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World J Gastroenterol. Sep 21, 2007; 13(35): 4776-4780
Published online Sep 21, 2007. doi: 10.3748/wjg.v13.i35.4776
Distribution of solitary lymph nodes in primary gastric cancer: A retrospective study and clinical implications
Cai-Gang Liu, Ping Lu, Yang Lu, Feng Jin, Hui-Mian Xu, Shu-Bao Wang, Jun-Qing Chen, Department of Surgical Oncology, First Affiliated Hospital of China Medial University, Heping, Shenyang110001, Liaoning Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Ping Lu, Department of Surgical Oncology, First Affiliated Hospital of China Medial University, Heping, Shenyang 110001, Liaoning Province, China. luping2999@yahoo.com.cn
Telephone: +86-24-81121999 Fax: +86-24-22834060
Received: April 27, 2007
Revised: June 13, 2007
Accepted: June 18, 2007
Published online: September 21, 2007

Abstract

AIM: To investigate the distribution pathway of metastatic lymph nodes in gastric carcinoma as a foundation for rational lymphadenectomy.

METHODS: We investigated 173 cases with solitary or single station metastatic lymph nodes (LN) from among 2476 gastric carcinoma patients. The location of metastatic LN, histological type and growth patterns were analyzed retrospectively.

RESULTS: Of 88 solitary node metastases cases, 65 were limited to perigastric nodes (N1), while 23 showed skipping metastasis. Among 8 tumors in the upper third stomach, 3 involved right paracardial LN (station number: No.1), and one in the greater curvature was found in No.1. In the 28 middle third stomach tumors, 10 were found in LN of the lesser curvature (No.3) and 6 in LN of the left gastric artery (No.7); 5 of the 20 cases on the lesser curvature spread to No.7, while 2 of the 8 on the greater curvature metastasized to LN of the spleen hilum (No.10). Of 52 lower third stomach tumors, 13 involved in No.3 and 19 were detected in inferior pyloric LN (No.6); 9 of the 29 cases along the lesser curvature were involved in No.6.

CONCLUSION: Transversal and skipping metastases of sentinel lymph nodes (SLN) are notable, and rational lymphadenectomy should, therefore, be performed.

Key Words: Gastric cancer, Metastatic lymph node, Lymph node dissection, Rational lymphadenectomy, Sentinel lymph node



INTRODUCTION

Lymphatic metastasis is the most important factor for prognosis of gastric carcinoma. To avoid missing positive lymph nodes, surgeons have performed an extensive radical lymphadenectomy for gastric cancer, a method which is also used when early tumors are present. As a result, patients that did not have lymph node metastasis have had to undergo operations and face potentially avoidable risks[1,2].

As the SLN concept gains acceptance, onco-surgery researchers are optimistic that the concept may serve as a breakthrough management tool to be used in gastric cancer; however, the concept is still considered to be at an investigative stage[3]. We studied the distribution pathway of solitary or positive lymph nodes limited to a single station to provide a foundation for undertaking rational lymphadenectomy for gastric carcinoma.

MATERIALS AND METHODS
Patients

One hundred and seventy-three patients were selected from the 2476 patients with gastric cancer for whom radical operations were performed at the first affiliated hospital of the China Medical University between 1980 and 2003. The criteria used for inclusion was: (1) D2 lymph node dissections had been performed[4]; (2) there were greater than 15 lymph nodes, and the resected specimens had been analyzed pathologically[5]; (3) patients with pT4 and M1 stage were excluded[5]; (4) patients’ medical records were complete. Among the 173 cases, 88 had solitary lymph metastasis and 85 involved a single station lymph node. Sixty-four of the 88 patients were male and 24 female. The average age of the patients in this group was 57.6 ± 7.2 years (range 30-80). With respect to tumor location, the tumor was found in the upper third stomach area (U) in 8 cases, in the middle third (M) in 28, and in the lower third (L) in 52. Amongst the 85 patients with single station node metastasis, 60 were male and 25 female. The average age of the patients in this group was 58.2 ± 8.3 years (range 32-76). In respect of tumor location; the tumor was in the U in 23 cases, in the M in 12, and in the L stomach areas in 50.

Reference standard

The location of the tumor, the classification of the lymph node and histological type were by the Japanese Classification of Gastric Carcinoma[6]. For classification, the symbol “No.” indicates lymph node station number and “N” indicates the lymph node group. The histological types included differentiated and undifferentiated. An “adjacent metastasis” was defined as when lymph node metastasis is limited to the tumor side of N1; “transversal metastasis” is limited to the region of N1 opposite the tumor; and a “skipping metastasis” indicates a lymph node metastasized outside of N1.

Histological growth patterns included massive, nest, and diffuse types[7].

Statistical methods

All data were analyzed using SPSS13.0 statistics software. The differences of the frequency distributions between the two groups of lymph nodes were determined by a χ2-test or by Fisher’s exact test. A χ2-test was adopted in the analysis of a single factor and a P value of less than 0.05 was considered statistically significant.

RESULTS
The distribution of metastatic nodes

Among the 88 patients with a solitary metastatic lymph node, in 65 (73.9%) the lymph nodes involved were within N1, and 23 (26.1%) were over N1. In 8 cases the tumor was in the U location, amongst which 6 (75%)were observed to be in N1 and 2 (25%) in N2. In 28 cases the tumor was in the M region, amongst which 19 (67.9%) were involved in N1 and 9 (32.1%) in N2. Among the 52 patients with L region cancers, 40 were found with solitary metastatic nodes in N1, 10 (19.2%) with nodes in N2 and 2 (3.9%) in N3 (Table 1).

Table 1 Distribution of metastatic lymph nodes (cases).
L tumors
M tumors
U tumors
SN1SSN2P valueSN1SSN2P valueSN1SSN2P value
No.120-322NS33NS
No.210-00-15NS
No.31311NS4101NS16NS
No.449NS51NS02NS
No.543NS11-00-
No.61921NS12NS03NS
No.745NS63NS11-
No.831-10-10-
No.910-01-01-
No.1000-20-01-
No.1110-00-01-
No.1200-01-00-
TOTAL5250-2812823

Comparisons were also made between cases with a solitary metastasis lymph node and single station nodes. No statistically significant difference was found with respect to the distribution of metastatic lymph nodes in the U, M and L regions using a χ2-test or Fisher’s exact test (Table 1).

Adjacent metastasis

In 7 of the 8 cases with a U region tumor, the tumor located at the side of the lesser curvature region. Amongst them, metastatic lymph nodes in 2 (28.6%) were detected within No.1. Among the 28 cases with a tumor in the M area, in 20 the tumor was observed in the lesser curvature region and in 8 in the greater curvature region. Metastatic lymph nodes in 10 of the 20 cases were found within No. 3, while 3 of the 8 were within No. 4.

Fifty-two cases had tumors in the L stomach area. Amongst these the tumors in 29 located at the lesser curvature region, 15 at the greater curvature side and 8 extended in a circle. Metastatic lymph nodes in 9 of the 29 cases were found within No.3, in 7 of the 15 within No.6, and in 3 of the 8 within No. 6 (Table 2 and Figure 1).

Figure 1
Figure 1 The metastatic pathway of SLN. Tumors are identified by circles and tumors extend in a circle in the lower third stomach.
Table 2 Distribution of solitary metastatic lymph nodes according to transversal zoning (cases).
L tumors
M tumors
U tumors
A1B2C3A1B2A1B2
No.10201112
No.20010001
No.339101001
No.42203201
No.51210100
No.67931000
No.71211501
No.80300101
No.91000000
No.100002000
No.110010000
Transversal metastasis

There was just one case with a tumor in the U area, and solitary metastatic lymph nodes were found within No.1. Twenty-nine patients had tumors at the lesser curvature side in the L area, and 9 (31%) of them were found to have metastatic lymph nodes within No.6. Of the 15 cases with tumors at the greater curvature side, in the L stomach area, 3 (20%) were involved in No.3 (Table 2 and Figure 1).

Skipping metastasis

Among the 8 cases with tumors in the U area of the lesser curvature region, one solitary metastatic lymph node (14.3% of total) was observed within No.7, and another node (14.3%) was found within No.8. In the M area, 5 (25%) of the 20 patients who had tumors at the lesser curvature side had metastatic lymph nodes within No.7, while a metastatic node was detected within No.10 in 2 (25%) of the 8 patients with a tumor in the greater curvature side. Among the 29 cases with a tumor in area L, the number of lymph node metastases involved in No.1, No.7 and No.8 were 2 (6.9%), 2 (6.9%) and 3 (10.3%), respectively (Table 2 and Figure 1).

Relationships among histological type, growth pattern, and distribution pattern of solitary lymph nodes

Comparing the 65 patients with metastasis within N1 and the 23 with a skipping metastasis, no statistical significance was found between histological type and the growth patterns of the two groups (Tables 3 and 4). Also, there was no significant difference between the adjacent metastasis group (39) and the transversal metastasis group (20) (Tables 5 and 6).

Table 3 Histological type and skipping metastasis (cases).
Group N1Group > N1P value
L tumors0.192
Differentiated224
Undifferentiated188
M tumors0.299
Differentiated33
Undifferentiated166
U tumors1.000
Differentiated31
Undifferentiated31
Total0.489
Differentiated288
Undifferentiated3715
Table 4 Histological growth pattern and skipping metastasis (cases).
Group N1Group > N1P values
L tumors0.087
Massive83
Nest213
Diffuse116
M tumors0.456
Massive22
Nest82
Diffuse95
U tumors0.645
Massive11
Nest20
Diffuse31
TOTAL0.051
Massive116
Nest315
Diffuse2312
Table 5 Histological type and transversal metastasis (cases).
TN1AN2P values
L tumors0.793
Differentiated811
Undifferentiated78
M tumors0.426
Differentiated03
Undifferentiated313
U tumors0.114
Differentiated03
Undifferentiated21
Total0.793
Differentiated817
Undifferentiated1222
Table 6 Histological growth pattern and transversal metastasis (cases).
TN1AN2P values
L tumors0.513
Massive62
Nest511
Diffuse46
M tumors0.453
Massive02
Nest26
Diffuse18
U tumors0.687
Massive10
Nest11
Diffuse12
TOTAL0.863
Massive74
Nest818
Diffuse616
DISCUSSION
The distribution pattern of solitary metastatic nodes

There is little clinical literature available on the lymphatic routes of the stomach[8-10]. After analyzing 51 cases, Kosaka et al[11] reported that 44 gastric carcinomas with solitary lymph node metastasis were involved within N1. Ichikura et al[12] analyzed 69 cases with solitary lymph node metastasis, and found that in 6 of the 28 cases that had a lesion along the lesser curvature region, lymph node metastasis was observed along the greater curvature region. Kikuchi[13] reported that skipping metastasis occurred in 14% of their patients with a solitary lymph node.

We investigated 173 cases with a solitary or single station metastatic lymph node from 2476 gastric cancer patients. First, 74.2% of the solitary metastasis lymph nodes were limited to within N1. The lesion found in each region had one or more adjacent lymph node stations where a metastasis was more frequently found. These lymph node stations were relatively certain for the lesion in each region. Second, the frequency of transversal lymph node metastases, referring to the lesion in each region, was also relatively high. For example, with reference to a lesion in the L region, 31% of patients with a primary tumor on the lesser curvature area involved No.6, while 20% with a lesion on the greater curvature involved No.3. Third, the frequency of skipping metastases in our study was 25.8%. The frequencies of metastases in N2 in regions U, M and L were 25%, 32.1% and 19.2%, respectively. We noted that the frequency of skipping metastasis in region M was 25%, that is, 25% of the lesions at the lesser curvature side were detected in No.7 and No.8, and 25% of the lesions at the greater curvature were found in No.10.

From the above results, it is apparent that the distribution patterns of solitary nodes in gastric carcinoma are basically adjacent metastases; however, transversal and skipping metastasis were also found. The histological type and growth patterns did not influence the distribution of solitary metastatic nodes.

The first possible nodes of metastasis along the route of lymphatic drainage from the primary lesion should be SLN[14]. However, because of the multidirectional and complicated lymphatic flow from the GI tract, when using methods that inject dyes or radioactive tracers, there is likely to be some bias in the description of the distribution pathway of SLN in gastric carcinoma[15-17]. By analyzing the location of solitary metastatic lymph nodes, the distribution pathway of SLN in gastric carcinoma can be accurately assessed.

Reasons for skipping metastasis

After analyzing the clinical records of 51 patients with solitary lymph node metastasis, Kosaka et al[11] reported 7 cases of lymph node metastases in N2-N3 without being in N1. Kosaka et al[11] suggested that the following could have a role in skipping metastasis: (1) occult metastases may remain unseen in a routine histopathological examination; (2) there may be a great number of lymphatic routes in the minor omentum; and (3) there may have been only a few perigastric nodes in those cases.

In this study, transversal and skipping metastasis were found to be notable. However, to date the reasons for the occurrence of skipping metastasis remain poorly understood. Chen et al[18] studied the dynamic role of stomach lymphatic flow from 138 infant corpses using 20% Prussian Blue Chloroform Solution as lymphatic dye. They reported that in 40 of 41 cases in which the drainage pointed at the greater curvature of the corpus gastricum, the lymphatic channel flowed directly to No.10. Therefore, with reference to lesions in a certain region, the so-called “skipping metastasis” of a SLN may be the first lymph node in the lymphatic drainage system. In cases where metastasis first occurs in N2 or N3, the function of N2 or N3 is considered to be the same as N1[14].

Clinical implications

In the past 23 years, 2476 patients with gastric cancer were treated at our hospital. Among them, for the 728 patients without metastatic lymph nodes an extended D1 dissection was also performed, and as a result some cases had complications connected with the dissection. A great achievement of gastric surgeons in the last century, one that deserves unequivocal respect, has been to establish radical surgery with extensive lymph node dissection for gastric cancer. However, we now need to proceed to another stage by improving post-operative function and quality of life after gastric cancer surgery without impairing long-term outcomes[19,20]. The concept of a “minimally invasive, curative, safe operation” has gradually gained acceptance[21,22]. Here, we have attempted to discover the distribution pathway of SLN in order to provide clinical data for rational lymphadenectomy.

Based on the study we suggest that: (1) for patients with U area cancer at the lesser curvature region, No.7 and No.8 should be treated in the same way as N1; (2) for patients with cancer in the M area in the lesser curvature region, No.7 should be treated in the same was as N1; (3) for patients with cancer in the M area at the greater curvature region, No.10 should be inspected more carefully, although No.10 can be regarded as the same as N3 for an M area cancer[6]; further, if No.10 is questionable, a resection of the spleen should be undertaken[4]; and 4) for patients with cancer in the L area at the lesser curvature region, No.1, No.7 and No.8 should be inspected more carefully.

COMMENTS
Background

The first possible nodes of metastasis along the route of lymphatic drainage from the primary lesion should be a sentinel lymph node (SLN). If a SLN is negative, patients can be considered to be without lymph node metastasis, and should not have to endure possible operations and face avoidable risks. The SLN concept is gaining greater acceptance, and thus clinicians and researchers can be optimistic that it may serve as a breakthrough management tool for use in gastric cancer.

Research frontiers

Many clinicians and researchers are presently undertaking studies of the distribution pathway of SLN in gastric carcinoma. However, because of the multidirectional and complicated lymphatic flow from the GI tract, there is likely to be some bias in the description of the distribution pathway of SLN in gastric carcinoma when using methods that inject dyes or radioactive tracers. The first possible sites of metastasis along the route of lymphatic drainage from the primary lesion are known as SLN. Therefore, a solitary metastatic lymph node could be regarded as SLN in gastric carcinoma. Some onco-surgery scholars have attempted to assess the distribution pathway of SLN in gastric carcinoma by analyzing the location of solitary metastatic lymph nodes.

Innovations and breakthroughs

Based on a large sample study, we described the distribution pathway of solitary metastatic lymph nodes and put forward concrete suggestions for lymph node dissection in gastric cancer.

Applications

We attempted to discover the distribution pathway of solitary metastatic lymph nodes in gastric cancer. Our results provide clinical data for rational lymphadenectomy and for experimental study of SLN.

Terminology

Minimally invasive surgery (MIS) is well recognized; however, rational lymphadenectomy operations are more focused on in this study. MIS is more about treatment of early gastric cancer, while rational lymphadenectomy is more about advanced gastric cancer.

Peer review

This manuscript presents a good overview of the distribution of lymph node metastasis in gastric cancer and should be of interest to GI researchers and clinicians.

Footnotes

Supported in part by the Gastric Cancer Laboratory of Chinese Medical University

S- Editor Liu Y L- Editor McGowan D E- Editor Liu Y

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