Müller Lukas, Kloeckner Roman, Heim Lorena, Moos Maximilian, Hahn Felix, Stoehr Fabian, Emrich Tilman, Graafen Dirk, Grunz Jan-Peter, Pinto Dos Santos Daniel, Weinmann Arndt, Foerster Friedrich, Mittler Jens, Marquardt Jens Uwe, Bäuerle Tobias, Mähringer-Kunz Aline
Department of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
Department of Radiology, University of Wisconsin, Madison, Wisconsin, United States of America.
PLoS One. 2025 Aug 22;20(8):e0330336. doi: 10.1371/journal.pone.0330336. eCollection 2025.
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related mortality, with portal vein tumor thrombosis (PVTT) being a common complication that significantly worsens prognosis. Recent studies have identified bone mineral density (BMD) as a prognostic factor in patients with HCC; however, its role in patients with PVTT remains unexplored. This retrospective study evaluated the prognostic value of BMD in 462 patients with HCC and PVTT treated between 2005 and 2020. BMD was measured via computed tomography attenuation at the first lumbar vertebra at the time of HCC diagnosis and PVTT onset, using an established threshold of 160 Hounsfield units (HU). Kaplan-Meier analysis assessed overall survival, and multivariate Cox regression adjusted for established prognostic factors. Median BMD was 136 HU (IQR: 113-160) at HCC diagnosis and 134 HU (IQR: 109-159) at PVTT onset. Patients with BMD ≥ 160 HU showed significantly longer overall survival both at HCC diagnosis (10.4 vs. 5.5 months, p < 0.001) and PVTT onset (8.5 vs. 4.7 months, p < 0.001). In multivariate analysis at both time points, BMD remained an independent predictor of survival, alongside tumor growth pattern, therapy, and Albumin-Bilirubin (ALBI) grade (alpha-fetoprotein reached significance only at time of PVTT diagnosis). These findings suggest that BMD independently predicts survival in HCC with PVTT and may enhance prognostic modeling and therapeutic decision-making.
肝细胞癌(HCC)是癌症相关死亡的第三大主要原因,门静脉肿瘤血栓形成(PVTT)是一种常见并发症,会显著恶化预后。最近的研究已将骨密度(BMD)确定为HCC患者的一个预后因素;然而,其在PVTT患者中的作用仍未得到探索。这项回顾性研究评估了2005年至2020年间接受治疗的462例HCC合并PVTT患者中BMD的预后价值。在HCC诊断和PVTT发病时,通过计算机断层扫描测量第一腰椎的衰减来测定BMD,使用既定的160亨氏单位(HU)阈值。Kaplan-Meier分析评估总生存期,并对既定的预后因素进行多变量Cox回归调整。HCC诊断时BMD的中位数为136 HU(IQR:113 - 160),PVTT发病时为134 HU(IQR:109 - 159)。BMD≥160 HU的患者在HCC诊断时(10.4个月对5.5个月,p < 0.001)和PVTT发病时(8.5个月对4.7个月,p < 0.001)均显示出显著更长的总生存期。在两个时间点的多变量分析中,BMD仍然是生存的独立预测因素,与肿瘤生长模式﹑治疗方法和白蛋白-胆红素(ALBI)分级一起(甲胎蛋白仅在PVTT诊断时具有统计学意义)。这些发现表明,BMD独立预测HCC合并PVTT患者的生存情况,并可能增强预后模型和治疗决策。