Abstract
Purpose
To evaluate the prevalence and extension of macrovascular invasion (MaVI) in a large cohort of hepatocellular carcinoma (HCC) patients and analyze the association between MaVI and overall survival (OS).
Methods
From 2011 to 2018, 2540 patients with newly diagnosed HCC who were managed in our institution were enrolled in this retrospective study. Tumor invasion of the intrahepatic branches of the portal or hepatic veins was defined as peripheral MaVI. Tumor invasion of the main portal vein or inferior vena cava was defined as central MaVI.
Results
MaVI prevalence was 16.2% (n = 411). Among patients with Barcelona Clinic Liver Cancer (BCLC) stage C and Child–Pugh class A, 165 patients presented with peripheral MaVI and 89 patients with central MaVI. The median OS was 13.2 months (95% confidence interval [CI]: 11.4–15.4) in the peripheral MaVI group and 6.6 months (95% CI: 3.6–9.5) in the central MaVI group (p < 0.001). In patients with BCLC stage C and Child–Pugh class B or BCLC stage D, 68 patients presented with peripheral MaVI and 89 patients with central MaVI. The median OS was 3.6 months (95% CI: 3.1–4.2) in the peripheral MaVI group and 2.8 months (95% CI: 2.1–3.4) in the central MaVI group (p = 0.674).
Conclusion
The extension of MaVI significantly affected patient survival only in those with BCLC stage C and Child–Pugh class A. In patients with BCLC stage C and Child–Pugh class B or BCLC stage D, survival was poor irrespective of MaVI status.
Similar content being viewed by others
Data availability
All data is available.
References
Marrero JA, Kulik LM, Sirlin CB et al (2018) Diagnosis, Staging, and Management of Hepatocellular Carcinoma: 2018 Practice Guidance by the American Association for the Study of Liver Diseases. Hepatology 68:723–750. https://doi.org/10.1002/hep.29913
EASL Clinical Practice Guidelines (2018) Management of hepatocellular carcinoma. J Hepatol 69:182–236. https://doi.org/10.1016/j.jhep.2018.03.019
Diaz-Gonzalez A, Reig M, Bruix J (2016) Treatment of hepatocellular carcinoma. Dig Dis 34:597–602. https://doi.org/10.1159/000445275
Shi J, Lai ECH, Li N et al (2010) Surgical treatment of hepatocellular carcinoma with portal vein tumor thrombus. Ann Surg Oncol 17:2073–2080. https://doi.org/10.1245/s10434-010-0940-4
Lau WY, Sangro B, Chen PJ et al (2013) Treatment for hepatocellular carcinoma with portal vein tumor thrombosis: the emerging role for radioembolization using yttrium-90. Oncology 84:311–318. https://doi.org/10.1159/000348325
Pawlik TM, Poon RT, Abdalla EK et al (2005) Hepatectomy for hepatocellular carcinoma with major portal or hepatic vein invasion: results of a multicenter study. Surgery 137:403–410. https://doi.org/10.1016/j.surg.2004.12.012
Guarino M, Cucchetti A, Pontillo G, et al; ITA.LI.CA Group (2021). Pattern of macrovascular invasion in hepatocellular carcinoma. Eur J Clin Invest. Mar 23:e13542. https://doi.org/10.1111/eci.13542
Oken M, Creech R, Tormey D et al (1982) Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 5:649–655
Llovet JM, Burroughs A, Bruix J (2003) Hepatocellular carcinoma. Lancet 362:1907–1917. https://doi.org/10.1016/S0140-6736(03)14964-1
Abou-Alfa GK, Pawlik TM, Shindoh J, et al (2017) Liver. In: AJCC Cancer Staging Manual, 8th ed, Amin MB (Ed), AJCC, Chicago. 287
American Joint Committee on Cancer (2010) American Joint Committee on Cancer Staging Manual, 7th ed, Edge SB, Byrd DR, Compton CC, et al (Eds), Springer, New York. 175
Pugh RN, Murray-Lyon IM, Dawson JL et al (1973) Transection of the oesophagus for bleeding oesophageal varices. Br J Surg 60:646–649. https://doi.org/10.1002/bjs.1800600817
Llovet JM, Ducreux M, Lencioni R et al (2012) EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol 56:908–943. https://doi.org/10.1016/j.jhep.2011.12.001
Omata M, Lesmana LA, Tateishi R et al (2010) Asian Pacific Association for the Study of the Liver consensus recommendations on hepatocellular carcinoma. Hepatol Int 4:439–474. https://doi.org/10.1007/s12072-010-9165-7
Bruix J, Sherman M (2011) American Association for the Study of Liver Diseases. Management of hepatocellular carcinoma: an update. Hepatology 53:1020–2. https://doi.org/10.1002/hep.24199
Yau T, Tang VY, Yao TJ et al (2014) Development of Hong Kong Liver Cancer staging system with treatment stratification for patients with hepatocellular carcinoma. Gastroenterology 146:1691–1700. https://doi.org/10.1053/j.gastro.2014.02.032
Edmonson H, Steiner P (1954) Primary carcinoma of the liver: a study of 100 cases among 48,900 necropsies. Cancer 7:462–503. https://doi.org/10.1002/1097-0142(195405)7:3%3c462::aid-cncr2820070308%3e3.0.co;2-e
Everhart JE, Wright EC, Goodman ZD et al (2010) Prognostic value of Ishak fibrosis stage: findings from the hepatitis C antiviral long-term treatment against cirrhosis trial. Hepatology 51:585–594. https://doi.org/10.1002/hep.23315
Vitale A, Farinati F, Pawlik TM et al (2019) The concept of therapeutic hierarchy for patients with hepatocellular carcinoma: a multicenter cohort study. Liver Int 39:1478–1489. https://doi.org/10.1111/liv.14154
Surveillance group; Diagnosis group; Staging group; Surgery group; Local ablation group; TACE/TARE/HAI group; Target therapy/systemic therapy group; Radiotherapy group; Prevention group; Drafting group Collaborators (2018) Management consensus guideline for hepatocellular carcinoma: 2016 updated by the Taiwan Liver Cancer Association and the Gastroenterological Society of Taiwan. J Formos Med Assoc 117:381-403. https://doi.org/10.1016/j.jfma.2017.09.007
Kokudo T, Hasegawa K, Matsuyama Y, Liver Cancer Study Group of Japan et al (2017) Liver resection for hepatocellular carcinoma associated with hepatic vein invasion: a Japanese nationwide survey. Hepatology 66:510–517. https://doi.org/10.1002/hep.29225
Chen ZH, Wang K, Zhang XP et al (2020) A new classification for hepatocellular carcinoma with hepatic vein tumor thrombus. Hepatobiliary Surg Nutr 9:717–728. https://doi.org/10.21037/hbsn.2019.10.07
Williet N, Clavel L, Bourmaud A et al (2017) Tolerance and outcomes of sorafenib in elderly patients treated for advanced hepatocellular carcinoma. Dig Liver Dis 49:1043–1049. https://doi.org/10.1016/j.dld.2017.06.008
Serper M, Taddei TH, Mehta R, VOCAL Study Group et al (2017) Association of provider specialty and multidisciplinary care with hepatocellular carcinoma treatment and mortality. Gastroenterology 152:1954–1964. https://doi.org/10.1053/j.gastro.2017.02.040
Giannini EG, Bucci L, Garuti F, Italian Liver Cancer (ITA.LI.CA) group et al (2018) Patients with advanced hepatocellular carcinoma need a personalized management: a lesson from clinical practice. Hepatology 67:1784–1796. https://doi.org/10.1002/hep.29668
Kokudo T, Hasegawa K, Matsuyama Y, Liver Cancer Study Group of Japan et al (2016) Survival benefit of liver resection for hepatocellular carcinoma associated with portal vein invasion. J Hepatol 65:938–943. https://doi.org/10.1016/j.jhep.2016.05.044
Finn RS, Qin S, Ikeda M, IMbrave150 Investigators et al (2020) Atezolizumab plus bevacizumab in unresectable hepatocellular carcinoma. N Engl J Med 382:1894–1905. https://doi.org/10.1056/NEJMoa1915745
American College of Radiology. CT/MRI Liver imaging reporting and data system v2018 Core. https://www.acr.org/Clinical-Resources/Reporting-and-Data-Systems/LI-RADS/CT-MRI-LI-RADS-v2018. Accessed Oct 2019
Tabrizian P, Jibara G, Shrager B et al (2015) Recurrence of hepatocellular cancer after resection: patterns, treatments, and prognosis. Ann Surg 261:947–955. https://doi.org/10.1097/SLA.0000000000000710
Shindoh J, Kawamura Y, Kobayashi Y et al (2021) Prognostic impact of surgical intervention after lenvatinib treatment for advanced hepatocellular carcinoma. Ann Surg Oncol. https://doi.org/10.1245/s10434-021-09974-0
Yao FY, Mehta N, Flemming J et al (2015) Downstaging of hepatocellular cancer before liver transplant: long term outcome compared to tumors within Milan criteria. Hepatology 61:1968–1977
Acknowledgements
The authors thank the Cancer Center, Kaohsiung Chang Gung Memorial Hospital, for the provision of HCC registry data. The authors thank Chih-Yun Lin and Nien-Tzu Hsu and the Biostatistics Center, Kaohsiung Chang Gung Memorial Hospital, for statistical work.
Funding
This study was supported by a grant CMRPG8J1281 from the Chang Gung Memorial Hospital-Kaohsiung Medical Center, Taiwan.
Author information
Authors and Affiliations
Corresponding authors
Ethics declarations
Ethics approval and consent to participate
The Institutional Review Board of Kaohsiung Chang Gung Memorial Hospital approved this study (reference number: 202000398B0) and waived the need for informed consent.
Conflict of interest
The authors declare no competing interests.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
423_2021_2370_MOESM1_ESM.jpg
Supplementary file1 A 59-year-old man with HBV-related HCC. CT showed a 17-cm HCC over the right liver and tumor thrombus inside the IVC (arrow). (JPG 63 KB)
423_2021_2370_MOESM2_ESM.jpg
Supplementary file2 A 65-year-old man with type 2 diabetes. HBsAg and anti-HCV were both negative. Coronal view of CT showing an HCC in S7–8 (10 cm) with right hepatic vein tumor thrombosis (arrow). (JPG 77 KB)
423_2021_2370_MOESM3_ESM.jpg
Supplementary file3 A 57-year-old man with HCV-related HCC. CT showed ill-defined infiltrating HCC in the right liver lobe, 12.9 cm in size, with tumor thrombosis in the right portal vein (Arrow). (JPG 54 KB)
423_2021_2370_MOESM4_ESM.jpg
Supplementary file4 A 57-year-old man with HCV-related HCC. CT showed ill-defined infiltrating HCC in the right liver lobe, 12.9 cm in size, with tumor thrombosis in the main portal vein (arrow). (JPG 54 KB)
423_2021_2370_MOESM5_ESM.pdf
Supplementary file5 A flow chart of the patients with MaVI and applied treatments among patients with BCLC Stage C and D. (PDF 73 KB)
Supplementary File6
(PNG 9755 KB)
423_2021_2370_MOESM6_ESM.tif
High Resolution Image Overall survival of all patients according to the presence of only HVTT or only PVTT. (TIF 200 KB)
Supplementary File7
(PNG 9755 KB)
423_2021_2370_MOESM7_ESM.tif
High Resolution Image Overall survival of patients with BCLC Stage C and Child–Pugh Class A according to the presence of only HVTT or only PVTT. (TIF 196 KB)
Supplementary File8
(PNG 9755 KB)
423_2021_2370_MOESM8_ESM.tif
High Resolution Image Overall survival of patients with BCLC Stage C and Child–Pugh Class B or BCLC Stage D according to the presence of only HVTT or only PVTT. (TIF 190 KB)
Supplementary File9
(PNG 6539 KB)
Supplementary File10
(PNG 6539 KB)
Supplementary File11
(PNG 6539 KB)
Supplementary File12
(PNG 6539 KB)
423_2021_2370_MOESM12_ESM.tif
High Resolution Image Overall survival for patients according to tumor number determined by pathology examination (TIF 150 KB)
Supplementary File13
(PNG 6539 KB)
423_2021_2370_MOESM14_ESM.docx
Supplementary file14 Comparison of the clinicopathologic features between patients undergoing LR with the pathology-confirmed absence of MaVI and those with pathology-confirmed peripheral MaVI (DOCX 20 KB)
Rights and permissions
About this article
Cite this article
Yen, YH., Li, WF., Kee, KM. et al. The characteristics of patients with macrovascular invasion in hepatocellular carcinoma: when East meets West. Langenbecks Arch Surg 407, 225–234 (2022). https://doi.org/10.1007/s00423-021-02370-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00423-021-02370-y