Comparison of capecitabine and 5-fluorouracil in chemoradiotherapy for locally advanced pancreatic cancer
- Yeon-Joo Kim†1,
- Woo Jin Lee†1,
- Sang Myung Woo†1,
- Tae Hyun Kim1Email author,
- Sung Sik Han1,
- Bo Hyun Kim1,
- Sung Ho Moon1,
- Sang Soo Kim1,
- Young Hwan Koh1,
- Sang Jae Park1,
- Joo Young Kim1,
- Dae Yong Kim1 and
- Joong Won Park1
© Kim et al.; licensee BioMed Central Ltd. 2013
Received: 28 March 2013
Accepted: 28 June 2013
Published: 3 July 2013
Although capecitabine has theoretical advantages in the pharmacokinetics, such as higher intratumoral and lower systemic concentration, relative to bolus 5-fluorouracil (5-FU), outcomes of chemoradiotherapy (CRT) with capecitabine or bolus 5-FU have not been directly compared in patients with locally advanced pancreatic cancer. Therefore, we retrospectively compared the outcomes, including toxicity, tumor response, and overall survival, of oral capecitabine plus radiotherapy (RT) with bolus 5-FU plus RT, in patients with locally advanced pancreatic cancer.
Between August 2006 and January 2012, 98 patients with locally advanced pancreatic cancer received CRT, with 52 receiving concurrent oral capecitabine and 46 receiving bolus injection of 5-FU. Primary tumor and overall response after CRT were evaluated radiologically, and toxicity, tumor response, and overall survival (OS) were compared in the two groups.
Baseline clinical parameters of the two groups were similar. The rates of ≥ Grade 3 hematologic (0% vs. 8.7%, p = 0.045) and non-hematologic (0% vs. 8.7%, p = 0.045) toxicities were significantly lower in the capecitabine group than in the 5-FU group. Primary tumor (30.7% vs. 28.2%, p = 0.658) and overall (13.7% vs. 15.2%, p = 0.273) response rates and median OS time (12.5 months vs. 11.6 months, p = 0.655) were similar in the two groups.
Capecitabine plus RT may be a safe and feasible regimen for patients with locally advanced pancreatic cancer, with similar efficacy and low rates of toxicities compared with bolus 5-FU plus RT.
Surgical resection is the only curative treatment for pancreatic cancer, but only 10–15% of patients have localized and resectable disease at diagnosis. Approximately 50% of pancreatic cancer patients present with distant metastatic disease and 30% present with localized and unresectable disease. The Gastrointestinal Tumor Study Group (GITSG) trials [1–3] showed that chemoradiotherapy (CRT) with bolus injection of 5-fluorouracil (5-FU) yielded a modest survival benefit when compared with radiotherapy (RT) or chemotherapy alone. Since then, CRT plus bolus 5-FU has been regarded as a standard therapy for patients with locally advanced pancreatic cancer. Despite recent advances in diagnostics and therapeutics, the prognosis of patients with locally advanced pancreatic cancer has remained poor, due to high rates of local progression and distant metastasis. Thus, various chemotherapeutic regimens, with various dosages and schedules and with or without RT, have been tested to improve survival [4–8].
Capecitabine, an oral prodrug of 5-FU, is absorbed by the gastrointestinal tract and metabolized to 5-FU by a cascade of three enzymes. Capecitabine is converted by carboxylesterase in the liver to 5′-deoxy-5-fluorocytidine (5′-DFCR), by cytidine deaminase in the liver and tumor tissue to 5′-deoxy-5-fluorouridine (5′-DFUR), and by thymidine phosphorylase (TP) to 5-FU in tumor tissue. TP is more concentrated in tumor tissue than in normal tissue, and is upregulated by radiation in tumor tissue but not in normal tissue. Thus, oral capecitabine can result in a higher intratumoral and lower systemic 5-FU concentration than bolus 5-FU [9, 10]. This improved therapeutic index, along with more favorable pharmacokinetics (similar to those of protracted infusion of 5-FU), and convenient oral administration without the need for central venous access and an ambulatory infusion pump, make capecitabine particularly appealing to use in conjunction with RT. To our knowledge, however, outcomes of CRT with capecitabine or bolus 5-FU have not been directly compared in patients with locally advanced pancreatic cancer. We therefore retrospectively compared the outcomes, including toxicity, tumor response, and overall survival, of oral capecitabine plus RT with bolus 5-FU plus RT, in patients with locally advanced pancreatic cancer.
Between August 2006 and January 2012, 52 patients with primary locally advanced pancreatic cancer underwent CRT with capecitabine under a phase II protocol. Eligibility criteria included: (1) pathologically confirmed pancreatic carcinoma; (2) unresectable disease (stage cT4) on computed tomography (CT)/positron-emission tomography (PET); (3) radiographically assessable disease; (4) age ≥ 18 years; (5) performance status of 0 to 1 on the Eastern Cooperative Oncology Group (ECOG) score; (6) adequate bone marrow (white blood cell count ≥ 2,000/mm3, hemoglobin ≥ 7.5 g/dL, platelet count ≥ 100,000/mm3), liver (total bilirubin ≤ 3.0 mg/dL), and renal (serum creatinine ≤ 1.5 mg/dL) function; and (7) oral intake (including J-tube feeding) of ≥ 1,500 calories/day. Patients with elevated bilirubin due to obstruction were stented and their bilirubin decreased to ≤ 3.0 mg/dL, and patients with biliary or gastroduodenal obstruction underwent drainage prior to study entry. Exclusion criteria included: (1) radiographic evidence of metastasis in the major viscera or peritoneal seeding on CT and/or PET; (2) previous history of RT adjacent to the planned field; (3) pregnancy or breast feeding; and (4) previous history of uncontrolled other malignancies within 2 years. All patients provided written informed consent before study enrollment and this trial was registered at clinicaltrials.gov (NCT00658840).
During the same study period, 46 patients who refused to participate in this protocol received CRT plus 5-FU, the routine clinical practice regimen in our institution for patients with locally advanced pancreatic cancer. This study was conducted in accordance with the guidelines of the institutional review boards of the National Cancer Center.
Capecitabine (n = 52), n (%)
5-FU (n = 46), n (%)
Mean ± SE
62.1 ± 1.3
65.0 ± 1.4
Tumor size* (cm)
Mean ± SE
4.0 ± 0.1
4.3 ± 0.2
CEA (ng/ mL)
Mean ± SE
6.4 ± 0.9
7.7 ± 1.7
Pretreatment CA 19–9 level (U/mL)
Mean ± SE
1179.6 ± 307.3
531.1 ± 130.6
Prior to RT, all patients underwent CT simulation, with their targets defined in accordance with the International Commission on Radiation Units and Measurements Report 50. The gross tumor volume (GTV) encompassed the gross tumor, as defined by contrast CT or PET scan. The clinical target volume (CTV) included the GTV and the volumes of regional lymph nodes, including the porta hepatic, pericholedochal, celiac, and pancreaticoduodenal nodes. The initial and boot planning target volume (PTV) included the CTV and GTV plus a 5–10 mm margin. All patients underwent three-dimensional treatment planning, such that the PTV would be encompassed by a 90% isodose volume of the prescribed dose.
An initial dose of 45 Gy in 25 fractions was delivered to the primary tumor and regional lymph nodes, followed by a boost of 10.8 Gy in 6 fractions to the gross tumor, 5 days a week. All patients received a total radiation dose of 55.8 Gy in 31 fractions.
Capecitabine or 5-FU was delivered concurrently with RT. The capecitabine group received an oral dose of 800 mg/m2 twice daily for the duration of RT with weekend breaks. The 5-FU group received two cycles of intravenous bolus injection of 5-FU (400 mg/m2/d) for 3 days in the first and fifth weeks of RT.
Treatment after CRT and evaluation
Following completion of CRT, patients were evaluated clinically and underwent CT scans of the abdomen, chest radiography, and serum CA 19–9 measurements to determine tumor response and resectability. Patients who had resectable disease after CRT was considered for surgical resection, whereas patients who still had unresectable disease were considered for gemcitabine based chemotherapy (1000 mg/m2over 30 minutes intravenously once weekly for 3 of every 4 weeks). Patients who refused further chemotherapy or had poor performance status received supportive care.
Serum samples for measurement of CA 19–9 were obtained from all patients within 2 weeks of the initiation of CRT (pre-treatment level) and 1 month after CRT (post-treatment level). The percent decrease in CA 19–9 concentration was calculated as: CA 19–9 percent decrease (%) = [(pre-treatment CA 19–9 – post-treatment CA 19–9)/pre-treatment CA 19–9] × 100. Tumor responses were determined by comparison of CT scans taken before and 1 month after CRT using the Response Evaluation Criteria in Solid Tumors guidelines . A complete response (CR) was defined as the disappearance of the primary tumor. A partial response (PR) was defined as ≥30% reduction in the longest diameter of the primary tumor. Progressive disease (PD) was defined as a ≥20% increase in the longest diameter of the primary tumor or the appearance of one or more new lesions. Stable disease (SD) was defined as a response that did not qualify as a PR or a PD. Objective response rates were calculated as the rate of CR + PR. Patients with CR or PR were considered “Responders”, and those with SD or PD were considered “Non-responders”. Toxicity was recorded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 3.0. Due to difficulties in accurately scoring lower grades of acute toxicity in patients with pancreatic cancer, only grade 3 or higher acute toxicities are compared.
Follow-up and statistical analysis
After completion of treatment, patients were given follow-up examinations every 2–4 weeks for the first 3 months, and then every 3 months. For most patients, follow-up evaluations at each visit included a physical examination, complete blood count, liver function test, serum CA 19–9 measurement, chest radiography, and dynamic CT scan of the abdomen and pelvis. Recurrence was proven by biopsy or cytology, and/or by radiological findings that indicated an increase in tumor size.
A pretreatment serum CA 19–9 of 400 U/mL, the significant cutoff point in our previous reports [13, 14], or a 40% decrease in CA 19–9, close to the median value for each group, was chosen as a cutoff point for comparison of patient survival rates. Parameters in the capecitabine and 5-FU groups were compared using chi-square tests, Fisher’s exact tests, and t-tests, as applicable. Overall survival (OS) was defined as the interval from the commencement of CRT to the date of death or last follow-up and its probability was calculated by the Kaplan–Meier method. Univariate and multivariate analyses were performed using the log rank test and Cox’s proportional hazard model, respectively, to evaluate prognostic factors associated with OS. All statistical tests were two-sided and were performed using STATA software (ver. 9.0; Stata Corp., College Station, TX). P values less than 0.05 were considered statistically significant.
Comparison of toxicities * between the capecitabine and 5-fluorouracil (5-FU) groups
Capecitabine (n = 52), n
5-FU (n = 46), n
Type of toxic effect
Treatment was well tolerated in both groups and there were no treatment-related deaths. The details of the distribution of toxicities between the capecitabine and 5-FU groups are summarized in Table 2. None of the patients in the capecitabine group developed Grade ≥3 toxicities, whereas 4 patients each (8.7%) in the 5-FU group developed Grade ≥3 hematologic and non-hematologic toxicities (p = 0.045 each).
Tumor response and overall survival
Tumor responses * in the capecitabine and 5-fluorouracil (5-FU) groups
Capecitabine (n = 51†), n (%)
5-FU (n = 46), n (%)
CA 19–9 percent decrease (%)
Mean ± SE
-1.9 ± 19.5
16.2 ± 15.8
Univariate analysis of factors influencing overall survival
Median (95% CI), months
CEA (ng/ mL)
Pretreatment CA 19–9 level (U/mL)
Primary tumor response
CA 19–9 percent decrease (%)
Multivariate analysis of factors influencing overall survival
CA 19–9 level (U/mL)
We found that the rates of Grade ≥3 hematologic (0% vs. 8.7%, p = 0.045) and non-hematologic (0% vs. 8.7%, p = 0.045) toxicities were significantly lower in the capecitabine group than in the 5-FU group. Lower toxicity rates may have been due to the pharmacodynamic advantages of oral capecitabine relative to bolus 5-FU . Capecitabine is a tumor-selective fluoropyrimidine carbamate that is converted to active 5-FU by TP, an enzyme of higher abundance in tumor than in normal tissue that is upregulated by radiation in tumor but not in normal tissue [9, 10]. Thus, theoretically, capecitabine could show lower rates of toxicity than bolus 5-FU. A previous study found that the rate of Grade ≥3 hematologic toxicity was lower in patients receiving capecitabine than 5-FU during preoperative CRT for locally advanced rectal cancer (1.5% vs. 7.8%, p = 0.04), similar to our results, but that rates of Grade ≥3 diarrhea (8.6% vs. 2.1%, p = 0.006) and hand-foot syndrome (2%vs. 0%, p = 0.061) were higher in the capecitabine group . However, a phase II trial of induction chemotherapy with gemcitabine and cisplatin followed by CRT with capecitabine in patients with locally advanced pancreatic cancer showed that the rates of Grade ≥3 diarrhea (5.4%) and hand-foot syndrome (0%) were low during CRT , similar to our findings. These findings implied that the lower rates of Grade ≥3 non-hematologic toxicity in the capecitabine than in the 5-FU group in our study maybe due to genetic differences in tolerability or susceptibility to capecitabine between Caucasians and Asians, as the conversion rate of tegafur to fluorouracil is different between Caucasians and Asians due to polymorphic differences in the CYP2A6 gene [18, 19]. However, due to the relatively small number of patients in the capecitabine group (n = 52), which may be insufficient to determine the overall actual toxicity rates thoroughly and low incidence of toxicities in western study treated with CRT with capecitabine , more comprehensive and larger-scale studies should be needed.
Protracted infusion of 5-FU and capecitabine, which prolongs the exposure of non-cycling tumor cells to 5-FU, may enhance cytotoxicity relative to bolus 5-FU. Protracted infusion of 5-FU or capecitabine during adjuvant CRT has been shown to improve relapse-free survival (RFS) and OS, compared with bolus 5-FU, in patients with rectal cancer [16, 21]. In contrast, the Intergroup 0144 study, which compared different 5-FU based chemotherapeutic regimens in rectal cancer, found that protracted and bolus infusion of 5-FU yielded similar RFS and OS, and our previous report  showed that capecitabine and bolus 5-FU resulted in similar radiologic and pathologic tumor responses in patients receiving preoperative CRT for rectal cancer. However, to date, it has been remained unclear whether chemotherapeutic regimens, among a protracted infusion of 5-FU, capecitabine, or bolus injection of 5-FU, can result in superior outcomes in patients with pancreatic cancer. We found that capecitabine, which mimics the protracted infusion of 5-FU, and bolus 5-FU yielded similar tumor responses and overall survival in patients with locally advanced pancreatic cancer.
A randomized trial found that, compared to5-FU, gemcitabine yielded better outcomes, including alleviation of disease-related symptoms and longer OS, in patients with advanced, symptomatic pancreatic cancer , and thus various dosages and schedules of gemcitabine based chemotherapy, with or without RT, have been tried to improve survival in locally advanced pancreatic cancer patients [4–6, 8]. These studies, however, showed that gemcitabine based chemotherapy, with or without oxaliplatin, paclitaxel, docetaxel, and tyrosine kinase inhibitors, resulted in high rates of severe toxicities, without survival benefits, compared to 5-FU. Thus, 5-FU continues to be used as a concurrent chemotherapeutic agent during CRT . To evaluate the effectiveness and safety of capecitabine, we compared outcomes, including toxicity, tumor response and overall survival, of RT plus capecitabine or bolus 5-FU, in patients with locally advanced pancreatic cancer.
This study was retrospective and thus had certain inherent limitations. First, it included relatively small numbers of patients in the capecitabine (n = 52) and 5-FU (n = 46) groups, which may have been insufficient to compare outcomes thoroughly. Second, this was a retrospective comparison study of two groups with different chemotherapeutic regimens, not a randomized trial. Thus, further larger scaled and comprehensive studies are required to accurately compare the outcomes of these two chemotherapy regimens in patients with locally advanced pancreatic cancer. However, in present study, the characteristics of patients in the two groups did not differ significantly, and each chemotherapeutic regimen was decided according to patient’s preferences.
In conclusion, we compared the outcomes of CRT with capecitabine or bolus 5-FU in patients with locally advanced pancreatic cancer. We found that CRT with capecitabine had low toxicity rates, but yielded similar tumor responses and overall survival compared with CRT with bolus 5-FU. These findings suggest that capecitabine may be a safe and feasible chemotherapy regimen in patients with locally advanced pancreatic cancer treated with CRT.
This work was supported by a National Cancer Center Grant (NCC-1310080, 1241110 and 1340940).
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