晚期癌症免疫检查点抑制剂相关性心肌炎的临床特征及预后影响。

IF 3 3区 医学 Q2 ONCOLOGY Investigational New Drugs Pub Date : 2023-12-01 Epub Date: 2023-10-30 DOI:10.1007/s10637-023-01400-4
Lan Xu, Manyi Xu, Wei Sun, Weiping Zhang, Zhengbo Song
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引用次数: 0

摘要

心肌炎是一种罕见的免疫相关不良事件,死亡率高,其临床特征和预后影响的报道很少。本研究旨在探讨免疫检查点抑制剂(ICI)治疗的晚期癌症(NSCLC)心肌炎的心脏参数与预后之间的关系。14名临床医生诊断为ICI相关心肌炎的患者被纳入研究分析。通过Cox单因素和多因素生存分析,确定了发展为严重心肌炎的潜在危险因素。还进行了生存分析,以探讨心肌炎患者的预后。在心肌炎患者中,较高的B型钠尿肽(BNP)水平(P=0.04)和传导阻滞(P=0.03)与进展为严重心肌炎有关。此外,高乳酸脱氢酶(LHD)水平(P=0.04)和2个月内心肌炎发作(P=0.02)是严重心肌炎的预后因素。所有患者的中位无进展生存期(PFS)时间和中位总生存期(OS)时间分别为5.9个月和18.5个月。然而,轻度和重度队列在PFS和OS方面没有统计学差异(PFS:4.5个月对8.5个月,P=0.017;OS:21.3个月对18.5个月,P=0.36)。我们发现心肌炎发生得越早,PFS预后越差(4.5个月和10.5个月,P=0.008),而OS没有差异(18.5个月对21.3个月,P=0.035)。与轻度心肌炎相比,严重心肌炎表现为BNP水平升高和心传导异常。此外,轻度和早期心肌炎患者的存活率往往较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical characteristics and prognostic impact of immune checkpoint inhibitor-associated myocarditis in advanced non-small cell lung cancer.

Myocarditis is a rare immune-related adverse events (irAEs) with high mortality rates, with few reports on its clinical characteristics and prognostic impact. This study designed to explore the associations between cardiac parameters and outcomes of myocarditis in advanced non-small cell lung cancer (NSCLC) who treated with immune checkpoint inhibitor (ICI). Fourteen patients diagnosed with ICI-associated myocarditis by clinicians were admitted to the study analysis. By Cox univariate and multivariate survival analyses, potential risk factors for the development of severe myocarditis were identified. Survival analysis was also performed to explore the prognosis of patients with myocarditis. Among patients with myocarditis, higher B-type natriuretic peptide (BNP) levels (P = 0.04) and conduction block (P = 0.03) were associated with progression to severe myocarditis. In addition, high lactate dehydrogenase (LHD) levels (P = .04) and myocarditis onset within 2 months (P = 0.02) were prognostic factors of severe myocarditis. The median progression-free survival (PFS) time and median overall survival (OS) time for all patients were 5.9 months and 18.5 months, respectively. However, there were no statistical differences between mild and severe cohorts in terms of PFS and OS (PFS: 4.5 vs. 8.5 months, P = 0.17; OS: 21.3 vs. 18.5months, P = 0.36). And we found that the earlier occurrence of myocarditis, worse PFS prognosis (4.5 months vs. 10.5 months, P = 0.008), while no difference in OS (18.5 months vs. 21.3 months, P = 0.35). Compared to mild myocarditis, severe myocarditis presented with higher BNP levels and cardiac conduction abnormalities. In addition, patients with mild and early myocarditis tended to have better survival rates.

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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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