Skip to main content
Log in

Liver Resection Is Justified in Patients with BCLC Intermediate Stage Hepatocellular Carcinoma without Microvascular Invasion

  • Original Article
  • Published:
Journal of Gastrointestinal Surgery Aims and scope

Abstract

Background

Large, multinodular (> 3 nodules and/or > 3 cm) hepatocellular carcinoma (HCC) is not an indication for liver resection based on the Barcelona Clinic Liver Cancer (BCLC) staging classification. We hypothesize that microvascular invasion (MVI) is a strong indication for surgery in these patients.

Methods

Between December 2009 and December 2010, a retrospective cohort of the patients with BCLC intermediate stage HCC undergoing surgical resection at Eastern Hepatobiliary Surgery Hospital was analyzed. Propensity score matching (PSM) was conducted to balance the patients with regard to their baseline characteristics. Survival analysis was performed according to the Kaplan–Meier method. Logistic regression was conducted to identify the predictors of MVI. Risk factors were evaluated using the Cox proportional hazards model.

Results

Among 323 patients, the MVI-negative group (26.0%) had a more favorable prognosis than did the MVI-positive group (5-year recurrence-free survival: 25.2% vs. 7.8%; 5-year overall survival: 49.5% vs. 24.0%). Similar results were identified after PSM. Compared with MVI-negative patients, MVI-positive patients experienced more early recurrence (< 2 years, P = 0.006), multinodular recurrence (P = 0.004), and extrahepatic recurrence (P = 0.026). Total bilirubin levels > 17.1 μmol/L, alpha fetal protein levels > 400 ng/mL, the presence of > 2 nodules, and the lack of a capsule were independent predictors of MVI.

Conclusions

In BCLC intermediate stage HCC, MVI predicted an adverse recurrence pattern and poor prognosis and has the potential to be used as a reference index when deciding whether to operate. Factors predictive of MVI could assist in choosing preoperative treatment and postoperative surveillance.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Abbreviations

HCC:

Hepatocellular carcinoma

BCLC:

Barcelona Clinic Liver Cancer

MVI:

Microvascular invasion

PSM:

Propensity score matching

AASLD:

American Association for the Study of Liver Diseases

EASL:

European Association for the Study of the Liver

MHCC:

Multiple nodular HCC

TACE:

Transarterial chemoembolization

IM:

Intrahepatic metastasis

MO:

Multicentric occurrence

ECOG:

Eastern Cooperative Oncology Group

AFP:

Alpha fetal protein

RFS:

Recurrence-free survival

OS:

Overall survival

TBIL:

Total bilirubin

ALB:

Albumin

RBC:

Red blood cell

HR:

Hazard ratio

CI:

Confidence interval

OR:

Odds ratio

References

  1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. 2018;68(1):7–30. doi:https://doi.org/10.3322/caac.21442.

  2. Islami F, Miller KD, Siegel RL, Fedewa SA, Ward EM, Jemal A. Disparities in liver cancer occurrence in the United States by race/ethnicity and state. CA: a cancer journal for clinicians. 2017;67(4):273–89. doi:https://doi.org/10.3322/caac.21402.

    Article  Google Scholar 

  3. Lu LC, Cheng AL, Poon RT. Recent advances in the prevention of hepatocellular carcinoma recurrence. Semin Liver Dis. 2014;34(4):427–34. doi:https://doi.org/10.1055/s-0034-1394141.

    Article  PubMed  Google Scholar 

  4. Colecchia A, Schiumerini R, Cucchetti A, Cescon M, Taddia M, Marasco G et al. Prognostic factors for hepatocellular carcinoma recurrence. World Journal of gastroenterology. 2014;20(20):5935–50. doi:https://doi.org/10.3748/wjg.v20.i20.5935.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Llovet JM, Bru C, Bruix J. Prognosis of hepatocellular carcinoma: the BCLC staging classification. Semin Liver Dis. 1999;19(3):329–38. doi:https://doi.org/10.1055/s-2007-1007122.

    Article  CAS  PubMed  Google Scholar 

  6. Heimbach JK, Kulik LM, Finn RS, Sirlin CB, Abecassis MM, Roberts LR et al. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology (Baltimore, Md). 2018;67(1):358–80. doi:https://doi.org/10.1002/hep.29086.

    Article  Google Scholar 

  7. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. Journal of hepatology. 2018;69(1):182–236. doi:https://doi.org/10.1016/j.jhep.2018.03.019.

    Article  Google Scholar 

  8. Forner A, Reig M, Bruix J. Hepatocellular carcinoma. Lancet (London, England). 2018;391(10127):1301–14. doi:https://doi.org/10.1016/s0140-6736(18)30010-2.

    Article  Google Scholar 

  9. Yang B, Zheng B, Yang M, Zeng Z, Yang F, Pu J et al. Liver resection versus transarterial chemoembolization for the initial treatment of Barcelona Clinic Liver Cancer stage B hepatocellular carcinoma. 2018. doi:https://doi.org/10.1007/s12072-018-9888-4.

  10. Liang L, Xing H, Zhang H, Zhong J, Li C, Lau WY et al. Surgical resection versus transarterial chemoembolization for BCLC intermediate stage hepatocellular carcinoma: a systematic review and meta-analysis. HPB : the official journal of the International Hepato Pancreato Biliary Association. 2018;20(2):110–9. doi:https://doi.org/10.1016/j.hpb.2017.10.004.

    Article  Google Scholar 

  11. Gehrau R, Mas V, Archer KJ, Maluf D. Molecular classification and clonal differentiation of hepatocellular carcinoma: the step forward for patient selection for liver transplantation. Expert review of gastroenterology & hepatology. 2011;5(4):539–52. doi:https://doi.org/10.1586/egh.11.48.

    Article  CAS  Google Scholar 

  12. Cong WM, Wu MC. New insights into molecular diagnostic pathology of primary liver cancer: Advances and challenges. Cancer letters. 2015;368(1):14–9. doi:https://doi.org/10.1016/j.canlet.2015.07.043.

    Article  CAS  PubMed  Google Scholar 

  13. Kim JM, Kwon CH, Joh JW, Park JB, Lee JH, Kim SJ et al. Intrahepatic metastasis is more risky than multiple occurrence in hepatocellular carcinoma patients after curative liver resection. Hepato-gastroenterology. 2015;62(138):399–404.

    CAS  PubMed  Google Scholar 

  14. Cong WM, Bu H, Chen J, Dong H, Zhu YY, Feng LH et al. Practice guidelines for the pathological diagnosis of primary liver cancer: 2015 update. World journal of gastroenterology. 2016;22(42):9279–87. doi:https://doi.org/10.3748/wjg.v22.i42.9279.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Wang H, Wu MC, Cong WM. Microvascular invasion predicts a poor prognosis of solitary hepatocellular carcinoma up to 2 cm based on propensity score matching analysis. Hepatology research. 2019;49:344–54. doi:https://doi.org/10.1111/hepr.13241.

  16. Rubin DB, Thomas N. Matching using estimated propensity scores: relating theory to practice. Biometrics. 1996;52(1):249–64.

    Article  CAS  Google Scholar 

  17. Hyun MH, Lee YS. Hepatic resection compared to chemoembolization in intermediate- to advanced-stage hepatocellular carcinoma: A meta-analysis of high-quality studies. 2018. doi:https://doi.org/10.1002/hep.29883.

  18. Guo H, Wu T, Lu Q, Li M, Guo JY, Shen Y et al. Surgical resection improves long-term survival of patients with hepatocellular carcinoma across different Barcelona Clinic Liver Cancer stages. Cancer management and research. 2018;10:361–9. doi:https://doi.org/10.2147/cmar.s152707.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Zhang W, Liu C, Tan Y, Jiang L, Yan L, Yang J et al. Role of liver resection in treating intermediate and advanced stage adolescent and young adult hepatocellular carcinoma patients: A propensity-matching cohort study. International journal of surgery (London, England). 2018;54(Pt A):259–64. doi:https://doi.org/10.1016/j.ijsu.2018.03.051.

    Article  Google Scholar 

  20. Forner A, Gilabert M, Bruix J, Raoul JL. Intermediate-stage HCC--upfront resection can be feasible. Nature reviews Clinical oncology. 2015;12(5). doi:https://doi.org/10.1038/nrclinonc.2014.122-c4.

  21. Zhong J-H, Lu S-D, Wang Y-Y, Ma L, Li L-Q. Intermediate-stage HCC—upfront resection can be feasible. Nature Reviews Clinical Oncology. 2015;12:295. doi:https://doi.org/10.1038/nrclinonc.2014.122-c3.

    Article  Google Scholar 

  22. Bolondi L, Burroughs A, Dufour JF, Galle PR, Mazzaferro V, Piscaglia F et al. Heterogeneity of patients with intermediate (BCLC B) Hepatocellular Carcinoma: proposal for a subclassification to facilitate treatment decisions. Semin Liver Dis. 2012;32(4):348–59. doi:https://doi.org/10.1055/s-0032-1329906.

    Article  CAS  PubMed  Google Scholar 

  23. Hiraoka A, Kumada T, Nouso K, Tsuji K, Itobayashi E, Hirooka M et al. Proposed New Sub-Grouping for Intermediate-Stage Hepatocellular Carcinoma Using Albumin-Bilirubin Grade. Oncology. 2016;91(3):153–61. doi:https://doi.org/10.1159/000447061.

    Article  CAS  PubMed  Google Scholar 

  24. Kimura H, Ohkawa K, Miyazaki M, Sakakibara M, Imanaka K, Tamura T et al. Subclassification of patients with intermediate-stage (Barcelona Clinic Liver Cancer stage-B) hepatocellular carcinoma using the up-to-seven criteria and serum tumor markers. Hepatology international. 2017;11(1):105–14. doi:https://doi.org/10.1007/s12072-016-9771-0.

    Article  PubMed  Google Scholar 

  25. Wei WX, Yang ZS, Lu LH, Li J, Lei ZQ, Wang K et al. Long-term survival after partial hepatectomy for sub-stage patients with intermediate stage hepatocellular carcinoma. International journal of surgery (London, England). 2018;56:256–63. doi:https://doi.org/10.1016/j.ijsu.2018.06.020.

    Article  Google Scholar 

  26. Wada H, Eguchi H, Noda T, Ogawa H, Yamada D, Tomimaru Y et al. Selection criteria for hepatic resection in intermediate-stage (BCLC stage B) multiple hepatocellular carcinoma. Surgery. 2016;160(5):1227–35. doi:https://doi.org/10.1016/j.surg.2016.05.023.

    Article  PubMed  Google Scholar 

  27. Nomoto S, Hishida M, Inokawa Y, Sugimoto H, Kodera Y. Management of hepatocellular carcinoma should consider both tumor factors and background liver factors. Hepatobiliary surgery and nutrition. 2014;3(2):82–5. doi:https://doi.org/10.3978/j.issn.2304-3881.2014.02.13.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Gao Q, Wang XY, Zhou J, Fan J. Multiple carcinogenesis contributes to the heterogeneity of HCC. Nature reviews Gastroenterology & hepatology. 2015;12(1):13. doi:https://doi.org/10.1038/nrgastro.2014.6-c1.

    Article  Google Scholar 

  29. Oikawa T, Ojima H, Yamasaki S, Takayama T, Hirohashi S, Sakamoto M. Multistep and multicentric development of hepatocellular carcinoma: histological analysis of 980 resected nodules. Journal of hepatology. 2005;42(2):225–9.

    Article  Google Scholar 

  30. Wang B, Xia CY, Lau WY, Lu XY, Dong H, Yu WL et al. Determination of clonal origin of recurrent hepatocellular carcinoma for personalized therapy and outcomes evaluation: a new strategy for hepatic surgery. Journal of the American College of Surgeons. 2013;217(6):1054–62. doi:https://doi.org/10.1016/j.jamcollsurg.2013.07.402.

    Article  PubMed  Google Scholar 

  31. Wang Z, Gong W, Shou D, Zhang L, Gu X, Wang Y et al. Clonal Origin of Hepatocellular Carcinoma and Recurrence After Liver Transplantation. Annals of transplantation. 2016;21:484–90.

    Article  CAS  Google Scholar 

  32. Huang C, Zhu XD, Ji Y, Ding GY, Shi GM, Shen YH et al. Microvascular invasion has limited clinical values in hepatocellular carcinoma patients at Barcelona Clinic Liver Cancer (BCLC) stages 0 or B. BMC cancer. 2017;17(1):58. doi:https://doi.org/10.1186/s12885-017-3050-x.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Shen J, Wen J, Li C, Wen T, Yan L, Li B et al. The prognostic value of microvascular invasion in early-intermediate stage hepatocelluar carcinoma: a propensity score matching analysis. BMC cancer. 2018;18(1):278. doi:https://doi.org/10.1186/s12885-018-4196-x.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Lei Z, Li J, Wu D, Xia Y, Wang Q, Si A et al. Nomogram for Preoperative Estimation of Microvascular Invasion Risk in Hepatitis B Virus-Related Hepatocellular Carcinoma Within the Milan Criteria. JAMA surgery. 2016;151(4):356–63. doi:https://doi.org/10.1001/jamasurg.2015.4257.

    Article  PubMed  Google Scholar 

  35. Schlichtemeier SM, Pang TC, Williams NE, Gill AJ, Smith RC, Samra JS et al. A pre-operative clinical model to predict microvascular invasion and long-term outcome after resection of hepatocellular cancer: The Australian experience. European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. 2016;42(10):1576–83. doi:https://doi.org/10.1016/j.ejso.2016.05.032.

    Article  CAS  Google Scholar 

  36. Li H, Zhang J, Zheng Z, Guo Y, Chen M, Xie C et al. Preoperative histogram analysis of intravoxel incoherent motion (IVIM) for predicting microvascular invasion in patients with single hepatocellular carcinoma. European journal of radiology. 2018;105:65–71. doi:https://doi.org/10.1016/j.ejrad.2018.05.032.

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Hua Yu and Zhen-Ying Cao (Department of Pathology, Eastern Hepatobiliary Surgery Hospital, Shanghai) for their advice regarding the pathological techniques used in this study.

Funding

We received funding from the National Natural Science Foundation of China (Grant No. 81472278 and No. 8150101732), the Funds for Creative Research Groups of the National Natural Science Foundation of China (Grant No. 81521091), and the Scientific Research Foundation of the Shanghai Municipal Commission of Health and Family Planning (Grant No. 20154Y0140) for this study.

Author information

Authors and Affiliations

Authors

Contributions

Conception: Wen-Ming Cong; study design: Wen-Ming Cong, Han Wang; administrative support: Meng-Chao Wu; data collection and acquisition: Han Wang, You-Wen Qian; data analysis: Han Wang; manuscript preparation: Han Wang, You-Wen Qian, Wen-Ming Cong; critical revision: Wen-Ming Cong; final approval of manuscript: all authors.

Corresponding author

Correspondence to Wen-Ming Cong.

Ethics declarations

Conflict of Interest

The authors declare that they have no conflict of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Supplementary Fig. 1

Cumulative overall survival after the first recurrence in patients with and without microvascular invasion (PNG 230 kb)

High resolution image (TIF 1210 kb)

Supplementary Fig. 2

Cumulative early recurrence-free survival (2A) and late recurrence-free survival (2B) in patients with and without microvascular invasion (PNG 293 kb)

High resolution image (TIF 1504 kb)

Supplementary Fig. 3

Cumulative recurrence-free survival (3A) and overall survival (3B) in patients with different degrees of risk for microvascular invasion (PNG 493 kb)

High resolution image (TIF 1616 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wang, H., Qian, YW., Wu, MC. et al. Liver Resection Is Justified in Patients with BCLC Intermediate Stage Hepatocellular Carcinoma without Microvascular Invasion. J Gastrointest Surg 24, 2737–2747 (2020). https://doi.org/10.1007/s11605-019-04251-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11605-019-04251-8

Keywords

Navigation