Abstract
Background/Aims
Preoperative lymph node staging in gastric cancer patients is important. The aim of this study was to assess the diagnostic accuracy of computed tomography (CT) in assessing lymph nodes in patients with gastric cancer.
Methods
A total of 56 patients had undergone standardized gastric resection with lymphadenectomy between October 2013 and June 2015 were reviewed retrospectively. The short axis diameter of the largest lymph node per station was recorded when reviewing the preoperative CT images. Diagnostic accuracy was calculated by comparing CT with histopathological findings.
Results
In 518 stations dissected at surgery, 56 included lymph nodes with metastasis. Among them, lymph nodes were visualized on preoperative CT in 26 stations. No lymph node was detected in 382 stations among 462 infiltration-negative stations. The cutoff of 12 mm had the highest accuracy rate of 0.896.
Conclusion
The accuracy of CT in the preoperative diagnosis of lymph node metastasis in patients with gastric cancer remains poor. Therefore, surgeons should pay attention to the visibility of lymph nodes on CT. Detection of lymph nodes on CT can be utilized for a more accurate diagnosis such as fine-needle aspiration biopsy.
Key Words: Computed tomography, Gastric cancer, Lymph node metastasis
Introduction
Accurate preoperative evaluation, especially for lymph node metastasis, is important for determining the therapeutic options of patients with gastric cancer. The National Comprehensive Cancer Network guidelines [1] state that perioperative chemotherapy or preoperative chemoradiation is the preferred approach for clinical stage II (T2-3/N+ or T4) or more advanced gastric cancers. The Japanese gastric cancer treatment guidelines 2010 (ver. 3) [2] recommend a D1 lymphadenectomy for cT1N0 tumors and a D2 lymphadenectomy for potentially curable T2-4 tumors as well as cT1N+ tumors. The revised Japanese Classification of Gastric Carcinoma [3] and the new TNM staging system [4] require the selective identification of single lymph nodes to differentiate between clinical N stages, thus further complicating evaluation.
At our institute, the most commonly used diagnostic method for lymph node staging of gastric cancer patients is 64-slice multidetector-row computed tomography (CT). So far, lymph nodes >10 mm in size are considered to be metastasis-positive in usual clinical settings [5]. Recently, since the adaptation of laparoscopic gastrectomy has been expanded and adapted for cT2-3N0 tumors, preoperative lymph node staging in gastric cancer patients has become more important.
The aim of this study was to assess the preoperative diagnostic accuracy of lymph node involvement in patients with gastric cancer using CT, and to define standard diagnostic criteria.
Methods
From October 2013 to June 2015, 80 consecutive patients underwent surgery for gastric cancer at St. Luke's International Hospital. Of those, patients with residual stomach cancer, those who underwent bypass surgery or probe laparotomy alone, and those who were treated with neoadjuvant chemotherapy were excluded. The present study included the remaining 56 patients who underwent standardized gastric resection with lymphadenectomy and who were reviewed retrospectively. All patients had been examined by CT before the surgery, and all tumors had been histopathologically diagnosed as adenocarcinomas of the stomach. The patients had undergone distal/total/proximal gastrectomy with standard lymph node dissection. The type of gastrectomy had been decided after considering the tumor location and progression according to the Japanese gastric cancer treatment guidelines 2010 (ver. 3) [2].
Two experienced radiologists (T.W., T.K.) who were blinded to the surgical or histopathological findings reviewed the axial CT images with a section thickness of 5 mm. The short axis diameter of the largest lymph node per station was measured and recorded. Some typical CT scan images are shown in Figure 1. The locations of the lymph nodes were based on the revised Japanese Classification of Gastric Carcinoma [3]. Diagnostic accuracy was calculated by comparing the CT scan with the histopathological findings.
First, we assessed the preoperative diagnostic accuracy of lymph node involvement per station and defined the standard diagnostic criteria. Although we usually use a cutoff value of 10 mm for the diagnosis of lymph node metastasis of gastric cancer, we evaluated the accuracy rate using various cutoff values in this study. Second, the diagnostic accuracy of lymph node involvement per patient (N0 or N+) was confirmed. Third, the distribution of lymph nodes visualized on CT and those with infiltration was investigated, and the diagnostic accuracy of lymph node metastasis in each station was confirmed.
The t test was used for comparisons of continuous data between two groups. A p value <0.05 was considered significant. Statistical analysis was performed using the SPSS statistical package, version 15.0 (SPSS Inc., Chicago, IL, USA).
Our study had approval of the institutional ethics review board, and written informed consent for preoperative staging with CT and surgery had been obtained from all patients.
Results
The characteristics of the 56 patients are summarized in Table 1. Histopathological lymph node metastases were present in 21 patients (37.5%). At surgery, 1,661 lymph nodes (median 28 lymph nodes per patient) were dissected, of which 152 (9.2%) were histopathologically infiltrated.
Table 1.
Median age, years (range) | 68 (51 – 93) |
Gender | |
Male | 35 |
Female | 21 |
Type of gastrectomy | |
Distal | 42 |
Total | 9 |
Proximal | 5 |
PT | |
T1 | 34 |
T2 | 8 |
T3 | 7 |
T4 | 7 |
pN | |
N0 | 35 |
N1 | 11 |
N2 | 1 |
N3 | 9 |
p stage | |
I | 36 |
II | 10 |
III | 5 |
IV | 5 |
Median number of dissected | |
lymph nodes (IQR) | 28 (20 ' 39) |
IQR, interquartile range.
When analyzed in terms of lymph node station, 518 stations were dissected at surgery, of which 56 (10.8%) included lymph node(s) with metastasis (Table 2). Among these 56 infiltrated lymph node stations, lymph nodes were visualized on the preoperative CT in 26 stations. On the other hand, no lymph node was detected in 382 stations among 462 infiltration-negative lymph node stations. The size of the lymph nodes visualized on CT was rational in infiltration-positive and -negative stations. The size of the largest lymph node visualized on CT was 11 mm in infiltration-negative stations.
Table 2.
Infiltration in dissected lymph node station |
||
---|---|---|
positive(n = 56) | negative (n = 462) | |
Number of stations on CT | ||
With visible lymph node | 26 | 80 |
Without visible lymph node | 30 | 382 |
Size of visible lymph nodes, mm | ||
Median | 6.5 | 5.3 |
Range | 1.4 ' 19 | 1.0 ' 11 |
The diagnostic accuracy of lymph node involvement per station is shown in Table 3. Using each cutoff value between 1 and 12 mm, all parameters, including sensitivity, specificity, positive predictive value, negative predictive value, and accuracy, are shown. Of these cutoff values, the cutoff of 12 mm had the highest accuracy rate of 0.896. To maximize sensitivity, when lymph nodes detected on CT were defined to be positive (cutoff = 1 mm), sensitivity was 0.464. To maximize specificity, when a lymph node <12 mm was defined to be negative on CT (cutoff = 12 mm), accuracy was 0.896 (specificity 1.000).
Table 3.
Cutoff, mm | Sensitivity | Specificity | PPV | NPV | Accuracy |
---|---|---|---|---|---|
12 | 0.036 | 1.000 | 1.000 | 0.895 | 0.896 |
10 | 0.054 | 0.994 | 0.500 | 0.896 | 0.892 |
8 | 0.179 | 0.970 | 0.417 | 0.907 | 0.884 |
5 | 0.357 | 0.894 | 0.290 | 0.920 | 0.836 |
1 | 0.464 | 0.827 | 0.245 | 0.927 | 0.788 |
PPV, positive predictive value; NPV, negative predictive value.
The diagnostic accuracy of lymph node involvement per patient is shown in Table 4. Among these cutoff values, the cutoff of 12 mm also had the highest accuracy rate of 0.661. To maximize sensitivity, when lymph nodes detected on CT were defined to be positive (cutoff = 1 mm), sensitivity was 0.905. To maximize specificity, when a lymph node <12 mm was defined to be negative on CT (cutoff = 12 mm), accuracy was 0.661 (specificity 1.000).
Table 4.
Cutoff, mm | Sensitivity | Specificity | PPV | NPV | Accuracy |
---|---|---|---|---|---|
12 | 0.095 | 1.000 | 1.000 | 0.648 | 0.661 |
10 | 0.143 | 0.886 | 0.429 | 0.633 | 0.607 |
8 | 0.381 | 0.743 | 0.471 | 0.667 | 0.607 |
5 | 0.714 | 0.257 | 0.366 | 0.600 | 0.429 |
1 | 0.905 | 0.171 | 0.396 | 0.750 | 0.446 |
PPV, positive predictive value; NPV, negative predictive value.
The distribution of lymph nodes and the diagnostic accuracy in each station are shown in Table 5. In stations #5 (suprapyloric) and #11 (splenic artery), there were some lymph node metastases, although preoperative CT could not detect them. Many swelled lymph nodes were visible on CT in stations #8a (common hepatic artery), #12a (proper hepatic artery), and #13 (posterior pancreatic head), regardless of the presence of metastasis.
Table 5.
Station1 | With visible LN on CT |
With infiltration, n | |
---|---|---|---|
n | median size, mm | ||
Perigastric | |||
#1 | 19 | 6.2 | 4 |
#2 | 0 | – | 0 |
#3 | 25 | 5.7 | 12 |
#4sa | 1 | 3.0 | 0 |
#4sb | 2 | 4.0 | 0 |
#4d | 20 | 4.7 | 11 |
#5 | 0 | – | 3 |
#6 | 12 | 4.9 | 10 |
Intermediate | |||
#7 | 6 | 5.7 | 4 |
#8a | 19 | 5.3 | 5 |
#9 | 2 | 9.3 | 3 |
#10 | 0 | – | 0 |
#11 | 0 | – | 1 |
#12a | 25 | 4.4 | 2 |
Distant | |||
#13 | 6 | 4.5 | 0 |
#14v | 1 | 6.3 | 1 |
#16 | 4 | 5.4 | 0 |
LN, lymph node.
According to the Japanese Classification of Gastric Carcinoma [3]. #1, right paracardial; #2, left paracardial; #3, lesser curvature; #4sa, short gastric arteries; #4sb, left gastroepiploic artery; #4d, greater curvature; #5, suprapyloric; #6, infrapyloric; #7, left gastric artery; #8a, common hepatic artery; #9, celiac artery; #10, splenic hilar; #11, splenic artery; #12a, proper hepatic artery; #13, posterior pancreatic head; #14v, superior mesenteric vein; #16, paraaortic.
Discussion
The accuracy of CT in the preoperative diagnosis of lymph node metastasis in gastric cancer patients in this study was poor. Our data failed to confirm a close correlation between size and infiltration using CT. Although multidetector-row CT scan is nevertheless the most widely used standard diagnostic tool, it is not considered the gold standard technique for N staging [6].
To improve the accuracy of the preoperative diagnosis of lymph node metastasis in gastric cancer patients, various methods have been reported. Although lymph nodes >8 mm in the short axis diameter are generally considered to be positive, different criteria have been proposed for assessing nodal status, including a size >6 mm plus round shape, a size >8 mm irrespective of axis, or a simple radiological detection of node [7,8]. A modified analytical technique on CT includes size and other characteristics such as marked enhancement, necrosis, shape, and fat content [9,10]. The accuracy in detecting lymph node metastasis with the conventional diagnostic tool is only around 60–80%, even when these other techniques are used [11]. In order to confirm the accuracy of preoperative imaging diagnosis for stage III gastric cancer, a validity study (JCOG 1302-A, “PRIMA-GC study”) is now ongoing in Japan.
Regarding other modalities, Kwee and Kwee reviewed the diagnostic accuracy of preoperative N staging by comparing endoscopic ultrasound, magnetic resonance imaging, positron emission tomography-CT, and CT [12]. In their study, the accuracy of N status diagnosis ranged from 40 to 90%. Although endoscopic ultrasound showed an accuracy similar to that of CT, the ultrasound is not objective and presents difficulty in evaluating lymph nodes that are located farther from the gastric wall. The diagnostic accuracy of magnetic resonance imaging is also poor. Low accuracy was also reported in positron emission tomography-CT studies due to the low sensitivity in detecting lymph node metastasis with fluorodeoxyglucose.
The limitation of our study was the small number of patients. However, if we analyze a larger number, the result may not change because the ability of CT to detect lymph nodes is very poor. Moreover, lymph node metastases were evaluated in each region, not for each lymph node individually, because it is hard to match the lymph nodes dissected during surgery with those evaluated on CT. The most important point in our study for clinical use may be the accurate diagnosis of clinical N status, not of individual nodal status. However, the diagnosis of lymph node metastases per patient (N0 or N+) was difficult to do on CT in this study.
Additional findings obtained from the analysis per station in our study were as follows: (1) In stations #5 (suprapyloric) and #11 (splenic artery), there were some lymph node metastases, although preoperative CT could not detect them. Therefore, surgeons should pay special attention to cases like these. (2) Many swelled lymph nodes were visible on CT in stations #8a (common hepatic artery), #12a (proper hepatic artery), and #13 (posterior pancreatic head), regardless of the presence of metastasis. There is a possibility of overtreatment with preoperative chemoradiotherapy or extended lymph node dissection if they are performed on the basis of the findings of #8a, #12a, or #13 lymph node swelling. Since lymph nodes are visible on CT, we can introduce endoscopic ultrasound-fine-needle aspiration biopsy for a more accurate diagnosis.
In conclusion, the accuracy of CT in the preoperative diagnosis of lymph node metastasis in patients with gastric cancer remains poor. Since lymph node metastases present at a certain frequency in gastric cancer patients, systematic dissection of lymph nodes must be performed at surgery, even when no lymph nodes are detected on preoperative CT. Gastric surgeons as well as radiologists should keep in mind that visible lymph nodes on CT are not necessarily metastatic and that lymph node detection on CT can be utilized to introduce endoscopic ultrasound-fine-needle aspiration biopsy.
Disclosure Statement
The authors have no conflicts of interest to declare in association with this study.
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