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        中國肝癌肝移植臨床實踐指南

        2014-07-07 10:07:00中華醫(yī)學(xué)會器官移植學(xué)分會
        中華移植雜志(電子版) 2014年2期
        關(guān)鍵詞:受者移植術(shù)肝移植

        中華醫(yī)學(xué)會器官移植學(xué)分會

        中華醫(yī)學(xué)會外科學(xué)分會移植學(xué)組

        中國醫(yī)師協(xié)會器官移植醫(yī)師分會

        1 前 言

        據(jù)統(tǒng)計中國每年超過30 萬人死于肝細(xì)胞肝癌(以下簡稱肝癌),占全球肝癌死亡人數(shù)的一半左右。而肝移植是被全世界認(rèn)可的治療終末期肝病最有效的手段之一。我國自20 世紀(jì)90 年代掀起第二次肝移植熱潮以來,肝移植事業(yè)發(fā)展迅猛,呈專業(yè)化和規(guī)?;l(fā)展態(tài)勢,在移植數(shù)量和質(zhì)量方面已接近或達(dá)到西方發(fā)達(dá)國家水平。截止2014 年4 月,中國肝移植注冊網(wǎng)站登記肝移植26 751 例。目前,肝移植在全國范圍內(nèi)已得到廣泛開展,亟待相關(guān)實踐指南來指導(dǎo)全國肝移植工作更規(guī)范、有效、安全地開展。中華醫(yī)學(xué)會器官移植學(xué)分會、中華醫(yī)學(xué)會外科學(xué)分會移植學(xué)組及中國醫(yī)師協(xié)會器官移植醫(yī)師分會組織專家制定肝癌肝移植臨床實踐指南,重點闡述肝移植受者選擇標(biāo)準(zhǔn)、術(shù)前降期治療、抗病毒治療、免疫抑制劑應(yīng)用、術(shù)后復(fù)發(fā)防治五部分內(nèi)容。本指南采用的循證醫(yī)學(xué)證據(jù)分級主要參考2001 牛津證據(jù)分級(詳見表1),推薦意見強(qiáng)度主要參考GRADE系統(tǒng)推薦分級等[1-2]。

        2 肝癌肝移植受者選擇標(biāo)準(zhǔn)(表2)

        供肝短缺是世界性難題,故應(yīng)將寶貴的供肝資源優(yōu)先分配給肝移植的最大獲益者。心臟死亡器官捐獻(xiàn)是中國現(xiàn)今拓展供肝來源的主要方向,而活體肝移植在有豐富移植經(jīng)驗的醫(yī)療單位已成為一項成熟技術(shù)[3]。1996 年Mazzaferro 等提出米蘭標(biāo)準(zhǔn)后,符合米蘭標(biāo)準(zhǔn)的肝癌肝移植受者獲得了長期存活[4-7]。但米蘭標(biāo)準(zhǔn)對肝癌大小和數(shù)目的限制過于嚴(yán)格,更重要的是忽略了腫瘤的生物學(xué)特性。如果根據(jù)米蘭標(biāo)準(zhǔn),中國大多數(shù)肝癌患者將失去肝移植機(jī)會。近年來國際上涌現(xiàn)出一些新的肝癌肝移植受者選擇標(biāo)準(zhǔn),如加州大學(xué)洛杉磯分校(University of California,San Francisco,UCSF)標(biāo)準(zhǔn)、Up-to-Seven標(biāo)準(zhǔn)等,這些新標(biāo)準(zhǔn)提出的共同目的是擴(kuò)大受者人群并取得與米蘭標(biāo)準(zhǔn)相似的移植生存率[8-9]。2008 年,中國提出的杭州標(biāo)準(zhǔn)是國際上首個引入腫瘤生物學(xué)特性和病理學(xué)特征的移植標(biāo)準(zhǔn),這是對以往標(biāo)準(zhǔn)局限于腫瘤形態(tài)學(xué)的巨大突破。研究證實,無論是尸體肝移植還是活體肝移植,符合杭州標(biāo)準(zhǔn)的肝癌受者均獲得滿意的術(shù)后生存率[10-15]。近年來,對于肝癌切除術(shù)后復(fù)發(fā)者,如符合肝移植準(zhǔn)入標(biāo)準(zhǔn),多數(shù)專家主張行搶救性肝移植[16-17];對于肝癌肝移植術(shù)后移植物失功者,再次肝移植應(yīng)審慎考慮[17-18]。

        表1 循證醫(yī)學(xué)證據(jù)分級

        表2 肝癌肝移植受者選擇標(biāo)準(zhǔn)

        3 肝癌肝移植術(shù)前降期治療(表3)

        肝癌肝移植術(shù)前腫瘤降期治療是通過一系列治療手段,減輕腫瘤負(fù)荷,降低分期,使超出肝癌肝移植受者選擇標(biāo)準(zhǔn)的患者能夠被納入移植標(biāo)準(zhǔn),獲得肝移植機(jī)會。降期治療主要適用于不符合現(xiàn)有肝癌肝移植標(biāo)準(zhǔn),且無門靜脈主干或下腔靜脈等大血管侵犯、無遠(yuǎn)處轉(zhuǎn)移的肝癌患者[17,19-21]。降期治療的方法主要有局部消融治療和肝動脈栓塞化療(transcatheter hepatic arterial chemoembolization,TACE)等[17,19,22]。局部消融治療包括射頻消融、微波消融、冷凍消融和經(jīng)皮無水乙醇注射等方法。降期治療的療效一般采用對比增強(qiáng)CT 和MRI,并結(jié)合甲胎蛋白(alpha fetal protein,AFP)水平變化進(jìn)行評估,評價指標(biāo)包括腫瘤大小、數(shù)目和AFP 水平等[22-28]。目前研究認(rèn)為多種治療方法的聯(lián)合應(yīng)用可達(dá)到更好的降期療效[29]。

        表3 肝癌肝移植術(shù)前降期治療

        4 肝癌肝移植受者抗病毒治療(表4)

        中國肝癌肝移植受者90%以上與乙型肝炎病毒(hepatitis B virus,HBV)感染相關(guān)。肝移植前HBV 載量高以及肝移植后乙型肝炎(以下簡稱乙肝)復(fù)發(fā)的受者,肝癌復(fù)發(fā)的風(fēng)險增加,因此對乙肝肝移植受者盡早行抗病毒治療,盡快降低HBV 水平,有助于降低移植術(shù)后乙肝復(fù)發(fā)率,提高受者長期生存率[30-32]。HBV 載量高的等待肝移植患者應(yīng)采用恩替卡韋等強(qiáng)效、高耐藥屏障核苷類似物(nucleostide analogues,NAs)。移植術(shù)中無肝期應(yīng)給予乙型肝炎免疫球蛋白(hepatitis B immunoglobulin,HBIG)。移植后的主要抗病毒治療方案為NAs 聯(lián)合低劑量HBIG,其中恩替卡韋或替諾福韋的聯(lián)合方案能更好地預(yù)防移植術(shù)后乙肝復(fù)發(fā)[33-38]。近年來,研究表明應(yīng)用無激素免疫抑制方案可降低移植術(shù)后乙肝復(fù)發(fā)率[39]。此外也有移植術(shù)后接種乙肝疫苗預(yù)防乙肝復(fù)發(fā)的報道,其臨床應(yīng)用尚有爭議[40-42]。中國丙型肝炎病毒(hepatitis C virus,HCV)感染患者呈增多趨勢,HCV RNA 陽性患者如肝功能Child-Pugh 評分≤7,術(shù)前宜進(jìn)行抗病毒治療,移植術(shù)后須經(jīng)病理確認(rèn)丙型肝炎復(fù)發(fā)后方可給予抗HCV 治療[43]。

        5 肝癌肝移植受者免疫抑制劑應(yīng)用(表5)

        鈣調(diào)磷酸酶抑制劑(calcineurin inhibitor,CNI)的應(yīng)用是肝移植后肝癌復(fù)發(fā)的獨立危險因素[44]。對于肝癌肝移植受者,腫瘤的復(fù)發(fā)風(fēng)險與其侵襲性及機(jī)體的免疫功能有關(guān),受者處于強(qiáng)免疫抑制狀態(tài)時其免疫監(jiān)視系統(tǒng)受到破壞,促進(jìn)腫瘤復(fù)發(fā)、轉(zhuǎn)移,而免疫抑制劑量不足則容易誘發(fā)排斥反應(yīng)。如何維持這一平衡,目前尚無定論[45-47]。肝癌肝移植受者目前尚不建議免疫抑制劑的全線撤除,但主張個體化的低劑量免疫抑制方案[45]。近年來臨床上有糖皮質(zhì)激素早期撤除、無糖皮質(zhì)激素及使用具有腫瘤抑制作用的mTOR 抑制劑(西羅莫司為代表)的成功應(yīng)用方案[48-51]。目前臨床上主要的免疫抑制方案為:①他克莫司或環(huán)孢素+嗎替麥考酚酯+糖皮質(zhì)激素;②白介素-2 受體阻滯劑+西羅莫司+嗎替麥考酚酯+糖皮質(zhì)激素;③白介素-2 受體阻滯劑+嗎替麥考酚酯+他克莫司/西羅莫司[52-55]。

        表4 肝癌肝移植受者抗病毒治療

        表5 肝癌肝移植受者免疫抑制劑應(yīng)用

        6 肝癌肝移植術(shù)后復(fù)發(fā)的防治(表6)

        文獻(xiàn)報道,肝癌肝移植術(shù)后5 年肝癌復(fù)發(fā)率可達(dá)20% ~57. 8%,故復(fù)發(fā)轉(zhuǎn)移的防治十分重要[56-57]。肝癌的形態(tài)學(xué)特征(大小、數(shù)目等)、分期、組織學(xué)分級以及生物學(xué)特性等應(yīng)作為術(shù)后用藥的重要參考,制定個體化治療方案。

        肝癌肝移植術(shù)后可能存在針對腫瘤的免疫逃逸,故應(yīng)給予受者一定療程的術(shù)后治療,以期盡可能地減少微小轉(zhuǎn)移灶,降低術(shù)后復(fù)發(fā)率。選用碘131美妥昔單抗放射免疫治療、索拉非尼治療以及系統(tǒng)性化療(如奧沙利鉑或阿霉素分別與氟尿嘧啶聯(lián)合使用),均可為部分受者提供一定的生存獲益[58-61]。

        對于肝移植術(shù)后肝癌復(fù)發(fā)轉(zhuǎn)移者,應(yīng)用索拉非尼治療,可延長受者生存期[17,62-64]。肺轉(zhuǎn)移灶如可切除,首選手術(shù)切除[65]。移植肝內(nèi)復(fù)發(fā)病灶的局部治療包括手術(shù)切除、TACE,局部消融等[66-68]。此外,有專家提出放療、再次肝移植等可作為治療的選擇。對于晚期患者,可考慮減少或停止免疫抑制劑的使用。

        表6 肝癌肝移植術(shù)后復(fù)發(fā)的防治

        編審專家組組長: 鄭樹森

        編審專家組成員( 按姓氏拼音排序) : 陳規(guī)劃、陳實、陳孝平、陳燕凌、陳知水、陳忠華、丁義濤、董家鴻、竇劍、竇科峰、杜國盛、段偉東、傅志仁、高杰、高良輝、何曉順、賀強(qiáng)、景鴻恩、李波、李立、李寧、李玉民、劉景豐、劉軍、盧實春、呂國悅、明英姿、彭承宏、彭貴主、彭志海、錢建民、沈巖、沈中陽、石承先、時軍、孫玉嶺、王偉林、溫浩、吳健、吳忠鈞、夏強(qiáng)、徐驍、嚴(yán)律南、楊廣順、楊家印、楊揚(yáng)、楊占宇、葉啟發(fā)、臧運(yùn)金、張峰、張珉、張水軍、鄭樹森、周琳、朱繼業(yè)、朱志軍

        執(zhí)筆: 徐驍、李建輝、高峰、陳峻、舒哲悅、方維佳、衛(wèi)強(qiáng)

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