Potthoff Andrej, Attia Dina, Pischke Sven, Mederacke Ingmar, Beutel Gernot, Rifai Kinan, Deterding Katja, Heiringhoff Karlheinz, Klempnauer Jürgen, Strassburg Christian P, Manns Michael P, Bahr Matthias J
Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany.
Department of Gastroenterology, Hepatology and Endemic Medicine, Beni Suef University, Beni Suef, Egypt.
Liver Int. 2015 Aug;35(8):2042-9. doi: 10.1111/liv.12816. Epub 2015 Mar 31.
A considerable proportion of patients receiving liver transplants for Budd-Chiari syndrome (BCS) suffer from myeloproliferative neoplasms (MPN). This study evaluated the long-term prognosis of liver-transplanted patients with BCS secondary to MPN and the effect of immunosuppression on MPN progression.
A total of 78 patients with BCS were evaluated between 1982 and 2013. Of those, 40 patients suffered from polycythaemia vera (PV) and essential thrombocythaemia (ET). One patient had primary myelofibrosis (PMF). All patients received the standard immunosuppressive regimen. We retrospectively evaluated the long-term survival, clinical course and laboratory parameters of patients with MPN.
Exactly 29/41 patients (71%) with MPN survived ≥ 3 years [mean age 36 ± 11 years; females n = 27 (93%)]. Mean follow-up after orthotopic liver transplantation (OLT) was 12.4 ± 7.3 years (range 3-28 years). Five- and 10-year survival rates were not significantly different in patients with and without MPN (P = 0.81 and P = 0.66 respectively) or in patients with PV and ET (P = 0.29 and P = 0.55 respectively). Thrombosis and bleeding developed in 7/29 (24%) long-term MPN survivors with no significant difference between ET and PV (P = 0.18). In the long-term follow-up, there was no evidence of progression to overt myelofibrosis or acute myeloid leukaemia (AML). In the uni- and multivariate Cox-regression analyses, MPN did not influence survival after OLT.
Budd-Chiari syndrome patients with and without underlying MPN had similar long-term survival rates after OLT. There was no evidence of enhanced progression of MPN after OLT secondary to immunosuppressive therapy. However, major haemorrhage and recurrent thrombosis contributed to morbidity and mortality after OLT in those patients.
相当一部分因布加综合征(BCS)接受肝移植的患者患有骨髓增殖性肿瘤(MPN)。本研究评估了继发于MPN的BCS肝移植患者的长期预后以及免疫抑制对MPN进展的影响。
1982年至2013年间共评估了78例BCS患者。其中,40例患有真性红细胞增多症(PV)和原发性血小板增多症(ET)。1例患有原发性骨髓纤维化(PMF)。所有患者均接受标准免疫抑制方案。我们回顾性评估了MPN患者的长期生存情况、临床病程和实验室参数。
确切地说,41例MPN患者中有29例(71%)存活≥3年[平均年龄36±11岁;女性n = 27例(93%)]。原位肝移植(OLT)后的平均随访时间为12.4±7.3年(范围3 - 28年)。有MPN和无MPN的患者5年和10年生存率无显著差异(分别为P = 0.81和P = 0.66),PV和ET患者之间也无显著差异(分别为P = 0.29和P = 0.55)。7/29例(24%)长期MPN存活者发生了血栓形成和出血,ET和PV之间无显著差异(P = 0.18)。在长期随访中,没有证据表明进展为明显的骨髓纤维化或急性髓系白血病(AML)。在单因素和多因素Cox回归分析中,MPN不影响OLT后的生存。
有或无潜在MPN的布加综合征患者在OLT后的长期生存率相似。没有证据表明OLT后由于免疫抑制治疗导致MPN进展加速。然而,大出血和复发性血栓形成导致这些患者OLT后的发病和死亡。