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最全證據(jù)!臨床治愈可顯著改善慢乙肝遠(yuǎn)期結(jié)局

 老國(guó)幾 2020-08-07

編者按臨床治愈的相關(guān)研究已進(jìn)入深入探索階段,最近慢乙肝臨床治愈珠峰工程項(xiàng)目年度工作會(huì)議上也傳來(lái)喜報(bào),從2018年珠峰項(xiàng)目啟動(dòng)以來(lái),已有超1400例患者實(shí)現(xiàn)臨床治愈(相關(guān)鏈接),是非常值得期待的。臨床治愈的持久性和復(fù)發(fā)因素以及臨床治愈與遠(yuǎn)期預(yù)后的關(guān)系一直是專家和患者都關(guān)注的重點(diǎn)問(wèn)題。肝霖君曾系統(tǒng)分析臨床治愈后慢乙肝患者持久性佳(相關(guān)鏈接)和可顯著改善遠(yuǎn)期結(jié)局的相關(guān)內(nèi)容(相關(guān)鏈接),這期系列分享將和大家整合最新證據(jù),并進(jìn)行系統(tǒng)回顧。

為了更系統(tǒng)地了解慢乙肝臨床治愈這十余年來(lái)的進(jìn)展情況,雨露肝霖將推出4篇臨床治愈系列文章,上期第3篇與大家分享了十年慢乙肝臨床治愈詳細(xì)研究結(jié)果(相關(guān)鏈接),今天最后1篇將為大家?guī)?lái)臨床治愈可顯著改善慢乙肝遠(yuǎn)期結(jié)局的最全證據(jù)。

01 慢乙肝患者獲得臨床治愈后持久應(yīng)答率高

現(xiàn)有國(guó)內(nèi)外指南均認(rèn)可臨床治愈作為慢乙肝抗病毒治療的理想結(jié)局。現(xiàn)有基于PEG IFNα的治療策略已可大大提升慢乙肝患者臨床治愈率,因此臨床治愈后的持久性和能否安全停藥也成為了大家重點(diǎn)關(guān)注的問(wèn)題。

最近慢乙肝臨床治愈峰會(huì)暨中國(guó)派高峰論壇第二場(chǎng)會(huì)議上,眾多專家也探討了這個(gè)問(wèn)題,均認(rèn)可慢乙肝臨床治愈后持久性佳,復(fù)發(fā)率低,復(fù)發(fā)率均< 10%(相關(guān)鏈接)。從下表的多項(xiàng)研究均可證實(shí)不論通過(guò)何種方式獲得臨床治愈,其持久性佳,基本維持在85%以上。

然而,我們知道NA單藥治療的HBsAg清除率極低,僅為 1-3%(相關(guān)鏈接)。因此,慢乙肝患者若想追求高臨床治愈率和持久應(yīng)答率,應(yīng)選擇基于PEG IFNα的治療方式。

最全證據(jù)!臨床治愈可顯著改善慢乙肝遠(yuǎn)期結(jié)局

02 臨床治愈可顯著改善慢乙肝患者遠(yuǎn)期結(jié)局

我國(guó)原發(fā)性肝癌中92%是HBV感染導(dǎo)致(相關(guān)鏈接),而慢乙肝患者的最終治療目標(biāo)是改善遠(yuǎn)期結(jié)局,如肝癌發(fā)生發(fā)展的風(fēng)險(xiǎn),從而提高生存率和生活質(zhì)量。肝霖君曾系統(tǒng)分析慢乙肝患者獲得HBsAg清除后肝癌發(fā)生風(fēng)險(xiǎn)顯著降低的相關(guān)研究。

為方便大家查看,我們匯總最新證據(jù),多項(xiàng)來(lái)自美國(guó)、加拿大、日本和中國(guó)的針對(duì)不同國(guó)家和地區(qū)人群的回顧性研究和薈萃研究顯示,慢乙肝患者獲得臨床治愈后5年累積肝癌發(fā)生率為1.5%左右,甚至更低,顯著低于未獲得臨床治愈的人群(> 5%)。這證實(shí)了慢乙肝患者獲得臨床治愈后可顯著改善遠(yuǎn)期結(jié)局。

最全證據(jù)!臨床治愈可顯著改善慢乙肝遠(yuǎn)期結(jié)局

參考文獻(xiàn):(可上下滑動(dòng)查看)

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[8] Han M, Jiang J, Hou J, et al. Sustained immune control in HBeAg-positive patients who switched from entecavir therapy to pegylated interferon-alpha2a: 1 year follow-up of the OSST study[J]. Antivir Ther, 2016, 21(4): 337-344.

[9] Yip TC, Chan HL, Wong VW, et al. Impact of age and gender on risk of hepatocellular carcinoma after hepatitis B surface antigen seroclearance[J]. J Hepatol. 2017 Nov;67(5):902-908.

[10] Tateda K, Suzuki F, Kobayashi M, et al. Predictive Factors Associated with Hepatocellular Carcinoma Incidence and Mortality after Hepatitis B Surface Antigen Seroclearance in Patients with Chronic Hepatitis B. AASLD2018 abstract (oral 213).

[11] Yip TC, Wong GL, Chan HL, et al. HBsAg seroclearance further reduces hepatocellular carcinoma risk after complete viral suppression with nucleos(t)ide analogues[J]. J Hepatol, 2019, 70(3): 361-370.

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[13] F. Liu, X.-W. Wang, L. Chen, et al. Systematic review with meta-analysis: development of hepatocellular carcinoma in chronic hepatitis B patients with hepatitis B surface antigen seroclearance[J]. Aliment Pharmacol Ther. 2016 Jun;43(12):1253-61.

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[15] Jiang JF, Sun J, Shi J, et al. Letter: hepatocellular carcinoma risk after hepatitis B surface antigen seroclearance[J]. Aliment Pharmacol Ther. 2017 May;45(9):1286-1288.

[16] Hannah S Choi, Ryan Anderson, Oliver Lenz, et al. Association between HBsAg loss and risk of hepatocellular carcinoma in chronic hepatitis B: a systematic review and Meta-analysis. AASLD2019. Abstracts (poster 671).

[17] Anderson RT, et al. Association Between Seroclearance of Hepatitis B Surface Antigen and Long-term Clinical Outcomes of Patients With Chronic HBV Infection: Systematic Review and Meta-analysis[J]. Clin Gastroenterol Hepatol, 2020.

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