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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.

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。

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