Prognostic Implications of Extranodal Extension in Relation to Colorectal Cancer Location

Chan Wook Kim; Jihun Kim; Yangsoon Park; Dong-Hyung Cho; Jong Lyul Lee; Yong Sik Yoon; In Ja Park; Seok-Byung Lim; Chang Sik Yu; Jin Cheon Kim

doi:10.4143/crt.2018.392

Cancer Research and Treatment > Volume 51(3); 2019 > Article

Kim, Kim, Park, Cho, Lee, Yoon, Park, Lim, Yu, and Kim: Prognostic Implications of Extranodal Extension in Relation to Colorectal Cancer Location

Original Article

Cancer Res Treat. 2019; 51(3): 1135-1143.

Published online: November 29, 2018

DOI: https://doi.org/10.4143/crt.2018.392

Prognostic Implications of Extranodal Extension in Relation to Colorectal Cancer Location

Chan Wook Kim, MD¹, Jihun Kim, MD², Yangsoon Park, MD², Dong-Hyung Cho, PhD³, Jong Lyul Lee, MD¹, Yong Sik Yoon, MD¹, In Ja Park, MD¹, Seok-Byung Lim, MD¹, Chang Sik Yu, MD¹, Jin Cheon Kim, MD, PhD¹

¹Department of Surgery, Institute of Innovative Cancer Research, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

²Department of Pathology, Institute of Innovative Cancer Research, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

³School of Life Science, Kyungpook National University, Daegu, Korea

Correspondence: Jin Cheon Kim, MD, PhD
Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Seoul 05505, Korea
Tel: 82-2-3010-3489 Fax: 82-2-474-9027 E-mail: jckim@amc.seoul.kr

Received July 9, 2018 Accepted November 18, 2018

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

This article has been corrected. See ERRATUM: Prognostic Implications of Extranodal Extension in Relation to Colorectal Cancer Location.

Abstract

Purpose

Extranodal extension (ENE) is closely associated with the aggressiveness of both colon and rectal cancer. This study evaluated the clinicopathologic significance and prognostic impact of ENE in separate populations of patients with colon and rectal cancers.

Materials and Methods

The medical records of 2,346 patients with colorectal cancer (CRC) who underwent curative surgery at our institution between January 2003 and December 2011 were clinically and histologically reviewed.

Results

ENE was associated with younger age, advanced tumor stage, lymphovascular invasion (LVI), and perineural invasion (PNI) in both colon and rectal cancer. ENE rates differed significantly in patients with right colon (36.9%), left colon (42.6%), and rectal (48.7%) cancers (right vs. left, p=0.037; left vs. rectum, p=0.009). The 5-year disease-free survival (DFS) rate according to ENE status and primary tumor site differed significantly in patients with ENE-negative colon cancer (80.5%), ENE-negative rectal cancer (77.4%), ENE-positive colon cancer (68.6%), and ENE-positive rectal cancer (64.2%) (p<0.001). Multivariate analysis showed that advanced tumor stage, ENE, LVI, PNI, and absence of adjuvant chemotherapy were independently prognostic of reduced DFS in colon and rectal cancer patients.

Conclusion

ENE is closely associated with the aggressiveness of colon and rectal cancers, with its frequency increasing from the right colon to the left colon to the rectum. ENE status is a significant independent predictor of DFS in CRC patients irrespective of tumor location. ENE might be more related with distally located CRC.

Key words: Colonic neoplasms, Rectal neoplasms, Extranodal extension, Prognosis

Introduction

Extranodal extension (ENE) of metastatic lymph nodes (LNs), which is indicated the extension of tumor cells beyond the nodal capsule into the perinodal adpose tissue, is an important prognostic factor in patients with several types of malignancies, including stomach, thyroid, bladder, and breast cancer [1-8]. ENE is also included in the American Joint Committee on Cancer (AJCC) eighth staging system for patients with penile cancer, vulvar cancer, and head and neck squamous cell carcinoma [9].

In contrast, ENE in patients with colorectal cancer (CRC) is not yet considered as TNM staging system. Nevertheless, a recent meta-analysis reported that the presence of ENE was an important prognostic factor in patients with node-positive CRC. However, this study, analyzed the prognostic effect of ENE in patients with CRC when considering colon and rectal cancers as only one entity.

It is unclear whether colon cancer and rectal cancer are biologically different malignancies or are the same malignancy at different locations. Accumulating evidence provide that colon and rectal cancer differed not only in etiologies, risk factors, anatomic site but in embryological origin, function, and metastatic patterns [10-12], suggesting that the prognostic implications of ENE should be investigated separately in patients with colon and rectal cancer [13]. Furthermore, right- and left-sided colon cancers may represent distinctive and different disease entities (two colon concept) [10,14]. Unfortunately, despite the difference according to location of CRC, little attention has been paid to the histologic feature of ENE. This study therefore assessed the clinicopathologic significance and prognostic impact of ENE in large, separate populations of patients with colon and rectal cancer.

Materials and Methods

1. Patients

The medical records of 2,346 patients with CRC having metastatic LNs who underwent surgery at Asan Medical Center (Seoul, Korea) between January 2003 and December 2011 were retrieved from the center’s database, and their clinical and histological characteristics were reviewed. All patients with node-positive CRC who had histologically proven adenocarcinoma and underwent curative resection (R0) were included. Patients with hereditary CRC (familial adenomatous polyposis and hereditary nonpolyposis CRC), multiple CRCs, and stage IV CRC were excluded. Also, we excluded were patients who received preoperative chemoradiotherapy or chmotherapy because tumor pathology may have been affected by preoperative treatment.

2. Evaluation

Before surgery, all patients underwent a staging workup, including colonoscopy, chest radiography, computed tomography (CT) of the abdomen and pelvis, and measurement of serum carcinoembryonic antigen (s-CEA) concentrations. Some patients also underwent positron emission tomography (PET) scanning and single contrast-enhanced magnetic resonance imaging (MRI) of the rectum and liver. s-CEA was measured by enzyme immunoassay (ELISA-2-CEA kit, CIS Bio International, Marcoule, France), with the normal concentration defined as ≤ 6 ng/mL. Tumors were pathologically staged in accordance with the AJCC cancer staging manual, eighth edition [9].

3. Histologic evaluation

The ENE status of all specimens was examined by two pathologists (J. Kim and Y. Park) and the final diagnosis was based on intradepartmental consultations with staff specialized in CRC. ENE was defined as cancer cells infiltrating the extranodal adipose tissue beyond the capsule of the LN (Fig. 1A). Tumor deposits (Fig. 1B) and tumor cells outside the LNs, continuous with the primary tumor (Fig. 1C), or confined to endolymphatic spaces (Fig. 1D) were not considered ENE. A tumor was considered ENE-positive when one or more of the metastatic LNs showed ENE, as described [15].

The distance between the tumor and the circumferential resection margin (CRM) was measured in millimeters. If CRM was found within 1mm of the tumor, we defined the positive CRM.

4. Adjuvant chemotherapy

Of the 2,346 patients in the study cohort, 2,151 (91.7%) received postoperative chemotherapy. Separate assessment of the 1,363 colon cancer patients showed that 1,273 (93.4%) received postoperative chemotherapy, including 105 (7.7%) who received 5-fluorouracil, 530 (38.9%) who received capecitabine, 517 (37.9%) who received oxaliplatin, 53 (3.9%) who received an oral pyrimidine analogue or oral 5-fluorouracil, and 68 (5.0%) who received chemotherapy at another hospital. The remaining 90 patients (6.6%) did not receive adjuvant chemotherapy.

Of the 983 rectal cancer patients, 878 (89.3%) received postoperative chemotherapy, including 303 (30.8%) who received 5-fluorouracil, 331 (33.7%) who received capecitabine, 108 (11.0%) who received oxaliplatin, 44 (4.5%) who received an oral pyrimidine analogue or oral 5-fluorouracil, and 92 (9.4%) who received chemotherapy at another hospital. The remaining 105 patients (10.7%) did not receive adjuvant chemotherapy. In addition, 382 (38.9%) rectal cancer patients received postoperative radiotherapy. Usually, our center recommended the postoperative radiotherapy for stage II or stage III mid to lower rectal cancer patients. For data analysis, patients who received intravenous 5-fluorouracil–based or capecitabine-/oxaliplatin-based chemotherapy were regarded as receiving complete adjuvant chemotherapy.

5. Follow-up

Standardized postoperative follow-up included clinical examinations, complete blood counts, blood chemistry tests, measurements of s-CEA levels, and chest radiography. Patients were followed up every 3 months for the first 2 postoperative years and every 6 months thereafter. Patients also underwent abdominal and pelvic CT scans every 6 months. Colonoscopy was performed within 1 year of surgery and then once every 2-3 years. If recurrence was suspected, patients were evaluated by CT, MRI, and/or PET scanning. Recurrence was diagnosed pathologically (by surgical resection or biopsy) and/or radiologically.

6. Statistical analysis

Categorical variables were compared using chi-square tests, and continuous variables were compared using independent sample t tests. The Kaplan-Meier method was used to compare disease-free survival (DFS). DFS was defined as the time from the date of the primary tumor surgical resection to the time of disease recurrence which was diagnosed pathologically or radiologically or death. Univariate and multivariate analyses of factors associated with DFS rates were performed using Cox proportional hazard regression models to estimate hazard ratios and 95% confidence intervals. All statistical tests were two-sided, and p < 0.05 was considered statistically significant. Statistical analyses were performed using SPSS ver. 21.0 for Windows (IBM Corp., Armonk, NY).

7. Ethical statement

This study protocol was approved by the institutional review board of Asan Medical Center (IRB No. 2018-1235). As this study was a retrospective analysis of routine clinical data, participants’ informed consent was waived by the institutional review board.

Results

1. Patient characteristics

Of the 2,346 patients included in this study, 1,363 (58.1%) were diagnosed with colon cancer and 983 (41.9%) with rectal cancer. A total patient group included 1,389 male (59.2%) and 957 female (40.8%). The mean age of these patients was 60±11 years (median age, 61; range, 19 to 89 years). All patients received curative intent surgery, with evidence of pathologic stage IIIA in 280 (11.9%), stage IIIB in 1,711 (72.9%), and stage IIIC in 355 (15.1%). ENE in a metastatic LN was detected in 551 (40.4%) colon cancer patients, including 195 (36.9%) patients with right colon cancer, 356 (42.6%) with left colon cancer, and 479 (48.7%) with rectal cancer (right vs. left, p=0.037; left vs. rectum, p=0.009). The mean follow-up interval was 60±32 months. The 5-year DFS rate in patients with right and left colon cancer differed significantly by ENE status, being highest in patients with ENE-negative left colon cancer (80.8%), followed by patients with ENE-negative right colon cancer (80.0%), ENE-positive left colon cancer (70.1%), and ENE-positive right colon cancer (65.6%) (p < 0.001) (Fig. 2A). However, the 5-year DFS rate in patients with colon and rectal cancer differed significantly by tumor site and ENE status, being 80.5%, 77.4%, 68.6%, and 64.2% in patients with ENE-negative colon cancer, ENE-negative rectal cancer, ENE-positive colon cancer, and ENE-positive rectal cancer, respectively (p < 0.001) (Fig. 2B).

2. Clinicopathologic characteristics according to ENE status in colon and rectal cancer patients

There were no significant differences in sex, s-CEA level, and histologic type between ENE-positive and ENE-negative colon and rectal cancer patients. However, ENE was more frequent in younger patients and those with higher T category, higher N category, lymphovascular invasion (LVI), and perineural invasion (PNI). ENE was more frequent in patients with left than right colon cancer (Table 1).

3. Prognostic factors of DFS in colon cancer patients

The 5-year DFS rate was significantly lower in ENE-positive than ENE-negative colon cancer (68.6% vs. 80.5%, p < 0.001). Univariate analysis showed that elevated s-CEA, pathologic stage, presence of ENE, presence of LVI, presence of PNI, and lack of adjuvant chemotherapy were associated with poorer DFS. Multivariate analysis showed that pathologic stage, presence of ENE, presence of LVI, presence of PNI, and lack of adjuvant chemotherapy were significant independent predictors of DFS (Table 2).

4. Prognostic factors of DFS in rectal cancer patients

The 5-year DFS rate was also significantly lower in ENE-positive than ENE-negative rectal cancer patients (64.1% vs. 77.4%, p < 0.001). Univariate analysis showed that elevated s-CEA, pathologic stage, presence of ENE, presence of LVI, and presence of PNI, positive of CRM and lack of adjuvant were associated with poorer DFS. Multivariate analysis showed that pathologic stage, presence of ENE, presence of LVI, presence of PNI, and lack of adjuvant chemotherapy were significant independent predictors of DFS (Table 2).

5. Recurrence patterns according to tumor location and ENE status

Recurrence patterns in colon cancer patients were unrelated to ENE status. LN recurrence was slightly higher in ENE-positive than in ENE-negative patients, but the difference was not statistically significant. In rectal cancer patients, however, LN and multiple route recurrences (e.g., hematogenous and LN, or hematogenous and peritoneal seeding) were significantly more frequent in ENE-positive than in ENE-negative patients (Table 3).

Discussion

This study investigated the clinical implications of ENE separately in patients with colon and rectal cancer who were treated at a single center during a 9 year period. We show that ENE is significantly associated with worse DFS in large cohort of patients with colon and rectal cancer, respectively, independent of the standard prognostic and predictive factors: pathologic stage, LVI, and PNI. Furthermore, ENE in both colon and rectal cancer significantly correlated with younger age, higher T category, higher N category, and occurrences of LVI and PNI. In general, patients with rectal cancer have a poorer prognosis than those with colon cancer [16]. However, we also found that 5-year DFS rates were poorer in ENE-positive colon cancer than in ENE-negative rectal cancer patients, being 77.4% in patients with ENE-positive colon cancer and 68.6% in patients with ENE-negative rectal cancer (p < 0.001). Taken together, these findings suggest that ENE is one of important indicators of prognosis and ENE can be considered a hallmark of tumor aggressiveness. In general, patients with left-sided CRC are younger than those with right-sided CRC [14]. As ENE is more frequent in the left-sided than the right-sided CRC, ENE may be associated with younger age.

ENE in metastatic LNs was found to be a well-known negative prognostic factor in patients with many other tumor types. Recently, ENE was reported to be a poor prognostic factor in patients with gastrointestinal tract cancers including esophageal [17], stomach [1], and colorectal [15,18] cancers.

CRC can be subdivided by site, namely, the proximal colon, distal colon, and rectum [10,14]. These sites differ in embryological origin, morphology, and physiology [11,14,19], and histological differences have been observed in proximal and distal CRC [20]. Epidemiologically, site-specific CRCs differ according to sex and age [21]. Consequently, primary rectal and colon cancers present with different recurrence patterns and prognosis, and may require different treatment modalities.

Genomic determinants are important predictors of tumor development and progression [22], and differ by tumor location. Two main syndromes resulting from germline mutations play a role in the occurrence of CRCs. In patients with familial adenomatous polyposis, tumors occur predominantly in the distal colon (~60%) and rectum (~25%) [23]. In patients with hereditary nonpolyposis colorectal cancer, however, tumors develop predominantly in the proximal colon (~55%) and rectum (~15%). Chromosomal instability has been associated with 60%-70% of CRCs, more frequently in the distal than in the proximal colon [24]. By contrast, the frequencies of CpG island methylator phenotype–high, high frequency of microsatellite instability, and BRAF mutations have been reported to increase in a retrograde manner from the rectum to the ascending colon [10]. Therefore, Yamauchi et al. insisted that the frequencies of molecular pathologic changes in CRC evolve gradually through bowel location, rather than after abruptly at the splenic flexure and rectosigmoid junction (continuum hypothesis) [10]. These findings suggested a close association between molecular subtype and site-specificity. Interestingly, this study showed that ENE rates increased significantly from patients with right colon cancer (36.9%) to left colon cancer (42.6%) to rectal cancer (48.7%) (right vs. left, p=0.037; left vs. rectum, p=0.009). These facts were that ENE was a common aggressive feature of CRC; however, it might be more related with distal part CRC. Considering continuum hypothesis, frequency of ENE increases from the right colon to the left colon to the rectum. However, genomic and molecular level investigation is required to verify our assertions.

Multivariate analyses showed that advanced tumor stage, ENE, LVI, PNI, and lack of adjuvant chemotherapy were independent poor prognostic factors for DFS in patients with colon cancer and rectal cancer. Pathologic tumor stage is a universally powerful prognostic factor [9], along with LVI or PNI [25,26]. Adjuvant chemotherapy significantly improves DFS and overall survival of patients with stage III CRC [27]. Our results showed that the prognostic impact of ENE in patients with colon and rectal cancer was same. However, we found that patients with ENE-negative rectal cancer had a better prognosis than those with ENE-positive colon cancer. In general, colon cancer is known to have a better survival rate than rectal cancer, but the survival rate of colon and rectal cancer can be reversed according to ENE status. Therefore, ENE status as well as tumor location may be an important prognostic indicator.

The limitations of this study include its retrospective design and its inclusion of patients who were treated at a single center, restricting the ability to generalize from study results. To our knowledge, however, this study is the first to report the prognostic effect of ENE separately in patients with colon cancer and rectal cancer by analyzing a relatively large patient cohort.

In conclusion, the occurrence of ENE is closely related to the aggressiveness of both colon and rectal tumors. ENE status is a significant independent prognostic factor regardless of tumor location. However, ENE might be more related with distally located CRC.

Conflicts of Interest

Conflict of interest relevant to this article was not reported.

Acknowledgments

This work was supported by a grant (to J.C. Kim) from the Korea Research Foundation (2016R1E1A1A02919844), Ministry of Science, ICT, and Future Planning, Republic of Korea.

Fig. 1.

Representative examples of lymph node metastasis patterns. (A) Tumor cells invading fat tissue (arrows) beyond the boundary of the lymph node (dashed line). Extranodal extension positive (×1.25 objective lens, scale bar=2 mm). (B) Tumor deposits with an invasive margin separate from the primary tumor. Extranodal extension negative (×1.25 objective lens, scale bar=2 mm). (C) Tumor cells outside the lymph node but in continuum with the primary tumor. Extranodal extension negative (×4 objective lens). (D) Tumor cells outside the lymph node but confined to endolymphatic spaces (arrow). Extranodal extension negative (×10 objective lens, scale bar=200 μm).

Fig. 2.

(A) Disease-free survival curves in patients with colon cancer according to tumor location (right colon vs. left colon) and extranodal extension (ENE) status (n=1,363). (B) Disease-free survival curves in patients with colon and rectal cancer according to tumor location (colon vs. rectum) and ENE status (n=2,346).

Table 1.

Clinicopathologic characteristics of patients with colorectal cancer with and without extranodal extension (n=2,346)

	Colon cancer (n=1,363)			Rectal cancer (n=983)
	ENE (–) (n=812)	ENE (+) (n=551)	p-value	ENE (–) (n=504)	ENE (+) (n=479)	p-value
Sex
Male	476 (58.6)	299 (54.3)	0.111	313 (62.1)	301 (62.8)	0.812
Female	336 (41.4)	252 (45.7)		191 (37.9)	178 (37.2)
Age (yr)	61±11	60±11	0.051	60±11	59±11	0.042
s-CEA level (ng/mL)	8.0±36.7	9.5±39.2	0.480	5.5± 12.7	6.2±15.0	0.385
Tumor location
RC	333 (41.0)	195 (35.4)	0.037
LC	479 (59.0)	356 (64.6)
pT category
T1	45 (5.6)	10 (1.8)	0.001	40 (7.9)	12 (2.5)	< 0.001
T2	63 (7.8)	32 (5.8)		82 (16.3)	41 (8.6)
T3	645 (79.7)	457 (83.1)		368 (73.0)	400 (83.7)
T4	56 (6.9)	51 (9.3)		14 (2.8)	25 (5.2)
pN category
N1	674 (83.0)	314 (57.0)	< 0.001	409 (81.2)	231 (48.2)	< 0.001
N2	138 (17.0)	237 (43.0)		95 (18.8)	248 (51.8)
pStage
IIIA	101 (12.4)	32 (5.8)	< 0.001	111 (22.0)	36 (7.5)	< 0.001
IIIB	658 (81.0)	391 (71.0)		353 (71.0)	309 (64.5)
IIIC	53 (6.5)	128 (23.2)		40 (7.9)	134 (28.0)
Histology
WD/MD	727 (89.5)	484 (87.8)	0.330	468 (92.9)	433 (90.4)	0.163
PD/SRC/Muc	85 (10.5)	67 (12.2)		36 (7.1)	46 (9.6)
LVI
No	519 (63.9)	322 (58.4)	0.037	338 (67.1)	253 (52.8)	< 0.001
Yes	290 (35.7)	229 (41.6)		166 (32.9)	226 (47.2)
Unknown	3 (0.4)	0
PNI
No	637 (78.4)	379 (68.8)	< 0.001	393 (78.0)	340 (71.0)	0.001
Yes	168 (20.7)	163 (29.6)		94 (18.7)	132 (27.6)
Unknown	7 (0.9)	9 (1.6)		17 (3.4)	7 (1.5)
Adjuvant CTx
Yes	729 (89.8)	489 (88.7)	0.545	425 (84.3)	409 (85.4)	0.643
No	83 (10.2)	62 (11.3)		79 (15.7)	70 (14.6)
Recurrence	140 (17.2)	160 (29.0)	< 0.001	98 (19.4)	161 (33.6)	< 0.001
Follow-up, median (range, mo)	61.7 (0.2-154.5)	60.8 (0.7-152.4)		63.4 (0.3-154.1)	59.9 (0.5-151.0)

Values are presented as number (%) or mean±standard deviation unless otherwise indicated. ENE, extranodal extension; s-CEA, serum carcinoembryonic antigen; RC, right colon; LC, left colon; WD, well-differentiated; MD, moderately differentiated; PD, poorly differentiated; SRC, signet ring cell; Muc, mucinous; LVI, lymphovascular invasion; PNI, perineural invasion; CTx, chemotherapy.

Table 2.

Univariate and multivariate analysis of factors prognostic of DFS in patients with node-positive colon and rectal cancer

Variable	Univariate analysis			Multivariate analysis
Variable	No. (%)	5-Year DFS rate	p-value	Hazard ratio	95% CI	p-value
Colon cancer (n=1,363)
Age (yr)
< 60	613 (45.0)	78.2	0.083	1		0.173
≥ 60	750 (55.0)	73.3		1.180	0.930-1.531
Sex
Female	588 (43.1)	76.1	0.862	-		-
Male	775 (56.9)	75.3		-	-
s-CEA
Normal	1,070 (78.5)	77.4	0.006	1		0.196
High	289 (21.2)	69.0		1.184	0.916-1.531
Histology
WD/MD	1,211 (88.8)	76.4	0.191	-		-
PD/Muc/SRC	152 (11.2)	70.0		-	-
Tumor location
RC	528 (38.7)	75.0	0.349	-		-
LC	835 (61.3)	76.2		-	-
pStage
Stage IIIA	133 (9.8)	93.3	< 0.001	1		0.002
Stage IIIB	1,049 (77.0)	76.1		3.125	1.535-6.362
Stage IIIC	181 (13.2)	60.5		3.930	1.837-8.406
ENE
Negative	812 (59.6)	80.5	< 0.001	1		0.001
Positive	551 (40.4)	68.6		1.490	1.180-1.882
LVI
Negative	841 (61.7)	80.2	< 0.001	1		0.001
Positive	519 (38.1)	68.0		1.479	1.170-1.870
PNI
Negative	1,016 (74.5)	79.9	< 0.001	1		< 0.001
Positive	331 (24.3)	62.3		1.624	1.275-2.068
Adjuvant CTx
No	145 (10.6)	60.8	< 0.001	1		< 0.001
Yes	1,218 (89.4)	77.3		0.529	0.383-0.731
Rectal cancer (n=983)
Age (yr)
< 60	471 (47.9)	72.6	0.236	-		-
≥ 60	512 (52.1)	68.9		-	-
Sex
Female	369 (37.5)	71.5	0.674	-		-
Male	614 (62.5)	70.3		-	-
s-CEA
Normal	785 (79.9)	72.2	0.025	1		0.559
High	197 (20.1)	64.2		1.089	0.818-1.451
Histology
WD/MD	901 (91.6)	71.4	0.162	-		-
PD/Muc/SRC	82 (9.4)	64.8		-	-
pStage
Stage IIIA	147 (15.0)	91.2	< 0.001	1		< 0.001
Stage IIIB	662 (67.3)	70.6		3.012	1.663-5.456
Stage IIIC	174 (17.7)	54.0		3.778	1.991-7.169
ENE
Negative	504 (51.3)	77.4	< 0.001	1		0.014
Positive	479 (48.7)	64.1		1.383	1.067-1.792
LVI
Negative	591 (60.1)	77.4	< 0.001	1		0.002
Positive	392 (39.9)	60.8		1.519	1.166-1.980
PNI
Negative	733 (74.6)	76.0	< 0.001	1		0.001
Positive	226 (23.0)	54.6		1.594	1.225-2.075
CRM
Negative	932 (94.8)	71.8	0.005	1		0.165
Positive	51 (5.2)	54.3		1.368	0.879-2.130
Adjuvant CTx
No	149 (15.2)	62.0	0.007	1		0.005
Yes	834 (84.8)	72.2		0.627	0.453-0.868

DFS, disease-free survival; CI, confidence interval; s-CEA, serum carcinoembryonic antigen; WD, well-differentiated; MD, moderately differentiated; PD, poorly differentiated; Muc, mucinous; SRC, signet ring cell; RC, right colon; LC, left colon; ENE, extranodal extension; LVI, lymphovascular invasion; PNI, perineural invasion; CTx, chemotherapy; CRM, circumferential resection margin.

Table 3.

Recurrence pattern according to tumor location and ENE status

	Colon cancer (n=296)			Rectal cancer (n=258)
	ENE (–) (n=137)	ENE (+) (n=159)	p-value	ENE (–) (n=98)	ENE (+) (n=161)	p-value
Hematogenous	77 (56.2)	75 (47.2)	0.121	70 (71.4)	98 (60.9)	0.084
Lymph node	26 (19.0)	41 (25.8)	0.163	17 (17.3)	31 (19.3)	0.702
Peritoneal seeding	17 (12.4)	23 (14.5)	0.606	4 (4.1)	8 (5.0)	0.742
Multiple route	11 (8.0)	17 (10.7)	0.435	2 (2.0)	14 (5.4)	0.168

Values are presented as number (%). ENE, extranodal extension.

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