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World Journal of Gastrointestinal Surgery logoLink to World Journal of Gastrointestinal Surgery
. 2022 May 27;14(5):442–451. doi: 10.4240/wjgs.v14.i5.442

Prognostic factors for patients with mass-forming intrahepatic cholangiocarcinoma: A case series of 68 patients

Jian Feng 1,2, Bin Liang 3, Hang-Yu Zhang 4, Zhe Liu 5, Kai Jiang 6, Xiang-Qian Zhao 7
PMCID: PMC9160678  PMID: 35734620

Abstract

BACKGROUND

Intrahepatic cholangiocarcinoma (ICC) is the second most common primary liver cancer in humans after hepatocellular carcinoma and a rare epithelial malignancy that results in a poor prognosis. According to the Liver Cancer Study Group of Japan classification, ICC can be divided into three types: Mass-forming (MF) type, periductal-infiltrating (PI) type, and intraductal-growth type. The MF type is the most common, accounting for 57.1-83.6% of ICCs. Nevertheless, little is known about the epidemiology and treatment of MF ICC.

AIM

To examine the prognostic factors for patients with MF ICC.

METHODS

We carried out a retrospective analysis of consecutive patients with MF ICC treated at the Faculty of Hepato-Pancreato-Biliary Surgery of Chinese PLA General Hospital between January 2008 and December 2018. According to the treatment received, the patients were divided into either a resection group or an exploration group.

RESULTS

The pooled 1-, 3-, and 5-year survival rates in the 68 patients with MF ICC were 66.5%, 36.3%, and 9.3%, respectively. Univariate analysis revealed that surgical resection (P < 0.001), nodal metastasis (P < 0.001), tumor location (P = 0.039), vascular invasion (P < 0.001), ascites (P < 0.001), and differentiation (P = 0.009) were significantly associated with the prognosis and survival of MF ICC. Multivariate analysis revealed that ascites (hazard ratio [HR] = 5.6, 95% confidence interval [CI]: 1.6-18.9, P = 0.006) and vascular invasion (HR = 2.5, 95%CI: 1.0-6.1, P = 0.045) were independent risk factors for MF ICC. The pooled 1-, 3-, and 5-year survival rates in the 19 patients of the exploration group were 5.3%, 5.3%, and 0, respectively. Among the 49 patients who underwent surgical resection, the pooled 1-, 3-, and 5-year survival rates were 93.5%, 49.7%, and 14.4%, respectively. Univariate and multivariate analyses revealed that vascular invasion (HR = 3.1, 95%CI: 1.2-8.5, P = 0.024) and nodal metastasis (HR = 3.2, 95%CI: 1.4-7.6, P = 0.008) were independent prognostic risk factors for surgical resection patients.

CONCLUSION

The prognosis of MF ICC patients is dismal, especially those with ascites or vascular invasion. Surgical resection is a key factor in improving overall survival in patients with MF ICC, and vascular invasion and lymph node metastasis affect the efficacy of surgical resection.

Keywords: Intrahepatic cholangiocarcinoma, Mass-forming, Treatment, Prognosis


Core Tip: This is a single-center, large-scale retrospective study on mass-forming intrahepatic cholangiocarcinoma (MF ICC) to examine the prognostic factors for MF ICC and improve the outcomes. The study found the patients with MF ICC with ascites and vascular invasion have a poor prognosis. Surgical resection is a key factor in improving overall survival in patients with MF ICC, and patients with vascular invasion and lymph node metastasis have poor surgical results.

INTRODUCTION

Intrahepatic cholangiocarcinoma (ICC) refers to a malignant tumor originating from the branching epithelial cells of the intrahepatic secondary bile duct and above, with a poor prognosis[1-2]. It has been reported that both the morbidity and mortality have gradually increased in recent years[1-4]. Surgical resection is currently the only potentially curative treatment for ICC[3-5], but the cure rates and survival of patients with ICC remain very low because of the high aggressiveness of the disease[6-7]. It has been reported that many factors influence the prognosis of surgical resection[8-11].

According to the Liver Cancer Study Group of Japan classification, ICC can be divided into three types: Mass-forming (MF) type, periductal-infiltrating (PI) type, and intraductal-growth (IG) type[11]. Among them, the MF type is the most common, accounting for 57.1-83.6% of ICCs[12-14].

Nevertheless, little is known about the epidemiology and treatment of MF ICC. Therefore, the aim of the present retrospective study was to analyze prognostic factors for patients with MF ICC.

MATERIALS AND METHODS

Study design

This was a retrospective analysis of consecutive patients with MF ICC treated at the Faculty of Hepato-Pancreato-Biliary Surgery of Chinese PLA General Hospital between January 2008 and December 2018. The study was approved by the Medical Ethics Committee of the Chinese PLA General Hospital.

Patients

The inclusion criteria were: (1) ≥ 18 years of age; (2) Hospitalized patients; (3) Confirmed as MF ICC by histopathological examination; and (4) No prior history of any malignancy. The exclusion criteria were: (1) Incomplete data; (2) Metastasis; (3) Hilar cholangiocarcinoma; (4) Cystadenocarcinoma; (5) PI ICC; or (6) IG ICC. The patients were divided into either a resection group or an exploration group according to the received treatment.

Treatments

All cases were discussed in tumor boards before any treatment. The indications for radical hepatectomy were: (1) No distant metastases preoperatively; (2) Preoperative imaging suggesting that the tumors could be completely resected, including eventual satellite lesions; (3) Child-Pugh grade A or B; and (4) Good cardiopulmonary function and no surgical or anesthetic contraindications.

The surgical principle was to achieve R0 resection. The pattern of hepatectomy was based on residual liver function, tumour size, and tumour-vessel relationship. Anatomic resection (AR) was the priority if feasible, while non-AR (NAR) was more frequently applied if the tumour was adjacent to major vascular structure. Surgical exploration was only performed in patients with extensive metastases in the liver, abdominal wall, and omentum. Lymph node dissection of the hepatoduodenal ligament was performed for patients with lymphadenectasis found by imaging or intraoperatively. Tumor and lymph node biopsies were performed in patients undergoing surgical exploration.

Data collection

General data and results of auxiliary examinations were recorded, including carbohydrate antigen 19-9 (CA19-9), hepatitis B virus (HBV), glutamic pyruvic transaminase (ALT), glutamic oxaloacetic transaminase, alkaline phosphatase, gamma-glutamyltransferase, and total bilirubin tests.

Follow-up

All patients were followed after surgery. Follow-up visits were performed once every 3 mo during the first year, once every 6 mo during the second and third years, and once a year later. Items checked during the follow-up visits included routine laboratory tests, tumor markers, chest roentgenogram, abdominal ultrasound, CT, and/or MRI examinations. The follow-up deadline was December 31, 2019, and the follow-up duration ranged from 1 to 82 mo, with a median duration of 13 mo.

Statistical analysis

All statistical analyses were performed using IBM SPSS Statistics ver. 21.0 (IBM Co, Armonk, NY, United States). Continuous data meeting a normal distribution are presented as the mean ± SD. Differences between the two groups were determined using independent sample t test. Continuous data not meeting a non-normal distribution are presented as the median (range). The non-parametric Mann-Whitney U test was used to determine the differences between the two groups. The chi-square test or the Fisher’s exact test was used for categorical data. Univariate Cox proportional hazard regression model analysis was used for survival data. Variables with P < 0.05 in univariate analysis were included in the multivariate Cox proportional hazard regression model. Kaplan-Meier analysis was used to calculate the survival rate. Log-rank method was used for group-wise comparison. Two-sided P values < 0.05 were considered statistically significant.

RESULTS

Characteristics of the patients

Among the 68 patients, 50 were male and 18 female, ranging from 24 to 74 years with a median age of 54. There were 40 patients with tumors in the right lobe of the liver and 28 with tumors in the left lobe of the liver. The median tumor diameter was 7.0 cm (range, 2.2-14.0). Twenty-eight (41.2%) patients had elevated CA 19-9 levels, five of whom had CA 19-9 > 1000 U/mL. Sixteen and four had concomitant hepatitis B and C viral infections, respectively. Fourteen cases were accompanied with ascites. The characteristics were similar between the two groups, except that the exploration group had higher levels of ALT (P = 0.031), higher frequencies of ascites (P < 0.001), nodal metastasis (P < 0.001), and vascular invasion (P < 0.001), and the tumors were mostly located in the left lobe (P < 0.001) (Table 1).

Table 1.

Baseline characteristics of the patients

Variable
All (n = 68)
Surgery (n = 49)
Exploration (n = 19)
P value
Age (yr) 54.3 ± 1.4 52.6 ± 1.7 58.6 ± 2.2 0.435
Gender, Male 50 (73.5%) 34 (69.4%) 16 (84.2%) 0.924
HBV infection 16 (23.5%) 13(26.5%) 3 (15.8%) 0.997
HCV infection 4 (5.9%) 2 (4.1%) 2 (10.5%) 0.314
Ascites 14 (20.6%) 1 (2.0%) 13(68.4%) < 0.001
Tumor size(cm) 6.9 ± 0.3 6.8 ± 0.4 7.63 ± 0.5 0.495
ALT (IU/L)(median) 1.8-92.1 (26) 1.8-92.1 (24.9) 23-76.3 (32.1) 0.031
AST (IU/L) (median) 9.6-74.2 (29) 9.6-74.2 (27.3) 18.2-61.9 (31) 0.142
ALP (U/L) (median) 13.4-280.5 (82.8) 13.4-280.5 (81.4) 45.3-109.9 (85.4) 0.149
GGT (U/L) (median) 11-325.6 (42.4) 11-325.6 (41.1) 28.9-104.7 (45.8) 0.512
TBIL (mg/dL) (median) 4.2-140.0 (18) 4.2-140 (18.1) 4.2-42.6 (17.8) 0.707
CA19-9 (U/mL) (median) 21-2000 (34.5) 21-1891 (36) 22-2000 (30) 0.104
Differentiation 0.536
Poor 30 (44.1%) 20 (40.8%) 10 (40.052.6
Poor-moderate 24 (35.3%) 19 (38.8%) 5 (26.3%)
Moderate 14 (20.6%) 10 (20.4%) 4 (21.1%)
Nodal metastasis 33 (48.5%) 14 (28.6%) 19 (100.0%) < 0.001
Tumor location < 0.001
Left lobe 28 (41.2%) 11 (22.4%) 17 (89.5%)
Right lobe 40 (58.8%) 38 (77.6%) 2 (10.5%)
Vascular invasion 31 (45.6%) 13 (26.5%) 19 (100.0%) < 0.001

HBV: Hepatitis B virus; HCV: Hepatitis C virus; ALT: Glutamic pyruvic transaminase; AST: Glutamic oxaloacetic transaminase; ALP: Alkaline phosphatase; GGT: Gamma-glutamyltransferase; TBIL: Total bilirubin; CA19-9: Carbohydrate antigen 19-9.

Survival

All patients were discharged successfully from the hospital. During follow-up, 48 patients died and 20 survived. Survival time ranged from 1 to 82 mo (median, 24 mo). The pooled 1-, 3-, and 5-year survival rates in the 68 patients with MF ICC were 66.5%, 36.3%, and 9.3%, respectively (Table 2). Univariate analysis revealed that surgical resection (P < 0.001), nodal metastasis (P < 0.001), tumor location (P = 0.039), vascular invasion (P < 0.001), ascites (P < 0.001), and differentiation (P = 0.009) were significantly associated with the prognosis and survival of MF ICC (Table 3). Multivariate analysis revealed that ascites (hazard ratio [HR] = 5.6, 95% confidence interval [CI]: 1.6-18.9, P = 0.006) and vascular invasion (HR = 2.5, 95%CI: 1.0-6.1, P = 0.045) were independent risk factors for MF ICC (Table 3).

Table 2.

Overall survival of the patients with mass-forming intrahepatic cholangiocarcinoma


All (n = 68)
Surgery (n = 49)
Exploration (n = 19)
P value
Follow-up (mo) 1-82 3-82 1-57
Survival < 0.001
1 yr 66.5% 93.5% 5.3%
3 yr 36.3% 49.7% 5.3%
5 yr 9.3% 14.4% 0.00%

Table 3.

Univariate and multivariate analyses of clinical and pathological factors for overall survival of 68 patients with mass-forming intrahepatic cholangiocarcinoma

Variable
Patients (n)
1 yr (%)
3 yr (%)
5 yr (%)
P value HR 95%CI P value
Age (yr) 0.278
≤ 54 35 71.8 39.8 13.5
>54 33 61.4 32.7 6.1
Gender 0.292
Male 50 62.2 34.2 9.7
Female 18 79.6 43.0 10.8
HBV infection 0.327
Yes 16 74.0 24.7 0
No 52 64.0 40.0 13.3
Ascites < 0.001 5.553 1.628-18.941 0.006
Present 14 0 0 0
Absent 54 84.0 45.8 11.8
Tumor size (cm) 0.230
≤ 7 41 64,3 49.0 10.1
> 7 27 70.2 12.5 6.3
CA 19-9 (IU/mL) 0.881
≤ 27 40 62.7 36.6 7.8
> 27 28 72.3 34.8 15.5
Differentiation 0.009 0.769 0.466-1.270 0.305
Poor 30 56.4 21.7 0
Poor-moderate 24 78.5 62.4 12.8
Moderate 14 66.1 23.6 23.6
Nodal metastasis < 0.001 2.294 0.983-5.353 0.055
Yes 35 97.0 64.0 21.7
No 33 37.8 9.1 0
Tumor location 0.032 2.186 0.801-5.965 0.127
Left lobe 28 40.9 28.6 0
Right lobe 40 86.8 43.9 12.4
Vascular invasion < 0.001 2.501 1.020-6.131 0.045
Yes 31 35.5 9.7 0
No 37 97.1 66.3 22.2
Group < 0.001 1.619 0.351-7.469 0.537
Resection 49 93.5 49.7 14.4
Exploration 19 5.3 5.3 0

HBV: Hepatitis B virus; CA19-9: Carbohydrate antigen 19-9.

Subgroup analysis

The pooled 1-, 3-, and 5-year survival rates in the 19 patients of the exploration group were 5.3%, 5.3%, and 0, respectively. Correspondingly, the pooled 1-, 3-, and 5-year survival rates in the 49 patients of the surgical resection group were 93.5%, 49.7%, and 14.4%, respectively. The survival rates of the resection group were significantly better than those of the exploration group (P < 0.001) (Figure 1). Table 4 presents the univariate and multivariate analyses of the factors associated with survival in the surgery group. Unlike the whole group of patients, univariate and multivariate analyses revealed that vascular invasion (HR = 3.1, 95%CI: 1.2-8.5, P = 0.024) and nodal metastasis (HR = 3.2, 95%CI: 1.4-7.6, P = 0.008) were independent prognostic risk factors for surgical resection patients.

Figure 1.

Figure 1

The resection group (blue line) vs the exploration group (green dashed line) (P < 0.001).

Table 4.

Univariate and multivariate analyses of clinical and pathological factors for overall survival of patients in the surgery group

Variable
Patients (n)
1 yr (%)
3 yr (%)
5 yr (%)
P value HR 95%CI P value
Age (yr) 0.633
≤ 54 27 92.3 48.6 21.2
> 54 22 95.0 50.7 9.5
Gender 0.441
Male 34 90.9 48.2 18.1
Female 15 100.0 54.0 13.5
HBV infection 0.063
Yes 13 92.3 30.8 0
No 36 94.0 57.1 22.5
Ascites 0.836
Present 1 0 0 0
Absent 48 93.4 49.6 14.4
Tumor size (cm) 0.044 1.273 0.485-3.339 0.624
≤ 7 28 92.9 69.6 16.9
> 7 21 94.1 33.6 8.4
CA 19-9 (IU/mL) 0.571
≤ 27 26 96.0 53.9 12.9
> 27 23 90.6 43.7 19.4
Differentiation 0.061
Poor 20 89.7 34.5 0
Poor-moderate 19 94.7 73.9 23.9
Moderate 10 100.0 35.7 35.7
Nodal metastasis 0.001 3.221 1.364-7.610 0.008
Yes 35 97.0 64.0 21.7
No 14 85.7 11.9 0
Tumor location 0.545
Left lobe 11 100.0 66.7 33.3
Right lobe 38 91.4 46.3 13.0
Vascular invasion < 0.001 3.148 1.160-8.544 0.024
Yes 12 83.3 16.7 0
No 37 97.1 66.3 22.2
Pattern of liver resection 0.773
AR resection 23 96.0 50.6 11.4
NAR resection 25 95.5 51.7 9.7
Resection margin(cm) 0.361
≤ 1 21 95.2 40.3 16.1
> 1 27 96.0 57.3 14.6

CA19-9: Carbohydrate antigen 19-9.

DISCUSSION

Little is known about the epidemiology and treatment of MF ICC. Therefore, this study aimed to examine the prognostic factors for patients with MF ICC. The results showed that the prognosis of MF ICC patients is dismal, especially those with ascites or vascular invasion. Resectable patients have a better prognosis, and vascular invasion and lymph node metastasis affected the efficacy of surgical resection. It is reported that the morbidity of ICC in males is 40-63.5%[14,16-18], and the age at diagnosis is mainly in the 6th decade of life, but ranges from 21 to 86 years[17-20]. Among the 68 cases in the current study, 50 were males, accounting for 73.5% of the patients, which was higher than that reported in the literature. The age of onset was 24-74 years with a median age of 54 years, which was consistent with literature reports but could still be a little younger than that in the literature. This discrepancy could be due to a number of reasons including genetics, environment, and methods of detection.

Many previous studies showed that HBV and hepatitis C virus (HCV) infections were associated with the occurrence of ICC. It has been reported that the rate of HBV infection ranges from 3.9% to 28.8% in ICC patients, and the rate of HCV infection ranges from 0.6% to 16.5%[20-22]. In the present study, the infection rates of HBV and HCV were 23.5% and 5.9%, respectively, which were similar to those reported in the literature. Currently, the relationship between HBV and ICC prognosis is still controversial. Pan et al[23] reported that the 1- and 3-year overall survival rates of patients with HBV infection was higher than that of patients without (67.6% and 47.2% vs 43.8% and 18.4%, respectively). Ahn et al[24] reported that HBV infection itself was not regarded as an independent prognostic factor. Tao et al[25] described that 1-, 3-, and 5-year cumulative survival rates of HBsAg-positive ICC patients are significantly lower than those of HBV-negative ICC patients. The present study found that there was no significant difference in survival between patients with HBV infection and those without. Nevertheless, among the 68 patients, the 5-year survival was 0 in patients with HBV infection, while it was 13.3% in those without HBV infection. In the surgery group, the 5-year survival was 0 in patients with HBV infection, while it was 22.5% in patients without HBV infection. These rates raise the question of the impact of HBV infection on the survival of ICC patients and further study is needed to investigate this point.

Surgical resection is the most important factor for long-term survival of ICC patients. In this study, the 5-year survival rate was 14.4% for patients in the resection group, while it was 0% for patients in the exploration group. The surgical approach required tumor-free surgical margins, i.e., R0 resection. The literature has reported that the R0 resection rate of ICC ranges from 24.1% to 92.8%[10,26], but the relationship between margins and survival is still controversial in patients with ICC. Bagante et al[13] deemed that patients with positive margins had a poor prognosis. Tang et al[16] reported that the prognosis in patients with margins > 1 cm was better than that of patients with margins ≤ 1 cm, while Bartsch et al[10] showed that the margin width was not related to prognosis. Other studies reported that no significant difference in survival was observed between patients with R0 resection and patients with R1 resection[7,27,28]. In the present study, the resection rate was 72.1% (49/68), and all resections were R0. Whether the margins were > 1 cm or not was not related to survival. Furthermore, there was no significant difference in 1-, 3-, and 5-year survival rates between AR and NAR resection (96.0%, 50.6%, and 11.4% vs 95.5%, 51.7%, and 9.7%, respectively). These results suggest that the objective is to achieve R0 no mater using AR or NAR resection. A number of studies have indicated that patients with positive lymph nodes have a poor prognosis[11,13,17,18]. Bagante et al[13] showed that the 5-year survival rate in patients with positive lymph nodes was 9.4%, while in patients with negative lymph nodes, it was 45.5%. In the present study, the 5-year survival rate in patients of the resection group and with positive lymph nodes was 0%, compared with 21.7%, in patients with negative lymph nodes. Lymph node metastasis could be an important prognostic factor for ICC. Nevertheless, there is still no definite conclusion as to whether resection of positive lymph nodes can extend survival or not[17,18,29,30].

Previous studies showed that vascular invasion was an important factor affecting the prognosis of ICC[27,31,32] . Our results revealed that the 3- and 5-year survival rates in the resection group with vascular invasion were 16.7% and 0%, respectively, compared with 66.3% and 22.2%, respectively, in patients without. The survival rate in patients without vascular invasion was higher than that of patients with vascular invasion. The multivariate analysis revealed that vascular invasion was an independent prognostic factor in patients with ICC.

In the present study, there was no significant difference in survival for left and right lobe tumors in the resection group. However, in the whole group of 68 patients, the resection rate of tumor in the right lobe was 95.0% (38/40), and that in the left lobe was 39.3% (11/28), indicating that the resection rate of tumors in the left lobe was low. Survival analysis also suggested that the survival rate was low for patients with tumors in the left lobe, which may be because tumors in the left lobe are more prone to metastasis through the ligament of the liver and stomach. In addition, we also noted that tumors in the left lobe could metastasize from the round ligament of the liver and sickle ligament of the liver to the abdominal wall. Nevertheless, further study is necessary for confirmation.

Data revealed that 25%-40% of the tumors with metastasis could not be dissected by surgical exploration for ICC patients whose tumors are considered to be removable before surgery. Therefore, laparoscopic examination should be performed before operation for patients with multicentric lesions, high CA19-9, suspected vascular infiltration, or peritoneal carcinomatosis[4]. In the present study, 19 patients (27.9%) underwent surgical exploration. Among the 40 cases with tumors in the right lobe of the liver, 5% (n = 2) underwent surgical exploration, while 60.7% (n = 17) underwent surgical exploration among the 28 patients with tumors in the left lobe of the liver, suggesting that the exploration rate was high for tumors in the left lobe of the liver. Among the 14 cases with preoperative ascites, there were 13 cases with abdominal metastasis and peritoneal metastasis. Therefore, we believe that routine laparoscopic exploration should be performed before operation for patients with tumors in the left lobe of the liver or with ascites in order to avoid meaningless laparotomy.

The present study is not without limitations. This was a retrospective, single-center study with a small sample size. In addition, it was limited to Chinese patients. Thus, the results should be validated using multicenter studies.

CONCLUSION

The prognosis of MF ICC patients is dismal, especially those with ascites or vascular invasion. Surgical resection is a key factor in improving overall survival in patients with MF ICC, and vascular invasion and lymph node metastasis affect the efficacy of surgical resection.

ARTICLE HIGHLIGHTS

Research background

The mass-forming (MF) type is the most common intrahepatic cholangiocarcinoma (ICC), accounting for 57.1%-83.6% of ICCs. Nevertheless, little is known about the epidemiology and treatment of MF ICC.

Research motivation

To improve the outcomes of ICC.

Research objectives

To examine the prognostic factors for patients with MF ICC.

Research methods

We carried out a retrospective analysis of consecutive patients with MF ICC. The patients were divided into either a resection group or an exploration group according to the treatment received.

Research results

The pooled 1-, 3-, and 5-year survival rates in the 68 patients with MF ICC were 66.5%, 36.3%, and 9.3%, respectively. Univariate analysis revealed that surgical resection (P < 0.001), nodal metastasis (P < 0.001), tumor location (P = 0.039), vascular invasion (P < 0.001), ascites (P < 0.001), and differentiation (P = 0.009) were significantly associated with the prognosis and survival of MF ICC. Multivariate analysis revealed that ascites (hazard ratio [HR] = 5.6, 95% confidence interval [CI]: 1.6-18.9, P = 0.006) and vascular invasion (HR = 2.5, 95%CI: 1.0-6.1, P = 0.045) were independent risk factors for MF ICC. The pooled 1-, 3-, and 5-year survival rates in the 19 patients of the exploration group were 5.3%, 5.3%, and 0, respectively. Among the 49 patients who underwent surgical resection, the pooled 1-, 3-, and 5-year survival rates were 93.5%, 49.7%, and 14.4%, respectively. Univariate and multivariate analyses revealed that vascular invasion (HR = 3.1, 95%CI: 1.2-8.5, P = 0.024) and nodal metastasis (HR = 3.2, 95%CI: 1.4-7.6, P = 0.008) were independent prognostic risk factors for surgical resection patients.

Research conclusions

The prognosis of MF ICC patients is dismal, especially those with ascites or vascular invasion. Surgical resection is a key factor in improving overall survival in patients with MF ICC, and vascular invasion and lymph node metastasis affect the efficacy of surgical resection.

Research perspectives

Surgical resection is a key factor in improving overall survival in patients with MF ICC, and vascular invasion and lymph node metastasis affect the efficacy of surgical resection.

Footnotes

Institutional review board statement: The study was approved by the Medical Ethics Committee of the Chinese PLA General Hospital.

Conflict-of-interest statement: All authors have no competing interests to disclose.

Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

Provenance and peer review: Unsolicited article; Externally peer reviewed.

Peer-review model: Single blind

Peer-review started: October 11, 2021

First decision: November 17, 2021

Article in press: April 20, 2022

Specialty type: Gastroenterology and hepatology

Country/Territory of origin: China

Peer-review report’s scientific quality classification

Grade A (Excellent): A

Grade B (Very good): B, B

Grade C (Good): 0

Grade D (Fair): 0

Grade E (Poor): 0

P-Reviewer: Andersen JB, Denmark; Jusakul A, Thailand; Pandya S, United States S-Editor: Wang LL L-Editor: Wang TQ P-Editor: Wang LL

Contributor Information

Jian Feng, Department of Hepatopancreatobiliary Surgery, Peking University Shougang Hospital, Beijing 100144, China; Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.

Bin Liang, Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.

Hang-Yu Zhang, Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.

Zhe Liu, Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.

Kai Jiang, Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China.

Xiang-Qian Zhao, Faculty of Hepato-Pancreato-Biliary Surgery, Institute of Hepatobiliary Surgery of Chinese PLA, Key Laboratory of Digital Hepatobiliary Surgery, Chinese PLA General Hospital, Beijing 100853, China. zhaoxq8014@163.com.

Data sharing statement

Additional date are available.

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