Angelico Roberta, Parente Alessandro, Manzia Tommaso Maria
Department of Experimental Medicine and Surgery, Liver Unit, Tor Vergata University of Rome, Rome, Italy.
Division of Abdominal Transplantation and Hepatobiliopancreatic Surgery, Bambino Gesù Children's Research Hospital IRCCS, Rome, Italy.
Transl Gastroenterol Hepatol. 2017 Sep 21;2:74. doi: 10.21037/tgh.2017.08.07. eCollection 2017.
Hepatocellular carcinoma (HCC) recurrence rate after liver transplantation (LT) is still up to 15-20%, despite a careful selection of candidates and optimization of the management within the waiting list. To reduce tumour recurrence, the currently adopted post-transplant strategies are based on the administration of a tailored immunosuppression (IS) regimen. Drug-induced depression of the immune system is essential in preventing graft rejection, however has a well-established association with oncogenesis. The immune system has a key role as a defending mechanism against cancer development, preventing vascular invasion and metastasis. Thus, IS drugs represent one of few modifiable non-oncological risk factors for tumour recurrence. In HCC recipients, a tailored IS therapy, with the aim to minimize drugs' doses, is essential to gain the optimal balance between the risk of rejection and the risk of tumour recurrence. So far, a complete withdrawal of IS drugs after LT is reported to be safely achievable in 25% of patients (defined as "operational tolerant"), without the risk of patient and graft loss. The recent identification of non-invasive "bio-markers of tolerance", which permit to identify patients who could successfully withdraw IS therapies, opens new perspectives in the management of HCC after LT. IS withdrawal could potentially reduce the risk of tumour recurrence, which represents the major drawback in HCC recipients. Herein, we review the current literature on IS weaning in patients who underwent LT for HCC as primary indication and we report the largest experiences on IS withdrawal in HCC recipients.
尽管在肝移植(LT)候选人的选择上十分谨慎,且在等待名单内对管理进行了优化,但肝细胞癌(HCC)肝移植后的复发率仍高达15%-20%。为降低肿瘤复发率,目前采用的移植后策略基于给予量身定制的免疫抑制(IS)方案。药物诱导的免疫系统抑制对于预防移植物排斥至关重要,但与肿瘤发生有着明确的关联。免疫系统作为抵御癌症发展、防止血管侵袭和转移的防御机制发挥着关键作用。因此,免疫抑制药物是肿瘤复发为数不多的可改变的非肿瘤学风险因素之一。在HCC肝移植受者中,旨在尽量减少药物剂量的量身定制的免疫抑制治疗对于在排斥风险和肿瘤复发风险之间取得最佳平衡至关重要。到目前为止,据报道25%的患者(定义为“手术耐受”)在肝移植后可安全地完全停用免疫抑制药物,且无患者和移植物丢失的风险。最近发现的非侵入性“耐受生物标志物”能够识别可成功停用免疫抑制治疗的患者,这为肝移植后HCC的管理开辟了新的前景。停用免疫抑制药物可能会降低肿瘤复发风险,而肿瘤复发是HCC肝移植受者的主要缺点。在此,我们回顾了以HCC为主要适应证接受肝移植患者免疫抑制药物撤减的当前文献,并报告了HCC肝移植受者免疫抑制药物撤减的最大规模经验。