San Miguel C, Fundora Y, Triguero J, Muffak K, Villegas T, Becerra A, Garrote D, Ferrón J A
General, Digestive Surgery, and Liver Transplantation Department, Virgen de las Nieves University Hospital, Granada, Spain.
General, Digestive Surgery, and Liver Transplantation Department, Virgen de las Nieves University Hospital, Granada, Spain.
Transplant Proc. 2015 Oct;47(8):2371-3. doi: 10.1016/j.transproceed.2015.08.020.
We describe an observational, retrospective study that included patients who underwent a liver transplantation (LT) for hepatocellular carcinoma (HCC) in our center between 2004 and 2012.
Clinical variables were recorded for donors and recipients as diagnosis and treatment, immunosuppressive therapy, toxicity, graft dysfunction, recurrence, and exitus. Fifty-eight patients were analyzed. The mean age was 57 ± 8 years. The viral etiology of HCC was 50% (n = 29), alcoholic 26% (n = 15), and others, 24% (n = 14). Regarding initial immunosuppressive strategy (IS), 51 patients (87.9%) were treated with standard regimen with corticosteroids (CS) and tacrolimus (TA), compared with 7 patients with impaired renal function (12.1%) who underwent a delayed therapy with calcineurin inhibitors (CNI) + mycophenolate mophetil (MMF) + CS. Concomitant use of anti-CD25 monoclonal antibodies was less than 10%. Regarding maintenance, 43 patients (74.1%) were treated with MMF + CNI versus 15 treated only with TA (25.9%).
Recurrence of HCC was approximately 12%: 7 patients (2 hepatic only, 5 also extra-hepatic). Exitus was established in 19 patients (32.75%); only 3 patients (5.17%) were attributable to HCC. Bivariate studies were conducted according to the initial IS (standard regimen versus delayed therapy) and maintenance therapy (MMF + TA versus TA alone), with no differences in any of them in recurrence, treatment toxicity, graft rejection, and dysfunction.
In our experience with the IS, we found no differences in the development of recurrent disease, treatment toxicity, development of graft dysfunction, or rejection. We believe that individualized immunosuppressive therapy in these patients is safe and effective.
我们描述了一项观察性回顾性研究,纳入了2004年至2012年间在我们中心因肝细胞癌(HCC)接受肝移植(LT)的患者。
记录供体和受体的临床变量,包括诊断与治疗、免疫抑制治疗、毒性、移植物功能障碍、复发和死亡情况。对58例患者进行了分析。平均年龄为57±8岁。HCC的病毒病因占50%(n = 29),酒精性病因占26%(n = 15),其他病因占24%(n = 14)。关于初始免疫抑制策略(IS),51例患者(87.9%)接受了含皮质类固醇(CS)和他克莫司(TA)的标准方案治疗,而7例肾功能受损患者(12.1%)接受了钙调神经磷酸酶抑制剂(CNI)+霉酚酸酯(MMF)+ CS的延迟治疗。抗CD25单克隆抗体的联合使用率低于10%。在维持治疗方面,43例患者(74.1%)接受了MMF + CNI治疗,15例仅接受TA治疗(25.9%)。
HCC复发率约为12%:7例患者(2例仅肝内复发,5例肝外也有复发)。19例患者(32.75%)死亡;仅3例患者(5.17%)死于HCC。根据初始IS(标准方案与延迟治疗)和维持治疗(MMF + TA与单独TA)进行了双变量研究,在复发、治疗毒性、移植物排斥和功能障碍方面均无差异。
根据我们在免疫抑制策略方面的经验,我们发现在复发性疾病的发生、治疗毒性、移植物功能障碍或排斥反应的发生方面没有差异。我们认为这些患者的个体化免疫抑制治疗是安全有效的。