Elevated preoperative CEA is associated with worse survival in stage I–III rectal cancer patients

Abstract

Background:

The objective of this investigation was to assess whether preoperative carcinoembryonic antigen (CEA) level is an independent predictor of overall survival in rectal cancer patients.

Methods:

All patients (n=504) undergoing a resection for stage I–III rectal cancer at the Kantonsspital St Gallen were included into a database between 1991 and 2008. The impact of preoperative CEA level on overall survival was assessed using risk-adjusted Cox proportional hazard regression models and propensity score methods.

Results:

In risk-adjusted Cox proportional hazard regression analyses, preoperative CEA level (hazard ratio (HR): 1.98, 95% confidence interval (CI): 1.36–2.90, P<0.001), distance from anal verge (<5 cm: HR: 1.93, 95% CI: 1.11–3.37; P=0.039), older age (HR: 1.07, 95% CI: 1.05–1.09; P<0.001), lower body mass index (HR: 0.94, 95% CI: 0.89–0.98; P=0.006), advanced tumour stage (stage II HR: 1.41, 95% CI: 0.85–2.32; stage III HR: 2.08, 95% CI: 1.31–3.31; P=0.004), R 1 resection (HR: 5.65, 95% CI: 1.59–20.1; P=0.005) and chronic kidney disease (HR: 2.28, 95% CI: 1.03–5.04; P=0.049) were all predictors for poor overall survival.

Conclusion:

This is one of the first investigations based on a large cohort of exclusively rectal cancer patients demonstrating that preoperative CEA level is a strong predictor of decreased overall survival. Preoperative CEA should be used as a prognostic factor in the preoperative assessment of rectal cancer patients.

Colorectal cancer is the malignancy with the fourth highest prevalence among females and males in the Western world with a lifetime risk of 1 in 20 persons (Parkin et al, 2005; Cancer-Statistics, 2010; Howlader et al, 2011). Among colorectal cancer patients, about 30% have a cancer of the rectum. Currently, the most important prognostic factor determining treatment strategy and outcomes in rectal cancer patients is tumour stage; however, the sole use of tumour stage to predict prognosis is imperfect.

Before rectal cancer resection, the guidelines of the National Comprehensive Cancer Network (NCCN) suggest routine measurement of preoperative carcinoembryonic antigen (CEA), mainly for monitoring postoperative surveillance (NCCN, 2012). However, there is persistent debate about the impact of an increased preoperative CEA as an independent predictive tumour marker in patients with rectal cancer.

Over 40 years ago, CEA was first described by Gold and Freedman and was subsequently identified as a prognostic tumour marker for colorectal cancer (Wanebo et al, 1978). Since then, postoperative measurement of CEA is an established tool in the follow-up surveillance of colorectal cancer patients (Kim et al, 2009; Lin et al, 2011; NCCN, 2012). Increased early postoperative CEA levels are often a sign of remaining cancer tissue, while a later increase is suggestive for cancer recurrence. Both, early and late increased postoperative CEA levels are associated with decreased survival (Yakabe et al, 2010; Lin et al, 2011). However, it is unknown whether elevated preoperative CEA levels among rectal cancer patients represents an independent prognostic marker for overall survival.

Therefore, the objective of the present study was to evaluate whether an elevated preoperative CEA level represents an independent prognostic factor in a sample of exclusively rectal cancer patients. The necessity of a focused analysis on a homogenous sample of rectal cancer patients is accentuated as current curative treatment strategies substantially differ between colon and rectal cancer (Lin et al, 2011; NCCN, 2012). To increase statistical power and to further elaborate the possible prognostic impact of CEA in a large cohort of exclusively stage I–III rectal cancer patients, both Cox proportional hazard regression analyses as well as propensity-scoring methods were applied.

Materials and Methods

The present study is based on the colorectal database of the Kantonsspital St Gallen, one of the largest tertiary care centres in Switzerland. Overall, 746 patients with histologically proven rectal cancer were identified from February 1994 to December 2008. Of these patients, 153 were excluded because of the presence of distant metastases (synchronous metastases) at the time of operation (American Joint Committee on Cancer (AJCC) stage IV), 19 patients due to urgent operation, 25 patients because tumour resection was performed transanally (5 of them with missing preoperative CEA levels) and 45 patients due to missing preoperative CEA levels. Figure 1 contains the patient selection flowchart. A total of 504 patients remained for further analyses. Patients were grouped into two groups according to preoperative CEA levels; C0-stage: patients with normal CEA levels (<5 ng ml⁻¹), C1-stage: patients with elevated CEA levels (⩾5 ng ml⁻¹; Locker et al, 2006). Carcinoembryonic antigen levels were determined uniformly the day before surgery in all patients. Therefore, in patients undergoing neoadjuvant radiochemotherapy, the CEA levels were measured post neoadjuvant radiochemotherapy.

Figure 1.

Patient selection.

Operative technique

The technique for surgical dissection has been earlier described in detail (Zaheer et al, 1998). The type of reconstruction was determined by the operating surgeon depending on tumour and anatomic circumstances. As a standardised procedure, anastomoses were performed after mobilisation of the splenic flexure in a double-stapled technique (Knight and Griffen, 1980). An air leak test was routinely performed by transanal insufflation of air with the anastomosis immersed in saline solution.

Data collection and definitions

Data on patients demographics, operative details, American Society of Anesthesiologists (ASA) score, cardiovascular disease, postoperative mortality, intra- and postoperative morbidity and histological results were gathered in an electronic database (access, Microsoft). Tumour height, defined as the distance between tumour and anal verge, was based on results of rigid rectosigmoidoscopy, endorectal sonography, MRI scans and/or colonoscopy and was considered in this rank order. Operation time was ascertained from the operation protocol. All patients had histologically proven adenocarcinoma of the rectum; in six patients two rectal cancers were simultaneously found. Neoadjuvant (radio) chemotherapy was routinely performed in patients with cT3/4 and/or cN+ tumours since 2004 according to the interdisciplinary tumour board decision (Sauer et al, 2004). According to the seventh edition of the AJCC, patients with a complete pathological response were included in stage I (AJCC, 2010). The indication for adjuvant treatment was based on the initial clinical stage (before the start of neoadjuvant radiochemotherapy), not on the final pathological disease stage (Sauer et al, 2004).

Follow-up

Starting 1 June 2007, the follow-up guidelines were as follows: clinical examination and CEA level measurement were obtained every 3 months during the first year and every 6 months for the second and third year after surgery. For the fourth and fifth year postsurgery, an annual clinical examination and CEA level measurement were performed. Moreover, a colonoscopy was done 1 and 4 years postoperatively. Thoraco-abdominal CT scans were performed yearly for 5 years, as well as recto-sigmoidoscopy and endorectal sonography every 6 months during the first 2 years (SGGSSG, 2007).

Before 1 June 2007, follow-up differed mainly in respect to the interval of the clinical examination and CEA level measurements, which were obtained semi-annually for the first 2 years and yearly thereafter for the third to fifth year postoperatively. Also, only one colonoscopy 3 years after resection was performed. Furthermore, either a liver sonography or an abdominal CT scan were performed annually during 5 years to rule out liver metastases in addition to a conventional yearly chest X-ray to detect lung metastases. Finally, recto-sigmoidoscopy was performed semi-annually during the first 2 years.

Statistical analysis

Statistical analyses were performed using the R statistical software (www.r-project.org). A two-sided P-value<0.05 was considered statistically significant. Continuous data are expressed as mean±standard deviation. For comparing proportions and continuous variables, χ² statistics and Mann–Whitney U tests were used, respectively.

First, CEA was assessed as a prognostic factor for overall survival in Cox regression analysis with and without risk-adjustment including a backward variable selection procedure based on the Akaike’s information criterion. The risk set included age, gender, body mass index, ASA classification, pre-existing cardiovascular disease, chronic obstructive pulmonary disease and kidney disease, AJCC tumour stage, distance to anal verge, neoadjuvant therapy, type of operation, resection status (R0 vs R1), operation time and adjuvant chemotherapy/chemoradiotherapy. A frailty term was included in the Cox regressions to adjust for hidden bias from unobserved variables (Govindarajulu et al, 2011).

Secondly, bipartite matched propensity score analyses as an additional, superior statistical method of adjusting for potential baseline confounding (Rosenbaum, 1985; Rubin, 1997; Boonpipattanapong and Chewatanakornkul, 2006; Fueglistaler et al, 2007) was used. The ‘MatchIt’ R package was used to match patients with a similar estimated propensity for C1-stage by simultaneously subclassifying and weighting them (Hansen and Klopfer Olsen, 2006). Afterwards, the baseline risk profiles of the matched patients were compared to assure that no major difference in baseline patient characteristics existed. Finally, the prognostic value of CEA for overall mortality was assessed in a Cox regression analysis with a frailty term for the subclasses and the weights of the bipartite matching propensity score analysis. The analysis was then repeated to assess disease-free survival (excluding four patients with a R1-resection).

Sensitivity analyses

Finally, various sensitivity analyses were performed. To exclude a potential bias caused by changes in staging procedures, subgroup analyses limited to patients operated before and after 2000 were performed. To adjust for the potential influence of a neoadjuvant therapy on the preoperative serum CEA levels, the prognostic value of CEA was assessed in subgroups of patients with and without neoadjuvant treatment. Finally, a sensitivity analysis including 20 patients with transanally resected tumours and available preoperative CEA measurements was performed.

Results

Patient characteristics and bias estimation

A total of 504 patients with histologically proven adenocarcinoma of the rectum with preoperative CEA measurement were included in the present analysis. Eleven patients had a complete pathological response and were included in stage I. Patients had a median follow-up time of 38.5 months ranging from 1 to 129 months (mean follow-up: 54.7 months). Mean CEA level was 5.8±16.7 ng ml⁻¹ with a range from 0.5 to 220 ng ml⁻¹. A total of 391 (77.6%) patients had a C0 stage (defined as preoperative CEA <5 ng ml⁻¹) and 113 patients (22.4%) had a C1-stage (defined as preoperative CEA ⩾5 ng ml⁻¹). Table 1 summarises the characteristics of the patients with C0-stage and C1-stage: In univariate analysis, patients with C1-stage were significantly older, had a higher ASA classification and AJCC stage, had more often a pre-existing cardiovascular disease, underwent less often neoadjuvant treatment, were less often operated with anterior resection with primary anastomosis and were more often transferred to the ICU postoperatively.

Table 1. Patient characteristics and potential bias for carcinoembryonic antigen elevation.

	Univariate analysis				Logistic regression for C-stage		Variable selection logistic regression for C-stage		Potential bias after weighted propensity score matching
	Total ( N =504)	C-stage I ( N =113)	C-stage 0 ( N =391)	P	OR (95% CI)	P a	OR (95% CI)	P a	Persisting bias b	P
Confounding variables
Age (years)	64.9±12.0	68.7±11.8	64.0±12.0	<0.001c	1.01 (0.99–1.03)	0.407	—		0.031	0.773c
Gender
Male	320 (63.5%)	74 (65.5%)	246 (62.9%)	0.617d	Reference	0.773	—		Reference	0.751d
Female	184 (36.5%)	39 (34.5%)	145 (37.1%)		0.93 (0.57–1.51)				0.033
Body mass index (kg m−2)	25.6±4.2	25.0±4.3	25.8±4.2	0.080c	0.96 (0.90–1.01)	0.108	0.96 (0.91–1.01)	0.119	−0.114	0.277c
ASA stage
II	392 (77.8%)	68 (60.2%)	324 (82.9%)	<0.001d	Reference	0.015	Reference	0.008	Reference	0.831d
III/IV	112 (22.2%)	45 (39.8%)	67 (17.1%)		2.06 (1.15–3.70)		2.13 (1.22–3.72)		−0.023
Cardiovascular disease
No	421 (83.5%)	81 (71.7%)	340 (87.0%)	<0.001d	Reference	0.133	Reference	0.087	Reference	0.828d
Yes	83 (16.5%)	32 (28.3%)	51 (13.0%)		1.64 (0.86–3.08)		1.71 (0.92–3.16)		−0.023
Chronic obstructive pulmonary disease
No	454 (90.1%)	98 (86.7%)	356 (91.0%)	0.176d	Reference	0.664	—		Reference	0.192d
Yes	50 (9.9%)	15 (13.3%)	35 (9.0%)		0.85 (0.39–1.77)				0.123
Chronic kidney disease
No	487 (96.6%)	107 (94.7%)	380 (97.2%)	0.195d	Reference	0.955	—		Reference	0.371d
Yes	17 (3.4%)	6 (5.3%)	11 (2.8%)		0.97 (0.28–3.04)				0.082
AJCC stage
I	185 (36.7%)	21 (18.6%)	164 (41.9%)	<0.001d	Reference	0	Reference	<0.001	Reference	0.764d
II	149 (29.6%)	37 (32.7%)	112 (28.6%)		2.54 (1.36–4.86)		2.62 (1.40–4.90)		−0.001
III	170 (33.7%)	55 (48.7%)	115 (29.4%)		4.32 (2.31–8.30)		4.48 (2.40–8.38)		0.060
Distance anal verge (cm)	7.7±3.9	7.8±4.2	7.6±3.9	0.644c	1.02 (0.95–1.09)	0.666	—		−0.077	0.477c
Neoadjuvant therapy
No	283 (56.2%)	77 (68.1%)	206 (52.7%)	0.004d	Reference	0.032	Reference		Reference	0.923d
Yes	221 (43.8%)	36 (31.9%)	185 (47.3%)		0.56 (0.32–0.95)		0.50 (0.31–0.82)	0.005	−0.010
Operation
Anterior resection	453 (89.9%)	94 (83.2%)	359 (91.8%)	0.007d	Reference	0.056	Reference	0.048	Reference	0.796d
Abdominal perineal excision	51 (10.1%)	19 (16.8%)	32 (8.2%)		2.15 (0.98–4.68)		1.97 (1.00–3.84)		−0.028
Operation time (hours)	3.1±1.2	3.0±1.0	3.0±1.3	0.542c	0.98 (0.80–1.20)	0.884	—		0.061	0.583c
Resection
R0	500 (99.2%)	112 (99.1%)	338 (99.2%)	0.901d	Reference	0.774	—		Reference	0.898d
R1	4 (0.8%)	1 (0.9%)	3 (0.8%)		0.69 (0.03–7.40)				−0.014
Adjuvant therapy
No	333 (66.1%)	79 (69.9%)	254 (65.0%)	0.328d	Reference	0.22	Reference	0.126	Reference	0.865d
Yes	171 (33.9%)	34 (30.1%)	137 (35.0%)		0.70 (0.40–1.23)		0.66 (0.39–1.12)		−0.018
Outcome variables
ICU postoperative
No	309 (61.3%)	55 (48.7%)	254 (65.0%)	0.002d			-
Yes	195 (38.7%)	58 (51.3%)	137 (35.0%)
Hospital stay (days)	23.5±13.5	24.4±13.8	22.8±13.2	0.416c			—

Abbreviations: AJCC=American Joint Committee on Cancer; ASA=American Society of Anesthesiologists.

n (%); mean±s.d.

Logistic regression (full model and backward variable selection) of baseline variables with odds ratios (OR) for C I-stage.

^aLikelihood ratio test.

^bPersisting potential bias after propensity score weighting, measured as standardised mean difference.

^ct-test.

^dχ²-test.

C-stage as a prognostic factor for overall and disease-free survival

An unadjusted Cox proportional hazards regression analysis revealed C1-stage as a statistically significant prognostic factor with an approximately 180% increased risk of mortality (hazard ratio (HR) of death=2.80, 95% confidence interval (CI)=1.95–4.02, P<0.001) (Table 2). The 5-year survival for patients with C1-stage was 46.7% (95% CI: 37.1–59.0%) compared with 81.0% (95% CI: 76.3–85.9%) for rectal cancer patients with C0-stage (Figure 2). In unadjusted Cox regression analyses, overall mortality was in addition to C1-stage dependent on age, body mass index, preexisting cardiovascular disease, chronic obstructive pulmonary disease, chronic kidney disease, ASA stage, AJCC stage, distance to anal verge, neoadjuvant treatment, adjuvant therapy, R0 vs R1 resection and type of operation (Table 2). After risk-adjusting the Cox regression analysis, C1-stage remained associated with an increased risk for overall mortality of 91% (HR of death=1.91, 95% CI=1.28–2.85, P=0.001). In a backward variable selection, C1-stage (HR of death=1.98, 95% CI=1.36–2.90, P<0.001) was confirmed as an independent predictor for increased overall mortality together with age, body mass index, chronic kidney disease, AJCC stage, R1 vs R0 resection and tumour distance from the anal verge. A forward variable selection yielded the same independent predictors.

Table 2. Prognostic factors for overall mortality.

	Unadjusted a		Cox regression, full model b		Cox regression, variable selection c
	HR (95% CI)	P d	HR (95% CI)	P d	HR (95% CI)	P d
C-stage
C-stage 0	Reference	<0.001	Reference	0.001	Reference	<0.001
C-stage I	2.80 (1.95–4.02)		1.91 (1.28–2.85)		1.98 (1.36–2.90)
Age (years)	1.08 (1.06–1.10)	<0.001	1.07 (1.05–1.09)	0.000	1.07 (1.05–1.09)	<0.001
Gender
Male	Reference	0.577	Reference	0.612	—
Female	0.91 (0.63–1.32)		0.94 (0.62–1.42)
BMI (kg m−2)	0.93 (0.89–0.97)	0.001	0.94 (0.89–0.99)	0.010	0.94 (0.89–0.98)	0.006
ASA stage
II	Reference	<0.001	Reference	0.235	—
III/IV	2.58 (1.79–3.73)		1.22 (0.77–1.95)
Cardiovascular disease
No	Reference	<0.001	Reference	0.641	—
Yes	2.27 (1.50–3.42)		1.04 (0.61–1.77)
Chronic obstructive pulmonary disease
No	Reference	0.003	Reference	0.553	—
Yes	2.21 (1.36–3.60)		1.03 (0.60–1.78)
Chronic kidney disease
No	Reference	0.002	Reference	0.106	Reference	0.049
Yes	4.04 (1.90–8.62)		2.01 (0.85–4.74)		2.28 (1.03–5.04)
AJCC stage
I	Reference	<0.001	Reference	0.006	Reference	0.004
II	1.80 (1.11–2.91)		1.36 (0.81–2.28)		1.41 (0.85–2.32)
III	2.66 (1.70–4.17)		2.12 (1.29–3.49)		2.08 (1.31–3.31)
Distance to anal verge
>10 cm	Reference	0.001	Reference	0.064	Reference	0.039
>5–10 cm	1.41 (0.85–2.33)		1.52 (0.88–2.63)		1.48 (0.88–2.49)
0–5 cm	2.38 (1.45–3.92)		1.97 (1.04–3.76)		1.93 (1.11–3.37)
Neoadjuvant therapy
No	Reference	0.199	Reference	0.671	—
Yes	0.79 (0.54–1.15)		0.98 (0.62–1.56)
Operation
Anterior resection	Reference	<0.001	Reference	0.117	Reference	0.095
Abd. perineal excision	2.57 (1.64–4.04)		1.54 (0.89–2.65)		1.55 (0.92–2.62)
Operation time (hours)	1.02 (0.90–1.17)	0.637	1.02 (0.88–1.19)	0.612	—
Resection
R0	Reference	0.027	Reference	0.023	Reference	0.005
R1	5.11 (1.51–17.3)		5.48 (1.50–20.0)		5.65 (1.59–20.1)
Adjuvant therapy
No	Reference	0.037	Reference	0.615	—
Yes	0.67 (0.45–0.99)		0.96 (0.60–1.54)

Abbreviations: AJCC=American Joint Committee on Cancer; ASA=American Society of Anesthesiologists.

Hazard ratios (HR) with 95% confidence intervals resulting from:

^aUnivariate, Cox proportional hazards regression analysis for overall mortality;

^bIndependent, full model Cox proportional hazards regression analysis for overall mortality;

^cIndependent, backward variable selection Cox proportional hazards regression analysis for overall mortality (confirmed by forward variable selection with identical results);

^dP-values from likelihood ratio tests.

Figure 2.

Kaplan–Meier curve for overall survival in unmatched analysis. Life tables for the number of rectal adenocarcinoma patients at risk are given below each plot. Survival curves are provided with 95% point-wise confidence intervals.

C-stage also served as a prognostic factor for disease-free survival. An unadjusted Cox proportional hazards regression analysis revealed C1-stage as a statistically significant prognostic factor with an approximately 163% increased risk for recurrence (HR of recurrence: 2.63, 95% CI: 1.89–3.65, P<0.001) (Table 3). After risk-adjusting in Cox regression analysis, C1-stage remained associated with an increased risk for recurrence of 117% (HR of recurrence: 2.17, 95% CI: 1.51–3.10, P<0.001). In a backward variable selection, C1-stage (HR of recurrence: 2.08, 95% CI: 1.48–2.94, P<0.001) was confirmed as an independent predictor for disease-free survival. The 5-year disease-free survival for patients with C1-stage was 38.9% (95% CI: 29.9–50.7%) compared with 72.3% (95% CI: 67.2–77.8%) for rectal cancer patients with C0-stage (Figure 3).

Table 3. Prognostic factors for disease-free survival.

	Unadjusted a		Cox regression, full model b		Cox regression, variable selection c
	HR (95% CI)	P d	HR (95% CI)	P d	HR (95% CI)	P d
C-stage
C-stage 0	Reference	<0.001	Reference	<0.001	Reference	<0.001
C-stage I	2.63 (1.89–3.65)		2.17 (1.51–3.10)		2.08 (1.48–2.94)
Age (years)	1.05 (1.03–1.07)	<0.001	1.04 (1.03–1.06)	<0.001	1.04 (1.03–1.06)	<0.001
Gender
Male	Reference	0.44	Reference	0.435	—
Female	0.88 (0.63–1.23)		0.89 (0.62–1.27)
BMI (kg m−2)	0.95 (0.91–0.99)	0.008	0.96 (0.92–1.00)	0.037	0.96 (0.92–1.00)	0.048
ASA stage
II	Reference	0.002	Reference	0.54	—
III/IV	1.74 (1.23–2.45)		0.92 (0.59–1.41)
Cardiovascular disease
No	Reference	0.006	Reference	0.605	—
Yes	1.75 (1.20–2.56)		1.07 (0.67–1.72)
Chronic obstructive pulmonary disease
No	Reference	0.002	Reference	0.191	—
Yes	2.12 (1.36–3.32)		1.29 (0.78–2.12)
Chronic kidney disease
No	Reference	0.02	Reference	0.137	—
Yes	2.68 (1.27–5.67)		1.83 (0.80–4.19)
AJCC stage
I	Reference		Reference	0	Reference	<0.001
II	1.49 (0.97–2.28)		1.18 (0.75–1.86)		1.26 (0.81–1.96)
III	2.56 (1.74–3.79)		2.15 (1.40–3.31)		2.20 (1.48–3.28)
Distance to anal verge
>10 cm	Reference	0	Reference	0.047	Reference	0.001
>5–10 cm	1.28 (0.82–2.00)		1.86 (1.07–3.23)		1.39 (0.88–2.19)
0–5 cm	2.22 (1.43–3.46)		1.29 (0.80–2.08)		2.19 (1.39–3.45)
Neoadjuvant therapy
No	Reference	0.746	Reference	0.258	—
Yes	0.98 (0.71–1.36)		1.22 (0.83–1.80)
Operation
Anterior resection	Reference	0.003	Reference	0.45	—
Abd. perineal excision	2.00 (1.29–3.11)		1.16 (0.69–1.94)
Operation time (hours)	1.05 (0.92–1.19)	0.437	1.03 (0.90–1.18)	0.551	—
Adjuvant therapy
No	Reference	0.589	Reference	0.587	—
Yes	0.93 (0.66–1.30)		1.07 (0.71–1.60)

Abbreviations: AJCC=American Joint Committee on Cancer; ASA=American Society of Anesthesiologists.

Hazard ratios (HR) with 95% confidence intervals resulting from:

^aUnivariate, Cox proportional hazards regression analysis for disease-free survival;

^bIndependent, full model Cox proportional hazards regression analysis for disease-free survival;

^cIndependent, backward variable selection Cox proportional hazards regression analysis for disease-free survival (confirmed by forward variable selection with identical results);

^dP-values from likelihood ratio tests.

Figure 3.

Kaplan–Meier curve for disease-free survival in unmatched analysis. Life tables for the number of rectal adenocarcinoma patients at risk are given below each plot. Survival curves are provided with 95% point-wise confidence intervals. Analysis limited to 500 patients with R0-resection.

Adjusting for patients characteristics with propensity score matching

To further corroborate the interesting findings from univariate and Cox proportional hazard regression analyses, the propensity score was estimated incorporating the patient characteristics listed in Table 1. The propensity for C1-stage was 0.33±0.17 compared with 0.19±0.14 for patients with C0-stage (P<0.001). After performing the propensity score-matching procedure, the score was practically identical for patients with C1-stage and C0-stage (0.33±0.17 vs 0.33±0.17, P=0.928). Figure 4 displays the distribution of the propensity score before and after matching for patients with C1-stage and C0-stage. The right columns of Table 1 summarise the persisting bias between the characteristics of patients with C1-stage and C0-stage after performing the propensity score-matching analysis. No significant differences in patient characteristics were found any more between C1-stage and C0-stage patients (Table 1), thus precluding bias of the observed variables.

Figure 4.

Distribution of propensity score before and after propensity score analysis. Left upper and lower panel show the distribution of the propensity score for patients with C1-stage and C0-stage before the matching procedure. Right upper and lower panel demonstrate the distribution of the propensity score after full propensity score matching.

Propensity score-matched prognostic factors for overall and disease-free survival

When performing a Cox regression analysis after the propensity score-matching procedure, C1-stage was a persistently significant predictor for overall mortality (HR=2.05, 95% CI=1.47–2.86, P<0.001). In the propensity score-matched analysis, the 5-year survival for patients with C1-stage was 46.7% (95% CI: 37.1–59.0%) compared with 71.5% (95% CI: 66.0–77.5%) for C0-stage patients (P<0.001) (Figure 5).

Figure 5.

Kaplan–Meier curve for overall survival in propensity score-matched analysis. Life tables for the number of rectal adenocarcinoma patients at risk are given below each plot. Survival curves are provided with 95% point-wise confidence interval.

When performing a Cox regression analysis after a propensity score-matching procedure, C1-stage remained a significant predictor for disease-free survival (HR: 1.90, 95% CI: 1.40–2.57, P<0.001). In the propensity score-matched analysis, the 5-year disease-free survival for patients with C1-stage was 38.9% (95% CI: 29.9–50.7%) compared with 62.8% (95% CI: 57.2–69.0%) for C0-stage patients (P<0.001) (Figure 6).

Figure 6.

Kaplan–Meier curve for disease-free survival in propensity score-matched analysis. Life tables for the number of rectal adenocarcinoma patients at risk are given below each plot. Survival curves are provided with 95% point-wise confidence intervals. Analysis limited to 500 patients with R0-resection.

Sensitivity analyses

In the present investigation, in 18 (13.5%) out of 133 patients who died, the cause of death remained unclear as no autopsy was performed, in 53 patients (39.9%) death was tumour related and in 62 patients (46.6%) death was not tumour related. In univariate analysis, the HR for cancer-specific survival was 2.33 (95% CI: 1.28–4.24, P=0.007) for C1-stage (elevated preoperative CEA level). In multivariable analysis after adjusting for AJCC stage, age, type of operation, distance of the tumour from the anal verge and R0 vs R1 resection, the HR for cancer-specific survival was 2.40 (95% CI: 1.26 to 4.59, P=0.008) for preoperative C1-stage.

In a subgroup analysis limited to the 323 patients with available data for postoperative CEA measurements, the preoperative C1-stage (HR: 1.86; 95% CI: 1.02–3.36, P=0.023), as well as the postoperative C1-stage (HR: 2.33; 95% CI: 1.01–5.41, P=0.038) were independent predictors for mortality in adjusted Cox-regression analysis.

In an additional subgroup analysis limited to 221 patients receiving neoadjuvant therapy, C1-stage did significantly increase the risk of mortality (HR: 2.59; 95% CI: 1.25–5.33, P=0.014). The risk of mortality (HR: 1.65; 95% CI: 1.05–2.58, P=0.033) in patients classified as C1-stage who did not receive neoadjuvant therapy was also significantly increased.

To address the potential influence of changing staging routines throughout the study period, a sensitivity analysis was performed in the subsets of patients operated prior and after the year 2000. In the subgroup analysis of 211 patients operated before the year 2000, C1-stage significantly increased the risk of mortality (HR: 1.72; 95% CI: 1.08–2.73, P=0.024). When analysing the 293 patients operated from 2000 onwards, C1-stage also significantly increased the risk of mortality (HR: 3.11; 95% CI: 1.70–5.67, P=0.001).

A total of 20 patients with transanally resected tumours and preoperative CEA level could have potentially been included in the present study, only one of them with C1-stage (5%). When performing a sensitivity analysis including these 20 patients, the results did not change relevantly (overall survival HR: 2.03 for C1-stage (95% CI: 1.45–2.83, P<0.001); disease-free survival HR: 2.18 for C1-stage (95% CI: 1.61–2.96, P<0.001)).

Discussion

The present investigation provides compelling evidence that an elevated preoperative CEA level in stage I–III rectal cancer patients is independently associated with a decreased overall, disease-free and cancer-specific survival. These survival benefits were found to be highly statistically significant in both multivariable Cox proportional hazard regression model as well as in propensity score-matched survival analyses and persistent in various subset analyses. Preoperative measurement of CEA level does provide important prognostic information.

A recent study published in the Journal of National Cancer Institute provides clear evidence that an increased preoperative CEA level is an independent prognostic factor for colon cancer patients (Thirunavukarasu et al, 2011). This population-based study assessed almost 18 000 patients from the Surveillance, Epidemiology and End Results database. C1-stage was found to have a 60% increased risk of overall mortality, however, the authors were not able to adjust for potentially important covariates like comorbidities and body mass index. Interestingly, in the present investigation on exclusively rectal cancer patients, the point estimate of the HR of overall mortality among C0-stage and C1-stage rectal cancer patients was even higher (HR of 1.98 in Cox proportional analyses), indicating a two-fold increase in risk of dying having a preoperative elevated CEA level. This finding is not only statistically significant but also highly clinically relevant.

The results of this investigation are partly supported by an earlier study performed by Park et al (2006). In contrast to the present study, they focused on perioperative changes in the serum CEA level measured in the preoperative and early postoperative period for predicting recurrence and survival in stage II and III rectal cancer patients. Park et al reported that stage II and III rectal cancer patients with pre- and postoperative normal CEA levels had a significantly better survival than patients with pre- and postoperative increased CEA levels (Park et al, 2006). Other studies investigating the influence of preoperative CEA levels were performed in more heterogeneous samples of colorectal cancer patients (Chapman et al, 1998; Diez et al, 2000; Takagawa et al, 2008; Sun et al, 2009), which differs from the present investigation involving exclusively rectal cancer patients. Although the authors of these studies concluded that a preoperative elevated CEA level is associated with poorer survival, two recent investigations among colorectal cancer patients did not find any significant association (Li et al, 2009; Lin et al, 2011).

Besides the prognostic capacity of preoperative CEA in colorectal cancer patients, postoperative measurement of CEA levels is also a valuable diagnostic tool. A persistently high CEA level or an early elevated postoperative CEA level is associated with precocious relapse while the majority of those tumours recur in the liver (Takagawa et al, 2008; Park et al, 2009; Lin et al, 2011). Suggestions to monitor postoperative CEA levels are not limited to patients with preoperatively elevated CEA but should be performed for all patients according to most guidelines. A secondary analysis of the TME trial of the Dutch ColoRectal Cancer group showed that 41% of patients with a preoperative normal CEA level developed an increased CEA level (>5 ng ml⁻¹) when they experienced a recurrent disease in the follow-up (Grossmann et al, 2007). Although most studies investigated pre- or postoperative CEA levels or both, Perez et al (2009) focused on CEA levels after neoadjuvant radiochemotherapy in rectal cancers. In their study, increased levels after neoadjuvant radiochemotherapy in rectal cancer patients was associated with poor survival. However, increased CEA levels before neoadjuvant radiochemotherapy was not associated with 5-year overall survival but showed decreased disease-free survival.

Limitations

The present study has several limitations that need to be addressed. First, this is a cohort study and not a randomised controlled trial. However, for the research question at hand, it is impossible to perform a randomised trial, and a cohort study is probably the best suited study design. Second, although extensive risk-adjustment was performed, a potential selection bias cannot fully be excluded with certainty in the present cohort study. However, in Cox proportional hazard regression analyses, propensity score analyses and different subset analyses, the differences in overall survival between patients with normal vs elevated preoperative CEA was not only statistically significant but also clinically relevant. Thus, it is likely that the observed differences are real.

Conclusions

The present investigation based on a large cohort of exclusively rectal cancer patients – one of the first in the literature – provides compelling evidence that an elevated preoperative CEA level is a strong and in our study independent predictor of overall survival. The findings of the present study increase the evidence that preoperative CEA measurement should be considered as an additional tool for preoperative tumour staging in addition to the TNM classification in stage I–III rectal cancer patients. A prospective, multicentre evaluation of the combination of preoperative CEA and TNM staging compared with histopathological staging alone might provide the highest evidence possible to further corroborate our findings.