- Open Access
Analysis of the recurrence risk factors for the patients with hepatocellular carcinoma meeting University of California San Francisco criteria after curative hepatectomy
© Soong et al; licensee BioMed Central Ltd. 2011
- Received: 31 October 2010
- Accepted: 27 January 2011
- Published: 27 January 2011
- Liver Transplantation
- Liver Resection
- Hepatic Resection
- Live Donor Liver Transplantation
- Donor Liver Transplantation
Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide, especially in the Asia pacific area . Liver transplantation is theoretically the best option because it cures both the tumor and the underlying liver disease. The overall survival rate at 5 years after liver transplantation was around 70-75%. In contrast, 5-year survival rates after liver resection were only 40% to 65%, and the 10-year survival rate was 29%. The high incidence of HCC recurrence following liver resection is a serious issue. The recurrent rate is as high as 50-60% at 3 years and 70-100% at 5 years. This high recurrent rate precludes long-term tumor-free survival of the patients with liver resection for HCC. However, liver transplantation is limited by a shortage of graft availability. Liver transplantation also has high perioperative risk, and long-term problems such as graft rejection and infections. Therefore, liver resection is still the primary selection treatment for many HCC patients, especially in areas lacking deceased liver.
Nevertheless, there is no doubt that for HCC, liver transplantation is a superior treatment option to liver resection, where long-term tumor-free survival is concerned. Adult-to-adult living donor liver transplantation is a well-established technique now. Liver transplantation for patients with HCC becomes feasible if a living donor wishes to donate part of the liver to save a member of the family. To optimize the benefit of living donor liver transplantation for HCC patients, the question of how to select the right patients to have liver transplantation is very important.
This study aims to identify the patients who accepted hepatectomy for a tumor/tumors and were within University of California San Francisco (UCSF) criteria, but had a poor 5-year disease-free survival rate (DFS). We analyze the pre-operative data of the patients and attempt to find the pre-operative risk factors of HCC recurrence. These risk factors could be indicators for clinical doctors to define and identify the patients with a high risk of tumor recurrence and to arrange liver transplantation rather than hepatectomy as the first treatment option.
After being discharged from the hospital, patients had regular follow-up checks at 2- to 3-month intervals. Liver function was tested and alfa-fetoprotein levels were measured at every visit. Abdominal ultrasonography was used for regular follow-up visits. If ultrasonography delivered a positive finding, liver dynamic computed tomography (CT) was used to define the nature of the tumor. Recurrence was defined as the presence of radiologically confirmed tumor by CT with/without elevation of AFP. If the CT finding was controversial, hepatic angiography and liver MRI was performed to confirm the nature of the tumor.
In group A, 302 cases developed early recurrence (≦1 yr), and 281 cases were late recurrence (>1 yr). In group B (n = 287) till last following up date (2009/6/30), there were 47 patients had recurrence (16.4%), the disease free interval ranged from 60.76 to 181.78 months.
The Chi-square or Fisher's Exact test was used to compare categorical variables as appropriate. Survival estimates were determined using Kaplan-Meier analysis; the results were compared by the log-rank test. Multivariate logistic regression analysis was used to identify independent factors associated with recurrence. For all statistical analysis, P < 0.05 was considered as significant. All statistical analysis was carried out using the Statistical Package for Social Science (SPSS13) for Windows.
Outcome of hepatectomy within UCSF criteria
Predictive factors for recurrence
Characteristics and Comparison of the two population study
DFS < 5 years
DFS ≧ 5 years
End-stage renal disease
≤ 5 cm
Pre-operative independent factors to predict tumor recurrence
independent risk factors in logstic regression
95% CI of odds ratio
The only therapies which are capable of providing cure for hepatocellular carcinoma patients are hepatic resection and liver transplantation. Despite the lack of a high-grade evidence base for either resection or transplantation, the result of these treatments provides 5-year survival rates of up to 70% in selected patients. These are clearly superior to the natural course of the disease [5–7]. Liver transplantation is theoretically the best resolution of HCC within UCSF criteria. Compared with patients under UCSF criteria undergoing liver transplantation, whose 5-year survival was 75%, our data revealed a 5-year survival rate of 56.8% for patients who underwent hepatectomy under the same criteria. The result is thus worse than for transplantation.
However, due to the problems of graft shortage, long waiting time, higher perioperative risk and long-term immunosupression, hepatectomy produces a considerable overall survival benefit for these patients. The major benefit of hepatic resection is that it can be performed without a waiting time. Furthermore, operative outcomes after hepatic resection have improved over recent decades in cirrhotic patients. The hospital mortality rate in experienced medical centers was less than 5% in selected patients. Similar to other series, we achieved a surgical mortality rate of 5.6%. Although hepatic resection is a safe therapeutic choice, the concern of the choice of hepatectomy in this group of patients is a higher risk of recurrence than transplantation.
The aims of this study were to find the recurrence risk factors for those patients with a tumor/tumors meeting UCSF criteria. This finding could assist both surgeon and patients in deciding whether they should immediately adopt primary liver transplantation. Those patients who did not have risk factors of recurrence could accept hepatectomy as their primary treatment. This may alleviate demand for liver graft or liver transplantation from living relatives. Furthermore, liver graft can be offered to high-risk group patients, so they don't need to explore salvage transplantation or drop out from the waiting list if they suffer recurrence or liver function deterioration. However, there has been some controversy regarding whether primary transplantation or salvage liver transplantation is the optimal treatment. Adam et al reported that primary liver transplantation is superior to salvage liver transplantation. Secondary liver transplantation has a poorer outcome, including higher mortality and morbidity, and higher recurrence than primary liver transplantation. However, Del Gaudio M. et al mentioned liver resection had a similar 5-year overall survival to primary liver transplantation under intention-to-treat analysis, although with an increased risk of recurrence in small HCC and well-compensated cirrhosis. Salvage transplantation is still a safe and effective approach in recurrent group.
Our data showed that liver function reserve was a key factor of early recurrence. AST > 34IU/L and albumin ≦ 3.5 were two important risk factors of recurrence. Chronic hepatitis is a key factor of liver cell mutation resulting in malignancy. Chronic hepatitis also influenced recurrence after hepatectomy. It has been reported that early tumor recurrence was related to cirrhosis, chronic active hepatitis and HCV positivity. In a large-scale multivariate analysis, the risk factors and outcome of early recurrence after resection of HCC included cirrhosis, hepatitis B/C, Child-Pugh score, transaminase level, albumin level, chronic active hepatitis. Patients with an elevated ALT level (>2× normal) had a risk not only of tumor recurrence, but also had a significantly higher risk of developing ascites and liver insufficiency. Therefore, primary liver transplantation for HCC patient with abnormal liver function may have clinical benefit.
Our data also showed that pre-operative AFP > 15 was an independent risk factor of recurrence. It has been reported that AFP was an independent prognostic indicator of overall survival and disease-free survival [10, 17, 18]. Vibert et al. mentioned that increasing AFP > 15 ng/ml/month while waiting for LT was the most relevant pre-operative prognostic factor for low overall and disease-free survival. AFP progression could be a pre-operative marker of tumor aggression . Therefore, primary liver transplantation may be considered for patients having AFP > 15 ng/ml. However, patients with both tumors >5 cm and serum AFP levels >1000 ng/mL had an 82% incidence of vascular invasion. Sakata, Shirai et al also reported that tumor sizes and serum AFP level, alone or in combination, were useful in predicting the presence or absence of vascular invasion before hepatectomy for HCC . Because vascular invasion was a poor prognostic factor of tumor recurrence both for hepatectomy and liver transplantation, liver transplantation for the patients with tumor size > 5 cm and marked elevation of AFP should be highly selected.
In almost all populations, HCC male/female prevalence ratio averaging between 2:1 and 4:1 was reported. A comprehensive review of literature revealed shortcomings associated with estrogen receptor (ER) and androgen receptor (AR) play an important role in normal liver and HCC. In our institution, male-to-female ratio is 3.6:1. The striking gender disparity is also the risk factor of recurrence after hepatectomy. Primary liver transplantation should be a treatment option for male patients.
In conclusion, hepatectomy or liver transplantation for HCC within UCSF criteria in deceased liver donor shortage areas is a difficult decision issue. In this study, male, AST > 34IU/L, albumin ≦ 3.5 g/dl, AFP > 15 ng/ml, tumor size >5 cm in diameter were the risk factors of tumor recurrence. For the patients without or with limited risk factors of tumor recurrence, hepatectomy rather than liver transplantation will be the first choice of treatment. For the patients with risk factors of tumor recurrence, primary liver transplantation rather than hepatectomy might be the option of treatment to achieve long-term disease-free survival although tumor recurrence can not be prevented completely.
Special thanks Mrs. Shu-fang Huang for data analysis and Mr. John Newman for language correction.
- Chuang SC, La Vecchia C, Boffetta P: Liver cancer: descriptive epidemiology and risk factors other than HBV and HCV infection. Cancer Letters. 2009, 286: 9-14. 10.1016/j.canlet.2008.10.040.View ArticlePubMedGoogle Scholar
- Hasegawa K, Kokudo N: Surgical treatment of hepatocellular carcinoma. Surgery Today. 2009, 39: 833-843. 10.1007/s00595-008-4024-z.View ArticlePubMedGoogle Scholar
- Park YK, Kim BW, Wang HJ, Kim MW: Hepatic resection for hepatocellular carcinoma meeting Milan criteria in Child-Turcotte-Pugh class a patients with cirrhosis. Transplantation Proceedings. 2009, 41: 1691-1697. 10.1016/j.transproceed.2008.07.146.View ArticlePubMedGoogle Scholar
- Yao FY: Liver transplantation for hepatocellular carcinoma: beyond the Milan criteria. American Journal of Transplantation. 2008, 8: 1982-1989. 10.1111/j.1600-6143.2008.02351.x.View ArticlePubMedGoogle Scholar
- Morris-Stiff G, Gomez D, de Liguori Carino N, Prasad KR: Surgical management of hepatocellular carcinoma: is the jury still out?. Surgical Oncology. 2009, 18: 298-321. 10.1016/j.suronc.2008.08.003.View ArticlePubMedGoogle Scholar
- Dawe RS: Hepatocellular carcinoma. Lancet. 2004, 363: 899-10.1016/S0140-6736(04)15751-6.View ArticlePubMedGoogle Scholar
- Baccarani U, Benzoni E, Adani GL, Avellini C, Lorenzin D, Sainz-Barriga M, Bresadola V, Uzzau A, Risaliti A, Beltrami CA, Bresadola F: Superiority of transplantation versus resection for the treatment of small hepatocellular carcinoma. Transplantation Proceedings. 2007, 39: 1898-1900. 10.1016/j.transproceed.2007.05.045.View ArticlePubMedGoogle Scholar
- Tanwar S, Khan SA, Grover VPB, Gwilt C, Smith B, Brown A: Liver transplantation for hepatocellular carcinoma. World Journal of Gastroenterology. 2009, 15: 5511-5516. 10.3748/wjg.15.5511.PubMed CentralView ArticlePubMedGoogle Scholar
- Yi NJ, Suh KS, Kim T, Kim J, Shin WY, Lee KU: Current role of surgery in treatment of early stage hepatocellular carcinoma: resection versus liver transplantation. Oncology. 2008, 75 (Suppl 1): 124-128. 10.1159/000173434.View ArticlePubMedGoogle Scholar
- Fong Y, Sun RL, Jarnagin W, Blumgart LH: An analysis of 412 cases of hepatocellular carcinoma at a Western center. Annals of Surgery. 1999, 229: 790-799. 10.1097/00000658-199906000-00005. discussion 799-800PubMed CentralView ArticlePubMedGoogle Scholar
- Tanaka S, Noguchi N, Ochiai T, Kudo A, Nakamura N, Ito K, Kawamura T, Teramoto K, Arii S: Outcomes and recurrence of initially resectable hepatocellular carcinoma meeting milan criteria: Rationale for partial hepatectomy as first strategy. Journal of the American College of Surgeons. 2007, 204: 1-6. 10.1016/j.jamcollsurg.2006.10.004.View ArticlePubMedGoogle Scholar
- Del Gaudio M, Ercolani G, Ravaioli M, Cescon M, Lauro A, Vivarelli M, Zanello M, Cucchetti A, Vetrone G, Tuci F: Liver transplantation for recurrent hepatocellular carcinoma on cirrhosis after liver resection: University of Bologna experience. American Journal of Transplantation. 2008, 8: 1177-1185. 10.1111/j.1600-6143.2008.02229.x.View ArticlePubMedGoogle Scholar
- Wakai T, Shirai Y, Yokoyama N, Nagakura S, Hatakeyama K: Hepatitis viral status affects the pattern of intrahepatic recurrence after resection for hepatocellular carcinoma. European Journal of Surgical Oncology. 2003, 29: 266-271. 10.1053/ejso.2002.1395.View ArticlePubMedGoogle Scholar
- Portolani N, Coniglio A, Ghidoni S, Giovanelli M, Benetti A, Tiberio GAM, Giulini SM: Early and late recurrence after liver resection for hepatocellular carcinoma: prognostic and therapeutic implications. Annals of Surgery. 2006, 243: 229-235. 10.1097/01.sla.0000197706.21803.a1.PubMed CentralView ArticlePubMedGoogle Scholar
- Bigourdan JM, Jaeck D, Meyer N, Meyer C, Oussoultzoglou E, Bachellier P, Weber JC, Audet M, Doffoel M, Wolf P: Small hepatocellular carcinoma in Child A cirrhotic patients: hepatic resection versus transplantation. Liver Transplantation. 2003, 9: 513-520. 10.1053/jlts.2003.50070.View ArticlePubMedGoogle Scholar
- Cunningham SC, Tsai S, Marques HP, Mira P, Cameron A, Barroso E, Philosophe B, Pawlik TM: Management of early hepatocellular carcinoma in patients with well-compensated cirrhosis. Annals of Surgical Oncology. 2009, 16: 1820-1831. 10.1245/s10434-009-0364-1.View ArticlePubMedGoogle Scholar
- Ikai I, Arii S, Kojiro M, Ichida T, Makuuchi M, Matsuyama Y, Nakanuma Y, Okita K, Omata M, Takayasu K, Yamaoka Y: Reevaluation of prognostic factors for survival after liver resection in patients with hepatocellular carcinoma in a Japanese nationwide survey. Cancer. 2004, 101: 796-802. 10.1002/cncr.20426.View ArticlePubMedGoogle Scholar
- Wu CC, Cheng SB, Ho WM, Chen JT, Liu TJ, P'Eng FK: Liver resection for hepatocellular carcinoma in patients with cirrhosis. British Journal of Surgery. 2005, 92: 348-355. 10.1002/bjs.4838.View ArticlePubMedGoogle Scholar
- Vibert E, Azoulay D, Hoti E, Iacopinelli S, Samuel D, Salloum C, Lemoine A, Bismuth H, Castaing D, Adam R: Progression of alphafetoprotein before liver transplantation for hepatocellular carcinoma in cirrhotic patients: a critical factor. American Journal of Transplantation. 2010, 10: 129-137. 10.1111/j.1600-6143.2009.02750.x.View ArticlePubMedGoogle Scholar
- Sakata J, Shirai Y, Wakai T, Kaneko K, Nagahashi M, Hatakeyama K: Preoperative predictors of vascular invasion in hepatocellular carcinoma. European Journal of Surgical Oncology. 2008, 34: 900-905. 10.1016/j.ejso.2008.01.031.View ArticlePubMedGoogle Scholar
- Ruggieri A, Barbati C, Malorni W: Cellular and molecular mechanisms involved in hepatocellular carcinoma gender disparity. International Journal of Cancer. 2010, 127: 499-504. 10.1002/ijc.25298.View ArticleGoogle Scholar
- Kalra M, Mayes J, Assefa S, Kaul AK, Kaul R: Role of sex steroid receptors in pathobiology of hepatocellular carcinoma. World Journal of Gastroenterology. 2008, 14: 5945-5961. 10.3748/wjg.14.5945.PubMed CentralView ArticlePubMedGoogle Scholar
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