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Failure patterns after curative resection for intrahepatic cholangiocarcinoma: possible implications for postoperative radiotherapy

BMC Cancer volume 19, Article number: 1108 (2019) Cite this article

Abstract

Background

To explore the patterns of failures and areas at highest risk of recurrence for postoperative intrahepatic cholangiocarcinoma (IHCC), with the aim to guide IHCC adjuvant radiotherapy.

Methods

Patients with IHCC who had undergone radical surgery at our institution from July 2010 to August 2017 were retrospectively analyzed. The survival and prognostic factors were analyzed by univariate and multivariate analysis. All sites of recurrence were found out and classified as the surgical margin, regional lymph nodes, liver remnant and distant metastasis. According to the recurring area at highest risk, the target volume of adjuvant radiotherapy was proposed.

Results

The median follow-up time was 23.5 months (2–85 months). The median recurrence free survival (RFS) and overall survival (OS) were 12.1 months and 24.8 months, respectively. Seventy-three (73/127, 57.5%) IHCC patients developed tumor recurrence. Initial recurrences occurred in the potential postoperative radiotherapy (PORT) volume, remnant liver and distant sits were 46 (46/73, 63.0%), 36 (36/73, 49.3%) and 22 (22/73, 30.1%) cases, respectively. Of the 46 patients whose initial recurrence inside the potential PORT volume, 29 (29/73, 39.7%) developed recurrence only inside the potential PORT volume, including 13 tumor bed recurrences, 7 lymph node metastases, and 9 with both tumor bed recurrences and lymph node metastases. The most common lymph node metastases sites were nodes around the abdominal aorta, followed by lymph nodes along the celiac artery, the common hepatic artery, and in the hepatoduodenal ligament.

Conclusions

High proportion of the recurrences occurred only inside the potential PORT volume, implying adjuvant radiotherapy might improve the local-regional control. Surgical margins and lymph node stations No.16a2, 9, 8, 12, 13, and 14 are suggested to be included in the radiation volume.

Peer Review reports

Background

Intrahepatic cholangiocarcinoma (IHCC) is an uncommon neoplasm, accounting for 5–10% of all cholangiocarcinomas [1, 2]. While prior studies estimated that IHCC occupied a minority of cholangiocarcinomas (CCAs) [2], more recent assessments reveal the incidence of IHCC seems to be rising across the world [3,4,5]. Owing to its intrahepatic location of IHCC, early symptoms are rare and most patients present with advanced tumors [6, 7]. IHCC has a dismal survival with limited treatment options and a very high rate of recurrence or metastatis [8, 9]. The mainstay of treatment of IHCC is surgical excision, definitive roles for adjuvant chemotherapy and radiotherapy have not been found, although both are used in daily practice [10, 11].

The literature on adjuvant radiation therapy for IHCC is sparse. In the few retrospective reports found in the English literature through Pubmed, the role of postoperative radiotherapy remains controversial. Shinohara et al. analyzed 3839 patients with IHCC revealed a better median OS with surgery and adjuvant radiotherapy than surgery alone (11 months vs 6 months, p = 0.014) [12]. Other two small size studies also proved the value of adjuvant therapy for postoperative IHCC [13, 14]. While a meta-analysis found a non-significant improvement in overall survival with adjuvant treatment (chemotherapy, radiation or both) compared with surgery alone [15]. Another study conducted by Hammad et al. reported that adjuvant radiotherapy was associated with an improved survival for patients with R1/R2 resection, but not for those with R0 resection [16]. To date, there is no prospective randomized study concerning the benefit of adjuvant radiotherapy on IHCC patients. Study on IHCC post-operative failure pattern might help to optimize adjuvant treatment strategies. If the rate of local recurrence is high, adjuvant radiotherapy might be engaged to improve local control. On the contrary, systematic chemotherapy should be considered if distant metastases are the predominant failure patterns.

In the present study, failure patterns of 127 postoperative IHCC patients were retrospectively analyzed, with the aim of providing more reference information for the design of adjuvant treatment.

Methods

Patients

This study was approved by the Institutional Review Board of the Second Affiliated Hospital, Zhejiang University School of Medicine (SAHZU). From July 2010 to August 2017, 182 patients had undergone surgery for intrahepatic cholangiocarcinoma at SAHZU, histopathology diagnosis were achieved after surgery. The medical records were retrospectively reviewed, 127 radical resection patients with at least 2-month follow-up were included. Data regarding the surgical resection performed and pathologic variables including sex, age, tumor staging, T classification, N classification, tumor differentiation, resection margins, tumor size, recurrence time, tumor markers, history of hepatitis, hypertension, diabetes, bile duct stone, jaundice, fever and postoperative chemotherapy were collected. Tumor staging was performed according to the guidelines of the American Joint Committee on Cancer (AJCC) Seventh edition [17] . Follow-up period ended on February 8, 2018. The diagnosis of recurrence is mainly based on imaging findings and clinical manifestations. RFS was measured from the day of operation to tumor recurrence, and OS from the day of operation to patient’s death or last follow-up. Long-term follow-up and patient status were determined by physician consult. Specific sites of first disease recurrence, time to disease recurrence, OS and RFS were analyzed.

Recurrence patterns

In the present study, the term “local-regional recurrence” was not used, as retroperitoneal lymph nodes recurrences are classified as distant metastases according to the 8th edition of the AJCC staging system. Instead, we use “potential volume of postoperative radiotherapy (PORT)” which including surgical margins, and high-risk lymphatic drainage area. The site(s) of initial disease recurrence, which determined from cross-sectional imaging studies (CT, MRI or PET-CT), were found out and classified as recurrences inside the potential PORT volume, residual liver, and distant recurrence. Biopsies for the recurrent lesions were encouraged. Radiologic evidence of tumor recurrence (suspicious new findings and progression of disease documented by serial imaging) was also accepted in patients who did not undergo biopsy. The date of initial disease recurrence was recorded as the time when the first suspicious radiologic finding was initially identified.

Statistical analysis

The correlation of patient characteristics with progression-free survival and overall survival were analyzed by Kaplan Meier analysis. Patient characteristics include tumor stage, T grade, lymph node status, tumor differentiation, nerve invasion, vascular invasion, tumor size, recurrence time, tumor markers, and history of hepatitis, schistosomiasis, hypertension, diabetes, gallstones, bile duct stones, Jaundice, fever, etc. Significance was evaluated using the log-rank test. Cox proportional hazards models was used for multivariate survival analysis. Statistical significance was defined as a p value< 0.05. IBM SPSS Statistics 19.0 was used for statistical analyses.

Results

Patient characteristics

The demographics of the 127 patients are summarized in Table 1. There were 64 men (50.4%) and 63 women (49.6%). The median patient age was 58 years old (range, 26–83 years old). Preoperative tumor markers examination was done in 125 cases, elevated CA-199 and CEA were detected in 82 (67.8%) and 36 (29.8%) cases, respectively. The mean tumor size was 4.5 cm (range 1.0–11.0 cm), of which 43 (33.9%) had a tumor size ≥5 cm. The differentiation of the IHCC was as follows: poor, 42 cases (33.1%); moderate, 52 cases (40.9%); well, 15 cases (11.8%); unkwon, 18 (14.2%). Distribution according to T stage was as follows: T1, 35 cases (27.6%); T2, 56 cases (44.1%); T3, 33 cases (26.0%); and T4, 3 cases (2.4%). Lymph nodes metastasis was found in 41 of the cases (32.3%). According to the tumor TNM staging, patients had stage I, II, III, and IV disease were 28 (22.0%), 34 (26.8%), 21 (16.5%), and 44 (34.6%) cases, respectively. Twenty eight patients received adjuvant chemotherapy.

Table 1 Intrahepatic cholangiocarcinoma patient characteristics
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Initial disease recurrence

Seventy-three (73/127, 57.5%) IHCC patients developed tumor recurrence. Disease progression was mainly documented by serial imaging in 65 patients (65/73, 89.0%), and 8 patients (8/73, 11.0%) had biopsy confirmation. Table 2 and Fig. 1 show the anatomic locations of all initial tumor progressions.

Table 2 Recurrent patterns of intrahepatic cholangiocarcinoma
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Fig. 1
figure 1

Initial recurrence pattern of intrahepatic cholangiocarcinoma (n = 73)

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Initial recurrences occurred in the potential PORT volume, remnant liver and distant sits were 46 (46/73, 63.0%), 36 (36/73, 49.3%) and 22 (22/73, 30.1%) cases, respectively. Among them, 20 cases had multiple sites of initial disease recurrence. Fifty-four patients had no evidence of disease at the last follow-up.

Of the 46 patients whose initial recurrence inside the potential PORT volume, 29 (29/73, 39.7%) developed recurrence only inside the potential PORT volume, including 13 tumor bed recurrences, 7 lymph node metastases, and 9 with both tumor bed recurrences and lymph node metastases. Three had synchronous recurrences at remnant liver, another 3 had synchronous recurrences at distant sites, and 11 had synchronous recurrences at remnant liver and distant sites.

Thirty-six patients developed initial recurrence in the remnant liver. Among them, 19 had remnant liver lesions as the only recurrences, 3 had synchronous recurrences in the potential PORT volume, another 3 had synchronous recurrences at distant sites, and 11 had synchronous recurrences at distant sites and the potential PORT volume.

Twenty-two had distant metastases at initial recurrence, 5 of them were distant metastases only (4 lung, 1 peritoneum), 3 had synchronous recurrences in the potential PORT volume, another 3 had synchronous remnant liver recurrences, and 11 had synchronous recurrences in the potential PORT volume and remnant liver.

Among the patients who received adjuvant chemotherapy, 17 patients relapsed. Seven patients relapsed inside the PORT volume, 7 patients relapsed outside the PORT volume, 3 patients relapsed both inside and outside the potential volume. The recurrence pattern was similar between patients received adjuvant therapy and the whole group.

The common sites of lymph node metastases were lymph nodes around the abdominal aorta (station No.16, n = 18), lymph nodes along the celiac artery (No.9, n = 13), lymph nodes along the common hepatic artery (No.8, n = 11), lymph nodes in the hepatoduodenal ligament (No. 12, n = 8), lymph nodes on the posterior aspect of the pancreatic head (No.13, n = 4), lymph nodes at the root of the mesenterium (No.14, n = 2). All patients with station No.16 recurrences had metastatic lesions at other lymph node stations or distant sites. Among them, 11 cases had lesions in No.16a2 with no metastases in No.16b1, 6 had lesions in No.16a2 and No.16b1. Only 1 case had lymph node metastases at station No.16b1 without lesion at No.16a2, but they had multiple metastatic nodes on the posterior aspect of the pancreatic head.

Follow-up and survival

The median follow-up time was 23.5 months (2–85 months), at the last follow-up on February 8, 2018, 59 patients were alive. The median recurrence free survival (RFS) and overall survival (OS) were 12.1 months and 24.8 months, respectively. In the univariate analysis of the entire cohort, improved survival was associated with age ≥ 55 years (RFS, 18.5 vs 10.0 months, p = 0.046; OS, 34.8 vs 18.6 months, p = 0.002) (Fig. 2), tumor size < 5 cm (RFS, 19.8 vs 6.7 months, p = 0.001; OS, 28.8 vs 21.5 months, p = 0.071) (Fig. 3), without lymph node metastasis (RFS, 21.2 vs 6.1 months, p < 0.001; OS, 40.2 vs 11.5 months, p < 0.001) (Fig. 4), without hepatitis (RFS, 17.6 vs 10.4 months, p = 0.005; OS, 25.2 vs 19.0 months, p = 0.079) (Fig. 5), early tumor staging (stage I and II vs stage III and IV, RFS, 30.2 vs 7.7 months, p < 0.001; OS, 45.5 vs 15.7 months, p < 0.001) (Fig. 6) and better tumor differentiation (poor vs moderate vs well, RFS, 6.7 vs 15.6 vs 51.7 months, p = 0.027; OS, 19.4 vs 28.8 months, not reached for well differentiation patients, p = 0.003) (Fig. 7). The results of the univariate analysis are summarized in Table 3. In the multivariate analysis, RFS of tumor size (RR 2.191; 95% confidence interval [CI] 1.257–3.817; p = 0.003) and tumor differentiation (RR 0.621; 95% confidence interval [CI] 0.408–0.947; p = 0.027) maintained significance. OS of age (RR 0.418; 95% confidence interval [CI] 0.236–0.740; p = 0.003) maintained significance.

Fig. 2
figure 2

Prognostic value of age in IHCC. Kaplan–Meier curves of RFS and OS in group with age less than 55 years old and equal to or more than 55 years old

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Fig. 3
figure 3

Prognostic value of tumor size in IHCC. Kaplan–Meier curves of RFS and OS in group with tumor size less than 5 cm and equal to or more than 5 cm

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Fig. 4
figure 4

Prognostic value of lymph node metastasis in IHCC. Kaplan–Meier curves of RFS and OS in group with lymph node metastasis and without lymph node metastasis

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Fig. 5
figure 5

Prognostic value of hepatitis in IHCC. Kaplan–Meier curves of RFS and OS in group with hepatitis and without hepatitis

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Fig. 6
figure 6

Prognostic value of tumor stage in IHCC. Kaplan–Meier curves of RFS and OS in group with tumor stage I, II and tumor stage III, IV

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Fig. 7
figure 7

Prognostic value of tumor differntiation in IHCC. Kaplan–Meier curves of RFS and OS in group with well, moderate and poor tumor differentiation

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Table 3 Univariate analyses for PFS and OS among 127 patients who underwent curative surgery for IHCC
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Discussion

This study analyzed the failure patterns of IHCC after curative resection. Tumor recurrences were found in up to 60% of the patients. Failures inside the potential PORT volume were found to be the most common sites of initial recurrences, followed by metastases in remnant liver and distant sits. Our findings implicate the possible benefits of postoperative radiotherapy for IHCC patients.

The frequency of postoperative failures in IHCC, including local-regional recurrence and remnant liver dissemination or distant metastases, has been reported to range from 53.5 to 80.0% [18,19,20,21,22]. Our result, with 57.5% of IHCC patients developed postoperative recurrence, was in line with the previous reports. For radiation oncologists, data on the specific patterns of recurrence can help to guide postoperative therapeutic approaches. According to the study by Hyder et al., the most common recurrent site after surgery of IHCC was intrahepatic [21]. While Doussot et al. reported a time dependent recurrence pattern. Recurrence within 24 months most often involved the liver (82.7%), and the most recurrences after 24 months were extrahepatic (61.1%) [22]. Recently, high local-regional recurrent rates as 62.5 and 68% of the total failures have been reported [18, 19]. The reported proportion of local-regional recurrence varies. Different statistical methods may explain for the inconsistent results. For example, margin recurrences usually be regarded as local failures, and might also be included in the intrahepatic failures. Furthermore, results could differ from whether initial recurrences or cumulative events are counted. In our study, recurrences in the potential PORT volume, i.e., surgical margins recurrence, regional and retroperitoneal lymph node metastasis, were found to be the most common relapse sites, accounting for 63% of the initial failures, which is consistent with the results of Song [18] and Luvira [19]. Chen et al. analyzed 320 surgical cases with clinically negative lymph node (T1–3N0M0) IHCC and observed 76 cases occurred lymph node metastasis (LNM) (76/320, 23.8%). And histological differentiation as well as tumor boundary and tumor size significantly correlated with LNM [23]. Postoperative local-regional recurrence for IHCC seems to be common, which imply the potential benefit of adjuvant radiotherapy, especially for those with high risk factors.

It is worthwhile pointing out that, up to 40% of the recurrences in our patient series occurred only inside the potential PORT volume, without lesions in remnant liver and distant sits. Similar figures could be found in the literature. In the report by Song et al. [18], the incidence of local-regional recurrence only as the first site of failure was 33%, which was the dominant pattern of failure for their patient series. Moreover, additional 18 (18/66, 27.3%) of their patients had non-regional lymph node metastases. Majority of such non-regional nodes could be inside the potential PORT volume, together with the above mentioned 33% of the cases, the proportion of recurrence only inside the radiation volume could be around 50%. In another study by Luvira et al. [19], recurrences only at surgical margin and regional lymph node account for 27.5% of the total failures. However, 15% patients had aortocaval regional lymph node metastases alone or with surgical margin and regional lymph node metastases. So, totally 42.5% of the patients had recurrences confined to the potential PORT volume. Taken together, about 40% of the IHCC patients recur strictly inside the potential PORT volume as the first site of failure. These findings suggest adjuvant radiotherapy might improve the local-regional control.

The target volume of adjuvant radiotherapy was proposed basing on the local recurrence pattern, mainly includes the tumor bed, and the corresponding high-risk lymphatic drainage area. According to our findings, the most common sites of lymph node metastases were stations No.16, 9, 8, 12, 13, and 14, these lymphatic drainage areas were suggested to be in the radiation volume (Fig. 8). As station No.16b1 metastases rarely recurred isolatedly, they relapsed as a consequent of lymph flow reflux after the metastases in the above mentioned node stations. We speculate that station No.16b1 metastases might be prevented or reduced if the area inside the proposed radiation volume is under well control. So, it might be suitable not to encompass station No.16b1 in the potential PORT volume. Since lymphatic drainage areas classified as distant metastases were included in the proposed radiation volume, the term “potential volume of PORT” was used instead of “local-regional recurrence”.

Fig. 8
figure 8

The potential PORT volume in 2 simulated cases. CTV: blue line, PTV: red line, Axial, coronal and sagittal views are shown for case 1 and case 2

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In our study, 44 patients developed recurrences outside the potential volume of PORT. For these patients, chemotherapy may be helpful. Until now, the role of chemotherapy in IHCC is still controversial. Miura et al. reported that there was no difference in the median OS between the observation group and the chemotherapy group after resection of intrahepatic cholangiocarcinoma (23 vs 20 months, P = 0.09) [24]. Edeline et al. conducted a phase III multicenter randomized controlled clinical trial of gemcitabine plus oxaliplatin in patients with intrahepatic cholangiocarcinoma after operation. One hundred ninety-six patients with intrahepatic cholangiocarcinoma were randomly divided into gemcitabine plus oxaliplatin group and observation group. They found longer RFS and OS in gemcitabine plus oxaliplatin group, but there was no statistical difference. In the chemotherapy group, grade III-IV side effects increased [25]. Schweitzer et al. divided 25 pairs of patients with intrahepatic cholangiocarcinoma after operation into adjuvant chemotherapy group and non-adjuvant chemotherapy group. The results showed that the total survival time of adjuvant chemotherapy group was significantly longer than that of non-adjuvant chemotherapy group [26]. Reames retrospectively analyzed 1154 patients with intrahepatic cholangiocarcinoma after radical resection, 347 (30%) received adjuvant chemotherapy, 184 of whom received gemcitabine-based chemotherapy. The results showed that chemotherapy did not change the prognosis of all patients with intrahepatic cholangiocarcinoma, but the subgroup with high risk of recurrence can benefit from chemotherapy [27]. A randomised, controlled, multicentre, phase 3 study (BILCAP) compared capecitabine with observation in resected biliary tract cancer and reported that capecitabine can improve overall survival in patients with resected biliary tract cancer when used as adjuvant chemotherapy [28]. Chemotherapy is not recommended as an adjuvant treatment for intrahepatic cholangiocarcinoma in this year’s NCCN guidelines. While this year’s ASCO clinical practice guidelines recommend capecitabine for 6 months after surgery for intrahepatic cholangiocarcinoma.

In this study, we found patients younger than 55 years old, tumor size larger than 5 cm, with later TNM stage, lymph node metastasis, and hepatitis were associated with poorer outcome. In previous reports, several prognostic factors were identified for IHCC patients, including tumor size, lymph node metastasis, TNM stage and tumor differentiation [29,30,31,32,33]. Our results were in accordance with the previous studies. As regards to the prognostic value of patient age and hepatitis history, controversial results were reported. In a retrospective study by Zhang et al. [34], in line with our result, hepatitis was found to be with poor prognosis in IHCC, while in the study by Zhou et al., hepatitis was a favorable prognostic factor [35]. The prognositic value of age was controversial, most study reported that age had no prognostic value in cholangiocarcinoma [34, 36,37,38]. Mavros et al. and Kato et al. found that older age was associated with worse prognosis [39, 40]. However, in our study, we found that patients with age < 55 years old had shorter RFS and OS than those with age ≥ 55 years old, which was in accordance with the results reported by Yamada et al. [41] Our data added some information in this respect, and the prognositic value of age is still uncertain.

Conclusions

This study analyzed the failure patterns after curative resection for intrahepatic cholangiocarcinoma. About two thirds of IHCC would recur after operation, with 60% of recurrences inside the potential volume of PORT. Importantly, up to 40% of the recurrences occurred only inside the potential PORT volume, without lesions in remnant liver and distant sits. Surgical margins and lymph node stations No.16a2, 9, 8, 12, 13, and 14 were the most common sites of recurrence, and should be included in the radiation volume. Our results implicate the possible benefits of postoperative radiotherapy for intrahepatic cholangiocarcinoma patients. As IHCC is a low incidence tumor type, prospective multicenter single arm clinical trial with radiation involved in the adjuvant therapies might be feasible.

Availability of data and materials

Datasets can be retrieved from authors by formal request from interested readers. Datasets will not be directly shared on public link as the national personal data protection act.

Abbreviations

AJCC:

American Joint Committee on Cancer

CCAs:

Cholangiocarcinomas

CI:

Confidence interval

IHCC:

Intrahepatic cholangiocarcinoma

LNM:

Lymph node metastasis

OS:

Overall survival

PORT:

Postoperative radiotherapy

RFS:

Recurrence free survival

RR:

Risk ratio

SAHZU:

Zhejiang University School of Medicine

SCI:

Science Citation Index

References

  1. Khan SA, Thomas HC, Davidson BR, Taylor-Robinson SD. Cholangiocarcinoma. Lancet. 2005;366(9493):1303–14.

    Article  Google Scholar 

  2. Nakeeb A, Pitt HA, Sohn TA, Coleman J, Abrams RA, Piantadosi S, Hruban RH, Lillemoe KD, Yeo CJ, Cameron JL. Cholangiocarcinoma. A spectrum of intrahepatic, perihilar, and distal tumors. Ann Surg. 1996;224(4):463–73 discussion 473-465.

    Article  CAS  Google Scholar 

  3. Malhi H, Gores GJ. Cholangiocarcinoma: modern advances in understanding a deadly old disease. J Hepatol. 2006;45(6):856–67.

    Article  CAS  Google Scholar 

  4. Endo I, House MG, Klimstra DS, Gonen M, D'Angelica M, Dematteo RP, Fong Y, Blumgart LH, Jarnagin WR. Clinical significance of intraoperative bile duct margin assessment for hilar cholangiocarcinoma. Ann Surg Oncol. 2008;15(8):2104–12.

    Article  Google Scholar 

  5. McGlynn KA, Tarone RE, El-Serag HB. A comparison of trends in the incidence of hepatocellular carcinoma and intrahepatic cholangiocarcinoma in the United States. Cancer Epidemiol Biomark Prev. 2006;15(6):1198–203.

    Article  Google Scholar 

  6. Berdah SV, Delpero JR, Garcia S, Hardwigsen J, Le Treut YP. A western surgical experience of peripheral cholangiocarcinoma. Br J Surg. 1996;83(11):1517–21.

    Article  CAS  Google Scholar 

  7. Chu KM, Lai EC, Al-Hadeedi S, Arcilla CE Jr, Lo CM, Liu CL, Fan ST, Wong J. Intrahepatic cholangiocarcinoma. World J Surg. 1997;21(3):301–5 discussion 305-306.

    Article  CAS  Google Scholar 

  8. Anderson CD, Pinson CW, Berlin J, Chari RS. Diagnosis and treatment of cholangiocarcinoma. Oncologist. 2004;9(1):43–57.

    Article  Google Scholar 

  9. Yang J, Yan LN. Current status of intrahepatic cholangiocarcinoma. World J Gastroenterol. 2008;14(41):6289–97.

    Article  Google Scholar 

  10. Bridgewater J, Galle PR, Khan SA, Llovet JM, Park JW, Patel T, Pawlik TM, Gores GJ. Guidelines for the diagnosis and management of intrahepatic cholangiocarcinoma. J Hepatol. 2014;60(6):1268–89.

    Article  Google Scholar 

  11. Konstantinidis IT, Arkadopoulos N, Ferrone CR. Surgical management of intrahepatic cholangiocarcinoma in the modern era: advances and challenges. Chin Clin Oncol. 2016;5(1):9.

    PubMed  Google Scholar 

  12. 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 

  13. Zheng X, Chen B, Wu JX, Jia AY, Rong WQ, Wang LM, Wu F, Zhao YT, Li YX, Wang WH. Benefit of adjuvant radiotherapy following narrow-margin hepatectomy in patients with intrahepatic cholangiocarcinoma that adhere to major vessels. Cancer Manag Res. 2018;10:3973–81.

    Article  CAS  Google Scholar 

  14. Jiang W, Zeng ZC, Tang ZY, Fan J, Zhou J, Zeng MS, Zhang JY, Chen YX, Tan YS. Benefit of radiotherapy for 90 patients with resected intrahepatic cholangiocarcinoma and concurrent lymph node metastases. J Cancer Res Clin Oncol. 2010;136(9):1323–31.

    Article  Google Scholar 

  15. Horgan AM, Amir E, Walter T, Knox JJ. Adjuvant therapy in the treatment of biliary tract cancer: a systematic review and meta-analysis. J Clin Oncol. 2012;30(16):1934–40.

    Article  Google Scholar 

  16. Hammad AY, Berger NG, Eastwood D, Tsai S, Turaga KK, Christian KK, Johnston FM, Pawlik TM, Gamblin TC. Is radiotherapy warranted following intrahepatic Cholangiocarcinoma resection? The impact of surgical margins and lymph node status on survival. Ann Surg Oncol. 2016;23(Suppl 5):912–20.

    Article  Google Scholar 

  17. Farges O, Fuks D, Le Treut YP, Azoulay D, Laurent A, Bachellier P, Nuzzo G, Belghiti J, Pruvot FR, Regimbeau JM. AJCC 7th edition of TNM staging accurately discriminates outcomes of patients with resectable intrahepatic cholangiocarcinoma: by the AFC-IHCC-2009 study group. Cancer. 2011;117(10):2170–7.

    Article  Google Scholar 

  18. Song S, Kim K, Chie EK, Kim S, Park HJ, Yi NJ, Suh KS, Ha SW. Locoregional recurrence after curative intent resection for intrahepatic cholangiocarcinoma: implications for adjuvant radiotherapy. Clin Transl Oncol. 2015;17(10):825–9.

    Article  CAS  Google Scholar 

  19. Luvira V, Eurboonyanun C, Bhudhisawasdi V, Pugkhem A, Pairojkul C, Luvira V, Sathitkarnmanee E, Somsap K, Kamsa-ard S. Patterns of recurrence after resection of mass-forming type intrahepatic Cholangiocarcinomas. Asian Pac J Cancer Prev. 2016;17(10):4735–9.

    PubMed  PubMed Central  Google Scholar 

  20. Gil E, Joh JW, Park HC, Yu JI, Jung SH, Kim JM. Predictors and patterns of recurrence after curative liver resection in intrahepatic cholangiocarcinoma, for application of postoperative radiotherapy: a retrospective study. World J Surg Oncol. 2015;13:227.

    Article  Google Scholar 

  21. Hyder O, Hatzaras I, Sotiropoulos GC, Paul A, Alexandrescu S, Marques H, Pulitano C, Barroso E, Clary BM, Aldrighetti L, et al. Recurrence after operative management of intrahepatic cholangiocarcinoma. Surgery. 2013;153(6):811–8.

    Article  Google Scholar 

  22. Doussot A, Gonen M, Wiggers JK, Groot-Koerkamp B, DeMatteo RP, Fuks D, Allen PJ, Farges O, Kingham TP, Regimbeau JM, et al. Recurrence patterns and disease-free survival after resection of intrahepatic Cholangiocarcinoma: preoperative and postoperative prognostic models. J Am Coll Surg. 2016;223(3):493–505 e492.

    Article  Google Scholar 

  23. Chen YX, Zeng ZC, Tang ZY, Fan J, Zhou J, Jiang W, Zeng MS, Tan YS. Prediction of the lymph node status in patients with intrahepatic cholangiocarcinoma: analysis of 320 surgical cases. Front Oncol. 2011;1:42.

    Article  Google Scholar 

  24. Miura JT, Johnston FM, Tsai S, George B, Thomas J, Eastwood D, Banerjee A, Christians KK, Turaga KK, Pawlik TM, et al. Chemotherapy for surgically resected intrahepatic Cholangiocarcinoma. Ann Surg Oncol. 2015;22(11):3716–23.

    Article  Google Scholar 

  25. Edeline J, Benabdelghani M, Bertaut A, Watelet J, Hammel P, Joly JP, Boudjema K, Fartoux L, Bouhier-Leporrier K, Jouve JL, et al. Gemcitabine and Oxaliplatin chemotherapy or surveillance in resected biliary tract Cancer (PRODIGE 12-ACCORD 18-UNICANCER GI): a randomized phase III study. J Clin Oncol. 2019;37(8):658–67.

    Article  CAS  Google Scholar 

  26. Schweitzer N, Weber T, Kirstein MM, Fischer M, Kratzel AM, Reineke-Plaass T, Lehner F, Manns MP, Vogel A. The effect of adjuvant chemotherapy in patients with intrahepatic cholangiocarcinoma: a matched pair analysis. J Cancer Res Clin Oncol. 2017;143(7):1347–55.

    Article  CAS  Google Scholar 

  27. Reames BN, Bagante F, Ejaz A, Spolverato G, Ruzzenente A, Weiss M, Alexandrescu S, Marques HP, Aldrighetti L, Maithel SK, et al. Impact of adjuvant chemotherapy on survival in patients with intrahepatic cholangiocarcinoma: a multi-institutional analysis. HPB (Oxford). 2017;19(10):901–9.

    Article  Google Scholar 

  28. Primrose JN, Fox RP, Palmer DH, Malik HZ, Prasad R, Mirza D, Anthony A, Corrie P, Falk S, Finch-Jones M, et al. Capecitabine compared with observation in resected biliary tract cancer (BILCAP): a randomised, controlled, multicentre, phase 3 study. Lancet Oncol. 2019;20(5):663–73.

    Article  CAS  Google Scholar 

  29. Wang Y, Li J, Xia Y, Gong R, Wang K, Yan Z, Wan X, Liu G, Wu D, Shi L, et al. Prognostic nomogram for intrahepatic cholangiocarcinoma after partial hepatectomy. J Clin Oncol. 2013;31(9):1188–95.

    Article  Google Scholar 

  30. Ribero D, Pinna AD, Guglielmi A, Ponti A, Nuzzo G, Giulini SM, Aldrighetti L, Calise F, Gerunda GE, Tomatis M, et al. Surgical approach for long-term survival of patients with intrahepatic Cholangiocarcinoma: a multi-institutional analysis of 434 patients. Arch Surg. 2012;147(12):1107–13.

    Article  Google Scholar 

  31. Farges O, Fuks D, Boleslawski E, Le Treut YP, Castaing D, Laurent A, Ducerf C, Rivoire M, Bachellier P, Chiche L, 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 830.

    Article  Google Scholar 

  32. de Jong MC, Nathan H, Sotiropoulos GC, Paul A, Alexandrescu S, Marques H, Pulitano C, Barroso E, Clary BM, Aldrighetti L, 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 

  33. Jiang W, Zeng ZC, Tang ZY, Fan J, Sun HC, Zhou J, Zeng MS, Zhang BH, Ji Y, Chen YX. A prognostic scoring system based on clinical features of intrahepatic cholangiocarcinoma: the Fudan score. Ann Oncol. 2011;22(7):1644–52.

    Article  CAS  Google Scholar 

  34. Zhang GW, Lin JH, Qian JP, Zhou J. Identification of risk and prognostic factors for patients with clonorchiasis-associated intrahepatic cholangiocarcinoma. Ann Surg Oncol. 2014;21(11):3628–37.

    Article  CAS  Google Scholar 

  35. Zhou HB, Wang H, Li YQ, Li SX, Wang H, Zhou DX, Tu QQ, Wang Q, Zou SS, Wu MC, et al. Hepatitis B virus infection: a favorable prognostic factor for intrahepatic cholangiocarcinoma after resection. World J Gastroenterol. 2011;17(10):1292–303.

    Article  Google Scholar 

  36. Yi B, Zhang BH, Zhang YJ, Jiang XQ, Zhang BH, Yu WL, Chen QB, Wu MC. Surgical procedure and prognosis of hilar cholangiocarcinoma. Hepatobiliary Pancreat Dis Int. 2004;3(3):453–7.

    PubMed  Google Scholar 

  37. Yi B, Zhang BH, Zhang YJ, Jiang XQ, Zhang BH, Yu WL, Cheng QB, Wu MC. Analysis of the relation between surgery and prognosis of hilar cholangiocarcinoma. Zhonghua Wai Ke Za Zhi. 2005;43(13):842–5.

    PubMed  Google Scholar 

  38. Kim HJ, Kang TU, Swan H, Kang MJ, Kim N, Ahn HS, Park SM. Incidence and prognosis of subsequent Cholangiocarcinoma in patients with hepatic resection for bile duct stones. Dig Dis Sci. 2018;63(12):3465–73.

    Article  Google Scholar 

  39. Mavros MN, Economopoulos KP, Alexiou VG, Pawlik TM. Treatment and prognosis for patients with intrahepatic Cholangiocarcinoma: systematic review and meta-analysis. JAMA Surg. 2014;149(6):565–74.

    Article  Google Scholar 

  40. Kato A, Naitoh I, Miyabe K, Hayashi K, Yoshida M, Hori Y, Natsume M, Jinno N, Asano G, Kato H, et al. An increased chromosome 7 copy number in endoscopic bile duct biopsy specimens is predictive of a poor prognosis in Cholangiocarcinoma. Dig Dis Sci. 2018;63(12):3376–81.

    Article  CAS  Google Scholar 

  41. Yamada T, Nakanishi Y, Okamura K, Tsuchikawa T, Nakamura T, Noji T, Asano T, Tanaka K, Kurashima Y, Ebihara Y, et al. Impact of serum carbohydrate antigen 19-9 level on prognosis and prediction of lymph node metastasis in patients with intrahepatic cholangiocarcinoma. J Gastroenterol Hepatol. 2018.

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Acknowledgements

The authors thank Prof. Kwok Cheung Lee from Georgetown University for language editing. We acknowledge the colleagues in medical records room of SAHZU for their help in providing the valuable medical records.

Funding

This study was funded by the National Natural Science Foundation of China (contracts 81572952), Scientific Research Project of Zhejiang Provincial Education Department (grant no. Y201636369), and Zhejiang University Research Foundation (grant no. 491020-I4161S). The funding had no role in the design of the study and collection, analysis, and interpretation of data and in the writing of the manuscript.

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Author notes

  1. Wei Yu and Chunxiu Hu contributed equally to this work.

Authors and Affiliations

  1. Department of Radiation Oncology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Jiefang Road 88, Hangzhou, 310009, People’s Republic of China

    Wei Yu, Chunxiu Hu, Yongjie Shui, Kui Wu, Lili Zhang, Chao Li, Jing Xu & Qichun Wei

  2. Ministry of Education Key Laboratory of Cancer Prevention and Intervention, Zhejiang University School of Medicine, Hangzhou, 310009, People’s Republic of China

    Wei Yu & Qichun Wei

  3. Department of Radiation Oncology, Zhejiang Quhua Hospital, Quzhou, 324000, People’s Republic of China

    Chunxiu Hu

  4. Department of Radiology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, People’s Republic of China

    Ying Chen

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  1. Wei Yu
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Contributions

WY participated in the design of the study, carried out the clinical data analysis and wrote the manuscript; CH participated in the design of the study, collected and interpreted the clinical data, and wrote part of the manuscript. YS participated in construction of the figures. KW and CL handled with the physics data. LZ polished the article. YC read the CT and MRI image. JX participated in the writing of discussion. QW conceived the study, analyzed the experimental and clinical data and wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Qichun Wei.

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Ethics approval and consent to participate

This study was approved by the Ethics Committee of SAHZU, and was carried out in accordance with the Declaration of Helsinki. Written informed consent was obtained from all patients.

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Not applicable.

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The authors declare that they have no competing interests.

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Yu, W., Hu, C., Shui, Y. et al. Failure patterns after curative resection for intrahepatic cholangiocarcinoma: possible implications for postoperative radiotherapy. BMC Cancer 19, 1108 (2019). https://doi.org/10.1186/s12885-019-6328-3

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  • DOI: https://doi.org/10.1186/s12885-019-6328-3

Keywords

  • Intrahepatic cholangiocarcinoma
  • Recurrence pattern
  • Target volume
  • Adjuvant radiotherapy

BMC Cancer

ISSN: 1471-2407

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