Suppr超能文献

意大利对等待肝移植的 HCV 患者同情使用索非布韦:一项全国真实体验。

The Italian compassionate use of sofosbuvir in HCV patients waitlisted for liver transplantation: A national real-life experience.

机构信息

Gastrohepatology Unit, AOU Città della Salute e della Scienza di Torino, Turin, Italy.

First Division of Gastroenterology, IRCCS Fondazione Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Milan, Italy.

出版信息

Liver Int. 2018 Apr;38(4):733-741. doi: 10.1111/liv.13588. Epub 2017 Oct 6.

Abstract

BACKGROUND & AIMS: This study aimed to assess the real-life clinical and virological outcomes of HCV waitlisted patients for liver transplantation (LT) who received sofosbuvir/ribavirin (SOF/R) within the Italian compassionate use program.

METHODS

Clinical and virological data were collected in 224 patients with decompensated cirrhosis and/or hepatocellular carcinoma (HCC) receiving daily SOF/R until LT or up a maximum of 48 weeks.

RESULTS

Of 100 transplanted patients, 51 were HCV-RNA negative for >4 weeks before LT (SVR12: 88%) and 49 negative for <4 weeks or still viraemic at transplant: 34 patients continued treatment after LT (bridging therapy) (SVR12: 88%), while 15 stopped treatment (SVR12: 53%). 98 patients completed SOF/R without LT (SVR12: 73%). In patients with advanced decompensated cirrhosis (basal MELD ≥15 and/or C-P ≥B8), a marked improvement of the scores occurred in about 50% of cases and almost 20% of decompensated patients without HCC reached a condition suitable for inactivation and delisting.

CONCLUSIONS

These real-life data indicate that in waitlisted patients: (i) bridging antiviral therapy can be an option for patients still viraemic or negative <4 weeks at LT; and (ii) clinical improvement to a condition suitable for delisting can occur even in patients with advanced decompensated cirrhosis.

摘要

背景与目的

本研究旨在评估意大利同情用药项目中接受索磷布韦/利巴韦林(SOF/R)治疗的等待肝移植(LT)的丙型肝炎病毒(HCV)患者的真实临床和病毒学结局。

方法

收集了 224 例失代偿性肝硬化和/或肝细胞癌(HCC)患者的临床和病毒学数据,这些患者接受每日 SOF/R 治疗,直至 LT 或最多 48 周。

结果

在 100 例接受移植的患者中,51 例在 LT 前 >4 周 HCV-RNA 阴性(SVR12:88%),49 例在 LT 前 <4 周或仍病毒血症:34 例患者在 LT 后继续治疗(桥接治疗)(SVR12:88%),而 15 例停止治疗(SVR12:53%)。98 例患者未接受 LT 完成 SOF/R 治疗(SVR12:73%)。在基线 MELD≥15 和/或 C-P≥B8 的晚期失代偿性肝硬化患者中,约 50%的患者评分明显改善,近 20%无 HCC 的失代偿患者达到可进行灭活和除名的条件。

结论

这些真实世界的数据表明,在等待移植的患者中:(i)桥接抗病毒治疗可能是 LT 时仍病毒血症或阴性 <4 周患者的一种选择;(ii)即使在晚期失代偿性肝硬化患者中,也可能出现适合除名的临床改善。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验