Skip to main content


We’d like to understand how you use our websites in order to improve them. Register your interest.

Intrahepatic cholangiocarcinoma – influence of resection margin and tumor distance to the liver capsule on survival



Intrahepatic cholangiocarcinoma (ICC) is often diagnosed in advanced stage. Aim of this study was to analyse the influence of resection margins and tumor distance to the liver capsule on survival and recurrence in a single center with a high number of extended resections.


From January 2008 to June 2018 data of all patients with ICC were collected and further analysed with Kaplan Meier Model, Cox regression or Chi2 test for categorical data.


Out of 210 included patients 150 underwent curative intended resection (71.4%). Most patients required extended resections (n = 77; 51.3%). R0-resection was achieved in 131 patients (87.3%) with minimal distances to the resection margin > 1 cm in 22, 0.5-1 cm in 11, 0.1–0.5 cm in 49 patients, and <  0.1 cm in 49 patients. Overall survival (OS) for margins > 0.5 cm compared to 0.5–0.1 cm or R1 was better, but without reaching significance. All three groups had significantly better OS compared to the irresectable group. Recurrence-free survival (RFS) was also better in patients with a margin > 0.5 cm than in the < 0.5–0.1 cm or the R1-group, but even without reaching significance. Different distance to the liver capsule significantly affected OS, but not RFS.


Wide resection margins (> 0.5 cm) should be targeted but did not show significantly better OS or RFS in a cohort with a high percentage of extended resections (> 50%). Wide margins, narrow margins and even R1 resections showed a significant benefit over the irresectable group. Therefore, extended resections should be performed, even if only narrow margins can be achieved.

Peer Review reports


Intrahepatic cholangiocarcinoma (ICC) is a rare tumor and the least frequent of all bile duct cancers. Its incidence especially in the western countries is rising in the last decades [1,2,3]. Because of its rarity, only few survival analyses exist in the literature identifying several risk factors for poor prognosis such as tumor size, multifocality, positive lymph nodes, metastases, vascular infiltration, incomplete resection or additional liver disease [4,5,6].

Currently, complete tumor resection is considered the only chance for cure. The role of positive or negative resection margin is extensively investigated in other primary or secondary liver malignancies such as colorectal liver metastases (CRLM) or hepatocellular carcinoma (HCC), but still controversial for ICC. Even between CRLM and HCC, the importance of minimal resection margin differs. While in CRLM the impact of the resection margin on long-term outcome is associated with the response to chemotherapy [7, 8], larger resection margins are associated with better survival for HCC patients [9]. Similarly, the extent of the resection margin has been suggested also to be important for ICC in single [10] or multicentre studies [11, 12]. However, the importance of the distance to the liver capsule has not been analysed for intrahepatic cholangiocarcinoma at all.

The aim of this current study was to investigate the influence of the distances to the resection margin as well as to the liver capsule on recurrence-free and overall survival as well as the pattern of recurrence in a single center.


All patients undergoing exploration for liver resection were collected in a prospective institutional database. Only patients who underwent explorative laparotomy for ICC between January 2008 and June 2018 qualified for this analysis. Patients with mixed ICC/HCC tumors were excluded from this analysis. Tumors with origin in the perihilar bile ducts recognizable by biliary intraepithelial neoplasia were excluded from the study. Data of eligible patients were transferred to a SPSS 23 (SPSS Inc. Released 2014, IBM SPSS Statistics for Windows, Version 23.0, IBM Armonk, NY, USA: IBM Corp.) database for further analysis.

All patients signed informed consent that data and follow-up will be collected anonymously and is potentially used for scientific analysis. Regarding to the regulations of the federal state law (state hospital law §36 & §37) and the independent ethics committee of Rheinland-Palatinate, no ethical approval was necessary for this study.

Staging procedures – surgery – follow up

Preoperative staging was based on high resolution computed tomography (CT) and/or magnetic resonance imaging (MRI) of good quality. If not previously performed elsewhere, we routinely performed colonoscopy and gastroscopy to exclude a primary gastrointestinal tumor. A preoperative biopsy does not belong to our routine work-up, but some patients were referred after histological proof of ICC.

All procedures were performed by the surgical HPB team. Surgery for ICC routinely includes a standard hilar lymphadenectomy. Follow-up was performed every 3 months for at least 2 years and based on CT-scan or MRI 3 months after surgery, and every 6 months thereafter. In between patients underwent ultrasound. After 2 years we recommended the patients to continue CT or MRI imaging every 6 months, but offered continuation of ultrasound as well. Whenever follow-up was performed outside our center due to the distance from their homes, we contacted the referring physician for all necessary information.

Data analysis

The surgical procedures, morbidity, mortality, histological results, recurrence-free and overall survival were analysed. Major and minor resections were classified according to the Brisbane-classification [13]: extended resections were defined as ≥5 resected segments and included mesohepatectomy, associating liver partition and portal vein ligation for staged hepatectomy (ALPPS) and all resections requiring the resection of surrounding organs or vessels.

The UICC 8th edition was used for disease staging [14]. Surgical morbidity was classified according to Clavien-Dindo [15], and mortality includes all in-hospital deaths as well as those occurring within 30- and 90-days from surgery.

Resection margins and tumor-relation to the liver capsule

The extent of the resection margin was grouped: > 2 cm, 1-2 cm, 0.5-1 cm, 0.1–0.5 cm, < 0.1 cm or R1.

In addition, the distance of the tumor to the liver capsule was quantified as “distant” (> 0.5 cm), “close/infiltration (< 0.5 cm)” or perforation. The distance of 0.5 cm was chosen because of a definition through our department of pathology that no detailed distance was given, if the distance exceeded 0.5 cm. Additionally, a group of patients showed centrally located ICC with dissemination/infiltration of the hepatic hilum. Because of the periductal dissemination and growth out of the liver parenchyma we defined these patients as own subgroup. The preoperative imaging, clinical and intraoperative features of these tumors (tumor diameter > 3 cm, located in second or third order bile ducts, imaging like a centrally located ICC) argued for them to be ICC involving the liver hilum, like described before [16, 17].

Statistical analysis

Only patients with complete data-sets were included in the statistical analyses. Statistics for categorial data was performed with the χ2-Test. The Kaplan Meier model was used for survival analyses, and the log rang test was used for the comparison of factors. Perioperative deaths were excluded from survival analyses. Multivariate analysis was performed using the Cox regression model.


Of 210 patients, who all underwent exploration for curative intended resection, 150 underwent liver resection with curative intent (71.4%). Reasons for irresectability (n = 60) were peritoneal carcinomatosis (n = 23), multifocal tumor dissemination (n = 15), locally advanced infiltration (n = 11) or cirrhosis/small for size liver remnant/poor quality of parenchyma (n = 11).

Gender was nearly equally distributed in the resection group (♀ n = 73; ♂ n = 77) with a median age of 64.2 years (IQR 56–73.7; range 32.3–84.4). The median BMI was 26.1 (IQR 23.8–29.3) while most patients were ASA II (n = 62) or III (n = 83) [ASA I n = 2, IV n = 3]. The majority of patients (n = 106) required major or even extended liver resections, and 131 patients underwent an R0 resection (87.3%). The majority of tumors was locally advanced (Table 1).

Table 1 Surgical procedures and histological outcome

Visceral and vascular extensions

In total, liver resection was extended in 102 cases by visceral and/or vascular resections in 61 patients. Neither the infiltration (p = 0.286) nor the resection of surrounding viscera (p = 0.26) were prognostic for the status of the resection margin (R0/R1). Also, the resection of surrounding vessels (e.g. portal vein, vena cava, p = 0.077) and the infiltration of such vessels (p = 0.389) had no influence on the margin status (R0 or R1).

Morbidity and mortality

Complications occurred in 69 patients (46%), of which 17 patients had minor complications (Dindo I + II). Treatment relevant complications (Dindo IIIa – IVb) occurred in 39 patients, and 13 patients (8.7%) died in the postoperative course due to sepsis (n = 3), liver (n = 4) or multi-organ (n = 6) failure. Twelve of these deaths occurred within 30 days, while one patient died within 90 days.

Factors associated with small resection margins and the distance to the liver capsule

A R0 resection was achieved in 131 patients (87.3%), and 19 resections were classified as R1, but none as R2. Subgroups according to established risk factors were analysed regarding their relevance for achieving a sufficient resection margin. Since the median resection margin reached 0.1 cm, patients were grouped for ≤0.1 cm vs. > 0.1 cm, and the association of the established risk factors were tested in cross tabulation: gender (p = 0.009), major resection (p = 0.004), extended resection (p = 0.029), vascular extension and reconstruction (p = 0.005), vascular infiltration (p = 0.047), tumor grading (G1 + 2 vs G3 + 4; p = 0.024) and T stage (p = 0.027) were significantly associated with resection margins.

The distance of the tumor to the liver capsule was analysed in the same way. Groups for cross tabulation were distant (n = 50), close/infiltration (n = 78) and perforation of the capsule (n = 11) in combination with the periductal dissemination growth type (n = 11). Significance was reached for extended resection (p <  0.001), T stage (p < 0.001), visceral extension (p < 0.001), visceral infiltration (p < 0.001), multifocality (p = 0.001) and UICC stage (UICC I + II vs. UICC III + IV; p = 0.002).

Tumor recurrence

Ninety-six patients (64%) developed a tumor recurrence within a median follow-up of 62.5 months. Most recurrences developed within the liver only (n = 42, 43.8%), while about a third of recurrences each were detected within and outside the liver (n = 29, 30.2%) or only outside the liver (n = 25, 26%). Different resection margins had no significant influence on the location of tumor recurrence (p = 0.354), neither had tumor distance to the liver capsule (p = 0.072).

The majority of recurrences (n = 60) was treated by palliative chemotherapy, and 12 patients only received best supportive care. Eleven patients qualified for repeat liver (n = 9) or extrahepatic (n = 2) resection, and another 6 patients underwent tumor ablation. In addition, four patients were treated by trans-arterial chemoembolization (TACE) and selective internal radiotherapy (SIRT), stereotactic irradiation or palliative surgery, once each, due to a limited intrahepatic but unresectable recurrence. Therapy of recurrence did not differ significantly regarding resection margins (p = 0.404) or distance to the liver capsule (p = 0.874).

Survival analysis

Influence of the extent of the resection margins and tumor distance to the liver capsule on overall survival

The median overall survival (OS) in an intention to treat analysis was 21.6 months with consecutive 1-, 3- and 5-year OS rates of 72, 29 and 16%, respectively. After excluding perioperative deaths, the median OS was 23.6 months with consecutive 1-, 3- and 5-year OS rates of 79, 32 and 17%, respectively.

A comparison of R0 versus R1 resections showed no significant survival difference (p = 0.655; Fig. 1a, Table 2). Also, the OS rates of the R1, < 0.1 cm and 0.1–0.5 cm groups were comparable (p = 0.732; Fig. 1b). A margin > 0.5 cm was associated with a longer OS, although the difference did not reach significance (p = 0.087; Fig. 2). All resected patients had a significantly better OS than patients with irresectable disease (p < 0.001; Fig. 2).

Fig. 1

a Kaplan Meier curve of the R0 and R1 resection groups comparing overall survival. p = 0.655; perioperative deaths were excluded. b Kaplan Meier curve comparing overall survival of the resection margin subgroups R1, < 0.1 cm and 0.1–0.5 cm with a comparable outcome. p = 0.732; perioperative deaths were excluded

Table 2 Overall and recurrence-free survival of the resection margin groups
Fig. 2

Kaplan Meier curve comparing overall survival of the > 0.5 cm, 0.5–0.1 cm, R1 resection and Irresectable group. Between the > 0.5 cm, 0.5–0.1 cm and R1 groups no significant difference in overall survival could be shown. But all of these groups had a favourable outcome compared to the Irresectable group (p < 0.001 for > 0.5 cm and 0.5–0.1 cm; p = 0.001 for R1); perioperative deaths were excluded

The tumor distance to the liver capsule had a significant influence on OS (p = 0.033; Table 3): the distant (p = 0.007) and close/infiltration groups (p = 0.032) had a significantly better OS compared to the periductal dissemination group, while no other cross testing led to significant differences.

Table 3 Overall and recurrence-free survival of tumor proximity to liver capsule groups

Influence of extent of the resection margins and tumor distance to the liver capsule on the recurrence-free survival

The median recurrence-free survival (RFS) was 9.7 months with a consecutive 1-, 3- and 5-year RFS rates of 38, 16 and 12%, respectively.

We observed a trend to a lower recurrence rate in case of a resection margin > 0.5 cm (p = 0.076), but the distance to the liver capsule did not reveal such a trend (p = 0.706).

The most favourable outcome was observed in patient with a resection margin > 0.5 cm (Table 2), who had a significantly longer RFS than patients with a smaller resection margin (p = 0.040; Fig. 3).

Fig. 3

Kaplan Meier curve for recurrence-free survival of the > 0.5 cm, the 0.5–0.1 cm and R1 resection group showing no significant difference. Perioperative deaths were excluded

Also, for the distance of the tumor to the liver capsule, we found a trend for a longer RFS, which however, did not reach statistical significance (p = 0.142, Table 3). All patients with a perforated liver capsule or a periductal dissemination recurred within 5-years from surgery (Table 3).

Multivariate analyses

Several parameters were tested in univariate analysis and included in multivariate analysis (Table 4). For overall survival beneath tumor distance to the liver capsule, age, major resection, tumor size (> 10 cm vs. < 10 cm) and N-stage showed to be independent predictors. For recurrence-free survival resection margin, tumor size (> 10 cm vs. < 10 cm), multifocality and M-stage were independent predictors.

Table 4 Univariate and multivariate analyses


We report on a single center cohort with a high number of extended resections and vascular or visceral extensions. The aim was to demonstrate the influence of resection margins and tumor distance to the liver capsule on survival and the pattern of recurrence. Neither resection margin width nor tumor distance to the liver capsule influenced the pattern of recurrence. For resection margins we were able to show that margins > 0.5 cm had a better long-term OS and RFS, but without reaching significance in direct comparison. Nevertheless, in multivariate analysis resection margins > 0.5 cm showed to be one independent predictor for RFS. In case of tumor distance to the liver capsule a significant impact on OS could be shown, while RFS was not influenced significantly. Multivariate analysis confirmed this finding with tumor distance to the liver capsule showed to be an independent predictor for OS.

Complete resection is the goal in oncologic surgery, but especially in liver surgery, different factors like multifocality or advanced tumor growth due to late diagnosis with or without infiltration of surrounding organs or structures may lead to borderline resectability and the necessity of extended resections [6, 18,19,20].

In the absence of treatment alternatives, we offer liver surgery whenever a tumor appears technically resectable. Due to the extent of ICC in many cases, more than half of our patients required extended resections regarding liver volume or perihepatic structures.

Even if liver surgery and extended liver resections have evolved over the last decades, intrahepatic cholangiocarcinoma has still a bad prognosis after resection with 5-year overall survival rates between 21 and 35% [4,5,6, 21, 22]. We achieved a 5-year survival of 17% which is most likely explained through our aggressive attitude. In our resection group, we had a total morbidity of 46% (Clavien-Dindo I – V). Major complications (Clavien-Dindo III – V) occurred in 34.7% of cases with a mortality of 8.7%, which is comparable to the literature [4, 23, 24], especially considering the fact that extended resections were performed frequently.

Surgery remains the only chance of cure taking into account, that ablation may also lead to complete tumor clearance. Because of the late onset of symptoms ICC is often diagnosed when ablation is not feasible or possible anymore. Therefore, ablation has its role in the treatment of recurrent ICC mainly [25].

Resection margins are important and because of their prevalence more often and better analyzed in liver surgery for colorectal liver metastasis (CRLM) or hepatocellular carcinoma (HCC). While for CRLM clear margins are most important in patients who do not respond well to chemotherapy [7, 8], Zhong and colleagues showed for HCC on 1932 patients that wide surgical margins > 1 cm significantly improve survival [9]. In contrast and respect of a much smaller cohort (n = 130) Field and colleagues presented a comparable overall and recurrence-free survival for narrow (< 0.5 cm) and wide (> 0.5 cm) groups for HCC [26]. For ICC especially, studies with large cohorts are lacking due to its low incidence. While the impact of resection margins on survival varied in smaller cohorts [10, 27,28,29], papers of Yeh and colleagues (n = 224, single-center, analyzed period of 30 years) with a larger and especially Spolverato and colleagues (multi-center [12 centers], analyzed period 23 years) with the largest cohort (n = 584) were able to show a significant influence on survival [11, 30]. In two meta-analysis of Li (comparing R0 vs R1) and Tang (comparing margins > 1 cm vs. < 1 cm) and colleagues, both were able to show significant survival benefits for the R0 respectively the > 1 cm groups [31, 32]. We were able to show a survival benefit for margins > 0.5 cm, but without statistical significance. The size of our cohort is not comparable to the beforementioned cohorts, which is of course a limitation of our analysis. Nevertheless, Yeh et al. analyzed a very long time period (30 years) in a single-center and Spolverato et al. a much longer time period (23 years) of a multi-center data. Therefore, our single center cohort with an analyzed period of ten and a half years is most probably more homogenous than the above-mentioned cohorts.

In addition, we performed many extended resections with either visceral and/or vascular extensions. Visceral or vascular extension did not influence R0 or R1 resection, but with the median margin width of 0.2 cm as cut off, gender, vascular extension, T stage, major or extended hepatic resection had significant influence. Gender was nearly balanced in our cohort. Interestingly, Spolverato and colleagues reported a strong impact of gender on resection margins as well (p < 0.001 [11];). Further analysis of our data showed that women had significantly more frequent tumors > 7 cm (median 6.4 cm) than men (p = 0.039). The T stage is an expression of infiltration depth including e.g. multifocality and higher T stages are more likely to be borderline resected. The same applies for vascular extension and both together explain the need for major or extended resection. These results are according to findings of Spolverato et al. as well [11].

Tumor recurrence is common after resection of ICC and the main reason for poor long-term survival. Most often recurrence is located isolated intrahepatically with up to 60%, followed by intra- and extrahepatic (ca. 20%) or isolated extrahepatic (ca. 20%) recurrence [33, 34]. The negative influence of narrow resection margins on recurrence or recurrence-free survival is demonstrated in different studies [6, 11, 27, 28]. Accordingly, we were able to show that margins > 0.5 cm led to a significant benefit for recurrence-free survival. Data on this special topic are scarce. Until 2017, no data of prospective randomized trials were available and the adjuvant treatment of ICC after resection was not standardized. Ercolani and colleagues showed that adjuvant treatment with Gemcitabine based mono or combined treatment led to a significant benefit in overall survival [35]. Wirasorn et al. were able to show beneath the general benefit of adjuvant treatment, that the combination of Gemcitabine and Capecitabine led to the best long-term outcome [36]. We did not apply any standard adjuvant chemotherapy until the first results of the BILCAP trial got available [37]. Capecitabine is now standard adjuvant treatment after resection. Some patients with unfavorable histological results were offered an individualized consultation with our oncologists and some were included in the early ACTICCA-trial. Alternative adjuvant treatment modalities like transarterial chemoembolization (TACE), radiation alone or chemotherapy in combination with radiation might play a role in the future [38,39,40]. We did not consider any of these alternatives as adjuvant treatment, because prospective randomized data does not exist, at least not yet.

We performed a multivariate analysis of several clinical and histological factors known for influencing OS and RFS for ICC. For OS tumor distance to the liver capsule showed to be an independent predictor while resection margins did not. Further age, major resection, tumor size and N-stage showed to be significant. Within the literature especially multifocality, N-stage or R-stage showed to be independent predictors for OS [4, 5, 22, 41]. Regarding RFS resection margins with a cut-off of 0.5 cm showed to be significant while tumor distance to the liver capsule did not. Further independent predictors for RFS were tumor size, multifocality and M-stage. Resection margins do not influence OS but RFS in our cohort with a high percentage of extended resections. This may be explained by the importance of tumor resection for OS, while recurrence is obviously and understandable depending on wider resection margins.

To the best of our knowledge the influence of tumor distance to the liver capsule on overall and disease-free survival has not been analysed yet. We were able to show a significant benefit for overall survival, especially for the distant and close/infiltration groups, but no influence on recurrence-free survival. In addition to distant, close/infiltration and perforation groups we specially classified a periductal dissemination type. We observed that some ICC deriving from centrally located bile ducts spread into the liver hilum without perforating the liver capsule. This special type is most likely comparable to the hilar type ICC described by Zhang and colleagues [16]. In their study the hilar type ICC had significant worse outcome compared to peripheral ICC (and perihilar cholangiocarcinoma), which matches our findings. All patients of the periductal dissemination group had a survival less than 3 years. One may argue that these tumors are perihilar cholangiocarcinoma. But as mentioned in the methods section, imaging, clinical and intraoperative features argued for these tumors to be ICC involving the liver hilum, as described by Zhang and Murakami et al. [16, 17]. Furthermore, the median diameter of these tumors was 5.7 cm (IQR 4.1–9.3; Mean 6.4 cm), which is highly uncommon, especially for resectable perihilar cholangiocarcinoma.

Complete tumor clearance with vascular and visceral extensions may explain why tumor distance to the liver capsule did not predict RFS in multivariate analysis. This is different in case of OS, imaginable especially due to the worse tumor biology in case of tumors with perforation of the liver capsule or the periductal dissemination type.


In conclusion, resection margins > 0.5 cm, < 0.1–0.5 cm or R1 resections showed no significant difference for overall and recurrence-free survival. All of these groups had a clear and significant benefit over irresectable tumors. Therefore exploration and if necessary extended resection should be considered, even if only narrow margins can be achieved. Tumor distance to the liver capsule showed an influence on overall and recurrence-free survival with disadvantages especially for the perforation or periductal dissemination groups.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.



Advanced liver partition and portal vein ligation for staged hepatectomy


American Society of Anaesthesiologists


Colorectal liver metastasis


Computed tomography


Hepatocellular carcinoma


Intrahepatic cholangiocarcinoma


Interquartile range


Magnetic resonance imaging


Overall survival


Recurrence-free survival


Selective internal radiotherapy


Trans-arterial chemoembolization


  1. 1.

    Gupta A, Dixon E. Epidemiology and risk factors: intrahepatic cholangiocarcinoma. Hepatobiliary Surg Nutr. 2017;6(2):101–4.

    Article  Google Scholar 

  2. 2.

    Razumilava N, Gores GJ. Cholangiocarcinoma. Lancet. 2014;383(9935):2168–79.

    Article  Google Scholar 

  3. 3.

    Shaib YH, Davila JA, McGlynn K, El-Serag HB. Rising incidence of intrahepatic cholangiocarcinoma in the United States: a true increase? J Hepatol. 2004;40(3):472–7.

    Article  Google Scholar 

  4. 4.

    Lang H, Sotiropoulos GC, Sgourakis G, Schmitz KJ, Paul A, Hilgard P, et al. Operations for intrahepatic cholangiocarcinoma: single-institution experience of 158 patients. J Am Coll Surg. 2009;208(2):218–28.

    Article  Google Scholar 

  5. 5.

    de Jong MC, Nathan H, Sotiropoulos GC, Paul A, Alexandrescu S, Marques H, et al. Intrahepatic cholangiocarcinoma: an international multi-institutional analysis of prognostic factors and lymph node assessment. J Clin Oncol. 2011;29(23):3140–5.

    Article  Google Scholar 

  6. 6.

    Bartsch F, Baumgart J, Hoppe-Lotichius M, Schmidtmann I, Heinrich S, Lang H. Visceral infiltration of intrahepatic cholangiocarcinoma is most prognostic after curative resection - retrospective cohort study of 102 consecutive liver resections from a single center. Int J Surg. 2018;55:193–200.

    Article  Google Scholar 

  7. 7.

    Andreou A, Aloia TA, Brouquet A, Dickson PV, Zimmitti G, Maru DM, et al. Margin status remains an important determinant of survival after surgical resection of colorectal liver metastases in the era of modern chemotherapy. Ann Surg. 2013;257(6):1079–88.

    Article  Google Scholar 

  8. 8.

    de Haas RJ, Wicherts DA, Flores E, Azoulay D, Castaing D, Adam R. R1 resection by necessity for colorectal liver metastases: is it still a contraindication to surgery? Ann Surg. 2008;248(4):626–37.

    PubMed  Google Scholar 

  9. 9.

    Zhong FP, Zhang YJ, Liu Y, Zou SB. Prognostic impact of surgical margin in patients with hepatocellular carcinoma: a meta-analysis. Medicine (Baltimore). 2017;96(37):e8043.

    Article  Google Scholar 

  10. 10.

    Ma KW, Cheung TT, She WH, Chok KS, Chan AC, Ng IO, et al. The effect of wide resection margin in patients with intrahepatic cholangiocarcinoma: a single-center experience. Medicine (Baltimore). 2016;95(28):e4133.

    Article  Google Scholar 

  11. 11.

    Spolverato G, Yakoob MY, Kim Y, Alexandrescu S, Marques HP, Lamelas J, et al. The impact of surgical margin status on long-term outcome after resection for intrahepatic Cholangiocarcinoma. Ann Surg Oncol. 2015;22(12):4020–8.

    Article  Google Scholar 

  12. 12.

    Farges O, Fuks D, Boleslawski E, Le Treut YP, Castaing D, Laurent A, et al. Influence of surgical margins on outcome in patients with intrahepatic cholangiocarcinoma: a multicenter study by the AFC-IHCC-2009 study group. Ann Surg. 2011;254(5):824–9 discussion 30.

    Article  Google Scholar 

  13. 13.

    Strasberg SM. Nomenclature of hepatic anatomy and resections: a review of the Brisbane 2000 system. J Hepato-Biliary-Pancreat Surg. 2005;12(5):351–5.

    Article  Google Scholar 

  14. 14.

    Brierley J, Gospodarowicz M, Wittekind C. International union against Cancer. TNM classification of malignant Tumours. 8th ed. Oxford: Wiley Blackwell; 2017.

    Google Scholar 

  15. 15.

    Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Ann Surg. 2004;240(2):205–13.

    Article  Google Scholar 

  16. 16.

    Zhang XF, Bagante F, Chen Q, Beal EW, Lv Y, Weiss M, et al. Perioperative and long-term outcome of intrahepatic cholangiocarcinoma involving the hepatic hilus after curative-intent resection: comparison with peripheral intrahepatic cholangiocarcinoma and hilar cholangiocarcinoma. Surgery. 2018;163(5):1114–20.

    Article  Google Scholar 

  17. 17.

    Murakami Y, Uemura K, Sudo T, Hashimoto Y, Nakashima A, Sueda T. Intrahepatic cholangiocarcinoma: clinicopathological differences between peripheral type and hilar type. J Gastrointest Surg. 2012;16(3):540–8.

    Article  Google Scholar 

  18. 18.

    Lam VW, Spiro C, Laurence JM, Johnston E, Hollands MJ, Pleass HC, et al. A systematic review of clinical response and survival outcomes of downsizing systemic chemotherapy and rescue liver surgery in patients with initially unresectable colorectal liver metastases. Ann Surg Oncol. 2012;19(4):1292–301.

    Article  Google Scholar 

  19. 19.

    van Dam RM, Lodewick TM, van den Broek MA, de Jong MC, Greve JW, Jansen RL, et al. Outcomes of extended versus limited indications for patients undergoing a liver resection for colorectal cancer liver metastases. HPB (Oxford). 2014;16(6):550–9.

    Article  Google Scholar 

  20. 20.

    Lafaro K, Grandhi MS, Herman JM, Pawlik TM. The importance of surgical margins in primary malignancies of the liver. J Surg Oncol. 2016;113(3):296–303.

    Article  Google Scholar 

  21. 21.

    Doussot A, Groot-Koerkamp B, Wiggers JK, Chou J, Gonen M, DeMatteo RP, et al. Outcomes after resection of intrahepatic Cholangiocarcinoma: external validation and comparison of prognostic models. J Am Coll Surg. 2015;221(2):452–61.

    Article  Google Scholar 

  22. 22.

    Sakamoto Y, Kokudo N, Matsuyama Y, Sakamoto M, Izumi N, Kadoya M, et al. Proposal of a new staging system for intrahepatic cholangiocarcinoma: analysis of surgical patients from a nationwide survey of the liver Cancer study Group of Japan. Cancer. 2016;122(1):61–70.

    Article  Google Scholar 

  23. 23.

    Bergeat D, Sulpice L, Rayar M, Edeline J, Merdignac A, Meunier B, et al. Extended liver resections for intrahepatic cholangiocarcinoma: friend or foe? Surgery. 2015;157(4):656–65.

    Article  Google Scholar 

  24. 24.

    Zhang XF, Bagante F, Chakedis J, Moris D, Beal EW, Weiss M, et al. Perioperative and long-term outcome for intrahepatic Cholangiocarcinoma: impact of major versus minor hepatectomy. J Gastrointest Surg. 2017;21(11):1841–50.

  25. 25.

    Shindoh J. Ablative therapies for intrahepatic cholangiocarcinoma. Hepatobiliary Surg Nutr. 2017;6(1):2–6.

    Article  Google Scholar 

  26. 26.

    Field WBS, Rostas JW, Philps P, Scoggins CR, McMasters KM, Martin RCG 2nd. Wide versus narrow margins after partial hepatectomy for hepatocellular carcinoma: balancing recurrence risk and liver function. Am J Surg. 2017;214(2):273–7.

    Article  Google Scholar 

  27. 27.

    Tamandl D, Herberger B, Gruenberger B, Puhalla H, Klinger M, Gruenberger T. Influence of hepatic resection margin on recurrence and survival in intrahepatic cholangiocarcinoma. Ann Surg Oncol. 2008;15(10):2787–94.

    Article  Google Scholar 

  28. 28.

    Murakami S, Ajiki T, Okazaki T, Ueno K, Kido M, Matsumoto I, et al. Factors affecting survival after resection of intrahepatic cholangiocarcinoma. Surg Today. 2014;44(10):1847–54.

    Article  Google Scholar 

  29. 29.

    Shimada K, Sano T, Sakamoto Y, Esaki M, Kosuge T, Ojima H. Surgical outcomes of the mass-forming plus periductal infiltrating types of intrahepatic cholangiocarcinoma: a comparative study with the typical mass-forming type of intrahepatic cholangiocarcinoma. World J Surg. 2007;31(10):2016–22.

    Article  Google Scholar 

  30. 30.

    Yeh CN, Hsieh FJ, Chiang KC, Chen JS, Yeh TS, Jan YY, et al. Clinical effect of a positive surgical margin after hepatectomy on survival of patients with intrahepatic cholangiocarcinoma. Drug Des Devel Ther. 2015;9:163–74.

    CAS  PubMed  Google Scholar 

  31. 31.

    Tang H, Lu W, Li B, Meng X, Dong J. Influence of surgical margins on overall survival after resection of intrahepatic cholangiocarcinoma: a meta-analysis. Medicine (Baltimore). 2016;95(35):e4621.

    CAS  Article  Google Scholar 

  32. 32.

    Li MX, Bi XY, Li ZY, Huang Z, Han Y, Zhao JJ, et al. Impaction of surgical margin status on the survival outcome after surgical resection of intrahepatic cholangiocarcinoma: a systematic review and meta-analysis. J Surg Res. 2016;203(1):163–73.

    Article  Google Scholar 

  33. 33.

    Spolverato G, Kim Y, Alexandrescu S, Marques HP, Lamelas J, Aldrighetti L, et al. Management and outcomes of patients with recurrent intrahepatic Cholangiocarcinoma following previous curative-intent surgical resection. Ann Surg Oncol. 2016;23(1):235–43.

    Article  Google Scholar 

  34. 34.

    Hyder O, Hatzaras I, Sotiropoulos GC, Paul A, Alexandrescu S, Marques H, et al. Recurrence after operative management of intrahepatic cholangiocarcinoma. Surgery. 2013;153(6):811–8.

    Article  Google Scholar 

  35. 35.

    Ercolani G, Vetrone G, Grazi GL, Aramaki O, Cescon M, Ravaioli M, et al. Intrahepatic cholangiocarcinoma: primary liver resection and aggressive multimodal treatment of recurrence significantly prolong survival. Ann Surg. 2010;252(1):107–14.

    Article  Google Scholar 

  36. 36.

    Wirasorn K, Ngamprasertchai T, Khuntikeo N, Pakkhem A, Ungarereevittaya P, Chindaprasirt J, et al. Adjuvant chemotherapy in resectable cholangiocarcinoma patients. J Gastroenterol Hepatol. 2013;28(12):1885–91.

    CAS  Article  Google Scholar 

  37. 37.

    Primrose JN, Fox R, Palmer DH, Prasad R, Mirza D, Anthoney DA, et al. Adjuvant capecitabine for biliary tract cancer: The BILCAP randomized study. ASCO 2017; Abstract 4006. 2017.

    Google Scholar 

  38. 38.

    Li J, Wang Q, Lei Z, Wu D, Si A, Wang K, et al. Adjuvant Transarterial chemoembolization following liver resection for intrahepatic Cholangiocarcinoma based on survival risk stratification. Oncologist. 2015;20(6):640–7.

    Article  Google Scholar 

  39. 39.

    Shinohara ET, Mitra N, Guo M, Metz JM. Radiation therapy is associated with improved survival in the adjuvant and definitive treatment of intrahepatic cholangiocarcinoma. Int J Radiat Oncol Biol Phys. 2008;72(5):1495–501.

    Article  Google Scholar 

  40. 40.

    Sur MD, In H, Sharpe SM, Baker MS, Weichselbaum RR, Talamonti MS, et al. Defining the benefit of adjuvant therapy following resection for intrahepatic Cholangiocarcinoma. Ann Surg Oncol. 2015;22(7):2209–17.

    Article  Google Scholar 

  41. 41.

    Wang Y, Li J, Xia Y, Gong R, Wang K, Yan Z, et al. Prognostic nomogram for intrahepatic cholangiocarcinoma after partial hepatectomy. J Clin Oncol. 2013;31(9):1188–95.

    Article  Google Scholar 

Download references


Not Applicable.


No funding was obtained for this study.

Author information




All authors critically revised the manuscript, approved the final version to be published, and agree to be accountable for all aspects of the work. FB: concept and design of the study, data acquisition, statistical analysis, draft of the manuscript, critically revision. JB: data acquisition. MH-L: data acquisition, follow-up. BKS: draft of the manuscript, critically revision. SH: draft of the manuscript, critically revision. HL: concept and design of the study, draft of the manuscript, critically revision.

Corresponding author

Correspondence to Hauke Lang.

Ethics declarations

Ethics approval and consent to participate

This article analysis retrospective data and does not contain any studies with human participants or animals performed by any of the authors. All patients signed informed consent that data and follow-up will be collected anonymously and is potentially used for scientific analysis. Regarding to the regulations of the federal state law (state hospital law §36 & §37) and the independent ethics committee of Rhineland-Palatinate, no ethical approval was necessary for this study.

Consent for publication

Not Applicable.

Competing interests

The authors declare that they have no financial or non-financial competing interests.

Additional information

Publisher’s Note

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

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Bartsch, F., Baumgart, J., Hoppe-Lotichius, M. et al. Intrahepatic cholangiocarcinoma – influence of resection margin and tumor distance to the liver capsule on survival. BMC Surg 20, 61 (2020).

Download citation


  • Intrahepatic cholangiocarcinoma
  • Cholangiocarcinoma
  • Resection margin
  • Tumor distance
  • Liver capsule
  • Overall survival
  • Recurrence