肝移植中的维持性免疫抑制疗法:意大利回顾性队列研究 CESIT 的结果。

IF 2.4 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Arianna Bellini, Marco Finocchietti, Alessandro Cesare Rosa, Lucia Masiero, Silvia Trapani, Massimo Cardillo, Marco Massari, Stefania Spila Alegiani, Silvia Pierobon, Eliana Ferroni, Martina Zanforlini, Olivia Leoni, Stefano Ledda, Donatella Garau, Marina Davoli, Antonio Addis, Valeria Belleudi
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引用次数: 0

摘要

目的调查肝移植术后维持性免疫抑制治疗的使用情况,并比较其在临床实践中的风险-效益情况:设计:回顾性多中心队列研究:地点:意大利四个大区(伦巴第大区、威尼托大区、拉齐奥大区、撒丁岛大区):方法:从国家移植信息系统和意大利四个大区的行政报销数据中整合数据。2009年至2019年期间,所有接受过肝移植手术的成年人都被识别出来,并被分为两组:肝硬化或肝细胞癌(HCC)。使用多变量考克斯模型(HR;95% CI)分析了多年来免疫抑制治疗的趋势,并对其有效性/安全性进行了比较:主要结果指标:死亡率、移植排斥/移植物失败、严重感染发生率、癌症、糖尿病、主要不良心血管事件和调脂药物的使用:研究包括肝硬化队列中的 750 名受试者和 HCC 队列中的 1159 名受试者。在研究期间,环孢素-CsA的使用率有所下降,而他克莫司与其他药物的联合疗法与单一疗法相比有所增加。总体而言,两组中使用他克莫司单药治疗的比例均略高于 40%,其次是他克莫司+霉酚酸酯(39.5%-肝硬化;30.6%-肝癌)和他克莫司+雷帕霉素分子靶点抑制剂(mTORi)(8.5%-肝硬化;13.3%-肝癌)。基于他克莫司的不同疗法在风险-效益方面无明显差异,只是与他克莫司+霉酚酸盐相比,接受他克莫司单药治疗的肝硬化患者的死亡风险更高(HR:2.07;1.17-3.65):该研究强调了肝移植后治疗模式随着时间的推移而发生的变化,即倾向于他克莫司与霉酚酸酯或mTORi联合使用,而非单药治疗。此外,研究还发现他克莫司单药治疗与肝硬化队列中死亡率升高之间存在潜在关联。为了更深入地研究这些发现并优化肝移植受者的治疗策略,有必要开展进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maintenance immunosuppressive therapy in liver transplantation: results from CESIT study, an Italian retrospective cohort study.

Objectives: To investigate the use of maintenance immunosuppressive treatments following liver transplantation and to compare their risk-benefit profiles in clinical practice.

Design: Retrospective multicentrer cohort study.

Setting: Four Italian regions (Lombardy, Veneto, Lazio, Sardinia).

Methods: Data were integrated from the national transplant information system and administrative claims data from four Italian regions. All adults who underwent incident liver transplantation between 2009 and 2019 were identified and categorised into two groups: cirrhosis or hepatocellular carcinoma (HCC). The trend of immunosuppressive treatment over years was analysed, and their effectiveness/safety profiles were compared using multivariate Cox models (HR; 95% CI).

Main outcome measures: Mortality, transplant reject/graft failure, incidence of severe infections, cancer, diabetes, major adverse cardiovascular events and lipid-modifying agents use.

Results: The study comprised 750 subjects in the cirrhosis cohort and 1159 in the HCC cohort. Over the study years, there was a decline in the use of cyclosporine-CsA, while combination therapy involving tacrolimus with other drugs increased compared with monotherapy. Overall, tacrolimus monotherapy use was slightly over 40% in both groups, followed by tacrolimus+mycophenolate (39.5%-cirrhosis; 30.6%-HCC) and tacrolimus+molecular target of rapamycin inhibitors (mTORi) (8.5%-cirrhosis; 13.3%-HCC). No significant differences emerged in risk-benefit profile of different tacrolimus-based therapies, except for a higher risk of mortality in cirrhosis subjects under tacrolimus monotherapy compared with tacrolimus+mycophenolate (HR: 2.07; 1.17 to 3.65).

Conclusions: The study highlights a shift over time in postliver transplant therapeutic patterns, favouring the use of tacrolimus in combination with mycophenolate or mTORi, rather than monotherapy. Moreover, a potential association between tacrolimus monotherapy and increased mortality in the cirrhosis cohort was identified. Further research is warranted to investigate these findings more deeply and to optimise treatment strategies for liver transplant recipients.

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来源期刊
BMJ Open
BMJ Open MEDICINE, GENERAL & INTERNAL-
CiteScore
4.40
自引率
3.40%
发文量
4510
审稿时长
2-3 weeks
期刊介绍: BMJ Open is an online, open access journal, dedicated to publishing medical research from all disciplines and therapeutic areas. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around fully open peer review and continuous publication, publishing research online as soon as the article is ready.
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