Concurrent analysis of human equilibrative nucleoside transporter 1 and ribonucleotide reductase subunit 1 expression increases predictive value for prognosis in cholangiocarcinoma patients treated with adjuvant gemcitabine-based chemotherapy.

BACKGROUND: The aim of this study was to investigate the predictive and prognostic values of intratumoural human equilibrative nucleoside transporter 1 (hENT1) and ribonucleotide reductase subunit 1 (RRM1) expression in advanced cholangiocarcinoma patients treated with adjuvant gemcitabine-based chemotherapy (AGC).
METHODS: Intratumoural hENT1 and RRM1 expression levels were investigated immunohistochemically in 127 patients with advanced cholangiocarcinoma who underwent surgical resection (68 with AGC and 59 without AGC). The impacts of hENT1 and RRM1 expression on survival were evaluated.
RESULTS: High intratumoural hENT1 and RRM1 expression levels were observed in 86 (68%) and 67 (53%) patients, respectively. In a multivariate analysis of 68 patients who received AGC, high hENT1 (P=0.044) and low RRM1 expression (P=0.009) were independently associated with prolonged disease-free survival (DFS), whereas low RRM1 expression (P=0.024) was independently associated with prolonged overall survival (OS). Moreover, concurrent high hENT1 and low RRM1 expression was a powerful independent predictor of prolonged DFS (P<0.001) and OS (P=0.001) when the combined classification of hENT1 and RRM1 was introduced.
CONCLUSIONS: Concurrent analysis of hENT1 and RRM1 expression may increase the predictive value of these biomarkers for survival of advanced cholangiocarcinoma patients treated with AGC.

Cholangiocarcinoma, including intra- and extrahepatic cholangiocarcinoma, is a relatively uncommon disease in the United States, accounting for 4410 deaths in 2012 (Siegel ). However, this disease is the sixth leading cause of cancer-related deaths in Japan, with >18 000 deaths reported in 2012 (National Cancer Center, Japan, 2014). Although surgical resection is the only curative treatment for cholangiocarcinoma, the 5-year overall survival (OS) rates of patients with resected cholangiocarcinoma are still 18–40%, even in high-volume centers (DeOliveira ; Murakami ; Nagino ). Therefore, several peri-operative therapeutic modalities, including adjuvant chemotherapy, have recently been proposed in order to improve the prognosis of patients with cholangiocarcinoma.

Since 2002, post-operative adjuvant gemcitabine-based chemotherapy (AGC) has been administered to patients with advanced cholangiocarcinoma (International Union Against Cancer (UICC) stages II–IV) in our institution, and we have previously reported a survival benefit associated with this therapy (Murakami , 2011, 2012). However, the efficacy of AGC varies among individuals, and the resulting survival rates are still unsatisfactory. To maximise the therapeutic benefit of adjuvant chemotherapy, identification of biomarkers that have predictive and prognostic value is important. Several clinical studies have revealed the predictive significance of intratumoural human equilibrative nucleoside transporter 1 (hENT1) for survival in pancreatic cancer patients treated with gemcitabine (Spratlin ; Giovannetti ; Farrell ; Maréchal ; Wei ; Greenhalf ). Moreover, our recent report demonstrated that hENT1 also predicts the survival of cholangiocarcinoma patients treated with AGC (Kobayashi ). Thus, hENT1 has been recognised as a relevant predictive biomarker for response to gemcitabine.

In addition, researchers have recently also become interested in identifying other candidates for predictive biomarkers related to gemcitabine sensitivity. In particular, the expression of ribonucleotide reductase subunit M1 (RRM1), which is involved in the production of deoxyribonucleotides for DNA synthesis, has been reported to be associated with gemcitabine resistance in several cancers (Ohtaka ; Akita ; Jordheim ; Gong ). In addition, we have recently demonstrated that combined analysis of hENT1 and RRM1 expression was a more powerful predictor than analysis of either target alone in pancreatic cancer (Nakagawa ). However, very few reports have revealed the predictive significance of RRM1 expression for gemcitabine resistance in cholangiocarcinoma. In addition, the predictive value of combined analysis of hENT1 and RRM1 expression in cholangiocarcinoma is still unclear. The aim of this study was to investigate the predictive and prognostic values of intratumoural hENT1 and RRM1 expression in advanced cholangiocarcinoma patients treated with AGC after surgical resection.

Materials and methods

Study design

Patients with advanced cholangiocarcinoma (UICC stages II, IIA, IIB, III, IIIA, IIIB, IV, IVA, and IVB) who underwent surgical resection with curative intent (R0 or R1 resection) at the Department of Surgery, Hiroshima University Hospital, Hiroshima, Japan between April 1989 and August 2012 were enrolled in this study. All patients had a confirmed pathological diagnosis. Patients who experienced post-operative mortality were excluded from this study. Formalin-fixed, paraffin-embedded tumour tissues from the resected specimens were collected from eligible patients, and immunohistochemical staining for detection of intratumoural hENT1 and RRM1 was performed. The influences of clinicopathological factors and hENT1 and RRM1 expression on survival were evaluated by univariate and multivariate analyses. Written informed consent was obtained from all patients for surgical treatment and pathological examinations, as required by institutional guidelines.

Surgical procedures and pathological assessment

Most patients with intrahepatic or perihilar cholangiocarcinoma underwent major hepatectomy, and all surgical procedures for perihilar cholangiocarcinoma included caudate lobectomy. Patients with distal cholangiocarcinoma usually underwent pancreatoduodenectomy with or without pylorus preservation. Dissection of the regional lymph nodes was performed for all patients. All resected specimens were examined histologically by specialised pathologists; each tumour was classified as well-differentiated, moderately differentiated, or poorly differentiated adenocarcinoma according to the predominant histology. Residual tumour (R factor) was considered R1 if histological infiltrating carcinoma was present at the proximal or distal bile duct transaction line, the hepatic transaction line, or the dissected peripancreatic soft-tissue margins. All patients with R2 resections were excluded from this study. Tumour stage, lymph node metastasis, and final stage were classified based on the 7th edition of the UICC tumour-node-metastasis (TMN) classification (Sobin ).

Adjuvant gemcitabine-based chemotherapy

The AGC regimen used in this study, which included two treatment options, has been reported previously (Murakami , 2011, 2012). First, intravenous chemotherapy consisted of gemcitabine 700 mg m−2 administered biweekly. Second, intravenous and oral chemotherapy consisted of intravenous gemcitabine 700 mg m−2 on day 1 and oral S-1 50 mg m−2 for 7 consecutive days. These regimens were repeated every 14 days for 10 cycles. None of the patients received radiation therapy during this study period. Patients who had to switch to other chemotherapies before the 10 cycles were completed because of recurrent disease were considered to have received AGC in our group classification. Patients who received gemcitabine-based chemotherapy because of recurrent disease after completion of AGC were also included in this group.

Immunohistochemistry for hENT1 and RRM1

Polyclonal rabbit antibodies against human hENT1 (Abnova Co., Taipei, Taiwan) and against human RRM1 (Abcam, Cambridge, UK) were used to evaluate hENT1 and RRM1 expression, respectively. Following antigen retrieval by autoclaving (100 °C for 10 min in Dako Target Retrieval Solution High pH 1 × for hENT1 or 121 °C, 10 min in 0.01 M citrate buffer for RRM1), sections were immersed in methanol containing 3% hydrogen peroxide for 15 min, incubated in protein blocking solution (Dako, Carpinteria, CA, USA) for 10 min, and incubated with anti-hENT1 antibodies (1 : 200 dilution) overnight at 4 °C or anti-RRM1 antibodies (1 : 150 dilution) for 60 min at room temperature. Samples were then incubated in labelled streptavidin-biotin polymer (Envision Plus, Dako, Hamburg, Germany) at room temperature for 60 min as a secondary antibody and immersed for 10 min in 0.01% 3,3-diaminobenzidine solution in 50 mM Tris-HCl buffer with 10 mM hydrogen peroxide as a substrate. Sections were counterstained with Mayer's haematoxylin, dehydrated, and mounted. Negative controls were provided by omitting the primary antibodies.

Two observers (HS and NK), blinded to clinical characteristics and outcomes, assessed and scored the expression of hENT1 and RRM1. In cases of disagreement, consensus was reached by joint review. Because hENT1 is strongly expressed in cell membranes of lymphocytes (Spratlin ; Farrell ), and RRM1 is strongly expressed in plasma and stromal cells (Ohtaka ; Akita ), these were used as internal positive controls. The intensities of hENT1 and RRM1 staining were scored as follows: grade 0, not stained; grade 1, weakly stained compared with the internal positive control; grade 2, stained as strongly as the internal positive control; and grade 3, strongly stained compared with the internal positive control. For evaluation of intratumoural hENT1 and RRM1 expression, if grade 2 or 3 staining was observed in >50% of tumour cells, the sample was considered to have high expression, and if grade 0 or 1 staining was observed in >50% of tumour cells, the sample was considered to have low expression (Figure 1). This cutoff value was determined on the basis of a previous report (Santini ).

Figure 1

Immunohistochemical analysis of human equilibrative nucleoside transporter 1 (hENT1) and ribonucleotide reductase subunit 1 (RRM1) expression in cholangiocarcinoma. These photomicrographs reveal (A) high hENT1 expression, (B) low hENT1 expression, (C) high RRM1 expression, (D) low RRM1 expression (original magnification, × 200; bar=50 μm). Positive internal controls is established by staining of lymphocytes and stromal cells (arrows).

Survival

Disease status was regularly assessed every 3 months by blood tests and computed tomography. If a patient had died, the survival time after surgery and cause of death were recorded. For surviving patients (as of 4 July 2013), postsurgical time and recurrence status were recorded. The failure event for OS was defined as death of any cause, whereas that for disease-free survival (DFS) was defined as disease recurrence, diagnosed based on imaging findings, or death of any cause. Survival time was measured from the date of operation to the date of the failure event or last follow-up evaluation.

Statistical analysis

Categorical clinicopathological variables were compared using the χ2-test and Fisher's exact test, as appropriate. Survival end points were estimated using the Kaplan–Meier method and compared by univariate log-rank (Mantel-Cox) test. The Cox proportional hazards model was applied to the multivariate survival analysis for factors found to be significant on univariate analysis. The UICC stage was excluded in the multivariate analysis, although it was significant by univariate analysis, because of its confounding with UICC pT factor and lymph node metastasis. P-values of <0.05 were considered statistically significant. Statistical analyses were performed by JMP software, version 10.2 (SAS Institute, Cary, NC, USA).

Results

Patient demographics and pathological assessment

A total of 132 consecutive patients with UICC stages II–IV cholangiocarcinoma underwent surgical resection (R0 or R1 resection) at our institution between April 1989 and August 2012. Of these 132 patients, 5 (3.7%) were excluded from this study because of operative deaths. In total, 127 cholangiocarcinoma patients were eligible for this study. This case series included 105 (83%) patients previously reported in our retrospective analysis of hENT1 expression in cholangiocarcinoma (Kobayashi ). Demographics and clinicopathological factors of enrolled patients are summarised in Table 1. The median age of these 127 patients was 69 years (range: 37–85 years). Lymph node metastasis was found in 65 (51%) patients, including 12 (9%) with para-aortic lymph node involvement. Finally, 32 (25%), 17 (13%), 24 (19%), 2 (2%), 7 (6%), 20 (16%), 6 (5%), 13 (10%), and 6 (5%) patients were diagnosed with stage II, IIA, IIB, III, IIIA, IIIB, IV, IVA, and IVB disease, respectively. All 12 patients with stage IV or IVB disease had para-aortic lymph node metastases detectable only by post-operative histological examination, but not by pre-operative-imaging examinations.

Table 1

Comparison of clinicopathological factors based on intratumoural hENT1 and RRM1 expression for all patients (n=127)

		No. of patients (%)			No. of patients (%)
		High hENT1	Low hENT1		High RRM1	Low RRM1
	Total no. of patients (%)	n=86 (68)	n=41 (32)	P-value	n=67 (53)	n=60 (47)	P-value
Ages(years)
<70	66 (52)	48 (56)	18 (44)	0.209	38 (57)	28 (47)	0.258
⩾70	61 (48)	38 (44)	23 (56)		29 (43)	32 (53)
Gender
Male	85 (67)	56 (65)	29 (71)	0.529	43 (64)	42 (70)	0.486
Female	42 (33)	30 (35)	12 (29)		24 (46)	18 (30)
Tumour location
Intrahepatic	20 (16)	13 (15)	7 (17)	0.251	14 (21)	6 (10)	0.02
Perihilar	60 (47)	37 (43)	23 (56)		24 (36)	36 (60)
Distal	47 (37)	36 (42)	11 (27)		29 (43)	18 (30)
AGC
Yes	68 (54)	45 (52)	23 (56)	0.69	35 (52)	33 (55)	0.755
No	59 (46)	41 (48)	18 (44)		32 (48)	27 (45)
Residual tumour
R0	95 (75)	64 (74)	31 (76)	0.885	54 (81)	41 (68)	0.112
R1	32 (25)	22 (26)	10 (24)		13 (19)	19 (32)
Pathological differentiation
Well	55 (43)	45 (52)	10 (24)	0.009	33 (49)	22 (37)	0.017
Moderately	49 (39)	29 (34)	20 (49)		28 (42)	21 (35)
Poorly	23 (18)	12 (14)	11 (27)		6 (9)	17 (28)
Lymph node metastasis
Present	65 (51)	47 (55)	18 (44)	0.257	36 (54)	29 (48)	0.544
Absent	62 (49)	39 (45)	23 (56)		31 (46)	31 (52)
UICC pT factor
T1	3 (2)	2 (2)	1 (2)	0.345	3 (4)	0 (0)	0.126
T2, 2a, 2b	62 (49)	38 (44)	24 (59)		32 (48)	30 (50)
T3	59 (46)	43 (50)	16 (39)		29 (43)	30 (50)
T4	3 (2)	3 (4)	0 (0)		3 (4)	0 (0)
UICC stages
II, IIA, IIB	73 (57)	49 (57)	24(58)	0.544	40 (60)	33 (55)	0.009
III, IIIA, IIIB	29 (23)	18 (21)	11(27)		9 (13)	20 (33)
IV, IVA, IVB	25 (20)	19 (22)	6(15)		18 (27)	7 (12)

Abbreviations: AGC=adjuvant gemcitabine-based chemotherapy; hENT1=human equilibrative nucleoside transporter 1; RRM1=ribonucleotide reductase subunit 1.

Delivery of AGC

Of the 127 patients, 68 (54%) received post-operative AGC, and 59 (46%) did not. In the 68 patients who received AGC, 60 (88%) patients received adjuvant gemcitabine plus S-1 chemotherapy, and 8 (12%) patients received gemcitabine alone. Sixty-one (90%) patients received 10 cycles of AGC, whereas the remaining 7 (10%) patients had to switch to other chemotherapies at 7 or 8 cycles of AGC because of recurrent disease. The median total dose of gemcitabine administered to the 68 patients was 17 000 mg (range: 7000–44 000 mg). No treatment-related deaths were reported in this case series. In the 59 patients without AGC, 55 (93%) patients received only surgical treatment, and 4 (7%) patients received adjuvant oral UFT chemotherapy.

Clinicopathological factors and intratumoural hENT1 and RRM1 expression

Potential correlations of hENT1 and RRM1 expression levels with each clinicopathological factor are shown in Table 1. High intratumoural hENT1 and RRM1 expression levels were observed in 86 (68%) and 67 (53%) patients, respectively. Significant differences in hENT1 expression were found among samples with varying states of pathological differentiation (P=0.009), and poorly differentiated adenocarcinoma samples were more likely to exhibit low RRM1 expression (P=0.017). In addition, the distribution of RRM1 expression was significantly different depending on the tumour location (P=0.020), pathological differentiation (P=0.017), and UICC stage (P=0.009). Other clinicopathological factors did not correlate with hENT1 or RRM1 expression.

Univariate survival analysis for patients with or without AGC

The median follow-up time after surgery was 81 months (range: 9–294 months) for all 127 patients. The 5-year DFS and OS rates for these patients were 26% and 33%, respectively. The results of univariate DFS and OS analyses for patients with or without AGC are shown in Table 2. In 68 patients who received AGC, pathological differentiation (P=0.003), UICC stage (P=0.042), hENT1 expression (P=0.005), and RRM1 expression (P=0.015) were significantly associated with DFS, and pathological differentiation (P=0.011), lymph node metastasis (P=0.009), UICC stage (P=0.012), hENT1 expression (P=0.036), and RRM1 expression (P=0.035) were also significantly associated with OS. In the 59 patients who did not receive AGC, residual tumour (P<0.001) and lymph node metastasis (P=0.037) were significantly associated with DFS, and residual tumour (P<0.001), pathological differentiation (P=0.049), lymph node metastasis (P=0.007), and UICC stage (P=0.017) were significantly associated with OS. However, both hENT1 and RRM1 expression were not significantly correlated with DFS (hENT1: P=0.796, RRM1: P=0.642) or OS (hENT1: P=0.913, RRM1: P=0.883) (Figures 2 and 3).

Table 2

Univariate DFS and OS analysis of prognostic factors in patients with cholangiocarcinoma who received AGC (n=68) and those who did not (n=59)

	AGC(+) (n=68)					AGC(−) (n=59)
		DFS		OS			DFS		OS
	N	5-Year survival (%)	P-value	5-Year survival (%)	P-value	N	5-Year survival (%)	P-value	5-Year survival (%)	P-value
Age (years)
<70	35	38	0.941	61	0.225	31	18	0.834	26	0.472
⩾70	33	36		30		28	14		15
Gender
Male	42	40	0.518	53	0.566	43	17	0.483	20	0.56
Female	26	19		35		16	13		21
Tumour location
Intrahepatic	12	20	0.129	56	0.479	8	25	0.56	13	0.841
Perihilar	36	43		49		24	17		27
Distal	20	33		39		27	13		16
Residual tumour
R0	53	42	0.077	50	0.11	42	23	0.001	29	<0.001
R1	15	16		36		17	0		0
Pathological differentiation
Well	28	54	0.003	62	0.011	27	27	0.187	34	0.049
Moderate, poor	40	20		32		32	4		7
Lymph node metastasis
Present	31	34	0.057	31	0.009	34	9	0.037	10	0.007
Absent	37	40		60		25	26		35
UICC pT factor
T1,2,2a,2b	34	43	0.216	56	0.126	31	21	0.092	27	0.167
T3,4	34	28		35		28	10		12
UICC stages
II, A, B	35	43	0.042	66	0.012	38	21	0.22	27	0.017
III, A, B, IV, A, B	33	30		25		21	8		10
hENT1 expression
High	45	45	0.005	55	0.036	41	18	0.796	24	0.913
Low	23	21		32		18	12		12
RRM1 expression
High	35	25	0.015	33	0.035	32	16	0.642	22	0.883
Low	33	47		59		27	16		19
Combined hENT1 and RRM1 classification
High hENT1/low RRM1	20	58	0.003	75	0.015	12	18	0.778	25	0.994
High hENT1/high RRM1	25	24		34		29	18		23
Low hENT1/low RRM1	13	19		32		15	13		13
Low hENT1/high RRM1	10	25		36		3	0		0
High hENT1/low RRM1	20	58	<0.001	75	0.001
The other three expression combinations	48	22		32

Abbreviations: AGC=adjuvant gemcitabine-based chemotherapy; DFS=disease-free survival; hENT1=human equilibrative nucleoside transporter 1; OS=overall survival; RRM1=ribonucleotide reductase subunit 1.

The other three expression combinations=high hENT1/high RRM1 expression or low hENT1/low RRM1 expression or low hENT1/high RRM1 expression. Values in bold represent P-values <0.05.

Figure 2

Disease-free survival (DFS) and overall survival (OS) curves stratified by intratumoural hENT1 expression. AGC (+) indicates subgroups of patients who received adjuvant gemcitabine-based chemotherapy; AGC (−) indicates subgroups of patients who did not receive adjuvant gemcitabine-based chemotherapy. (A) DFS curves in AGC (+) patients (P=0.005). (B) DFS curves in AGC (−) patients (P=0.796). (C) OS curves in AGC (+) patients (P=0.036). (D) OS curves in AGC (−) patients (P=0.913).

Figure 3

DFS and OS curves stratified by intratumoural RRM1 expression. AGC (+) indicates subgroups of patients who received adjuvant gemcitabine-based chemotherapy; AGC (−) indicates subgroups of patients who did not receive adjuvant gemcitabine-based chemotherapy. (A) DFS curves in AGC (+) patients (P=0.015). (B) DFS curves in AGC (−) patients (P=0.642). (C) OS curves in AGC (+) patients (P=0.035). (D) OS curves in AGC (−) patients (P=0.883).

Each of the 68 patients who received AGC was classified into four groups based on hENT1 and RRM1 expression levels as follows: high hENT1/low RRM1 expression (n=20), high hENT1/high RRM1 expression (n=25), low hENT1/low RRM1 expression (n=13), and low hENT1/high RRM1 expression (n=10), which was significantly associated with both DFS (P=0.003) and OS (P=0.015) by univariate analysis (Figure 4). Moreover, patients with high hENT1/low RRM1 expression experienced significantly longer DFS and OS than those with high hENT1/high RRM1 expression (DFS: P=0.001, OS: P=0.006), low hENT1/low RRM1 expression (DFS: P<0.001, OS: P=0.002), and low hENT1/high RRM1 expression (DFS: P<0.001, OS: P=0.003). On the basis of these findings, we further categorised these 68 patients who received AGC into the high hENT1/low RRM1 expression (n=20) group and low hENT1 and/or high RRM1 group (n=48) for comparative purposes. This combined classification was significantly associated with both DFS (P<0.001) and OS (P=0.001) by univariate analysis.

Figure 4

DFS and OS curves stratified by combined analysis of intratumo AGC (+) indicates subgroups of patients who received adjuvant gemcitabine-based chemotherapy; AGC (−) indicates subgroups of patients who did not receive adjuvant gemcitabine-based chemotherapy. (A) DFS curves in AGC (+) patients (P=0.003). (B) DFS curves in AGC (−) patients (P=0.778). (C) OS curves in AGC (+) patients (P=0.015). (D) OS curves in AGC (−) patients (P=0.994).

On the other hand, each of the 59 patients who did not received AGC was also classified into four groups: high hENT1/low RRM1 expression (n=12), high hENT1/high RRM1 expression (n=29), low hENT1/low RRM1 expression (n=15), and low hENT1/high RRM1 expression (n=3), which was not significantly associated with both DFS (P=0.778) and OS (P=0.994) by univariate analysis.

Multivariate survival analysis for patients who received AGC

Multivariate analysis including separated hENT1 and RRM1 expression for 68 patients who received AGC identified well-differentiated (HR, 0.37; 95% CI, 0.17–0.76; P=0.007), high hENT1 expression (HR, 0.49; 95% CI, 0.24–0.98; P=0.044), and low RRM1 expression (HR, 0.41; 95% CI, 0.21–0.80; P=0.009) as independent factors for prolonged DFS and well-differentiated (HR, 0.45; 95% CI, 0.19–0.98; P=0.045), absence of lymph node metastasis (HR, 0.39; 95% CI, 0.18–0.81; P=0.011), and low RRM1 expression (HR, 0.43; 95% CI, 0.20–0.89; P=0.024) as independent prognostic factors for prolonged OS (Table 3, model 1).

Table 3

Multivariate DFS and OS analysis of prognostic factors in patients who received AGC (n=68)

	DFS			OS
	HR	95% CI	P-value	HR	95% CI	P-value
Model 1—multivariate analysis including separated hENT1 and RRM1 expression
Pathological differentiation
Well	0.37	0.17–0.76	0.007	0.45	0.19–0.98	0.045
Moderate, poor	1			1
Lymph node metastasis
Present				1	0.18–0.81	0.011
Absent				0.39
hENT1 expression
High	0.49	0.24–0.98	0.044	0.55	0.26–1.21	0.135
Low	1			1
RRM1 expression
High	1	0.21–080	0.009	1	0.20–0.89	0.024
Low	0.41			0.43
Model 2—multivariate analysis including combined hENT1 and RRM1 classification
Pathological differentiation
Well	0.38	0.17–0.77	0.007	0.49	0.21–1.05	0.066
Moderate, poor	1			1
Lymph node metastasis
Present				1	0.18–0.81	0.012
Absent				0.39
Combined hENT1 and RRM1 classification
High hENT1/low RRM1	0.22	0.08–0.51	<0.001	0.22	0.07–0.60	0.001
The other three expression combinations	1			1

Abbreviations: AGC=adjuvant gemcitabine-based chemotherapy; CI=confidence interval; DFS=disease-free survival; HR=hazard ratio; hENT1=human equilibrative nucleoside transporter 1; OS=overall survival; RRM1=ribonucleotide reductase subunit 1.

The other three groups=high hENT1/high RRM1 expression or low hENT1/low RRM1 expression or low hENT1/high RRM1 expression. Values in bold represent P-values <0.05

Furthermore, multivariate analysis including combined hENT1 and RRM1 classification was performed among the 68 patients who received AGC. Well-differentiated (HR, 0.38; 95% CI, 0.17–0.77; P=0.007) and high hENT1/low RRM1 expression (HR, 0.22; 95% CI, 0.08–0.51; P<0.001) were identified as independent factors of prolonged DFS, and absence of lymph node metastasis (HR, 0.39; 95% CI, 0.18–0.81; P=0.012) and high hENT1/low RRM1 expression (HR, 0.22; 95% CI, 0.07–0.60; P=0.001) were identified as independent factors for prolonged OS (Table 3, model 2).

Discussion

As some clinical studies, including one randomised controlled trial, have revealed that gemcitabine-based chemotherapy provides a survival advantage for patients with unresectable biliary cancer (Okusaka ; Valle ), gemcitabine has also been recognised as a key anticancer drug in adjuvant chemotherapy for resectable cholangiocarcinoma. Indeed, our previous studies have revealed that use of AGC was independently associated with prolonged survival (Murakami , 2011, 2012). On the basis of these findings, we believe that AGC can provide a survival benefit for patients with resectable cholangiocarcinoma, and identification of biomarkers that could predict the clinical outcome of AGC may contribute to further optimisation of adjuvant chemotherapy for cholangiocarcinoma. The current study and our previous study (Kobayashi ) has revealed the predictive significance of hENT1 in advanced cholangiocarcinoma patients who received AGC in the adjuvant setting. These results suggested that hENT1 expression could be used as a predictive marker for the efficacy of AGC. In contrast to hENT1, however, reports investigating the predictive and prognostic values of intratumoural RRM1 expression with immunochemical staining in biliary cancer are extremely rare. To the best of our knowledge, this is the first clinical report concurrently investigating hENT1 and RRM1 expression in cholangiocarcinoma patients treated with AGC.

In this study, 68% and 53% of patients with cholangiocarcinoma had high intratumoural hENT1 and RRM1 expression, respectively. One analysis by Fisher of data from 63 patients who underwent surgical resection for biliary malignancies found that 81% of patients exhibited high RRM1 expression, which was slightly higher than that observed in the current study. Moreover, the current study revealed significant correlations between RRM1 expression and some clinicopathological factors, although no previous reports including a sufficient number of patients have previously demonstrated these correlations. Therefore, further, larger-scale studies on RRM1 expression in cholangiocarcinoma are needed.

RRM1 is the large subunit of human ribonucleotide reductase. In cellular replication, ribonucleotide reductase catalyses the production of deoxynucleotide triphosphates, which are necessary for DNA synthesis. Gemcitabine is currently the most potent and most widely used ribonucleotide reductase inhibitor, and some clinical studies on gastrointestinal and other cancers treated with gemcitabine have demonstrated the significant correlation between increased RRM1 expression and gemcitabine resistance (Ohtaka ; Akita ; Jordheim ; Gong ; Nakagawa ). However, only a few studies on cholangiocarcinoma, which generally included only a small number of patients, have revealed the predictive significance of RRM1 expression in the palliative setting. The analysis by Ohtaka of data from 12 patients with recurrent biliary carcinoma treated with gemcitabine alone found a trend towards a better response rate in patients with low RRM1 expression compared with those with high RRM1 expression. The analysis by Nakamura of data from 10 patients with advanced biliary carcinoma demonstrated significant associations of low RRM1 expression with gemcitabine sensitivity and improved OS. In contrast, no previous study in the adjuvant setting has evaluated the impact of RRM1 expression on the efficacy and/or prognosis of cholangiocarcinoma patients treated with gemcitabine. The current study revealed that high RRM1 expression was independently associated with poor DFS and OS in patients treated with AGC, but not in those who did not receive AGC. These results suggested that RRM1 expression could be a relevant predictive marker of survival in cholangiocarcinoma patients treated with AGC. On the other hand, some basic studies have demonstrated that increased expression of RRM1 decreases the formation of metastasis and inhibits the development of carcinogen-induced lung tumours (Fan ; Gautam ; Gautam and Bepler 2006). Indeed, a significant correlation between high RRM1 expression and improved outcomes has been reported in a few studies of lung cancer in patients who underwent surgery alone (Bepler ; Zheng ). However, no significant difference was found in the current study between RRM1 expression and survival of cholangiocarcinoma patients who did not receive AGC. The possible causes of this discrepancy are differences in cancer type and/or the small number of patients in this study. In addition, patients who did not receive AGC were selected without randomisation and their post-operative courses were slightly different (a few patients received adjuvant oral UFT chemotherapy). Therefore, further basic and clinical studies on the role of RRM1 in the growth and proliferation of cholangiocarcinoma cells are needed.

As both hENT1 and RRM1 were associated with survival in patients treated with AGC, the combined hENT1 and RRM1 classification was introduced in this study to reinforce the predictive values of these targets. The current results demonstrated that patients with high hENT1 and low RRM1 experienced longer DFS and OS compared with the other three groups. In addition, these patients had markedly reduced HRs compared with analyses of separated hENT1 and RRM1 expression. On the basis of these findings, the combined hENT1 and RRM1 classification enabled us to increase the predictive value of these targets for prognosis in cholangiocarcinoma patients treated with AGC compared with either factor alone and may contribute to the optimisation of adjuvant chemotherapy for resected cholangiocarcinoma.

This study has some inherent limitations owing to the small number of patients analysed and the study's retrospective nature. First, patients who did not receive AGC (the control group in the current study) were selected without randomisation. Second, oral fluoropyrimidines were administered to some of the patients treated with and without gemcitabine in the current study. However, we believe this supplement had no effect on the results of this study, because prior studies have revealed that hENT1 and RRM1 work as a predictive marker of gemcitabine but not fluoropyrimidine (Farrell ; Fujita ; Greenhalf ). Third, some other biomarkers, including deoxycytidine kinase, 5′-nucleotidase, cytidine deaminase, and ribonucleotide reductases subunit 2, have been reported to be associated with response to gemcitabine in pancreatic cancer (Giovannetti ; Fujita ; Maréchal ). The role of these candidates as potential predictive markers in cholangiocarcinoma is still unclear. Further prospective, large-scale, randomised studies are needed to overcome these limitations.

In conclusion, both intratumoural hENT1 and RRM1 expression levels were closely associated with the survival of patients with advanced cholangiocarcinoma treated with AGC after surgical resection. In addition, combined analysis of hENT1 and RRM1 expression was more useful for prediction of AGC efficacy than either factor alone. These findings warrant further investigations to establish appropriate post-operative treatments for resectable cholangiocarcinoma, which can be optimised based on hENT1 and RRM1 expression levels.