Department of Pathology, Humanitas Clinical and Research Center, Rozzano, Italy.
Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hepatology. 2020 Jan;71(1):183-195. doi: 10.1002/hep.30814. Epub 2019 Aug 9.
We investigated the clinical significance of a vascular growth pattern of hepatocellular carcinoma (HCC), the vessels that encapsulate tumor clusters (VETC), previously linked to HCC metastatic dissemination. VETC was assessed in a large multi-institutional cohort of 541 resected HCCs from Italy, Korea and Japan, and matched against a full spectrum of clinical and pathological variables. The VETC phenotype (defined as ≥ 55% tumor area by CD34 immunostaining) was easily reproducible and reliably detectable in whole sections and small-sized tissues of tissue microarray. VETC HCCs represented 18.9% of the whole series, the lowest proportion occurring in the cohort with smallest tumors (8.7%, Japanese series). VETC was significantly associated with several clinical and pathological features such as high alfa-fetoprotein (AFP) level, tumor size greater than 5 cm, poor differentiation, macrotrabecular pattern, less compact pattern, less inflammatory infiltrates, and frequent microvascular invasion. VETC was associated with early recurrence (hazard ratio [HR]: 1.52 [1.06-2.19], P = 0.023), disease-free survival (HR: 1.66 [1.21-2.27], P = 0.002), and overall survival (HR: 2.26 [1.37-3.72], P = 0.001) at multivariable analysis. VETC affected the survival in HCC patients stratified for etiology (hepatitis C virus/hepatitis B virus), vascular invasion, and specific molecular phenotypes (β-catenin/GS+). This distinct vascular pattern was enriched in the recently reported macrotrabecular massive HCC subtype, which was seen in 7.8% (42 of 541) of patients and associated with high AFP levels and poor differentiation. Conclusion: The VETC pattern was found to be easily detectable in a consistent fraction of HCC and a powerful pathological finding affecting survival. This study suggests that the heterogeneous pattern of angiogenesis is involved in HCC behavior.
我们研究了一种与肝细胞癌(HCC)转移扩散相关的血管生长模式,即包裹肿瘤簇的血管(VETC),此前已将其与 HCC 转移扩散联系起来。我们在一个由来自意大利、韩国和日本的 541 例 HCC 患者组成的大型多机构队列中评估了 VETC,并与一系列全面的临床和病理变量进行了匹配。VETC 表型(定义为 CD34 免疫染色的肿瘤面积≥55%)在整个切片和组织微阵列的小组织中易于重现和可靠检测。VETC HCC 占整个系列的 18.9%,在肿瘤最小的队列中(日本系列为 8.7%)比例最低。VETC 与多种临床和病理特征显著相关,如高甲胎蛋白(AFP)水平、肿瘤大小大于 5cm、分化差、大小梁模式、不太紧凑模式、炎症浸润较少和微血管侵犯频繁。VETC 与早期复发(风险比[HR]:1.52[1.06-2.19],P=0.023)、无病生存(HR:1.66[1.21-2.27],P=0.002)和总生存(HR:2.26[1.37-3.72],P=0.001)相关。多变量分析显示,VETC 影响病因(丙型肝炎病毒/乙型肝炎病毒)、血管侵犯和特定分子表型(β-连环蛋白/GS+)分层的 HCC 患者的生存。这种独特的血管模式在最近报道的大小梁巨块型 HCC 亚型中更为丰富,该亚型见于 541 例患者中的 7.8%(42 例),与高 AFP 水平和低分化相关。结论:VETC 模式在 HCC 中的一个一致比例中易于检测,是影响生存的有力病理发现。本研究表明,血管生成的异质性模式参与了 HCC 的行为。