To report the results of stereotactic body radiotherapy (SBRT) for unresectable primary or recurrent cholangiocarcinoma.
From January 2005 through August 2013, 58 patients with unresectable primary (n = 28) or recurrent (n = 30) cholangiocarcinoma treated by SBRT were retrospectively analyzed. The median prescribed dose was 45 Gy in 3 fractions (range, 15 to 60 Gy in 1-5 fractions). Patients were treated by SBRT only (n = 53) or EBRT + SBRT boost (n = 5). The median tumor volume was 40 mL (range, 5 to 1,287 mL).
The median follow-up duration was 10 months (range, 1 to 97 months). The 1-year, 2-year overall survival rates, and median survival were 45%, 20%, and 10 months, respectively. The median survival for primary group and recurrent group were 5 and 13 months, respectively. Local control rate at 1-year and 2-year were 85% and 72%, respectively. Disease progression-free survival rates at 1-year and 2-year were 26% and 23%, respectively. In univariate analysis, ECOG performance score (0-1 vs. 2-3), treatment volume (<50 vs. ≥50 mL), and pre-SBRT CEA level (<5 vs. ≥5 ng/mL) were significant in overall survival rate. In multivariate analysis, ECOG score (p = 0.037) and tumor volume (p = 0.030) were statistically significant. In the recurrent tumor group, patients with >12 months interval from surgery to recurrence showed statistically significant higher overall survival rate than those with ≤12 months (p = 0.026). Six patients (10%) experienced ≥grade 3 complications.
SBRT can be considered as an effective local modality for unresectable primary or recurrent cholangiocarcinoma.
Cholangiocarcinoma is a rare malignancy originating from the epithelial cells of the bile ducts. It is classically classified as intrahepatic and extrahepatic tumor according to their anatomical origins. Currently, surgical resection provides the only possibility of cure. However, the majority of patients present with unresectable disease and therefore have dismal prognosis. Resectability rates are generally low, usually less than 30% [
Stereotactic body radiotherapy (SBRT) can be a promising treatment modality, which involves the delivery of very high doses with high precision. In this study, we present the clinical outcomes and toxicity associated with SBRT for unresectable or recurrent cholangiocarcinoma.
We retrospectively reviewed the records of 58 patients with unresectable primary (n = 28) or recurrent (n = 30) cholangiocarcinoma who were treated with SBRT at our institution between January 2005 and August 2013. Primary tumors were found in liver (n = 27) or liver + enlarged lymph node (n = 1). Recurrent tumors were found in liver (n = 12), para-aortic lymph node (n = 17), or liver + enlarged lymph node (n = 1). All patients presented the Eastern Cooperative Oncology Group (ECOG) performance status of 0-3 and assessed by computed tomography (CT), magnetic resonance imaging, or positron emission tomography/computed tomography before SBRT. The decision 'inoperable tumor' and the following decision for SBRT was made in an interdisciplinary tumor board. The diagnosis was confirmed by histology or image study. The demographic data as well as the tumor and therapy data of the patients are depicted in
Five patients received EBRT followed by SBRT boost. The patients were selected by radiation oncologist's discretion. Total 38-44 Gy (median, 40 Gy) of EBRT was delivered with conventional fractionation (2 Gy). EBRT was administered via 3-dimensional conformal RT. All patients underwent CT simulation in the supine position with arms elevated above the head. A CMS XiO treatment planning system (CMS Inc., St. Louis, MO, USA) was utilized for EBRT, delivered by using a linear accelerator (Siemens, Erlangen, Germany) with 10- or 15-MV photon beams.
Contrast-enhanced CT with 2-mm slice thickness was performed for SBRT planning, with each patient in the supine position with both arms raised above the head. All patients were immobilized by using a customized vacuum cushion fixed in a stereotactic body frame (Smithers Medical Products Inc., North Canton, OH, USA). Diaphragmatic movements were reduced by using an abdominal compression device attached to the frame. SBRT dose planning and delivery were performed by using the On-Target planning system and CyberKnife (Accuray Inc., Sunnyvale, CA, USA) in 31 patients and the Eclipse treatment planning system and RapidArc (Varian Medical Systems Inc., Palo Alto, CA, USA) in 27 patients. The gross tumor volume (GTV) was defined as the visible lesion detected on CT. A thin-slice CT was performed with a slice thickness of 2 mm at 3 seconds per slice. These relatively slow CT images included respiratory movement of the target; therefore, the tumor volumes used during planning were larger than the GTVs and are referred to as internal target volumes (ITVs). The planning target volume (PTV) included an expansion of the ITV by 2-mm anteroposteriorly, 2-mm laterally, and 4-mm craniocaudally. Radiation doses were prescribed at 70%-80% isodose line of the maximum dose in CyberKnife and at 92%-99% in RapidArc to cover at least 95% of the PTVs.
Individualized prescribed doses, doses per fraction, and numbers of fractions were determined based on tumor size, location, patient performance, and organs at risk. Prescribed doses for SBRT only patients were 30-60 Gy (median, 45 Gy) in 3-5 fractions (median, 3 fractions). Prescribed doses for EBRT + SBRT patients were 15-18 Gy (median, 16 Gy) in 1 fraction. The SBRT doses were converted to the biologically equivalent dose at a fraction size of 2 Gy (BED2Gy) using a linear quadratic equation, BED = total dose × (1 + dose per fraction / α/β). The converted dose BED2Gy (α/β = 10) ranged from 48 to 150 Gy (median, 86 Gy).
Tumor response was assessed as described in the Response Evaluation and Criteria in Solid Tumors (RECIST) v.1.1 at 3 months after SBRT completion. Local failure was defined as an increase in tumor size or the development of a new lesion in the radiation field. Distant failure was defined as the development of a new lesion in non-targeted liver or beyond the liver.
Acute and late toxicities were defined based on patient's symptoms, laboratory findings, and diagnostic findings that developed before or after 3 months post-SBRT, respectively. Toxicities were scored using the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) v.4.03.
Survival and disease control were calculated from the start date of RT by using the Kaplan-Meier method. Various variables were evaluated from patient records for prognostic factor analysis. Log-rank analysis was used to compare prognostic factors. Those found to influence prognosis in univariate analysis were entered into multivariate analysis with the Cox proportional hazard regression model by using a backward conditional stepwise procedure to determine whether they acted independently. The Pearson chi-square test was used to compare incidences between two groups. All calculations were done with SPSS ver. 13.0 (SPSS Inc., Chicago, IL, USA), and p-values of <0.05 were considered significant.
Follow-up durations ranged from 1 to 97 months (median, 10 months), and 50 patients (86%) had died at the time of the analysis. The 1-year and 2-year overall survival rates and median survival were 45%, 20%, and 10 months, respectively. Disease progression-free survival rates at 1-year and 2-year were 26% and 23%, respectively, with a median time to disease progression of 5 months. Local control rate at 1-year and 2-year were 85% and 72%, respectively (
In the recurrent tumor group, univariate analysis showed that treatment volume (<50 vs. ≥50 mL) and time interval from surgery to recurrence (≤12 vs. >12 months) were significant factors for overall survival. The median survival of the patients with recurrence ≤12 months from the date of initial surgery was 8 months, whereas the median survival of those with recurrence >12 months was 17 months (p = 0.007). In multivariate analysis, time interval to recurrence was the only significant prognostic factor (p = 0.026) for overall survival.
Seventeen patients (29%) experienced nausea, vomiting, abdominal pain, and systemic discomfort of grade 1 or 2 during treatment. During follow-up, 6 patients (10%) experienced a severe complication above grade 3. Of the 6 patients, three patients with grade 3 complication were managed by medication and recovered. Of the 3 patients with grade 4 complication, 2 patients with cholangitis and bile duct stenosis were hospitalized and successfully managed by medication and percutaneous transhepatic biliary drainage, respectively. One patient with gastric perforation was recommended to receive surgical treatment. However, she refused the surgery and expired. Details for toxicities are summarized in
Among the 58 patients, 54 patients were assessable for the radiological response 3 months after SBRT completion. Four out of 54 patients experienced a complete response, 18 patients a partial response, 27 patients a stable disease, and 5 patients experienced disease progression. The overall RECIST response rate was 38% (complete response 5%; partial response 31%) with a stable disease rate of 47%.
The general approach for unresectable cholangiocarcinoma has been conventional EBRT with or without chemotherapy. Most of studies concerning EBRT are retrospective, nonrandomized, often combine gall bladder cancers with intrahepatic and extrahepatic cholangiocarcinoma, and involve small numbers of patients. In spite of limitations, they usually reported high rate of local recurrence (36%-72%) as a main treatment failure pattern with median survival of 9.5-15.8 months [
In terms of complications, we report 10% (6 of 58 pts) of severe complications (
This study suggests that SBRT can be considered as an effective local modality for unresectable primary or recurrent cholangiocarcinoma. Especially, patients with small and indolent recurrent cholangiocarcinoma are favorable candidates for salvage SBRT. Further, a well-controlled prospective study is necessary to confirm the optimal dose and constraints for SBRT in a large number of patients.
No potential conflict of interest relevant to this article was reported.
Kaplan-Meier survival analysis for overall survival (OS), disease progression-free survival (DPFS), and local control (LC) rates for all patients (n = 58). SBRT, stereotactic body radiotherapy.
Kaplan-Meier overall survival (OS) graph for patients with primary (n = 28) versus recurrent (n = 30) cholangiocarcinoma. SBRT, stereotactic body radiotherapy.
Kaplan-Meier overall survival (OS) difference in patients with small (<50 mL) tumor and large (≥50 mL) tumor. SBRT, stereotactic body radiotherapy.
Baseline patient and tumor characteristics (n = 58)
ECOG, Eastern Cooperative Oncology Group; PALN, para-aortic lymph node; LN, lymph node; SBRT, stereotactic body radiotherapy; EBRT, external beam radiation therapy; BED2Gy, biologically equivalent dose in 2 Gy/fraction.
a)Interval from surgery to recurrence includes recurrent tumor group only.
Prognostic factors affecting LC and OS rates on univariate analysis
LC, local control; OS, overall survival; ECOG, Eastern Cooperative Oncology Group; SBRT, stereotactic body radiotherapy; CEA, carcinoembryonic antigen; CA19-9, carbohydrate antigen 19-9; BED2Gy, biologically equivalent dose in 2 Gy/fraction; NS, non-specific.
a)Interval from surgery to recurrence includes recurrent tumor group only.
Severe complications above grade 3 (CTCAE v.4.03) after SBRT
CTCAE v.4.03, Common Terminology Criteria Adverse Events version 4.03; SBRT, stereotactic body radiotherapy; RT, radiotherapy; BED2Gy, biologically equivalent dose in 2 Gy/fraction; PALN, para-aortic lymph node; PTBD, percutaneous transhepatic biliary drainage.