Skip Navigation
Skip to contents

Cancer Res Treat : Cancer Research and Treatment

OPEN ACCESS

Articles

Page Path
HOME > Cancer Res Treat > Volume 51(1); 2019 > Article
Original Article Hepatic Resection Provides Survival Benefit for Selected Intermediate-Stage (BCLC-B) Hepatocellular Carcinoma Patients
Zhang Zhaohui, MD, Shen Shunli, PhD, Chen Bin, PhD, Li Shaoqiang, PhD, Hua Yunpeng, PhD, Kuang Ming, PhD, Liang Lijian, PhD, Peng Bao Gang, PhD
Cancer Research and Treatment : Official Journal of Korean Cancer Association 2019;51(1):65-72.
DOI: https://doi.org/10.4143/crt.2018.038
Published online: February 26, 2018

Department of Hepatic Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China

Correspondence: Peng Bao Gang, PhD Department of Hepatic Surgery, First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China
Tel: 86-20-87755766-8214 Fax: 86-20-87755766-8663 E-mail: pengbaogang@medmail.com.cn
*Zhang Zhaohui and Shen Shunli contributed equally to this work.
• Received: January 12, 2018   • Accepted: February 20, 2018

Copyright © 2019 by the Korean Cancer Association

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

  • 8,603 Views
  • 371 Download
  • 19 Web of Science
  • 18 Crossref
  • 21 Scopus
prev next
  • Purpose
    The intermediate stage of hepatocellular carcinoma (HCC) (Barcelona Clinic Liver Cancer [BCLC] B) comprises a highly heterogeneous population, and the treatment strategy is still controversial. Because of the heterogeneity, a subclassification of intermediate-stage HCCs was put forward by Bolondi according to the ‘beyond Milan and within up-to-7’ criteria and Child-Pugh score. In this study, we aim to analyze the prognosis of BCLC-B stage HCC patients who received hepatic resection according to the Bolondi’s subclassification.
  • Materials and Methods
    One thousand and one hundred three patients diagnosedwith HCC and treatedwith hepatic resectionwere enrolled in our hospital between 2006 and 2012. According to Bolondi’s subclassification, the BCLC-B patients were divided into four groups. Recurrence-free survival (RFS) and overall survival (OS) were analyzed.
  • Results
    According to Bolondi’s subclassification, the BCLC-B patients were divided into four groups: B1 (n=41, 18.7%), B2 (n=160, 73.1%), B3 (n=11, 5.0%), and B4 (n=7, 3.2%). Significant difference was observed between B1 and other groups (B1 vs. B2, p=0.022; B1 vs. B3, p < 0.001; B1 vs. B4, p < 0.001), but no difference for B2 vs. B4 (p=0.542) and B3 vs. B4 (p=0.542). In addition, no significant differences were observed between BCLC-A and BCLC-B1 group for both RFS (p=0.087) and OS (p=0.643). In multivariate analysis, BCLC-B subclassification was not a risk factor for both OS (p=0.263) and RFS (p=0.892).
  • Conclusion
    In our study, HCC patients at B1 stagewere benefited from hepatic resection and had similar survival to BCLC-A stage patients. Our study provided rationality of hepatic resection for selected BCLC-B stage HCC patients instead of routine transarterial chemoembolization.
Hepatocellular carcinoma (HCC) is the fifth most prevalent neoplasm and the third most frequent cause of cancer mortality in the world [1]. Despite improvements in diagnosis and treatment of surgical techniques and perioperative care, the prognosis of HCC remains far from satisfactory [2].
The Barcelona Clinic Liver Cancer (BCLC) system is widely used for prognosis prediction and treatment strategy selection [3,4]. According to the criteria, hepatic resection and liver transplantation are recommended for early stage tumors (stage 0 and stage A), while patients on intermediate-stage are only suitable for palliative treatment, like transarterial chemoembolization (TACE). However, the intermediate stage of HCC (BCLC stage B) comprises a highly heterogeneous population, and the treatment strategy is still controversial [5].
According to the BCLC staging system, the hepatic resection should not be recommended to the patients with BCLC-B patients, while retrospective studies have demonstrated that hepatic resection is superior to palliative treatments (TACE) for BCLC-B patients [6,7]. A research group in Italy analyzed the treatment selection and prognosis of 405 HCC cases in the BCLC stage B by the Italian Liver Cancer group [8]. Only 40% of HCC cases in the BCLC stage B underwent TACE. However, TACE couldn’t obviously prolong overall survival (OS) than hepatic resection (median survival, 27 months vs. 37 months). Similarly, Vitale et al. [9] conducted a retrospective study involving 2090 HCC cases in the different BCLC stage patients who were enrolled between 2000 and 2012 by the Italian Liver Cancer group. They revealed that BCLC-B patients may benefit most from hepatic resection than non-surgical treatments. The focus of disputes is the heterogeneity of BCLC-B patients over tumor load, age, liver function, and possible comorbidities.
Because of the heterogeneity, a subclassification of intermediate-stage HCCs was put forward by Bolondi et al. [10] in 2012 according to the ‘beyond Milan and within up-to-7’ criteria, Child-Pugh score, patient’s performance status (tumor-related) and portal vein thrombosis. The novel concept divided the BCLC-B patients into four subgroups (Table 1). Different from the recommendation of classical BCLC staging system, this system recommends liver transplantation or hepatic resection as the first treatment option for B1 patients. It recommends sorafenib or TACE for B2-B4 patients, which is consistent with the classical BCLC staging system. However, the usefulness of the subclassification of BCLC-B is also controversial. Weinmann et al. [11] analyzed 254 BCLC-B patients receiving TACE. The median OS for stage B1-B4 were 28.5, 22.8, 12.3, and 5.9 months, but the log-rank test showed no significant survival differences in subclassification. On the contrary, another study conducted by Giannini et al. [12] assessed the prognosis of 269 untreated HCC patients observed in the period 1987-2012. They found the median survival progressively decreased from stage B1 (25 months) through stages B2 (16 months) and B3 (9 months), to stage B4 (5 months, p < 0.001) and a significantly different survival between contiguous stages. Furthermore, a recent study reported a modified Bolondi's subclassification system (Kinki criteria) [13] combining B2 and B3 group, but no more studies verified the effectiveness of Kinki criteria.
In this study, we aim to analyze the prognosis of BCLC-B stage HCC patients who received hepatic resection according to the Bolondi’s subclassification and explore the rationality of hepatic resection for BCLC-B HCC patients.
1. Study population
Patients diagnosed with HCC and received hepatectomy were enrolled in our hospital between 2006 and 2012. The final diagnosis of HCC was confirmed by pathological examination of the specimen. All patients were > 18 years of age, with complete clinical and laboratory data. We collected the clinicopathological variables including sex, age, hepatitis B surface antigen (HBsAg), α-fetoprotein (AFP), capsulation, lymphatic metastasis, tumor size. As for platelet count, we used the standard of 150/mm3 as the cutoff value [14,15]. The following criteria were considered to help diagnose HCC : a history of chronic hepatitis,the imaging tests (computed tomography [CT] or magnetic resonance imaging scan of the abdomen) and the level of AFP. The exclusion criteria were as follows: (1) patients with mixed HCC and cholangiocarcinoma; (2) patients with no follow-up data; and (3) patients receiving TACE or Sorafenib before or after operation.
2. Subclassification of BCLC-B stage
Patients were divided into three groups: BCLC-A, BCLC-B, and BCLC-C according to the American Association for the Study of the Liver Guidelines (AASLD) [16]. And patients with Child-Pugh A and B liver function, multifocal HCC (two to three tumors > 3 cm in maximal diameter or more than three tumors regardless of size) and lacking of vascular invasion comprise the intermediate-stage disease (BCLC-B) [10]. Furthermore, a novel classification system proposed by Bolondi divided the BCLC-B patients into four subgroups from B1 to B4 (Table 1).
In terms of the modified Bolondi's subclassification system, the subclasses B1, B2, and B3 refer to Child-Pugh scores of 5-7 points and ‘in’ in terms of the ‘up-to-7’ criteria; subclass B2 refers to Child-Pugh scores of 5-7 points with ‘out’ of the ‘up-to-7’ criteria, and subclass B3 refers to Child-Pugh scores of 8-9 points with either ‘in’ or ‘out’ of the ‘up-to-7’ criteria, respectively.
3. Surgical procedures
Hepatic resection, including subsegmentectomy, segmentectomy, bisegmentectomy, trisegmentectomy, right trisectionectomy, right hepatectomy, and left hepatectomy, was performed as proposed by the Committee of the International Hepato-Pancreato-Biliary Association of Brisbane 2000 system [17]. Tumor thrombectomy or combined diaphragmatic resection was performed when necessary.
4. Follow-up
Patients were regularly followed up at outpatient clinics. Patients received a physical examination, liver ultrasound, chest X-ray, and serum AFP test at each follow-up. Abdominal CT scan was performed every 6-12 months or when recurrence was suspected. Recurrence was defined as the emergence of clinical, radiological, and/or pathologic diagnosis of the tumor from a previous origin locally or distantly. Once recurrence was confirmed, salvage treatments, including further surgery, percutaneous ablation, or transcatheter arterial chemoembolization, were selected as needed.
5. Statistical analysis
Recurrence-free survival (RFS) was calculated from the date of surgery to the date of recurrence, and OS from the date of surgery to the date of HCC-associated death. Survival curves among groups were calculated by the Kaplan-Meier method. Univariate analysis of prognostic variables was performed by log-rank test and multivariate analysis by Cox proportional-hazards model. A p-values of < 0.05 was considered to be statistically significant. All statistical analyses were performed using package of rms in R ver. 2.14.1 (http://www.r-project.org/).
6. Ethical statement
Informed consent was obtained, and procedures were carried out with prior approval of the Ethics Committee of the First Affiliated Hospital of Sun Yat-sen University (Guangzhou, China).
1. Patients
A total of 1,103 patients were eligible for the study. The median age at diagnosis was 50 years (range, 21 to 79 years), and there were 970 men and 133 women. HBsAg was positive in 946 patients (85.7%). Increased AFP (≥ 400 ng/mL) was found in 560 cases (50.8%), and 299 patients (27.1%) had a low platelet count (< 150×109/L). And 718 patients (65.1%) had tumors larger than 5 cm. As to lymphatic metastasis, lymphatic metastasis was found in 73 patients (6.6%). Details of features are shown in Table 2. The follow-up time ranged from 4 to 131 months. Seventeen point six percent patients were lost to follow-up.
2. Survival according to BCLC-stage
The median RFS and OS were 12 months and 30 months. According to the BCLC stage, we classified the HCC patients into three stages: BCLC-A (n=530, 48.1%), BCLC-B (n=219, 19.9%), and BCLC-C (n=354, 32.1%). The median survival was 92 months in the BCLC-A, 30 months in BCLC-B, and 10 months in BCLC-C, respectively. Furthermore, the median RFS was 36 months in the BCLC-A, 9 months in BCLC-B, and 4 months in BCLC-C, respectively. A significant difference was observed between BCLC stage by log-rank test (p < 0.05) (Fig. 1A and B).
3. Bolondi’s subclassification
According to Bolondi’s subclassification, the BCLC-B patients were divided into four groups: B1 (n=41, 18.7%), B2 (n=160, 73.1%), B3 (n=11, 5.0%), and B4 (n=7, 3.2%). Most of the patients (n=201, 91.8%) were B1 group or B2 group. The median survival was 75 months, 28 months, 9.5 months, and 8 months for B1-B4 group. Results from the log-rank test showed that obvious difference was observed between B1 group and other groups (B1 vs. B2, p=0.022; B1 vs. B3, p < 0.001; B1 vs. B4, p < 0.001), but no difference for B2 vs. B4 (p=0.542), B3 vs. B4 (p=0.542), and B2 vs. B3 (p=0.645) (Fig. 2A).
In addition, the median RFS was 21 months, 8 months, 3 months and 4 months for B1-B4 groups. And results from the log-rank test showed significant survival differences for B1 vs. B2 (p=0.041) and B1 vs. B3 (p=0.024), but no difference for the B2 vs. B3 (p=0.274) and B3 vs. B4 (p=0.483) (Fig. 2B).
In multivariate analysis, Bolondi’s subclassification had no significant effect for RFS (p=0.892) and OS (p=0.263). Tumor size was the only independent risk predictor of OS (hazard ratio [HR], 2.74; 95% confidence interval [95% CI], 1.58 to 4.74; p < 0.001) for BCLC-B patients. In addition, tumor size (HR, 2.31; 95% CI, 1.42 to 3.74; p=0.001) and sex (HR, 0.36; 95% CI, 0.15 to 0.82) were independent risk predictors p=0.015) for RFS (Table 3).
4. Modified Bolondi’s subclassification system (Kinki criteria)
The median OS for modified subclassification is 58 months, 14 months and 9 months, and the median RFS is 29 months, 5 months and 3 months. Although obvious difference was observed between B1 and other groups for OS (B1 vs. B2, p < 0.001; B1 vs. B3, p < 0.001) and RFS (B1 vs. B2, p=0.478; B1 vs. B3, p < 0.001), there was still no obvious difference for RFS (p=0.722) and OS (p=0.337) between B2 and B3 according to Kinki criteria (Fig. 2C and D).
5. BCLC-A stage vs. BCLC-B1 group
Subsequently, the 1-, 3-, and 5-year OS rate was 88, 71, and 68% for BCLC-A stage and 92%, 78%, and 66% for BCLC-B1 subclassification. Correspondingly, the 1-, 3-, and 5-year recurrence rate was 70%, 56%, and 48% for BCLC-A stage and 59%, 40%, and 32% for BCLC-B1 subclassification. The log-rank test revealed that no significant differences were observed between BCLC-A and BCLC-B1 group for both RFS (p=0.087) and OS (p=0.643) (Fig. 1C and D).
The BCLC staging system, endorsed by European Association for the Study of Liver (EASL) and AASLD, provides prognostic score and guidance for therapeutic decisions for HCC patients based on tumor staging criteria, liver function and health status [18,19]. Intermediate stage HCC (BCLC-B) patients are a very heterogeneous population in terms of tumor size, tumor number and liver function [13]. On account of the heterogeneity, increasing researchers have begun to create a novel subclassification system to improve the staging-treatment association. In 2012, Bolondi et al. [10] proposed an innovative classification system. Thereafter, many studies had been carried out to prove the effectiveness of Bolondi’s subclassification. A recent study designed by Ciria et al. [20], involving 80 BCLC-B patients received TACE and hepatic resection between 2007 and 2012, revealed that overall survival was 40% with a median follow-up of 29.5 months (0.07-96.9) and 5-year survival rates were 62.9%, 28.1%, and 15.4%, respectively (p=0.004) for B1, B2, and B3-4 stages.
In our study, we found the overall survival trends were remarkable in B1 stages, but no difference for the test B2 vs. B3 and B3 vs. B4. In addition, Bolondi’s subclassification had no significant effect for RFS (p=0.892) and OS (p=0.263) in multivariate analysis. This illustrates that Bolondi’s subclassification cannot totally distinguish the BCLC-B patients who received hepatic resection, especially the subclass B2 to B4. For this reason, a research from Kinki University School of Medicine in Japan put forward a novel classification system by modifying the Bolondi’s subclassification [13]. In this modified Bolondi’s subclassification system (Kinki criteria), the biggest change is putting B2 and B3 group together. Then patients with intermediate-stage HCC are classified into 3 groups. Further analysis of validity of the Kinki criteria by Arizumi et al. [21] with 425 HCC patients who underwent TACE, and the result revealed that the median overall survival was 3.9 years in the BCLC subclass B1 group, 2.5 years in the B2 group, and 1.1 years in the B3 group (p < 0.001), and survival curves were stratified with significant differences. In our study, there was no obvious difference for RFS (p=0.722) and OS (p=0.337) between B2 and B3 according to Kinki criteria (Fig. 2C and D). Therefore,both of the two subclassifications may be not suitable to distinguish BCLC-B2-B4 patients who received hepatic resection. And these findings stress once again that BCLC stage B is a heterogeneous category.
Although TACE was considered as the main treatment for those patients, it is not always the case in the clinical work because of the heterogeneity. Several groups proposed that therapeutic approach is different according to subclassification. As it is recently stated in a study from the Italian Liver Cancer Group in which TACE for BCLC-B was analyzed on 405 patients, "TACE cannot be considered the best approach for BCLC stage B patients who represent a heterogeneous population and are often suitable for more aggressive therapies, which lead to a better survival” [8]. Similarly, Zhong et al. [6] reported a wide single center experience with similar results. In fact, with deepened understanding of liver cirrhotic and improved operative techniques, hepatic resection may be a much more feasible and safe choice for some BCLC-B patients. In our study, we found that the BCLC-B1 patients with hepatic resection had a better prognosis than the B2-B4 patients and no significant difference in RFS and OS between the BCLC-A and the subclass B1 group. Although many studies believed the only TACE is indicated for intermediate-stage HCC [22,23], a recent randomized controlled trial (RCT) conducted by Yin et al. [24], including 173 patients with multinodular HCC, revealed that there were no significant differences in the 30-day and in the 90-day mortality between the hepatic resection and TACE groups for BCLC-B patients. However, the hepatic resection group had significantly better overall survive than the TACE group. In addition, a meta-analysis including 50 retrieved papers shows a statistically significantly higher overall survival in hepatic resection group than in TACE group in HCC within the BCLC stage B alone (HR, 0.48; 95% CI, 0.25 to 0.90) [25]. Furthermore, in the research of Ciria et al. [20], no significant difference were found in the HCC patients with BCLC-B1 who underwent live resection with those who received TACE treatment for 5-year survival rate (63.2% vs. 62.5%). Therefore, in our opinion, Bolondi’s subclassification may be used to the selection of part of BCLC-B patients who may benefit from hepatic resection. On the other hand, as for patients in the subclass B2-B4, TACE may be a more appropriate treatment, which could reduce the risk of liver failure.
Some limitations have been found in our study. Firstly, the main limitation is the retrospective nature, which may result in selection bias. We have been carrying on a prospective multicenter RCT comparing hepatic resection versus TACE+ radiofrequency ablation for BCLC-B stage HCC patients (RCT: NCT02616926). Secondly, owing to the severe liver function injury and huge tumor burden, there are only six and five patients who received hepatic resection for subclass B3 and B4 and 18.6% patients were lost to follow up in BCLC-B stage HCC patients, which may cause a statistical discrepancy. This is why the median survival of B4 group longer than the B3 group in our study.
In our study, we stress once again that BCLC stage B is a heterogeneous category and the overall survival trends were remarkable in B1 stages according to Bolondi’s subclassification for HCC patients with hepatic resection. In addition, no significant difference in RFS and OS between the BCLC-A and the B1 stages were found, suggesting that some BCLC-B patients may benefit from hepatic resection. Therefore, our study provided rationality of hepatic resection for selected BCLC-B stage HCC patients instead of routine TACE.

Conflict of interest relevant to this article was not reported.

Acknowledgements
This work was supported by Sun Yat-Sen University Clinical Research 5010 Program (Grant number: 2015012).
Fig. 1.
(A) Overall survival according to the Barcelona Clinic Liver Cancer (BCLC) staging system. (B) Recurrence-free survival according to the BCLC staging system. (C) Overall survival of BCLC-A and BCLC-B1. (D) Recurrence-free survival of BCLC-A and BCLC-B1.
crt-2018-038f1.jpg
Fig. 2.
(A) Overall survival according to the Bolondi’s classification. (B) Recurrence-free survival according to the Bolondi’s classification. (C) Overall survival according to the modified Bolondi’s classification (Kinki criteria). (D) Recurrence-free survival according to the modified Bolondi’s classification (Kinki criteria).
crt-2018-038f2.jpg
Table 1.
Proposed subclassification of BCLC-B patients published
Subclassification B1 B2 B3 B4
Child-Pugh points 5-6-7 5-6 7 8-9
Beyond Milan and within Up-to-Seven criteria In Out Out Out
ECOG (tumour-related) PST 0 0 0 0-1
Portal vein thrombosis No No No No

BCLC, Barcelona Clinic Liver Cancer; ECOG, Eastern Cooperative Oncology Group; PST, performance status test.

Table 2.
Main clinical characteristics of patients
Variable All (n=1,103) BCLC-A (n=530) BCLC-B (n=219)
BCLC-C (n=354)
BCLC-B1 (n=41) BCLC-B2 (n=160) BCLC-B3 (n=11) BCLC-B4 (n=7)
Sex
 Male 970 444 39 148 11 5 323
 Female 133 86 2 12 0 2 31
Age (yr)
 < 50 521 251 17 75 2 2 174
 ≥ 50 582 279 24 85 9 5 180
PLT (×109/L)
 < 150 299 149 15 33 1 2 99
 ≥ 150 804 381 26 127 10 5 255
HBsAg
 Negative 157 89 3 19 1 1 44
 Positive 946 441 38 141 10 6 310
AFP (ng/mL)
 < 400 543 293 23 77 4 3 143
 ≥ 400 560 237 18 83 7 4 211
Capsulation
 Capsulated 812 421 36 131 9 7 208
 Noncapsulated 291 109 5 29 2 0 146
Lymphatic metastasis
 Absent 1,030 524 39 150 9 7 301
 Present 73 6 2 10 2 0 53
Tumor size (cm)
 < 5 385 249 41 19 1 4 71
 ≥ 5 718 281 0 141 10 3 283

BCLC, Barcelona Clinic Liver Cancer; PLT, platelet; HBsAg, hepatitis B surface antigen; AFP, α-fetoprotein.

Table 3.
Multivariable regression results for overall survival and recurrence-free survival
Characteristic Overall survival
Recurrence-free survival
HR (95% CI) p-value HR (95% CI) p-value
Sex 0.56 (0.24-1.32) 0.184 0.36 (0.15-0.82) 0.015
Age 0.95 (0.62-1.45) 0.799 0.98 (0.68-1.42) 0.915
PLT 0.77 (0.47-1.24) 0.288 1.27 (0.82-1.97) 0.289
HBsAg 1.02 (0.53-1.93) 0.960 1.09 (0.63-1.89) 0.764
AFP 1.37 (0.88-2.11) 0.160 1.44 (0.99-2.08) 0.052
Capsulation 1.51 (0.90-2.55) 0.120 1.11 (0.70-1.77) 0.643
Bolondi’s subclassification 1.31 (0.82-2.10) 0.263 0.97 (0.65-1.46) 0.892
Lymphatic metastasis 2.01 (0.81-4.98) 0.131 1.49 (0.70-3.20) 0.299
Tumor size 2.74 (1.58-4.74) < 0.001 2.31 (1.42-3.74) 0.001

HR, hazard ratio; CI, confidence interval; PLT, platelet; HBsAg, hepatitis B surface antigen; AFP, α-fetoprotein.

  • 1. Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893–917. ArticlePubMed
  • 2. Pang Q, Qu K, Zhang JY, Song SD, Liu SS, Tai MH, et al. The prognostic value of platelet count in patients with hepatocellular carcinoma: a systematic review and meta-analysis. Medicine (Baltimore). 2015;94:e1431ArticlePubMedPMC
  • 3. Forner A, Llovet JM, Bruix J. Hepatocellular carcinoma. Lancet. 2012;379:1245–55. ArticlePubMed
  • 4. Llovet JM, Di Bisceglie AM, Bruix J, Kramer BS, Lencioni R, Zhu AX, et al. Design and endpoints of clinical trials in hepatocellular carcinoma. J Natl Cancer Inst. 2008;100:698–711. ArticlePubMedPDF
  • 5. Chang WT, Kao WY, Chau GY, Su CW, Lei HJ, Wu JC, et al. Hepatic resection can provide long-term survival of patients with non-early-stage hepatocellular carcinoma: extending the indication for resection? Surgery. 2012;152:809–20. ArticlePubMed
  • 6. Zhong JH, Ke Y, Gong WF, Xiang BD, Ma L, Ye XP, et al. Hepatic resection associated with good survival for selected patients with intermediate and advanced-stage hepatocellular carcinoma. Ann Surg. 2014;260:329–40. ArticlePubMed
  • 7. Choi SH, Choi GH, Kim SU, Park JY, Joo DJ, Ju MK, et al. Role of surgical resection for multiple hepatocellular carcinomas. World J Gastroenterol. 2013;19:366–74. ArticlePubMedPMC
  • 8. Farinati F, Vanin V, Giacomin A, Pozzan C, Cillo U, Vitale A, et al. BCLC stage B hepatocellular carcinoma and transcatheter arterial chemoembolization: a 20-year survey by the Italian Liver Cancer group. Liver Int. 2015;35:223–31. ArticlePubMed
  • 9. Vitale A, Burra P, Frigo AC, Trevisani F, Farinati F, Spolverato G, et al. Survival benefit of liver resection for patients with hepatocellular carcinoma across different Barcelona Clinic Liver Cancer stages: a multicentre study. J Hepatol. 2015;62:617–24. ArticlePubMed
  • 10. 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;32:348–59. ArticlePubMed
  • 11. Weinmann A, Koch S, Sprinzl M, Kloeckner R, Schulze-Bergkamen H, Duber C, et al. Survival analysis of proposed BCLC-B subgroups in hepatocellular carcinoma patients. Liver Int. 2015;35:591–600. ArticlePubMed
  • 12. Giannini EG, Moscatelli A, Pellegatta G, Vitale A, Farinati F, Ciccarese F, et al. Application of the intermediate-stage subclassification to patients with untreated hepatocellular carcinoma. Am J Gastroenterol. 2016;111:70–7. ArticlePubMedPDF
  • 13. Kudo M, Arizumi T, Ueshima K, Sakurai T, Kitano M, Nishida N. Subclassification of BCLC B stage hepatocellular carcinoma and treatment strategies: proposal of modified Bolondi's subclassification (Kinki Criteria). Dig Dis. 2015;33:751–8. ArticlePubMed
  • 14. Maithel SK, Kneuertz PJ, Kooby DA, Scoggins CR, Weber SM, Martin RC 2nd, et al. Importance of low preoperative platelet count in selecting patients for resection of hepatocellular carcinoma: a multi-institutional analysis. J Am Coll Surg. 2011;212:638–48. ArticlePubMedPMC
  • 15. Lim C, Compagnon P, Sebagh M, Salloum C, Calderaro J, Luciani A, et al. Hepatectomy for hepatocellular carcinoma larger than 10 cm: preoperative risk stratification to prevent futile surgery. HPB (Oxford). 2015;17:611–23. ArticlePubMedPMC
  • 16. Bruix J, Sherman M; American Association for the Study of Liver Diseases. Management of hepatocellular carcinoma: an update. Hepatology. 2011;53:1020–2. ArticlePubMedPMC
  • 17. Sutherland F, Harris J. Claude Couinaud: a passion for the liver. Arch Surg. 2002;137:1305–10. ArticlePubMed
  • 18. Dhir M, Melin AA, Douaiher J, Lin C, Zhen WK, Hussain SM, et al. A review and update of treatment options and controversies in the management of hepatocellular carcinoma. Ann Surg. 2016;263:1112–25. ArticlePubMed
  • 19. EASL-EORTC clinical practice guidelines: management of hepatocellular carcinoma. J Hepatol. 2012;56:908–43. ArticlePubMed
  • 20. Ciria R, Lopez-Cillero P, Gallardo AB, Cabrera J, Pleguezuelo M, Ayllon MD, et al. Optimizing the management of patients with BCLC stage-B hepatocellular carcinoma: modern surgical resection as a feasible alternative to transarterial chemoemolization. Eur J Surg Oncol. 2015;41:1153–61. ArticlePubMed
  • 21. Arizumi T, Ueshima K, Iwanishi M, Minami T, Chishina H, Kono M, et al. Validation of a modified substaging system (Kinki Criteria) for patients with intermediate-stage hepatocellular carcinoma. Oncology. 2015;89 Suppl 2:47–52. ArticlePubMed
  • 22. Adhoute X, Penaranda G, Raoul JL, Bourliere M. Hepatocellular carcinoma scoring and staging systems. Do we need new tools? J Hepatol. 2016;64:1449–50. ArticlePubMed
  • 23. Dufour JF, Bargellini I, De Maria N, De Simone P, Goulis I, Marinho RT. Intermediate hepatocellular carcinoma: current treatments and future perspectives. Ann Oncol. 2013;24 Suppl 2:ii24–9. ArticlePubMedPDF
  • 24. Yin L, Li H, Li AJ, Lau WY, Pan ZY, Lai EC, et al. Partial hepatectomy vs. transcatheter arterial chemoembolization for resectable multiple hepatocellular carcinoma beyond Milan Criteria: a RCT. J Hepatol. 2014;61:82–8. ArticlePubMed
  • 25. Qi X, Wang D, Su C, Li H, Guo X. Hepatic resection versus transarterial chemoembolization for the initial treatment of hepatocellular carcinoma: a systematic review and meta-analysis. Oncotarget. 2015;6:18715–33. ArticlePubMedPMC

Figure & Data

REFERENCES

    Citations

    Citations to this article as recorded by  
    • Overexpression of tousled-like kinase 2 predicts poor prognosis in HBV-related hepatocellular carcinoma patients after radical resection
      Bang Liu, Ling-Ling Lu, Li Yu, Xuan Mei, Jia Liu, Jiao-Long Zheng, Xiao-Ling Zhou, Hai-Yan Lin, Xiu-Ling Zhu, Dong-Liang Li
      Frontiers in Genetics.2024;[Epub]     CrossRef
    • Prognostic significance of early and multiple recurrences after curative resection for hepatocellular carcinoma
      Akihiro Tanemura, Daisuke Noguchi, Toru Shinkai, Takahiro Ito, Aoi Hayasaki, Kazuyuki Gyoten, Takehiro Fujii, Yusuke Iizawa, Yasuhiro Murata, Naohisa Kuriyama, Masashi Kishiwada, Shugo Mizuno
      BMC Surgery.2024;[Epub]     CrossRef
    • TAC score better predicts survival than the BCLC following resection of hepatocellular carcinoma
      Henrique A. Lima, Yutaka Endo, Zorays Moazzam, Laura Alaimo, Chanza Shaikh, Muhammad M. Munir, Vivian Resende, Alfredo Guglielmi, Hugo P. Marques, François Cauchy, Vincent Lam, George A. Poultsides, Irinel Popescu, Sorin Alexandrescu, Guillaume Martel, It
      Journal of Surgical Oncology.2023; 127(3): 374.     CrossRef
    • Multiplication of tumor maximum diameter and number as a new surgical indicator for Barcelona Clinic Liver Cancer intermediate‐stage hepatocellular carcinoma
      Yuji Morine, Yu Saito, Shinichiro Yamada, Hiroki Teraoku, Yuhei Waki, Takayuki Noma, Tetsuya Ikemoto, Mitsuo Shimada
      Hepatology Research.2023; 53(6): 531.     CrossRef
    • Clinical consensus statement: Establishing the roles of locoregional and systemic therapies for the treatment of intermediate-stage hepatocellular carcinoma in Canada
      Jason K. Wong, Howard J. Lim, Vincent C. Tam, Kelly W. Burak, Laura A. Dawson, Prosanto Chaudhury, Robert J. Abraham, Brandon M. Meyers, Gonzalo Sapisochin, David Valenti, Setareh Samimi, Ravi Ramjeesingh, Amol Mujoomdar, Ilidio Martins, Elijah Dixon, Maj
      Cancer Treatment Reviews.2023; 115: 102526.     CrossRef
    • Advances in post-operative prognostic models for hepatocellular carcinoma
      Ziqin He, Xiaomin She, Ziyu Liu, Xing Gao, Lu Lu, Julu Huang, Cheng Lu, Yan Lin, Rong Liang, Jiazhou Ye
      Journal of Zhejiang University-SCIENCE B.2023; 24(3): 191.     CrossRef
    • Preoperative alpha fetoprotein, total bilirubin, fibrinogen, albumin, and lymphocytes predict postoperative survival in hepatocellular carcinoma
      Jia Xu, Shu An, Ying Lu, Laisheng Li, Zhi‐Qi Wu, Hua‐Guo Xu
      Cancer Medicine.2023; 12(12): 13319.     CrossRef
    • Liver resection versus transarterial chemoembolisation for the treatment of intermediate hepatocellular carcinoma: a systematic review and meta-analysis
      Aleksandar Bogdanovic, Jelena Djokic Kovac, Predrag Zdujic, Uros Djindjic, Vladimir Dugalic
      International Journal of Surgery.2023; 109(5): 1439.     CrossRef
    • Surgical resection versus transarterial chemoembolization for patients with hepatocellular carcinoma beyond Milan criteria: prognostic role of tumor burden score
      Shu-Yein Ho, Po-Hong Liu, Chia-Yang Hsu, Yi-Hsiang Huang, Hao-Jan Lei, Jia-I Liao, Chien-Wei Su, Ming-Chih Hou, Teh-Ia Huo
      Scientific Reports.2023;[Epub]     CrossRef
    • Clinical outcome of surgical resection for multifocal T2-T3 hepatocellular carcinoma up to 3 nodules: a comparative analysis with a single nodule
      Sehyeon Yu, Hye-Sung Jo, Young-Dong Yu, Yoo jin Choi, Dong-Sik Kim
      Journal of Liver Cancer.2023; 23(2): 377.     CrossRef
    • Pretreatment Non-Invasive Biomarkers as Predictors to Estimate Portal Vein Tumor Thrombosis (PVTT) Risk and Long-Term Survival in HBV-Related Hepatocellular Carcinoma Patients Without PVTT
      Bang Liu, Jia Liu, Xuan Mei, Zhi-Qiang Zhang, Jian Fang, Li-Li Zhou, Jiao-Long Zheng, Hai-Yan Lin, Xiu-Ling Zhu, Dong-Liang Li
      Journal of Hepatocellular Carcinoma.2023; Volume 10: 2367.     CrossRef
    • Tumor Burden Score and Serum Alpha-fetoprotein Subclassify Intermediate-Stage Hepatocellular Carcinoma
      Henrique A. Lima, Yutaka Endo, Laura Alaimo, Zorays Moazzam, Muhammad Musaab Munir, Chanza Shaikh, Vivian Resende, Alfredo Guglielmi, Hugo P. Marques, François Cauchy, Vincent Lam, George A. Poultsides, Irinel Popescu, Sorin Alexandrescu, Guillaume Martel
      Journal of Gastrointestinal Surgery.2022; 26(12): 2512.     CrossRef
    • Comparison of 10 noninvasive models for predicting overall survival in patients with intermediate-stage hepatocellular carcinoma
      Wei-Fan Hsu, Kai-Chih Chang, Te-Hong Chen, Chien-Hung Lin, Ying-Chun Lin, Ming-Hung Tsai, Pei-Yu Chen, Hung-Wei Wang, Chia-Sheng Chu, Cheng-Yuan Peng
      Medicine.2021; 100(33): e27000.     CrossRef
    • Hepatic Resection Versus Transarterial Chemoembolization for Intermediate-Stage Hepatocellular Carcinoma: A Cohort Study
      Linbin Lu, Peichan Zheng, Zhixian Wu, Xiong Chen
      Frontiers in Oncology.2021;[Epub]     CrossRef
    • Hepatocellular carcinoma surveillance, early detection and survival in a privately insured US cohort
      Vincent L. Chen, Amit G. Singal, Elliot B. Tapper, Neehar D. Parikh
      Liver International.2020; 40(4): 947.     CrossRef
    • Complex treatment of hepatocellular carcinoma at early (BCLC-A) and intermediate (BCLC-B) stages
      B. N. Kotiv, I. I. Dzidzava, S. A. Alent’yev, A. V. Smorodsky, K. I. Makhmudov, A. A. Apollonov, S. A. Soldatov, P. N. Zubarev
      Annaly khirurgicheskoy gepatologii = Annals of HPB Surgery.2020; 25(2): 55.     CrossRef
    • A simple and clinically applicable model to predict liver-related morbidity after hepatic resection for hepatocellular carcinoma
      Jonggi Choi, So-Hyun Kim, Seungbong Han, Danbi Lee, Ju Hyun Shim, Young-Suk Lim, Han Chu Lee, Young-Hwa Chung, Yung Sang Lee, Sung-Gyu Lee, Ki-Hun Kim, Kang Mo Kim, Leonidas G Koniaris
      PLOS ONE.2020; 15(11): e0241808.     CrossRef
    • BCLC-B Subclassification and the Hong Kong Liver Cancer System in Intermediate Hepatocellular Carcinoma
      Larisse Longo, Laura B. Rodrigues de Freitas, Deivid Santos, Ivana Grivicich, Mário R. Álvares-da-Silva
      American Journal of Clinical Oncology.2019; 42(5): 466.     CrossRef

    • PubReader PubReader
    • ePub LinkePub Link
    • Cite
      CITE
      export Copy Download
      Close
      Download Citation
      Download a citation file in RIS format that can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Reference Manager.

      Format:
      • RIS — For EndNote, ProCite, RefWorks, and most other reference management software
      • BibTeX — For JabRef, BibDesk, and other BibTeX-specific software
      Include:
      • Citation for the content below
      Hepatic Resection Provides Survival Benefit for Selected Intermediate-Stage (BCLC-B) Hepatocellular Carcinoma Patients
      Cancer Res Treat. 2019;51(1):65-72.   Published online February 26, 2018
      Close
    • XML DownloadXML Download
    Hepatic Resection Provides Survival Benefit for Selected Intermediate-Stage (BCLC-B) Hepatocellular Carcinoma Patients
    Image Image
    Fig. 1. (A) Overall survival according to the Barcelona Clinic Liver Cancer (BCLC) staging system. (B) Recurrence-free survival according to the BCLC staging system. (C) Overall survival of BCLC-A and BCLC-B1. (D) Recurrence-free survival of BCLC-A and BCLC-B1.
    Fig. 2. (A) Overall survival according to the Bolondi’s classification. (B) Recurrence-free survival according to the Bolondi’s classification. (C) Overall survival according to the modified Bolondi’s classification (Kinki criteria). (D) Recurrence-free survival according to the modified Bolondi’s classification (Kinki criteria).
    Hepatic Resection Provides Survival Benefit for Selected Intermediate-Stage (BCLC-B) Hepatocellular Carcinoma Patients
    Subclassification B1 B2 B3 B4
    Child-Pugh points 5-6-7 5-6 7 8-9
    Beyond Milan and within Up-to-Seven criteria In Out Out Out
    ECOG (tumour-related) PST 0 0 0 0-1
    Portal vein thrombosis No No No No
    Variable All (n=1,103) BCLC-A (n=530) BCLC-B (n=219)
    BCLC-C (n=354)
    BCLC-B1 (n=41) BCLC-B2 (n=160) BCLC-B3 (n=11) BCLC-B4 (n=7)
    Sex
     Male 970 444 39 148 11 5 323
     Female 133 86 2 12 0 2 31
    Age (yr)
     < 50 521 251 17 75 2 2 174
     ≥ 50 582 279 24 85 9 5 180
    PLT (×109/L)
     < 150 299 149 15 33 1 2 99
     ≥ 150 804 381 26 127 10 5 255
    HBsAg
     Negative 157 89 3 19 1 1 44
     Positive 946 441 38 141 10 6 310
    AFP (ng/mL)
     < 400 543 293 23 77 4 3 143
     ≥ 400 560 237 18 83 7 4 211
    Capsulation
     Capsulated 812 421 36 131 9 7 208
     Noncapsulated 291 109 5 29 2 0 146
    Lymphatic metastasis
     Absent 1,030 524 39 150 9 7 301
     Present 73 6 2 10 2 0 53
    Tumor size (cm)
     < 5 385 249 41 19 1 4 71
     ≥ 5 718 281 0 141 10 3 283
    Characteristic Overall survival
    Recurrence-free survival
    HR (95% CI) p-value HR (95% CI) p-value
    Sex 0.56 (0.24-1.32) 0.184 0.36 (0.15-0.82) 0.015
    Age 0.95 (0.62-1.45) 0.799 0.98 (0.68-1.42) 0.915
    PLT 0.77 (0.47-1.24) 0.288 1.27 (0.82-1.97) 0.289
    HBsAg 1.02 (0.53-1.93) 0.960 1.09 (0.63-1.89) 0.764
    AFP 1.37 (0.88-2.11) 0.160 1.44 (0.99-2.08) 0.052
    Capsulation 1.51 (0.90-2.55) 0.120 1.11 (0.70-1.77) 0.643
    Bolondi’s subclassification 1.31 (0.82-2.10) 0.263 0.97 (0.65-1.46) 0.892
    Lymphatic metastasis 2.01 (0.81-4.98) 0.131 1.49 (0.70-3.20) 0.299
    Tumor size 2.74 (1.58-4.74) < 0.001 2.31 (1.42-3.74) 0.001
    Table 1. Proposed subclassification of BCLC-B patients published

    BCLC, Barcelona Clinic Liver Cancer; ECOG, Eastern Cooperative Oncology Group; PST, performance status test.

    Table 2. Main clinical characteristics of patients

    BCLC, Barcelona Clinic Liver Cancer; PLT, platelet; HBsAg, hepatitis B surface antigen; AFP, α-fetoprotein.

    Table 3. Multivariable regression results for overall survival and recurrence-free survival

    HR, hazard ratio; CI, confidence interval; PLT, platelet; HBsAg, hepatitis B surface antigen; AFP, α-fetoprotein.


    Cancer Res Treat : Cancer Research and Treatment
    Close layer
    TOP