Gastroenterology Research and Practice
Volume 2016 (2016), Article ID 5620765, 7 pages
http://dx.doi.org/10.1155/2016/5620765

Research Article

Clinicopathologic Significance of Extranodal Tumor Extension in Colorectal Adenocarcinoma with Regional Lymph Node Metastasis

Hyunsung Kim,¹ Abdul Rehman,¹ Yumin Chung,¹ Kijong Yi,¹ Young Chan Wi,¹ Yeseul Kim,¹ Kiseok Jang,¹ Se Min Jang,² and Seung Sam Paik¹

¹Department of Pathology, College of Medicine, Hanyang University, Seoul 04763, Republic of Korea
²Department of Pathology, College of Medicine, Konyang University, Daejeon 35365, Republic of Korea

Received 6 January 2016; Revised 30 March 2016; Accepted 31 March 2016

Academic Editor: Nicola Silvestris

Copyright © 2016 Hyunsung Kim et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. This study investigated the clinicopathologic significance of extranodal tumor extension in colorectal adenocarcinoma with lymph node metastasis. Method. Included were 419 patients who underwent curative resection for primary colorectal adenocarcinoma. Results. Extranodal tumor extension was observed more frequently in tumors with ulceroinfiltrative gross type (), higher histologic grade (), high grade tumor budding (), vascular invasion (), perineural invasion (), tumor deposit (), high ratio of metastatic/total lymph nodes (), and high pN stage (). Overall survival was significantly different between an extranodal tumor extension (−) group and an extranodal tumor extension (+) group for both N1 () and N2 homogeneous staging (). Both overall () and disease-free survival () were significantly different between the two groups in an N1a homogeneous group and overall survival was significantly different () in an N2b homogeneous group. Conclusion. Our study demonstrated that extranodal tumor extension was a useful prognostic factor for colorectal adenocarcinoma with lymph node metastasis, especially in homogeneous pN staging groups.

1. Introduction

Colorectal cancer is one of the most common cancers and the second leading cause of cancer-related deaths in the United States [1, 2]. According to cancer statistics, in 2012, South Korea had 28,988 new cases of colorectal cancer: 17,445 (60.2%) in men and 11,543 (39.8%) in women, with a male : female ratio of 1.5 : 1. The crude incidence rate was 57.6 per 100,000 and the crude mortality rate was 16.2 per 100,000 people in South Korea [3].

TNM classification is widely used to evaluate cancer staging and make treatment decisions [4]. Although the TNM staging system has been modified continuously, outcomes of patients with colorectal cancer differ, even among patients with tumors within the same stage [5]. Because colorectal cancer prognosis is still poor, the need for new prognostic factors including histopathological features and molecular subtypes that can stratify patients into different risk group is warranted [5].

The presence of lymph node metastasis and the number of metastatic lymph nodes are useful prognostic factors for colorectal adenocarcinoma [6]. In the 6th American Joint Committee on Cancer (AJCC) TNM staging system, metastatic nodal status was subdivided into N1 and N2 by number of metastatic lymph nodes. In the 7th AJCC TNM staging system, the N category was subdivided more precisely into N1a, N1b, N2a, and N2b within the N1 and N2 categories, according to number of metastatic lymph nodes and presence of pericolonic tumor deposits, which is considered N1c [7]. Extranodal tumor extension (ENTE) to metastatic lymph nodes is widely regarded as a poor prognostic factor for many other solid cancers [8]. A few studies have demonstrated the prognostic value of ENTE in colorectal adenocarcinoma with lymph node metastasis [6, 9, 10]. However, the prognostic impact of ENTE within homogeneous pN staging groups has not been reported.

This study investigated the prognostic significance of ENTE in colorectal cancer with lymph node metastasis. We retrospectively reviewed a consecutive series of 419 patients with colorectal adenocarcinoma who underwent curative resection for primary cancer and evaluated the correlation between ENTE and clinicopathologic factors and investigated survival rates in homogeneous pN staging groups.

2. Materials and Methods

2.1. Patients and Specimens

From an institutional database, 419 patients who had undergone curative resection for primary colorectal adenocarcinoma from January 2005 to December 2010 at the Department of Surgery, Hanyang University Hospital, were selected. Excluded were patients who had received neoadjuvant or adjuvant chemotherapy or radiotherapy or those with recurrent colorectal cancer or fewer than 12 lymph nodes. Medical records were reviewed to define clinical characteristics including age, gender, date of surgery, date of last follow-up, date of first local recurrence, and date of first distant metastasis. This study was approved by the Institutional Review Board of the Hanyang University Hospital (HYUH 2015-05-023). Two surgical pathologists (Hyunsung Kim and Seung Sam Paik) reviewed all hematoxylin and eosin stained slides and pathology reports to confirm diagnoses and define clinicopathologic characteristics. TNM staging and other pathologic parameters were determined according to a protocol for examining specimens from patients with primary carcinoma of the colon and rectum [11]. Pathologic data collected included age, gender, tumor size, gross type, tumor location, histologic grade, tumor budding, vascular invasion, perineural invasion, tumor deposit, ratio of metastatic lymph nodes/total lymph nodes (MLN/TLN), pT category, pN category, and status of distant metastasis. All slides of resected lymph nodes were reviewed to determine ENTE. ENTE was defined as a perforation of the nodal capsule by tumor tissue with extranodal growth and evaluated as present or absent [9]. Representative microphotos are in Figure 1. Tumor cell nodule that was discontinuous with the tumor or without surrounding lymphoid tissue was considered a tumor deposit and excluded.

(a)

(b)

Figure 1: Representative microphotos of lymph node metastasis without extranodal tumor extension (a) and with extranodal tumor extension (b) (hematoxylin and eosin, ×20).

2.2. Statistical Analysis

Statistical analysis was performed using SPSS software version 21 (IBM Corp., Armonk, NY, USA). Mann-Whitney and chi-square tests were used to examine associations among ENTE and clinicopathologic parameters of age, gender, tumor size, macroscopic growth pattern, tumor location, histologic grade, tumor budding, presence of lymphovascular invasion or perineural invasion, MLN/TLN ratio, invasion depth (T) category, regional lymph nodes metastasis (N) category, and distant metastasis (M) category. Overall survival rate and disease-free survival rate were determined using the Kaplan-Meier method, and the log-rank test was used to compare groups according to N category. A Cox proportional hazard regression model was used to evaluate the prognostic significance in univariable and multivariable analyses. was considered statistically significant.

3. Results

3.1. Clinicopathologic Characteristics of Patients

Selected were 419 patients who underwent curative resection for primary colorectal cancer between January 2005 and December 2010. Their clinicopathologic information is in Table 1. Median follow-up was 53 (range: 1–117) months. Mean age at surgery was 63.4 (±11.4) years with 257 (61.3%) men and 162 (38.7%) women with a male : female ratio of 1.59 : 1. Pathological evaluation revealed that 31 tumors (7.4%) were histological grade 1, 196 (46.8%) were grade 2, 168 (40.1%) were grade 3, and 24 (5.7%) were grade 4. By pT stage, 35 (8.4%) were pT1, 42 (10.0%) were pT2, 263 (62.8%) were pT3, 52 (12.4%) were pT4a, and 27 (6.4%) were pT4b. By pN stage, 180 (43.0%) were N0, 48 (11.5%) were N1a, 55 (13.1%) were N1b, 9 (2.1%) were N1c, 62 (14.8%) were N2a, and 65 (15.5%) were N2b. Distant metastasis was identified in 29 (7%) patients. The mean number of removed lymph nodes was 29.2 (±15.78) and of mean metastatic lymph nodes was 3.6 (±6.83).

Table 1: Baseline patient characteristics ().

Factors
Value (%)

Number of patients
419 (100%)

Mean age at surgery (years)
63.4 (±11.4)

Sex

    Male
257 (61.3%)

    Female
162 (38.7%)

Histologic grade

    Grade 1
31 (7.4%)

    Grade 2
196 (46.8%)

    Grade 3
168 (40.1%)

    Grade 4
24 (5.7%)

Pathologic characteristics

    pT

        1
35 (8.4%)

        2
42 (10.0%)

        3
263 (62.8%)

        4a
52 (12.4%)

        4b
27 (6.4%)

    pN

        0
180 (43.0%)

        1a
48 (11.5%)

        1b
55 (13.1%)

        1c
9 (2.1%)

        2a
62 (14.8%)

        2b
65 (15.5%)

    M

        0
390 (93.0%)

        1a
25 (6.0%)

        1b
4 (1.0%)

Mean number of removed LNs
29.2 (±15.78)

Mean number of metastatic LNs
3.6 (±6.83)

LNs: lymph nodes.

3.2. Correlation among ENTE and Clinicopathologic Parameters

Of the 419 patients, 230 (54.9%) showed lymph node metastasis with 108 (47.0%) with ENTE in metastatic lymph node(s). Correlation among ENTE and clinicopathologic parameters of colorectal adenocarcinoma is in Table 2. ENTE was observed more frequently in tumors with ulceroinfiltrative gross type (), higher histologic grade (), high grade tumor budding (), vascular invasion (), perineural invasion (), tumor deposit (), high MLN/TLN ratio (), and high pN stage ().

Table 2: Correlations between ENTE and clinicopathologic factors in colorectal adenocarcinoma with regional lymph node metastasis ().

Factors

ENTE
value

Negative (%)
Positive (%)

()
()

Age (year)

0.476†

    Mean (±SD)
230
62.66 (±10.30)
63.43 (±12.82)

Gender

0.857‡

    Male
137
72 (52.6%)
32 (47.4%)

    Female
93
50 (53.8%)
43 (46.2%)

Tumor size

0.477†

    Mean (±SD)
230
5.13 (±2.06)
5.33 (±2.12)

Gross type

0.026‡

    UI
127
59 (46.5%)
68 (53.5%)

    UF & P
103
63 (61.2%)
40 (38.8%)

Location

0.275‡

    Colon
134
67 (50.0%)
67 (50.0%)

    Rectum
96
55 (57.3%)
41 (42.7%)

Histologic grade

0.012‡

    Low grade
101
63 (62.4%)
38 (37.6%)

    High grade
129
59 (45.7%)
70 (54.3%)

Tumor budding

0.003‡

    Low grade
111
70 (63.1%)
41 (36.9%)

    High grade
119
52 (43.7%)
67 (56.3%)

Vascular invasion

<0.001‡

    Absent
158
96 (60.8%)
62 (39.2%)

    Present
72
26 (36.1%)
46 (63.9%)

Perineural invasion

0.015‡

    Absent
69
45 (65.2%)
24 (34.8%)

    Present
161
77 (47.8%)
84 (52.2%)

Tumor deposit

<0.001‡

    Absent
158
101 (63.9%)
57 (36.1%)

    Present
72
21 (29.2%)
51 (70.8%)

MLN/TLN

<0.001†

    Mean ratio (%)
230
15.30 (±14.43)
31.81 (±25.46)

T stage

0.211‡

    T1
2
1 (50.0%)
1 (50.0%)

    T2
15
11 (73.3%)
4 (26.7%)

    T3
148
81 (54.7%)
67 (45.3%)

    T4
65
29 (44.6%)
36 (55.4%)

N stage

<0.001‡

    N1
103
75 (72.8%)
28 (27.2%)

    N2
127
47 (37.0%)
80 (63.0%)

Distant metastasis

0.741‡

    Absent
204
109 (53.4%)
95 (46.6%)

    Present
26
13 (50.0%)
13 (50.0%)

SD: standard deviation; †Mann-Whitney test; ‡chi-square test; UI: ulceroinfiltrative; UF: ulcerofungating; P: polypoid; MLN/TLN: metastatic lymph nodes/total lymph nodes.

3.3. Correlation among ENTE and Overall and Disease-Free Survival in Colorectal Adenocarcinoma

The 5-year survival rate was 74% in the ENTE (−) group and 52% in the ENTE (+) group with a significant difference between the ENTE (−) and ENTE (+) groups in both overall and disease-free survival ( and , log-rank test) (Figures 2(a) and 2(b)). In univariate analyses, ENTE showed a significant effect on both overall survival and disease-free survival ( and , log-rank test). In multivariate analyses, ENTE was an independent prognostic factor for overall survival (, log-rank test). However, ENTE was not an independent prognostic factor for disease-free survival (, log-rank test) (Table 3).

Table 3: Univariable and multivariable analyses in colorectal adenocarcinoma with regional lymph node metastasis ().

Variable
Univariable analysis
Multivariable analysis

HR (95% CI)
value
HR (95% CI)
value

Overall survival

    ENTE (absent versus present)
2.484 (1.603–3.848)
<0.001
1.676 (1.065–2.637)
0.026

    Vascular invasion
3.095 (2.034–4.710)
<0.001
2.469 (1.595–3.822)
<0.001

    Perineural invasion
1.806 (1.086–3.002)
0.023
1.078 (0.631–1.841)
0.785

    Tumor deposit
3.778 (2.477–5.763)
<0.001
2.850 (1.839–4.416)
<0.001

    Tumor budding (low grade versus high grade)
1.990 (1.284–3.084)
0.002
1.704 (1.087–2.672)
0.020

Disease-free survival

    ENTE (absent versus present)
1.866 (1.171–2.973)
0.009
1.357 (0.821–2.244)
0.234

    Vascular invasion
2.967 (1.858–4.738)
<0.001
1.211 (0.722–2.029)
0.468

    Perineural invasion
1.410 (0.834–2.384)
0.200
1.154 (0.651–2.042)
0.624

    Tumor deposit
2.205 (1.373–3.542)
<0.001
0.937 (0.556–1.580)
0.807

    Tumor budding (low grade versus high grade)
1.244 (0.769–2.012)
0.375
0.888 (0.524–1.503)
0.658

HR: hazard ratio; CI: confidence interval; ENTE: extranodal tumor extension.

(a)

(b)

Figure 2: Significant difference between ENTE (−) and ENTE (+) groups in overall survival (a) and disease-free survival (b) () (Kaplan-Meier method with log-rank test).

3.4. Survival Analyses by Homogeneous pN Staging Groups

To analyze the effect of ENTE in homogeneous pN groups, we grouped the patients with lymph node metastasis into N1 and N2 according to the 6th AJCC staging system and further subdivided them without ENTE and with ENTE. A significant difference was seen in overall survival between the ENTE (−) and ENTE (+) groups in both the N1 () and N2 (, log-rank test) homogeneous groups (Figures 3(a) and 3(b)). However, no significant difference was seen in disease-free survival between ENTE (−) and ENTE (+) groups in the N1 () or N2 (, log-rank test) homogeneous group (data not shown). We also grouped patients with lymph node metastasis into N1a, N1b, N2a, and N2b according to the 7th AJCC staging system and further subdivided them into without ENTE and with ENTE. The N1a homogeneous group showed significant differences in both overall () and disease-free survival (, log-rank test) between ENTE (−) and ENTE (+) groups (Figures 3(c) and 3(d)). However, the N1b homogeneous group showed no significant difference in overall () or disease-free (, log-rank test) survival between the ENTE (−) and ENTE (+) groups (data not shown). In the N2a homogeneous group, no significant difference was seen in overall survival () or disease-free survival (, log-rank test) between the ENTE (−) and ENTE (+) groups (data not shown). In the N2b homogeneous group, overall survival was significantly different between the ENTE (−) and ENTE (+) groups (, log-rank test) (Figure 3(e)). However, disease-free survival was not significantly different between the ENTE (−) and ENTE (+) groups (, log-rank test) (Figure 3(f)).

(a)

(b)

(c)

(d)

(e)

(f)

Figure 3: In N1 and N2 homogeneous group analyses, a significant difference was seen between ENTE (−) and ENTE (+) groups in overall survival (a and b). In N1a and N1b homogeneous group analyses, a significant difference was seen in overall survival (c) and disease-free survival (d) by N1a staging group between ENTE (−) and ENTE (+) groups. In N2a and N2b homogeneous group analyses, a significant difference was seen in overall survival (e) of N2b staging group between ENTE (−) and ENTE (+) groups. No significant difference was seen in disease-free survival (f) (Kaplan-Meier method with log-rank test).

4. Discussion

ENTE in metastatic lymph nodes is widely regarded as a poor prognostic factor in many malignancies including gastric cancer [4, 12], bladder cancer [13, 14], papillary thyroid carcinoma [15], penile carcinoma [8], breast cancer [16], non-small cell lung cancer [17], and prostate cancer [18]. Lee et al. and Choi et al. reported that ENTE is associated with advanced T and N stages and is an independent factor for poor prognosis in gastric cancer [4, 12]. Fleischmann et al. and Fajkovic et al. reported that ENTE is an independent prognostic factor for bladder cancer patients with lymph node metastasis, especially with disease recurrence [13, 14]. Distant recurrence is higher in papillary thyroid carcinoma patients with ENTE than in patients without ENTE [15]. Wang et al. found that the degree of ENTE is associated with poor outcome in patients with penile carcinoma [8]. Shigematsu et al. found that ENTE in sentinel lymph node(s) is an independent predictor of nonsentinel lymph node metastasis and of poor prognosis in breast cancer with sentinel lymph node metastasis [16]. Lee et al. showed that ENTE is significantly higher in women with adenocarcinomas of advanced stage, vascular invasion, or p53 expression and that ENTE is associated with poor 5-year survival rate in patients with surgically resected non-small cell lung cancer [17]. Fleischmann et al. reported that ENTE is an indicator lesion for advanced or aggressive prostate tumors with poor outcomes [18].

A few studies have investigated the prognostic value of ENTE in colorectal cancer [6, 9, 10]. Komuta et al. found that ENTE in metastatic lymph node(s) is a poor prognostic factor in a study of 84 patients with colorectal cancer. However, in that study, no significant association was found between ENTE and clinicopathologic parameters and no statistically significant difference was seen in recurrence or survival between pN categories according to the sixth AJCC staging [10]. Yano et al. investigated ENTE in a study of 155 patients with Duke stage C colorectal adenocarcinoma and suggested that ENTE can be a more critical prognostic factor than other parameters such as T status, lymphovascular invasion, and number of positive lymph nodes [9]. Puppa et al. studied pericolonic tumor deposits and extracapsular tumor extension and concluded that the value of ENTE as an independent prognostic factor of stage III cancer is of borderline significance [6].

We found that ENTE was more frequent in cancers with well-known adverse histopathologic features such as higher histologic grade, high grade tumor budding, vascular invasion, perineural invasion, tumor deposit, and pT and pN stages. These results suggested that ENTE was closely associated with aggressive clinical behavior of colorectal adenocarcinoma with lymph node metastasis. In survival analyses, Kaplan-Meier survival curves revealed a significant difference between ENTE (−) and ENTE (+) patients in both overall survival and disease-free survival. These results suggested that ENTE is a poor prognostic factor for colorectal adenocarcinoma with lymph node metastasis.

The prognostic impact of ENTE in homogeneous pN staging groups of colorectal cancer has not been reported. In subgroup analyses by homogeneous pN staging groups, significant differences were seen in overall survival between ENTE (−) and ENTE (+) groups in both N1 and N2 staging groups and overall and disease-free survival in the N1a staging group with and without ENTE. In the N2b homogeneous group, overall survival was significantly different between the ENTE (−) and ENTE (+) groups. These results suggested that ENTE is an important prognostic factor in homogeneous pN staging groups. Therefore, careful pathological examination should be done to detect ENTE in metastatic lymph nodes and pathology reports should specify the presence of ENTE in colorectal adenocarcinoma with lymph node metastasis.

Our study had several limitations in patient selection and definite criteria for ENTE. Neoadjuvant treatment is a well-known effective therapy for colorectal adenocarcinoma that is essential for some patients. However, we could not determine the clinicopathologic correlations between neoadjuvant treatment and ENTE and excluded all patients who received neoadjuvant or adjuvant chemotherapy or radiotherapy. We defined ENTE as perforation of the nodal capsule by tumor tissue with extranodal growth and evaluated ENTE as present or absent. However, this definition cannot be applied in all cases. For example, some lymph nodes have no fibrous tissue covering the lymphoid tissue. Komuta et al. also graded the amount of ENTE by the number of tumor cells in the extranodal space [10]. Definite criteria and grading of ENTE and more studies with a large number of patients are needed.

In conclusion, our study demonstrated that the presence of ENTE was an important prognostic factor in homogeneous pN staging groups. The prognostic effect of ENTE as number of metastatic lymph nodes with ENTE or thickness of ENTE in metastatic lymph nodes should be validated in further studies. We recommend that the number of metastatic lymph nodes and the presence of ENTE be considered in determining the pN stage of colorectal cancer.

Competing Interests

The authors declare that they have no competing interests.

References

F. Coppedè, A. Lopomo, R. Spisni, and L. Migliore, “Genetic and epigenetic biomarkers for diagnosis, prognosis and treatment of colorectal cancer,” World Journal of Gastroenterology, vol. 20, no. 4, pp. 943–956, 2014.

V. W. Chen, M.-C. Hsieh, M. E. Charlton et al., “Analysis of stage and clinical/prognostic factors for colon and rectal cancer from seer registries: Ajcc and collaborative stage data collection system,” Cancer, vol. 120, no. 23, pp. 3793–3806, 2014.

K.-W. Jung, Y.-J. Won, H.-J. Kong et al., “Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2012,” Cancer Research and Treatment, vol. 47, no. 2, pp. 127–141, 2015.

I.-S. Lee, Y.-S. Park, M.-H. Ryu et al., “Impact of extranodal extension on prognosis in lymph node-positive gastric cancer,” British Journal of Surgery, vol. 101, no. 12, pp. 1576–1584, 2014.

G. Puppa, A. Sonzogni, R. Colombari, and G. Pelosi, “TNM staging system of colorectal carcinoma: a critical appraisal of challenging issues,” Archives of Pathology and Laboratory Medicine, vol. 134, no. 6, pp. 837–852, 2010.

G. Puppa, P. Maisonneuve, A. Sonzogni et al., “Pathological assessment of pericolonic tumor deposits in advanced colonic carcinoma: relevance to prognosis and tumor staging,” Modern Pathology, vol. 20, no. 8, pp. 843–855, 2007.

S. Edge, D. R. Byrd, C. C. Compton, A. G. Fritz, F. L. Greene, and A. Trotti, Eds., AJCC Cancer Staging Manual, Springer, New York, , NY, USA, 7th edition, 2010.

J.-Y. Wang, Y. Zhu, S.-X. Tang et al., “Prognostic significance of the degree of extranodal extension in patients with penile carcinoma,” Asian Journal of Andrology, vol. 16, no. 3, pp. 437–441, 2014.

H. Yano, Y. Saito, Y. Kirihara, and J. Takashima, “Tumor invasion of lymph node capsules in patients with Dukes C colorectal adenocarcinoma,” Diseases of the Colon and Rectum, vol. 49, no. 12, pp. 1867–1877, 2006.

K. Komuta, S. Okudaira, M. Haraguchi, J. Furui, and T. Kanematsu, “Identification of extracapsular invasion of the metastatic lymph nodes as a useful prognostic sign in patients with resectable colorectal cancer,” Diseases of the Colon and Rectum, vol. 44, no. 12, pp. 1838–1844, 2001.

M. K. Washington, J. Berlin, P. Branton et al., “Protocol for the examination of specimens from patients with primary carcinoma of the colon and rectum,” Archives of Pathology and Laboratory Medicine, vol. 133, no. 10, pp. 1539–1551, 2009.

W. H. Choi, S. Kim, J. Shen et al., “Prognostic significance of perinodal extension in gastric cancer,” Journal of Surgical Oncology, vol. 95, no. 7, pp. 540–545, 2007.

A. Fleischmann, G. N. Thalmann, R. Markwalder, and U. E. Studer, “Extracapsular extension of pelvic lymph node metastases from urothelial carcinoma of the bladder is an independent prognostic factor,” Journal of Clinical Oncology, vol. 23, no. 10, pp. 2358–2365, 2005.

H. Fajkovic, E. K. Cha, C. Jeldres et al., “Extranodal extension is a powerful prognostic factor in bladder cancer patients with lymph node metastasis,” European Urology, vol. 64, no. 5, pp. 837–845, 2013.

S. Moritani, “Impact of invasive extranodal extension on the prognosis of patients with papillary thyroid carcinoma,” Thyroid, vol. 24, no. 12, pp. 1779–1783, 2014.

H. Shigematsu, K. Taguchi, H. Koui, and S. Ohno, “Clinical significance of extracapsular invasion at sentinel lymph nodes in breast cancer patients with sentinel lymph node involvement,” Annals of Surgical Oncology, vol. 22, no. 7, pp. 2365–2371, 2015.

Y.-C. Lee, C.-T. Wu, S.-W. Kuo, Y.-T. Tseng, and Y.-L. Chang, “Significance of extranodal extension of regional lymph nodes in surgically resected non-small cell lung cancer,” Chest, vol. 131, no. 4, pp. 993–999, 2007.

A. Fleischmann, S. Schobinger, R. Markwalder et al., “Prognostic factors in lymph node metastases of prostatic cancer patients: the size of the metastases but not extranodal extension independently predicts survival,” Histopathology, vol. 53, no. 4, pp. 468–475, 2008.