Naymagon Leonard, Tremblay Douglas, Zubizarreta Nicole, Moshier Erin, Schiano Thomas, Mascarenhas John
Tisch Cancer Institute, Icahn School of Medicine At Mount Sinai, One Gustave L. Levy Place, Box 1079, New York, NY, 10029, USA.
Department of Population Health Science and Policy/Tisch Cancer Institute, Icahn School of Medicine At Mount Sinai, New York, NY, USA.
J Thromb Thrombolysis. 2020 Oct;50(3):652-660. doi: 10.1007/s11239-020-02052-4.
Non-cirrhotic portal vein thrombosis (ncPVT) most often occurs in the setting of intraabdominal proinflammatory processes. Less often, ncPVT may result from primary hematologic thrombophilia (most commonly JAK2V617F). Although these etiologic categories are pathophysiologically distinct, they are treated similarly using anticoagulation. We conducted a retrospective assessment of outcomes among ncPVT patients harboring JAK2V617F, and compared them to outcomes among patients with other etiologies for ncPVT, to determine whether anticoagulation alone is adequate therapy for JAK2V617F associated PVT. Outcomes were complete radiographic resolution (CRR) of PVT, recanalization (RC) of occlusive PVT, and development of significant portal hypertension (SPH). Three-hundred-thirty ncPVT patients seen between 1/2000 and 1/2019, including 37 harboring JAK2V617F (JAK2), 203 with other evident etiology (OE) for PVT, and 90 with no evident etiology (NE) for PVT followed for a median 29 months (53, 21, and 32 months respectively). Outcomes among the JAK2 cohort were dismal relative to the other groups. CRR rates were 8%, 31%, and 55% for the JAK2, NE, and OE cohorts respectively (multivariable HR JAK2:OE = 0.15 (0.05, 0.49), p = 0.0016). RC rates were 16%, 33%, and 49% for the JAK2, NE, and OE cohorts respectively (multivariable HR for RC JAK2:OE = 0.24 (0.09, 0.63), p = 0.0036). SPH rates were 49%, 32%, and 17% for the JAK2, NE, and OE cohorts respectively (multivariable HR for SPH JAK2:OE = 1.23 (0.62, 2.42), p = 0.5492). Given the strikingly poor outcomes among patients harboring JAK2V617F, anticoagulation alone does not appear to be adequate therapy for this cohort. Further investigation into thrombolysis and/or thrombectomy as an adjunct to anticoagulation is merited in this high-risk group.
非肝硬化门静脉血栓形成(ncPVT)最常发生于腹腔内促炎过程中。较少见的情况是,ncPVT可能由原发性血液系统血栓形成倾向(最常见的是JAK2V617F)引起。尽管这些病因在病理生理学上有所不同,但使用抗凝治疗时它们的治疗方法相似。我们对携带JAK2V617F的ncPVT患者的预后进行了回顾性评估,并将其与其他病因导致的ncPVT患者的预后进行比较,以确定单纯抗凝是否是治疗JAK2V617F相关门静脉血栓形成(PVT)的充分疗法。观察的预后指标包括PVT的完全影像学消退(CRR)、闭塞性PVT的再通(RC)以及严重门静脉高压(SPH)的发生情况。在2000年1月至2019年1月期间共诊治了330例ncPVT患者,其中37例携带JAK2V617F(JAK2组),203例有其他明确病因(OE组),90例无明确病因(NE组),随访时间中位数分别为29个月(JAK2组53个月、OE组21个月、NE组32个月)。与其他组相比,JAK2组的预后很差。JAK2组、NE组和OE组的CRR率分别为8%、31%和55%(多变量风险比JAK2:OE = 0.15(0.05, 0.49),p = 0.0016)。JAK2组、NE组和OE组的RC率分别为16%、33%和49%(多变量风险比JAK2:OE = 0.24(0.09, 0.63),p = 0.0036)。JAK2组、NE组和OE组的SPH率分别为49%、32%和17%(多变量风险比JAK2:OE = 1.23(0.62, 2.42),p = 0.5492)。鉴于携带JAK2V617F的患者预后明显较差,单纯抗凝似乎不是该组患者的充分疗法。对于这个高危组,值得进一步研究将溶栓和/或血栓切除术作为抗凝辅助治疗的效果。