| Home | E-Submission | Sitemap | Contact Us |  
Radiation Oncology Journal > Volume 37(4); 2019 > Article
Lee, Lee, Lee, Lee, Yu, Jang, and Kim: Retrospective analysis of intensity-modulated radiotherapy and three-dimensional conformal radiotherapy of postoperative treatment for biliary tract cancer



This study was conducted to compare the outcome of three-dimensional conformal radiotherapy (3D-CRT) and intensity-modulated radiotherapy (IMRT) for the postoperative treatment of biliary tract cancer.

Materials and Methods

From February 2008 to June 2016, 57 patients of biliary tract cancer treated with curative surgery followed by postoperative 3D-CRT (n = 27) or IMRT (n = 30) were retrospectively enrolled.


Median follow-up time was 23.6 months (range, 5.2 to 97.6 months) for all patients and 38.4 months (range, 27.0 to 89.2 months) for survivors. Two-year recurrence-free survival is higher in IMRT arm than 3D-CRT arm with a marginal significance (25.9% vs. 47.4%; p = 0.088). Locoregional recurrence-free survival (64.3% vs. 81.7%; p = 0.122) and distant metastasis-free survival (40.3% vs. 55.8%; p = 0.234) at two years did not show any statistical difference between two radiation modalities. In the multivariate analysis, extrahepatic cholangiocarcinoma, poorly-differentiated histologic grade, and higher stage were significant poor prognostic factors for survival. Severe treatment-related toxicity was not significantly different between two arms.


IMRT showed comparable results with 3D-CRT in terms of recurrence, and survival, and radiotherapy toxicity for the postoperative treatment of biliary tract cancer.


Biliary tract cancer, which consists of cholangiocarcinoma and gallbladder cancer, is well known for its poor prognosis. The reported 5-year overall survival rate is around 5%–30% [1-5]. Surgical excision is the treatment of choice for all detectable biliary tract cancer, but complete resection rates are not high enough to achieve cure and recurrence following surgery is common, either at local or distant sites [6-8]. Accordingly, adjuvant treatment is recommended following surgical management, although optimal strategy is not clearly determined [9]. Recently, intensity-modulated radiotherapy (IMRT) has become an alternative to three-dimensional conformal radiotherapy (3D-CRT) in upper gastrointestinal cancers, such as pancreas and periampullary cancer for its ability to decrease the treatment related toxicity while successfully achieve dose escalation [10]. Similar to pancreas cancer, biliary tract cancer is also surrounded by number of critical organs and subsequent treatment related toxicity is severe. There are trials of adjuvant radiotherapy utilizing 3D-CRT and IMRT, but endpoints did not focus on the survival and/or toxicity of the two modalities [11,12]. In the multicenter retrospective studies, long-term local control was achieved with higher radiation dose (≥50–54 Gy), without significant difference in acute adverse events in postoperative radiotherapy of biliary tract cancer, and this might encourage the extended use of IMRT for its feasibility of dose escalation [13,14]. To the best of our knowledge, there was no study which directly compared the results of postoperative treatment of resectable biliary tract cancer in terms of radiotherapy technique, in this case, 3D-CRT versus IMRT. Therefore, the purpose of this study is to compare the outcome of 3D-CRT and IMRT in postoperative treatment of biliary tract cancer.

Materials and Methods

Between February 2008 and April 2016, collectively 57 biliary tract cancer patients whose medical records assembled from three medical institutions were reviewed retrospectively. This study was approved by the Institutional Review Board of The Catholic University of Korea Catholic Medical Center (No. VC18RESI0014). The eligibility criteria were: (1) histologically confirmed bile duct or gallbladder adenocarcinoma; (2) received curative surgery followed by adjuvant radiotherapy within 60 days; (3) planned and completed at least 45 Gy of postoperative radiotherapy; (4) no evidence of distant metastasis.
Clinical staging work-up included physical examination, complete blood count, blood chemistry for evaluation of jaundice and liver function, level of tumor marker CA19-9, chest and abdominal computed tomography (CT), and positron emission tomography/computed tomography (PET/CT) along with magnetic resonance image (MRI) of the abdomen if feasible. The 8th edition of the American Joint Committee on Cancer staging system was used for both clinical and pathological staging.

1. Treatment

All patients were treated with curative surgery. Surgical procedure was selected based on tumor site and extent, listed as follows: 18 liver lobectomy with bile duct resection, 11 pylorus-preserving pancreaticoduodenectomy, 10 bile duct resection, 16 cholecystectomy, 1 extended hepatectomy with bile duct resection, and 1 common bile duct total segmental resection with Roux-en-Y hepaticojejunostomy. The interval between surgery and radiotherapy ranged from 18 to 60 days, median 39 days. Contrast-enhanced simulation CT was acquired to generate the radiotherapy planning. Radiotherapy was planned using 3D-CRT techniques in 27 (47.4%) patients, and IMRT planning techniques in 30 (52.6%) patients.
In 2 of 3 institutions, all 16 patients were treated with 3D-CRT plans. The other institution used both planning method for 21 patients until May 2014. Twenty patients enlisted since August 2014 were treated with IMRT. The differences between institutions and treatment period were not statistically significant.
For 3D-CRT plans, target was delineated based on the postoperative tumor bed and draining lymph nodes. An 1-cm margin was added to make up for set-up errors. A 3- or 4-field box beam arrangement was used with anterior-posterior, posterior-anterior, and right and left lateral beams. For IMRT, the clinical target volume (CTV) was generated which encompassed the postoperative tumor bed and draining lymph nodes. The planning target volume (PTV) was expanded from CTV by 0.5 to 1 cm to every dimension, accounting for set-up error and organ movement.
The 3D-CRT was delivered with 6–15 MV photons using the linear accelerator. TomoTherapy (Accuray Inc., Sunnyvale, CA, USA) was utilized to deliver IMRT plan. Vac-Lock and wing board were used to ensure the immobilization of patients in IMRT and 3D-CRT, respectively. At least 45 Gy of radiation dose was prescribed, and up to 56.9 Gy was delivered depending on initial tumor extent, gross or microscopic residual diseases, and relationship with surrounding organs at risk (OAR). Dose-volume histograms were produced for the PTV and all the OARs. The optimization was constrained to deliver greater than 95% of the prescription dose to the PTV. Quantitative Analysis of Normal Tissue Effects in Clinics (QUANTEC) parameters were used to evaluated the dosimetric doses to OAR. Concurrent chemotherapy was utilized in all but one patient, due to poor general condition. The 5-fluorouracil (5-FU) was the most commonly used regimen, 400 to 600 mg/m2 injected intravenously once a week during the radiotherapy. Adjuvant chemotherapy was delivered to 13 patients, using FL (5-FU and leucovorin) or FP (5-FU and cisplatin) regimen.

2. Statistical analyses

The primary endpoint was to determine overall survival (OS), recurrence-free survival (RFS), locoregional recurrence-free survival (LRFS), and distant metastasis-free survival (DMFS), of 3D-CRT and IMRT. Pearson chi-square test was used to analyze the distribution of variables. Kaplan-Meier method was used to calculate the actuarial OS, RFS, LRFS, and DMFS rates. OS was defined as the time from operation to date of death or the last day of follow-up. RFS was defined as the time from operation to date of disease progression, death, or the last day of follow-up. LRFS and DMFS were defined as the time from operation to date of locoregional recurrence and distant metastasis, respectively. Univariate and multivariate analysis was performed for prognostic factors using the log-rank test and Cox proportional hazards model. p-values less than 0.05 were considered statistically significant. Statistical analysis was performed with R version 3.2.1 (http://www.R-project.org).


Patient and tumor characteristics are shown in Table 1. The median age of all patients at the time of diagnosis was 60 years, ranging from 47 to 79 years. Age, sex, pathologic stage, histologic grade, residual disease, and total radiation dose were distributed between 3D-CRT and IMRT groups with no significant difference. The mean interval between surgery and radiotherapy differed significantly between groups, 39.7 days in 3D-CRT and 32.8 days in IMRT group (p = 0.013).

1. Recurrence and survival

The median follow-up time for all patients was 23.6 months (range, 5.2 to 97.6 months). As for the survivors, median follow-up time was 38.4 months (range, 27.0 to 89.2 months). Median OS time for all patients, 3D-CRT, and IMRT group were 23.6, 31.3, and 21.7 months, respectively. The 3-year OS rates were 40.7% in 3D-CRT group and 43.3% in IMRT group (p =0.957) (Fig. 1). Two-year RFS (25.9% vs. 47.4%; p=0.088), LRFS (64.3% vs. 81.7%; p = 0.122), and DMFS (40.3% vs. 55.8%; p = 0.234) rates showed no statistical difference between 3D-CRT and IMRT arms (Fig. 2).

2. Risk factors for recurrence and survival

The prognostic factors of OS, RFS, LRFS, and DMFS in the univariate analysis are shown in Table 2. Age older than 60 and poor histologic grade were factors associated with poor outcome in the OS and RFS. Intrahepatic cancer presented better RFS compare to other types of cholangiocarcinoma (p = 0.043). The radiotherapy modality was not a significant risk factor of survival in the univariate analysis. In the multivariate analysis, tumor site, histology, and stage were significant prognostic factors for OS. Other factors associated with RFS, LRFS, and DMFS are listed in Table 3.

3. Toxicity

Toxicity was assessed with the Common Terminology Criteria for Adverse Events v4.0. Grade 3 and 4 hematologic toxicities occurred in 9 patients, 5 in 3D-CRT and 4 in IMRT group, respectively. There was a case of grade 3 liver abscess in IMRT group, which occurred 8 months after radiotherapy. All other cases of toxicity were reported during the radiotherapy or within 1 month of completion. A patient in 3D-CRT group was hospitalized with grade 3 sepsis 1 month after the treatment, while the other one in IMRT group complained of grade 3 nausea and vomiting during the adjuvant radiotherapy.

Discussion and Conclusion

The standard adjuvant therapy of biliary tract cancer is not established due to low incidence of disease entity and resultant lack of prospective randomized controlled trial. Even retrospective studies directly comparing the treatment result biliary tract cancer survival analysis was reported by Fuller et al. [20], compared 24 IMRT and 24 3D-CRT patients, including 14 (29%) unresectable cases. The median survival was 17.6 and 9.0 months, respectively in IMRT and 3D-CRT groups, although statistical significance was not stated. Grade 2 or higher gastrointestinal toxicity was also lower in IMRT group, even with higher mean radiation dose (Table 4).
In this study, 30 IMRT cases and 27 3D-CRT cases were compared after surgical resection of biliary tract cancer. Radiation dose between two groups were not different (50.3 Gy of IMRT vs. 50.6 Gy of 3D-CRT). The 3-year OS did not show statistical difference (p = 0.957) and the RFS showed the tendency of favoring IMRT (p = 0.088), although still not statistically significant. The treatment volume was smaller in IMRT owing to reduced PTV margin, yet drew the similar results in survival and toxicity compared with 3D-CRT.
Limitations of this study should be acknowledged. First of all, the retrospective nature of this study weakens the authority of clinical implication. The rarity of disease entity itself and low resectability caused by initially advanced disease status make it difficult to conduct a prospective randomized controlled trial. Even though this study comprised the medical records from three different territorial institutions, the number of patient was not large enough to analyze by the subsites of cholangiocarcinoma and gallbladder cancer separately. In addition, resectable cases regardless of pathologic stage were included, causing further heterogeneity of patient population. The uneven patient distribution between 3D-CRT and IMRT group could also have affected the result. Finally, the follow-up duration was relatively short to assess the late recurrences and complications.
Nevertheless, the value of this study still stands being the first report of comparison between 3D-CRT and IMRT in biliary tract cancer solely in adjuvant setting, to the best of our knowledge. According to our data, IMRT did not show superior result over 3D-CRT. However, IMRT has proven to be a safe and effective modality of postoperative treatment in biliary tract cancer that is non-inferior to 3D-CRT. Since IMRT is a relatively newer modality in biliary tract cancer radiotherapy and being more commonly used in clinics, a prospective randomized controlled trial is expected to clarify the role of adjuvant radiotherapy with IMRT.


Conflict of Interest

No potential conflict of interest relevant to this article was reported.


The authors wish to acknowledge the financial support of the St. Vincent’s hospital, research institute of medical science (No. SVHR-2019-08). This work was supported by a grant from the National R&D Program for the Ministry of Science and ICT, Republic of Korea (No. 2017R1C1B5015762).

Fig. 1.
Kaplan-Meier overall survival curves of intensity-modulated radiotherapy (IMRT) arm and three-dimensional conformal radiotherapy (3D-CRT) arms.
Fig. 2.
Kaplan-Meier recurrence-free survival curves of intensity-modulated radiotherapy (IMRT) arm and three-dimensional conformal radiotherapy (3D-CRT) arms.
Table 1.
Patients’ characteristics
Characteristic 3D-CRT (n = 27) IMRT (n = 30) p-value
Age at diagnosis (yr) 62.5 ± 8.2 61.4 ± 9.4 0.889
Sex 0.462
 Male 17 (63.0) 16 (53.3)
 Female 10 (37.0) 14 (46.7)
Tumor site 0.083
 Intrahepatic cholangiocarcinoma 15 (55.6) 8 (26.7)
 Extrahepatic cholangiocarcinoma 6 (22.2) 12 (40.0)
 Gallbladder carcinoma 6 (22.2) 10 (33.3)
Presence of jaundice at diagnosis 0.400
 No 17 (63.0) 22 (73.3)
 Yes 10 (37.0) 8 (26.7)
Histologic grade 0.642
 Well differentiated 4 (14.8) 6 (20.0)
 Moderately differentiated 19 (70.4) 17 (56.7)
 Poorly differentiated 4 (14.8) 7 (23.3)
Residual disease 0.160
 R0 resection 15 (55.6) 22 (73.3)
 R1 resection 12 (44.4) 8 (26.7)
Lymphovascular invasion 1.000
 No 10 (40.0) 12 (40.0)
 Yes 15 (60.0) 18 (40.0)
Perineural invasion 0.097
 No 7 (28.0) 15 (50.0)
 Yes 18 (72.0) 15 (50.0)
Stage 0.451
 I 2 (7.4) 1 (3.3)
 II 9 (33.3) 13 (43.3)
 III 14 (51.9) 16 (53.3)
 IV 2 (7.4) 0 (0.0)
Adjuvant chemotherapy 0.025
 No 17 (63.0) 27 (90.0)
 Yes 10 (37.0) 3 (10.0)
Radiotherapy interval (day) 39.7 ± 10.0 32.8 ± 10.1 0.008
Radiation dose (Gy) 50.6 ± 2.8 50.3 ± 3.5 0.237

Values are presented as mean ± standard deviation or number (%).

3D-CRT, three-dimensional conformal radiotherapy; IMRT, intensity-modulated radiotherapy.

Table 2.
Analyses of factors associated with overall survival
HR (95% CI) p-value HR (95% CI) p-value
Age (yr) 0.019 0.086
 ≤60 1 1
 >60 2.164 (1.136–4.123) 0.497 (0.224–1.104)
Tumor site 0.076 -
 Intrahepatic 1 -
 Extrahepatic 0.969 (0.484–1.939) 0.929 -
 Gallbladder 0.359 (0.143–0.901) 0.029 -
Tumor grade 0.068 0.024
 Well differentiated 1 1
 Moderate differentiated 0.771 (0.328–1.815) 0.552 0.443 (0.175–1.120) 0.085
 Poorly differentiated 2.031 (0.754–5.468) 0.161 1.438 (0.524–3.946) 0.480
Lymphovascular invasion 0.033 -
 No 1 -
 Yes 2.099 (1.060–4.156) -
Perineural invasion 0.003 0.001
 No 1 1
 Yes 3.132 (1.490–6.582) 3.761 (1.695–8.345)
Stage 0.093 0.023
 I 1 1
 II 1.944 (0.432–8.750) 0.386 1.262 (0.152–10.450) 0.829
 III 2.033 (0.407–8.855) 0.345 1.435 (0.186–11.056) 0.729
 IV 117.735 (1.512–91.091) 0.019 16.529 (1.320–207.008) 0.030

HR, hazard ratio; CI, confidence interval.

Table 3.
Analyses of factors associated with recurrence-free survival
HR (95% CI) p-value HR (95% CI) p-value
Radiotherapy modality 0.093 -
 3D-CRT 1 -
 IMRT 0.581 (0.308–1.096) -
Age (yr) 0.022 0.019
 ≤60 1 1
 >60 2.089 (1.111–3.927) 2.347 (1.147–4.800)
Tumor site 0.003 0.072
 Intrahepatic 1 1
 Extrahepatic 0.690 (0.344–1.384) 0.296 0.425 (0.189–0.957) 0.039
 Gallbladder 0.242 (0.097–0.607) 0.002 0.513 (0.167–1.577) 0.244
Tumor grade 0.032 0.019
 Well differentiated 1 1
 Moderate differentiated 0.779 (0.334–1.018) 0.564 1.137 (0.419–3.084) 0.801
 Poorly differentiated 2.384 (0.890–6.388) 0.084 4.339 (1.322–14.239) 0.016
Lymphovascular invasion 0.025 -
 No 1 -
 Yes 2.208 (1.106–4.406) -
Perineural invasion 0.004 0.02
 No 1 1
 Yes 2.885 (1.416–5.877) 2.968 (1.190–7.401)
Jaundice 0.059 0.06
 No 1 1
 Yes 1.860 (0.916–3.543) 2.149 (0.970–4.764)

HR, hazard ratio; CI, confidence interval; 3D-CRT, three-dimensional conformal radiotherapy; IMRT, intensity-modulated radiotherapy.

Table 4.
Key studies comparing 3D-CRT and IMRT in biliary tract cancers
Study Year Treatment Median F/U (mo) Tumor site No. of patients RT dose (Gy) Median endpoint (mo)
Jia et al. [15] 2014 IMRT vs. surgery 24 Intrahepatic 14 vs. 24 50–60 OS: 21.8 vs. 15.0 (p = 0.049)
RFS: 12.5 vs. 5.5 (p = 0.049)
Fuller et al. [20] 2009 IMRT vs. 3D-CRT 34 Biliary adenocarcinoma 24 vs. 24 59 vs. 48 (p = 0.0001) Survival: 17.6 vs. 9.0
Current study 2019 IMRT vs. 3D-CRT 24 Biliary tract 30 vs. 27 50.3 vs. 50.6 (p = 0.760) OS: 21.7 vs. 31.3 (p = 0.957)
RFS: 14.5 vs. 16.5 (p = 0.088)

3D-CRT, three-dimensional conformal radiotherapy; IMRT, intensity-modulated radiotherapy; F/U, follow-up; RT, radiotherapy; OS, overall survival; RFS, recurrence-free survival.


1. Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin 2012;62:10–29.
crossref pmid
2. Nagorney DM, Kendrick ML. Hepatic resection in the treatment of hilar cholangiocarcinoma. Adv Surg 2006;40:159–71.
crossref pmid
3. de Jong MC, Nathan H, Sotiropoulos GC, et al. Intrahepatic cholangiocarcinoma: an international multi-institutional analysis of prognostic factors and lymph node assessment. J Clin Oncol 2011;29:3140–5.
crossref pmid
4. Zaydfudim VM, Rosen CB, Nagorney DM. Hilar cholangiocarcinoma. Surg Oncol Clin N Am 2014;23:247–63.
crossref pmid
5. Yoshioka Y, Ogawa K, Oikawa H, et al. Factors influencing survival outcome for radiotherapy for biliary tract cancer: a multicenter retrospective study. Radiother Oncol 2014;110:546–52.
crossref pmid
6. Hasegawa S, Ikai I, Fujii H, Hatano E, Shimahara Y. Surgical resection of hilar cholangiocarcinoma: analysis of survival and postoperative complications. World J Surg 2007;31:1256–63.
crossref pmid pdf
7. Kim MY, Kim JH, Kim Y, Byun SJ. Postoperative radiotherapy appeared to improve the disease free survival rate of patients with extrahepatic bile duct cancer at high risk of loco-regional recurrence. Radiat Oncol J 2016;34:297–304.
crossref pmid pmc pdf
8. Koo TR, Eom KY, Kim IA, et al. Patterns of failure and prognostic factors in resected extrahepatic bile duct cancer: implication for adjuvant radiotherapy. Radiat Oncol J 2014;32:63–9.
crossref pmid pmc pdf
9. Cereda S, Belli C, Reni M. Adjuvant treatment in biliary tract cancer: to treat or not to treat? World J Gastroenterol 2012;18:2591–6.
crossref pmid pmc
10. Taremi M, Ringash J, Dawson LA. Upper abdominal malignancies: intensity-modulated radiation therapy. Front Radiat Ther Oncol 2007;40:272–88.
crossref pmid
11. Wang SJ, Lemieux A, Kalpathy-Cramer J, et al. Nomogram for predicting the benefit of adjuvant chemoradiotherapy for resected gallbladder cancer. J Clin Oncol 2011;29:4627–32.
crossref pmid pmc
12. Ben-Josef E, Guthrie KA, El-Khoueiry AB, et al. SWOG S0809: a phase II intergroup trial of adjuvant capecitabine and gemcitabine followed by radiotherapy and concurrent capecitabine in extrahepatic cholangiocarcinoma and gallbladder carcinoma. J Clin Oncol 2015;33:2617–22.
crossref pmid
13. Hayashi K, Isohashi F, Ogawa K, et al. Postoperative external irradiation of patients with primary biliary tract cancer: a multicenter retrospective study. Anticancer Res 2015;35:6231–7.
14. Im JH, Seong J, Lee J, et al. Postoperative radiotherapy dose correlates with locoregional control in patients with extrahepatic bile duct cancer. Radiat Oncol J 2014;32:7–13.
crossref pmid pmc pdf
15. Jia AY, Wu JX, Zhao YT, et al. Intensity-modulated radiotherapy following null-margin resection is associated with improved survival in the treatment of intrahepatic cholangiocarcinoma. J Gastrointest Oncol 2015;6:126–33.
pmid pmc
16. Sun XN, Wang Q, Gu BX, et al. Adjuvant radiotherapy for gallbladder cancer: a dosimetric comparison of conformal radiotherapy and intensity-modulated radiotherapy. World J Gastroenterol 2011;17:397–402.
crossref pmid pmc
17. Milano MT, Chmura SJ, Garofalo MC, et al. intensity-modulated radiotherapy in treatment of pancreatic and bile duct malignancies: toxicity and clinical outcome. Int J Radiat Oncol Biol Phys 2004;59:445–53.
crossref pmid
18. Yovino S, Poppe M, Jabbour S, et al. Intensity-modulated radiation therapy significantly improves acute gastrointestinal toxicity in pancreatic and ampullary cancers. Int J Radiat Oncol Biol Phys 2011;79:158–62.
crossref pmid
19. Prasad S, Cambridge L, Huguet F, et al. Intensity modulated radiation therapy reduces gastrointestinal toxicity in locally advanced pancreas cancer. Pract Radiat Oncol 2016;6:78–85.
crossref pmid
20. Fuller CD, Dang ND, Wang SJ, et al. Image-guided intensity-modulated radiotherapy (IG-IMRT) for biliary adenocarcinomas: initial clinical results. Radiother Oncol 2009;92:249–54.
crossref pmid
Editorial Office
Department of Radiation Oncology, Samsung Medical Center,
Proton Therapy Center, B2, 81, Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea
Tel : +82-2-3410-3617
E-mail: rojeditor@gmail.com, roj@kosro.or.kr
Copyright © The Korean Society for Radiation Oncology.                      Developed in M2PI
Close layer
prev next