SARS-CoV-2 感染对慢性肝病患者肝细胞癌发病率和治疗策略的影响。

IF 2.5 Q2 GASTROENTEROLOGY & HEPATOLOGY
Lung-Yi Mak, Matthew Shing Hin Chung, Xue Li, Francisco Tsz Tsun Lai, Eric Yuk Fai Wan, Celine Sze Ling Chui, Franco Wing Tak Cheng, Esther Wai Yin Chan, Ching Lung Cheung, Ivan Chi Ho Au, Xi Xiong, Wai-Kay Seto, Man-Fung Yuen, Carlos King Ho Wong, Ian Chi Kei Wong
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引用次数: 0

摘要

背景:目的:确定严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)感染对慢性肝病患者肝细胞癌(HCC)发病率和治疗策略的影响:方法:从香港的电子健康数据库中找到了一组回顾性的全港慢性阻塞性肺病患者。在 2020 年 1 月 1 日至 2022 年 10 月 25 日期间确诊感染 SARS-CoV-2 [冠状病毒病 2019 (COVID-19)+CLD] 的患者被识别出来,并与未感染 SARS-CoV-2 的患者(COVID-19-CLD)按倾向分数进行 1:1 配对。对每位患者进行随访,直至死亡、出现结果事件或 2022 年 11 月 15 日。主要结果为 HCC 发病率。次要结局包括全因死亡率、肝脏不良结局以及针对 HCC 的不同治疗策略(根治性治疗、非根治性治疗和姑息治疗)。根据 SARS-CoV-2 感染的急性期(20 天内)和急性期后(21 天或更长)进一步进行了分层分析。通过泊松回归模型估算了发病率比(IRRs):在队列中的 193589 名 CLD 患者(95% 以上为非肝硬化)中,55163 名 COVID-19+CLD 患者和 55163 名 COVID-19-CLD 患者经过 1:1 倾向分数匹配后被纳入队列。中位随访249天后,与COVID-19-CLD相比,COVID-19+CLD与发生HCC的风险增加无关(IRR:1.19,95%CI:0.99-1.42,P = 0.06),但接受HCC姑息治疗的风险更高(IRR:1.60,95%CI:1.46-1.75,P < 0.001)。在感染的急性期和急性期后,COVID-19+CLD 与全因死亡风险增加相关(急性期:IRR:7.06,95%CI:1.46-1.75,P<0.001):IRR:7.06,95%CI:5.78-8.63,P <0.001;急性期后:IRR:1.24,95%CI:5.78-8.63,P <0.001:IRR:1.24,95%CI:1.14-1.36,P <0.001)和不良肝功能结果(急性期:IRR:1.98,95%CI:1.14-1.36,P <0.001):急性期:IRR:1.98,95%CI:1.79-2.18,P <0.001;急性期后:IRR:1.24,95%CI:1.14-1.36,P <0.001:结论:与COVID-19-CLD相比,SARS-CLD患者在急性期的IRR为1.98,95%CI为1.79-2.18,P<0.001;急性后期的IRR为1.24,95%CI为1.13-1.35,P<0.001:结论:虽然感染SARS-CoV-2的CLD患者罹患HCC的风险并没有增加,但与未感染SARS-CoV-2的患者相比,他们更有可能接受姑息治疗。SARS-CoV-2感染的不利影响在急性期后仍然存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of SARS-CoV-2 infection on incidence and treatment strategies of hepatocellular carcinoma in people with chronic liver disease.

Background: Chronic liver disease (CLD) was associated with adverse clinical outcomes among people with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.

Aim: To determine the effects of SARS-CoV-2 infection on the incidence and treatment strategy of hepatocellular carcinoma (HCC) among patients with CLD.

Methods: A retrospective, territory-wide cohort of CLD patients was identified from an electronic health database in Hong Kong. Patients with confirmed SARS-CoV-2 infection [coronavirus disease 2019 (COVID-19)+CLD] between January 1, 2020 and October 25, 2022 were identified and matched 1:1 by propensity-score with those without (COVID-19-CLD). Each patient was followed up until death, outcome event, or November 15, 2022. Primary outcome was incidence of HCC. Secondary outcomes included all-cause mortality, adverse hepatic outcomes, and different treatment strategies to HCC (curative, non-curative treatment, and palliative care). Analyses were further stratified by acute (within 20 d) and post-acute (21 d or beyond) phases of SARS-CoV-2 infection. Incidence rate ratios (IRRs) were estimated by Poisson regression models.

Results: Of 193589 CLD patients (> 95% non-cirrhotic) in the cohort, 55163 patients with COVID-19+CLD and 55163 patients with COVID-19-CLD were included after 1:1 propensity-score matching. Upon 249-d median follow-up, COVID-19+CLD was not associated with increased risk of incident HCC (IRR: 1.19, 95%CI: 0.99-1.42, P = 0.06), but higher risks of receiving palliative care for HCC (IRR: 1.60, 95%CI: 1.46-1.75, P < 0.001), compared to COVID-19-CLD. In both acute and post-acute phases of infection, COVID-19+CLD were associated with increased risks of all-cause mortality (acute: IRR: 7.06, 95%CI: 5.78-8.63, P < 0.001; post-acute: IRR: 1.24, 95%CI: 1.14-1.36, P < 0.001) and adverse hepatic outcomes (acute: IRR: 1.98, 95%CI: 1.79-2.18, P < 0.001; post-acute: IRR: 1.24, 95%CI: 1.13-1.35, P < 0.001), compared to COVID-19-CLD.

Conclusion: Although CLD patients with SARS-CoV-2 infection were not associated with increased risk of HCC, they were more likely to receive palliative treatment than those without. The detrimental effects of SARS-CoV-2 infection persisted in post-acute phase.

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来源期刊
World Journal of Hepatology
World Journal of Hepatology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.10
自引率
4.20%
发文量
172
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