checkpoint inhibitors (ICIs) are a cornerstone in cancer treatment but they can induce immune-related adverse events (irAEs). Furthermore, patients with pre-existing autoimmune and/or inflammatory disease (AID) have been excluded from clinical trials. The objective of this study is to evaluate the efficacy and safety of ICIs in patients with cancer and AID.

MATERIALS & METHODS: This is an observational, retrospective study carried out at the Medical Oncology Department of Hospital Universitario Puerta de Hierro, Majadahonda, Madrid between January 2016 and December 2018.

RESULTS

A total of 202 cancer patients treated with ICIs were included, 15 (7, 4%) of them had pre-existing autoimmune diseases. The most frequent pre-existing AID were thyroid diseases (33.3%): autoimmune hypothyroidism, Graves-Basedow disease and Hashimoto's thyroiditis. Three patients had psoriasis, two antinuclear antiboides + polyarthritis, one rheumatoid arthritis, another latent autoimmune diabetes in adults, another systemic lupus erythematosus and the last one, a polymyalgia rheumatica. In this series, the majority of patients (73.33%) did not experience any flare up of their autoimmune disease. In patients who had AID flare up, this was treated with corticosteroids. The most frequent cause of immunotherapy discontinuation was tumor progression (40%). A total of 20% of patients had to discontinue immunotherapy due to toxicity.

CONCLUSION

In our series, AID flare ups or irAEs in patients with pre-existing AID who receive immunotherapy are not very common and can often be controlled without interrupting treatment. Prospective studies are needed to establish the incidence of irAEs in patients with pre-existing autoimmune conditions, evaluate risk-benefit and elaborate management clinical guidelines in this population.

摘要

目的

免疫检查点抑制剂(ICIs)是癌症治疗的基石,但它们可诱发免疫相关不良事件(irAEs)。此外,患有自身免疫性和/或炎性疾病(AID)的患者被排除在临床试验之外。本研究的目的是评估ICIs在患有癌症和AID的患者中的疗效和安全性。

材料与方法

这是一项于2016年1月至2018年12月在马德里马亚达翁达市铁之门大学医院医学肿瘤科开展的观察性、回顾性研究。

结果

共纳入202例接受ICIs治疗的癌症患者,其中15例(7.4%)患有既往自身免疫性疾病。最常见的既往AID是甲状腺疾病(33.3%):自身免疫性甲状腺功能减退症、格雷夫斯-巴塞多氏病和桥本甲状腺炎。3例患者患有银屑病,2例抗核抗体阳性+多关节炎,1例类风湿关节炎,1例成人潜伏性自身免疫性糖尿病,1例系统性红斑狼疮,最后1例是风湿性多肌痛。在该系列中,大多数患者(73.33%)未出现自身免疫性疾病的任何发作。在出现AID发作的患者中,采用皮质类固醇进行治疗。免疫治疗中断的最常见原因是肿瘤进展(40%)。共有20%的患者因毒性不得不停止免疫治疗。

结论

在我们的系列研究中,接受免疫治疗的既往患有AID的患者出现AID发作或irAEs并不常见,且通常可在不中断治疗的情况下得到控制。需要进行前瞻性研究以确定既往患有自身免疫性疾病的患者中irAEs的发生率,评估风险效益,并为该人群制定详细的管理临床指南。