Literature DB >> 26912060

Prognostic value of three different lymph node staging systems in the survival of patients with gastric cancer following D2 lymphadenectomy.

Chen Jian-Hui1,2, Cai Shi-Rong1,2, Wu Hui1,2, Chen Si-le1,2, Xu Jian-Bo1,2, Zhai Er-Tao1,2, Chen Chuang-Qi1,2, He Yu-Long3,4.   

Abstract

The log odds of positive lymph nodes (LODDS) was defined as the log of the ratio between the number of positive lymph nodes and the number of negative lymph nodes, which is a novel and promising nodal staging system for gastric cancer. Here, we aimed to compare the prognostic effect of pN, lymph node ratio (LNR) and LODDS. The association between overall survival and pN, LNR and LODDS was retrospectively analysed. The discriminatory ability and monotonicity of gradients (linear trend χ (2) score), homogeneity ability (likelihood ratio test) and prognostic stratification ability (Akaike information criterion [AIC] and receiver operating characteristic [ROC] curve) were compared among three lymph node staging systems. The pN, LNR and LODDS were all identified as independent prognostic factors for gastric cancer patients in the multivariate analysis. LODDS showed the best prognostic performance (linear trend χ (2) score 266.743, likelihood ratio χ (2) test score 427.771, AIC value 5670.226, area under the curve (AUC) 0.793), followed by LNR and pN. In patients with different levels of retrieved lymph nodes (≤10, 11-14, 15-25 and >25), LODDS was the most powerful for prognostic prediction and discrimination of the heterogeneity among the subgroups. Significant differences in survival were observed among patients in different LODDS subgroups after being classified according to the pN and LNR classifications. LODDS appears to be a more powerful system for predicting the overall survival of gastric cancer patients, as compared to LNR and pN, and may serve as an alternative nodal staging system for gastric cancer.

Entities:  

Keywords:  Gastric cancer; Log odds of positive lymph nodes; Lymph node ratio; Nodal system; Prognosis

Mesh:

Year:  2016        PMID: 26912060      PMCID: PMC4999458          DOI: 10.1007/s13277-015-4191-7

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


Introduction

According to the GLOBOCAN 2012 database, 952,000 new cases of gastric cancer and 723,000 cases of gastric cancer-related death are reported worldwide, which correspond to the total malignant cases of 8.5 and 10.1 %, respectively. Lymph node metastasis is known to be one of the most important prognostic factors for gastric cancer. Although the lymph node staging system, based on the extent of lymph node metastasis, was abandoned in the latest guideline of the Japanese Gastric Cancer Association (JGCA) [1], the prognostic ability of the lymph node staging system of the Union for International Cancer Control (UICC) remains controversial. Some authors indicated that the latest lymph node classification, as part of UICC staging, is influenced by the number of retrieved lymph nodes [2]. Moreover, certain studies suggested that the ratio-based lymph node system, which evaluates the ratio of metastatic lymph nodes and total retrieved lymph nodes, was theoretically superior to the involved number-based lymph node system, as the former system considers information of both metastatic and the total retrieved lymph nodes [3, 4]. The favourable results obtained from a comparison of survival with the ratio-based lymph node system suggest that this system may serve as an alternative to the traditional one. However, some studies indicated that patients with the same LNR staging had different survival outcomes, along with changes in the total number of retrieved lymph nodes, particularly when the LNR value was 0 or 1 [5]. Log odds of positive nodes (LODDS) is a novel, promising lymph node staging system and is defined as the log of the ratio of the number of positive lymph nodes and the total number of retrieved lymph nodes. The LODDS system has a better discrimination ability for patients without metastatic lymph nodes and has been considered as a more reliable method than the pN or LNR systems for prognostic evaluation in gastric cancer patients [6, 7]. Till now, there is no study to compare the prognostic significance of pN, LNR and LODDS systems together in Asian patients after D2 lymphadenectomy. In the present study, we aimed to compare the prognostic performance of the pN, LNR and LODDS lymph node staging systems and to determine the most appropriate lymph node staging system for predicting overall survival in gastric cancer patients.

Materials and methods

Patients and surveillance

Between January 1994 and December 2008, all the cases diagnosed with gastric adenocarcinoma after radical surgery in the Department of Gastrointestinal Surgery of the First Affiliated Hospital, Sun Yat-sen University, China, were retrospectively analysed. The eligibility criteria were as follows: patients with gastric adenocarcinoma diagnosed via a histopathologic examination; patients receiving R0 resection and D2 lymphadenectomy, or extensive lymphadenectomy if necessary; patient death due to cancer and patients with complete follow-up data. The exclusion criteria were as follows: patients with a history of malignant tumours at other sites or gastric stump cancer. patients who were diagnosed with distant metastasis preoperatively or during the operation, patients who received neoadjuvant chemotherapy or radiochemotherapy and patients who died due to postoperative complications. In total, 935 patients were included in this study. Written informed consent was obtained from all the patients preoperatively. The study was approved by the Ethics Committees of The First Affiliated Hospital of Sun Yat-sen University. All the cases were followed up every 3 months in the first 2 years, every half year in the after 3 years and every year thereafter. Follow-up program consisted of physical examination, serum tumour markers, chest X-ray, annual gastroscope, abdominal CT scan or ultrasound every 6 months. The last follow-up was in December 2014. The median follow-up time was 56 months.

Lymph node classifications

Lymph nodes were classified according to the seventh edition of the UICC/AJCC tumour-node-metastasis (TNM) system, based on the number of metastatic lymph nodes: N0, negative; N1, 1–2 positive lymph nodes; N2, 3–6 positive lymph nodes; N3, >6 positive lymph nodes. The LNR was defined as the ratio between the metastatic lymph nodes and total retrieved lymph nodes. The LNR ranged from 0 to 1 and was stratified at intervals of 0.1; it was used to compare the overall survival among each interval and among adjacent subgroups with similar survival outcomes. The LNR system was classified as follows: LNR0, 0; 0.01 < LNR1 ≤ 0.1; 0.1 < LNR2 ≤ 0.25 and LNR3 > 0.25. LODDS was defined as log ([pLN + 0.5] / [nLN + 0.5]), where pLN is the number of positive lymph nodes and nLN is the number of negative lymph nodes; 0.5 was added to both the numerator and denomination to avoid singularity. A similar method was performed to stratify LODDS, with an interval of 0.5. Thus, LODDS was classified as follows: LODDS1 ≤ −1.5, −1.5 < LODDS2 ≤ −1.0, −1.0 < LODDS3 ≤ 0.0 and LODDS4 > 0.0.

Statistical analysis

The overall survival rate was calculated according to the life table method, and the log-rank test was used to assess statistical differences between groups. Survival curves were established using the Kaplan-Meier method. All the parameters that were statistically significant in the univariate analysis were included in the multivariate Cox proportional hazard model. With the Cox proportional hazard model, the likelihood ratio (χ 2) test was used to measure homogeneity between groups, whereas the Akaike information criterion (AIC) was adopted to minimise any potential bias when comparing different prognostic systems. The AIC was defined by a −2 log maximum likelihood +2, multiplied by the number of parameters in the model. The discriminatory ability and monotonicity of gradients were measured using the linear trend χ 2 test. The accuracy of the prognostic evaluation of different staging systems was compared using receiver operating characteristic (ROC) curve analysis and the area under the curve (AUC). The accepted level of statistical significance was defined as P < 0.05. The statistical analysis was performed using the SPSS 18.0 statistical package (SPSS Inc., Chicago, IL).

Results

Clinicopathological characteristics and survival analysis

In total, 935 patients were enrolled, including 636 men and 299 women, with a mean age of 57.5 years (range, 24–87 years). The gastric cancer was located in the lower part of the stomach (44.7 %) in most cases, followed by the upper portion (31.6 %), middle portion (21.7 %) and the entire stomach (2.0 %). Moreover, the average number of total retrieved lymph nodes was 24.9 per case (range, 0–140). The mean number of involved lymph nodes in our cohort was 4.61 (range, 0–124). Among 18.6 % of the patients, lymph node retrieval was insufficient. The 5-year survival rate of our cohort was 54.0 %, with a median overall survival time of 53.3 months (range, 1.3–148.4 months). Table 1 shows the demographics and survival results of our study.
Table 1

Clinicopathological characteristics and survival analysis of 935 patients with gastric cancer following radical gastrectomy

VariablePatients (%)5-year survival rate χ 2 value (log-rank test) P value
Age (years)7.67670.006
 <60526 (56.3 %)57.2 %
 ≧60409 (43.7 %)49.9 %
Sex3.1900.074
 Male636 (68.0 %)52.0 %
 Female299 (32.0 %)58.2 %
Tumour site30.575<0.001
 Upper295 (31.6 %)43.1 %
 Middle203 (21.7 %)60.1 %
 Lower418 (44.7 %)60.0 %
 Whole19 (2.0 %)26.3 %
Tumour size79.694<0.001
 <5 cm613 (65.6 %)63.4 %
 ≧5 cm322 (34.4 %)36.0 %
Gross type69.323<0.001
 Borrmann I + II351 (37.5 %)71.5 %
 Borrmann III + IV584 (62.5 %)43.4 %
Degree of differentiation12.898<0.001
 Well/moderately340 (36.4 %)61.1 %
 Pooly/undifferentiated595 (63.6 %)50.0 %
Seventh T stage (UICC)159.378<0.001
 T1 162 (17.3 %)86.4 %
 T2 125 (13.4 %)74.3 %
 T3 330 (35.3 %)52.4 %
 T4 318 (34.0 %)31.1 %
Seventh N stage (UICC)281.440<0.001
 N0364 (38.9 %)81.6 %
 N1172 (18.4 %)56.4 %
 N2199 (21.3 %)40.2 %
 N3200 (21.4 %)18.0 %
LNR stage368.726<0.001
 LNR0364 (38.9 %)81.6 %
 LNR1143 (15.3 %)63.6 %
 LNR2197 (21.1 %)42.6 %
 LNR3231 (24.7 %)14.3 %
LODDS stage428.720<0.001
 LODDS1277 (29.6 %)87.0 %
 LODDS2170 (18.2 %)65.9 %
 LODDS3385 (41.2 %)37.7 %
 LODDS4103 (11.0 %)7.0 %
Number of LN retrieved16.801<0.001
 <15174 (18.6 %)42.0 %
 ≧15761 (81.4 %)56.7 %
Clinicopathological characteristics and survival analysis of 935 patients with gastric cancer following radical gastrectomy

Survival impact of pN, R stage and LODDS

The survival curves of patients according to pN, LNR and LODDS were all significantly different (Fig. 1a–c) (all, P < 0.001). In the univariate analysis, age, tumour location, tumour size, gross type, histological type, number of retrieved lymph nodes, pN, LNR and LODDS were significantly correlated with overall survival (Table 2). All the potential prognostic factors identified in the univariate analysis were included in the multivariate analysis. All the three lymph node staging systems (pN, LNR and LODDS) were identified as significantly independent prognostic factors of overall survival in our cohort (Table 3).
Fig. 1

Kaplan-Meier analysis of overall survival (OS) for cases with gastric cancer according to different lymph node staging systems: a survival curves of patients according to the pN system, b survival curves of patients according to the LNR system and c survival curves of patients according to the LODDS system

Table 2

Univariate analysis of overall survival in gastric cancer

Parameters χ 2 valueHazard ratio95 % CIa P value
Age7.6191.2931.077–1.5510.006
Gender3.1830.074
Tumour location29.540<0.001
 Upper
 Middle12.3930.6320.489–0.816<0.001
 Lower17.2460.6450.525–0.794<0.001
 Whole3.4801.6790.974–2.8940.062
Tumour size75.3772.2511.874–2.703<0.001
Gross type65.0282.3931.936–2.959<0.001
Histological type12.7351.4301.175–1.741<0.001
T stage134.757<0.001
 T1
 T2 4.7731.7161.057–2.7870.029
 T3 42.4843.6452.470–5.377<0.001
 T4 91.6556.4494.403–9.446<0.001
Insufficient retrieved lymph nodes16.4840.6370.512–0.792<0.001
pN101.762<0.001
 pN0 (reference)
 pN1 11.4131.7161.254–2.3470.001
 pN2 37.0782.4611.842–3.289<0.001
 pN3 94.8074.2553.161–5.648<0.001
rN191.740<0.001
 rN0 (reference)
 rN1 20.9622.4071.653–3.506<0.001
 rN2 70.5924.0502.922–5.612<0.001
 rN3 174.15112.7568.739–18.618<0.001
LODDS427.771<0.001
 LODDS1 (reference)
 LODDS227.1662.6971.857–3.917<0.001
 LODDS3123.2865.7774.239–7.874<0.001
 LODDS4272.25519.59413.761–27.900<0.001

CI a confidence interval

Table 3

Multivariate analysis of overall survival in gastric cancer for the different lymph node staging systems

ParametersMultivariate analysis 1Multivariate analysis 2Multivariate analysis 3
HR95 % CIa p ValueHR95 % CIa p ValueHR95 % CIa P value
Age1.3691.139–1.6460.0011.4091.171–1.695<0.0011.3401.1141.6120.002
Gender
Tumour location
 Upper
 Middle
 Lower
 Whole
Tumour size1.3201.087–1.6030.0051.2571.034–1.5270.021
Gross type1.2921.024–1.6300.0311.3461.069–1.6850.01213451.073–1.6860.010
Histological type
T stage<0.001
 T1 (reference)
 T2 1.0930.664–1.7990.7281.0700.648–1.7650.7921.0290.625–1.6930.911
 T3 1.7611.150–2.6940.0091.7221.127–2.6330.0121.8181.197–2.7590.005
 T4 2.2241.440–3.433<0.0012.1731.409–3.350<0.0012.3631.550–3.603<0.001
Insufficient retrieved lymph nodes0.4880.389–0.612<0.0010.6220.499–0.776<0.0010.7480.597–0.938<0.001
pN<0.001
 pN0 (reference)
 pN1 1.6971.241–2.3200.001
 pN2 2.6101.951–3.491<0.001
 pN3 4.9873.704–6.714<0.001
rN<0.001
 rN0 (reference)
 rN1 1.6171.142–2.290.007
 rN2 2.4861.843–3.353<0.001
 rN3 5.7024.280–7.596<0.001
LODDS<0.001
 LODDS1 (reference)
 LODDS22.1441.457–3.153<0.001
 LODDS33.8402.765–5.333<0.001
 LODDS412.0358.234–17.590<0.001

CI a confidence interval

Kaplan-Meier analysis of overall survival (OS) for cases with gastric cancer according to different lymph node staging systems: a survival curves of patients according to the pN system, b survival curves of patients according to the LNR system and c survival curves of patients according to the LODDS system Univariate analysis of overall survival in gastric cancer CI a confidence interval Multivariate analysis of overall survival in gastric cancer for the different lymph node staging systems CI a confidence interval

Comparison of prognostic ability among pN, R stage and LODDS

To identify the most appropriate system of representing lymph node involvement for the evaluation of overall survival in gastric cancer patients, we adopted the linear trend χ 2 score to evaluate the discriminatory ability and monotonicity of gradients, the likelihood ratio (χ 2) test to assess homogeneity ability and AIC value and ROC curve to compare the prognostic ability among the systems. We observed that LODDS had the highest linear trend χ 2 score and likelihood ratio (χ 2) test score, lowest AIC value and largest AUC (Table 4). Therefore, we considered that the LODDS was superior to LNR and pN.
Table 4

Prognostic ability comparison among the different lymph node staging systems for gastric cancer

Linear trend χ 2 scoreLikelihood ratio χ 2 testAIC valueROC area
Seventh UICC pN215.021280.8265769.0370.767
rN262.177367.9085706.2940.793
LODDS266.743427.7715670.2260.793
Prognostic ability comparison among the different lymph node staging systems for gastric cancer To elucidate the reason for the superiority of LODDS compared to pN and LNR, we created scatter plots of the relationship between LODDS and the number or ratio of lymph node involvement. As shown in Fig. 2a, b, the LODDS value increased with the number and the ratio of metastatic lymph nodes, indicating close relationships between LODDS and pN, as well as LNR. However, these correlations were not linear. When the number of lymph nodes involved was ≤10 or when the ratio of lymph node metastasis was <0.2, the curves of pN and LNR increased at a slower rate as compared to the LODDS, indicating that LODDS could be superior to pN and LNR in the prediction of long-term overall survival of the cases mentioned above. Moreover, when the ratio of lymph node metastasis was 0 or 1, the LODDS score was heterogeneous, indicating that the LODDS system had the potential to indicate different survival outcomes for patients with the same LNR stage, especially for cases with an LNR score of 0 or 1.
Fig. 2

Scatter plots of the relationship between LODDS and the number or ratio of lymph nodes involved: a scatter plots of the relationship between LODDS and the number of metastatic lymph nodes and b scatter plots of the relationship between LODDS and LNR

Scatter plots of the relationship between LODDS and the number or ratio of lymph nodes involved: a scatter plots of the relationship between LODDS and the number of metastatic lymph nodes and b scatter plots of the relationship between LODDS and LNR

Correlation among the total number of retrieved lymph nodes, pN, LNR and LODDS

A Pearson test was conducted to evaluate the correlation of the total number of retrieved lymph nodes with the pN, LNR and LODDS systems. A strong relationship was observed between the total number of retrieved lymph nodes and the number or ratio of metastatic lymph nodes (r = 0.214 and 0.077, P < 0.001 and 0.018, respectively). However, there was no association between the number of retrieved lymph nodes and LODDS (r = −0.038, P = 0.251). The results of Pearson analysis indicated that LODDS was positively correlated with pN and LNR (r = 0.868 and 0.888, P < 0.001 and <0.001, respectively), whereas a strong relationship was present between pN and LNR (r = 0.938, P < 0.001).

Evaluation of the prognostic value of different lymph node staging systems with different levels of retrieved lymph nodes

To assess the prognostic abilities of pN, LNR and LODDS with different levels of retrieved lymph nodes, all the patients were divided into four groups according to the number of retrieved lymph nodes: group 1 (≤10, n = 93), group 2 (11–14, n = 81), group 3 (15–25, n = 405) and group 4 (>25, n = 356). As shown in Table 5, pN, LNR and LODDS showed prognostic stratification abilities among the different subgroups. We further compared the prognostic performance among the groups. We noted that in all four groups, the LODDS system had the highest linear trend χ 2 score, likelihood ratio (χ 2) test score and lowest AIC value, followed by the LNR system and pN system. Similarly, the LODDS system had the largest AUC in group 1 and group 3. However, in group 2 and group 4, the LNR system had the largest AUC, followed by the LODDS and pN systems (Table 6).
Table 5

Evaluation of the prognostic value of the different lymph node systems with different levels of retrieved lymph nodes

Number5-year survival rate χ 2 value P value
Retrieved LN (≦10)93
Seventh UICC pN staging9.7920.020
 pN0 47 (50.5 %)61.7 %
 pN1 25 (26.9 %)40.0 %
 pN2 18 (19.4 %)33.3 %
 pN3 3 (3.2 %)0.0 %
pN ratio39.029<0.001
 rN0 47 (50.5 %)74.5 %
 rN1 5 (5.4 %)40.0 %
 rN2 15 (16.1 %)33.3 %
 rN3 26 (28.0 %)11.5 %
LODDS64.853<0.001
 LODDS14 (4.3 %)100.0 %
 LODDS242 (45.2 %)73.8 %
 LODDS335 (37.6 %)28.6 %
 LODDS412 (12.9 %)0.0 %
Retrieved LN (11–14)81
Seventh UICC pN staging33.848<0.001
 pN0 34 (42.0 %)91.2 %
 pN1 18 (22.2 %)27.8 %
 pN2 16 (19.8 %)25.0 %
 pN3 13 (16.0 %)23.1 %
pN ratio61.503<0.001
 rN0 34 (42.0 %)91.2 %
 rN1 9 (11.1 %)55.6 %
 rN2 18 (22.2 %)33.3 %
 rN3 20 (24.7 %)5.0 %
LODDS66.012<0.001
 LODDS13 (3.7 %)100.0 %
 LODDS231 (38.3 %)90.3 %
 LODDS334 (42.0 %)35.3 %
 LODDS413 (16.0 %)0.0 %
Retrieved LN (15–25)405
Seventh UICC pN staging101.302<0.001
 pN0 164 (40.5 %)79.9 %
 pN1 77 (40.5 %)57.1 %
 pN2 104 (25.7 %)41.3 %
 pN3 60 (14.8 %)18.3 %
pN ratio117.273<0.001
 rN0 164 (40.5 %)79.9 %
 rN1 62 (15.3 %)61.3 %
 rN2 96 (23.7 %)47.9 %
 rN3 83 (20.5 %)16.9 %
LODDS135.377<0.001
 LODDS1147 (36.3 %)85.7 %
 LODDS248 (11.9 %)52.1 %
 LODDS3175 (43.2 %)42.3 %
 LODDS435 (8.6 %)11.4 %
Retrieved LN (>25)356
Seventh UICC pN staging150.634<0.001
 pN0 119 (33.4 %)84.0 %
 pN1 53 (14.9 %)71.6 %
 pN2 60 (16.9 %)46.7 %
 pN3 124 (34.8 %)17.7 %
pN ratio160.727<0.001
 rN0 119 (33.4 %)84.0 %
 rN1 69 (19.4 %)68.1 %
 rN2 67 (18.8 %)40.3 %
 rN3 101 (28.4 %)13.9 %
LODDS173.033<0.001
 LODDS1123 (34.6 %)87.8 %
 LODDS249 (13.8 %)57.1 %
 LODDS3141 (39.6 %)34.8 %
 LODDS443 (12.1 %)7.0 %
Table 6

Comparison of prognostic value of the different pN staging systems with different levels of retrieved lymph nodes for gastric cancer

Linear trend χ 2 scoreLikelihood ratio χ 2 testAIC valueROC area
Retrieved LN (≦10)
 Seventh UICC pN9.5779.776410.0230.669
 rN28.11338.959384.1980.792
 LODDS29.65764.653370.8190.804
Retrieved LN (11–14)
 Seventh UICC pN24.72033.769306.7130.829
 rN39.79561.343292.0890.889
 LODDS49.66165.832290.8300.877
Retrieved LN (15–25)
 Seventh UICC pN80.198101.1102109.7850.747
 rN88.779117.0452099.3590.760
 LODDS95.421135.1262082.6450.763
Retrieved LN (>25)
 Seventh UICC pN111.970150.2291851.2480.809
 rN113.450160.3001848.6280.813
 LODDS114.897172.5731840.3840.810
Evaluation of the prognostic value of the different lymph node systems with different levels of retrieved lymph nodes Comparison of prognostic value of the different pN staging systems with different levels of retrieved lymph nodes for gastric cancer

Survival analysis of the pN and LNR subgroups according to the LODDS stratification

To evaluate the survival impact of the LODDS stratification as per the pN and LNR systems, all the distinct prognostic cohorts stratified according to the pN or LNR systems were analysed based on different LODDS stratifications. We observed that the LODDS could discriminate among N0, N1, N2 and N3, regardless of whether the pN or LNR system was used, suggesting that LODDS had excellent prognostic discriminatory ability to assess the current lymph node system. All the survival data and statistical results were shown in Table 7.
Table 7

Survival analysis of pN stage and rN systems according to the LODDS staging system

Number5-year survival rate χ 2 value P value
UICC pN
UICC pN0 22.895<0.001
 LODDS1267 (73.4 %)89.9 %
 LODDS297 (26.6 %)67.0 %
UICC pN1 28.892<0.001
 LODDS110 (5.8 %)90.0 %
 LODDS268 (39.3 %)64.7 %
 LODDS394 (54.3 %)46.8 %
 LODDS41 (0.6 %)0.0 %
UICC pN2 11.0040.004
 LODDS26 (3.0 %)83.3 %
 LODDS3184 (92.9 %)40.2 %
 LODDS48 (4.1 %)12.5 %
UICC pN3 17.658<0.001
 LODDS3106 (53.0 %)26.8 %
 LODDS494 (47.0 %)9.6 %
rN
rN0 22.895<0.001
 LODDS1267 (73.4 %)89.9 %
 LODDS297 (26.6 %)67.0 %
rN1 9.2650.010
 LODDS110 (6.8 %)90.0 %
 LODDS274 (50.7 %)69.2 %
 LODDS362 (42.5 %)50.4 %
rN2 6.3660.012
 LODDS219 (9.7 %)73.7 %
 LODDS3177 (90.3 %)40.1 %
rN3 22.961<0.001
 LODDS3126 (55.0 %)17.6 %
 LODDS4103 (45.0 %)9.7 %
Survival analysis of pN stage and rN systems according to the LODDS staging system

Discussion

Information on lymph node involvement in gastric cancer has a great clinical impact on treatment decisions and survival assessment. The number-based lymph node staging system of UICC classification (seventh edition) was widely used, although a principle flaw is that the prognostic accuracy is influenced by the number of total retrieved lymph nodes [8, 9]. The most recent NCCN guideline recommends that D2 lymphadenectomy should be used to remove an adequate number of lymph nodes (no less than 15); however, some studies reported that ≥15 lymph nodes are harvested in only 29 and 60.2 % of cases in the USA [10] and China [11]. Moreover, the optimal number of retrieved lymph nodes to avoid stage migration remains unclear in some studies [12, 13]. Hence, in cases where the number of tested lymph nodes was insufficient, the staging migration phenomenon may occur. The LNR system considers both the information of nodal involvement and total lymph nodes tested and can theoretically overcome the limitations of number-based nodal system. Most authors indicated that LNR was superior to the pN system due to the presence of a larger power for minimising staging migration [14]. A recent large cohort study (nearly 9000 cases) on gastric cancer in Korea [15] concluded that the LNR system is a better alternative for predicting long-term survival and compensating for the stage migration effect. However, due to some limitations, it cannot be considered as an alternative to the current pN staging. First, there is no difference among the patients with negative lymph nodes between the pN and LNR systems, indicating that LNR does not have the ability to distinguish the difference in survival in pN0 patients. Moreover, the cut-off value of LNR reported in several studies is varied [14, 16, 17]. In addition, the patients in the same LNR stage may have different survival outcomes, with a different number of tested lymph nodes [18]. LODDS—a novel system for assessing the status of lymph node involvement—is an alternative option for the evaluation of metastatic lymph nodes to predict overall survival; however, this system has only been investigated in cases of colon cancer and breast cancer. Following the report of Sun [6] who emphasised the favourable prognostic impact of LODDS in gastric cancer, some studies in China and North America have validated its use for prognostic purposes. Another study [11] proposed a new tumour-LODDS-metastasis (TLM) classification, which was based on the LODDS system, and was superior to the TNM and tumour-ratio-metastasis (TRM) classifications in the prognostic assessment of cases following D2 lymphadenectomy. Some studies did not note any superiority of LODDS over the pN or LNR systems [10, 19]. Yu [20] indicated the LODDS system may reflect a false survival outcome for patients with gastric cancer, with a reduced true hazard ratio of the N status against survival. An ideal lymph node staging system should satisfy three conditions [21]: decreased patient survival with increasing stage (monotonicity), similar survival within a group (homogeneity) and difference in survival between groups (distinctiveness). To our knowledge, the present study is the first to compare the above three conditions among the pN, LNR and LODDS systems. In multivariate Cox regression analysis in the present study, the pN, LNR and LODDS systems were all found to be independent parameters for overall survival. Moreover, the LODDS system had the highest linear trend χ 2 score, likelihood ratio (χ 2) test score, largest AUC and lowest AIC value, indicating that the LODDS system was superior to both the pN system and LNR system. Theoretically, the LODDS system was superior to the pN system in minimising stage migration, particularly in cases where the number of analysed lymph nodes was insufficient [22]. We further interpret that this novel system had a remarkable robustness in terms of the prognostic effect and discrimination ability at different levels of tested lymph nodes. As shown in Table 5, when the number of retrieved lymph nodes was insufficient (≤10 or 11–14), the LODDS system had the best performance in homogeneity, discriminatory ability, monotonicity of gradients and accuracy of the prognosis evaluation, followed by the LNR system and pN system. Moreover, in the present study, the pN and LNR systems were positively correlated with the number of retrieved lymph nodes. However, unlike that reported in the study of Qiu [11], we found that there was no relationship between the number of tested lymph nodes and the LODDS system, indicating that the LNR and pN systems were affected by the total number of tested lymph nodes, whereas the LODDS system was unaffected. Moreover, Aurello [23] reported that the LODDS system was a function of the number of negative lymph nodes, whereas the LNR system was a function of the number of total retrieved lymph nodes; hence, theoretically, the LODDS system was superior to the LNR system. Jiao [24] explained that cases with an increasing number of tested lymph nodes may reflect better survival, particularly in patients with node-negative gastric cancer. For patients with an LNR value 0 or 1, the LNR system had no discriminatory power. As shown in Fig. 2b, the LODDS system can distinguish patients with an LNR value 0 or 1, which accounted for 39.6 % of the total number of patients. Moreover, using the log-rank test, we noted that LODDS had the ability to distinguish between patients with different pN or LNR systems into distinct prognostic groups. This evidence strongly suggests that the LODDS system may be the most reliable method for lymph node classification in gastric cancer. Our study had certain limitations. First, all data was obtained from a single institution, and this may not reflect the status in other centres in China. Moreover, the method of calculation in the LODDS system was complicated, which may limit the clinical application of the LODDS system. In conclusion, the pN, LNR and LODDS systems appear to be independent prognostic factors, as determined by the multivariate analysis. Although the LODDS system was more complex, it showed prognostic superiority over both the pN and LNR systems in our study. It can discriminate survival differences of gastric cancer patients with negative lymph nodes and an insufficient number of retrieved lymph nodes. Hence, the LODDS system should be considered as a novel and promising lymph node staging system for gastric cancer in the future.
  23 in total

1.  Evaluation of the prognostic value of the metastatic lymph node ratio for gastric cancer.

Authors:  Bao-Yan Zhang; Jing Yuan; Zhen-Shuang Cui; Zhong-Wu Li; Xiang-Hong Li; You-Yong Lu
Journal:  Am J Surg       Date:  2013-10-12       Impact factor: 2.565

2.  Prognostic impact of lymph node retrieval and ratio in gastric cancer: a U.S. single center experience.

Authors:  Joyce Wong; Shams Rahman; Nadia Saeed; Hui-Yi Lin; Khaldoun Almhanna; Ravi Shridhar; Sarah Hoffe; Kenneth L Meredith
Journal:  J Gastrointest Surg       Date:  2013-10-16       Impact factor: 3.452

3.  The impact of calculation procedure on the hazard ratio of N classifications.

Authors:  Cunjun Yu; Zhu Ying; Wenping Chen
Journal:  Ann Surg Oncol       Date:  2011-06-03       Impact factor: 5.344

4.  Does a minimum number of 16 retrieved nodes affect survival in curatively resected gastric cancer?

Authors:  A Biondi; D D'Ugo; F C M Cananzi; V Papa; A Borasi; F Sicoli; M Degiuli; G Doglietto; R Persiani
Journal:  Eur J Surg Oncol       Date:  2015-04-08       Impact factor: 4.424

5.  Cancer of the esophagus and esophagogastric junction: data-driven staging for the seventh edition of the American Joint Committee on Cancer/International Union Against Cancer Cancer Staging Manuals.

Authors:  Thomas W Rice; Valerie W Rusch; Hemant Ishwaran; Eugene H Blackstone
Journal:  Cancer       Date:  2010-08-15       Impact factor: 6.860

6.  Prognostic value of metastatic lymph node ratio as an additional tool to the TNM stage system in gastric cancer.

Authors:  X-J Wu; R-L Miao; Z-Y Li; Z-D Bu; L-H Zhang; A-W Wu; X-L Zong; S-X Li; F Shan; X Ji; H Ren; J-F Ji
Journal:  Eur J Surg Oncol       Date:  2015-04-03       Impact factor: 4.424

7.  Metastatic lymph node ratio successfully predicts prognosis in western gastric cancer patients.

Authors:  Onur C Kutlu; Mitchell Watchell; Sharmila Dissanaike
Journal:  Surg Oncol       Date:  2015-03-24       Impact factor: 3.279

8.  Prognostic value of number of examined lymph nodes in patients with node-negative gastric cancer.

Authors:  Xu-Guang Jiao; Jing-Yu Deng; Ru-Peng Zhang; Liang-Liang Wu; Li Wang; Hong-Gen Liu; Xi-Shan Hao; Han Liang
Journal:  World J Gastroenterol       Date:  2014-04-07       Impact factor: 5.742

9.  The tumor-log odds of positive lymph nodes-metastasis staging system, a promising new staging system for gastric cancer after D2 resection in China.

Authors:  Miao-zhen Qiu; Hui-juan Qiu; Zhi-qiang Wang; Chao Ren; De-shen Wang; Dong-sheng Zhang; Hui-yan Luo; Yu-hong Li; Rui-hua Xu
Journal:  PLoS One       Date:  2012-02-14       Impact factor: 3.240

10.  Prognostic significance of metastatic lymph node ratio in patients with gastric cancer: an evaluation in north-East of iran.

Authors:  Ali Taghizadeh-Kermani; Seyede Zeinab Yahouiyan; Mohsen AliAkbarian; Mehdi Seilanian Toussi
Journal:  Iran J Cancer Prev       Date:  2014
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  14 in total

1.  The prognostic value of lymph nodes count on survival of patients with node-negative gastric cancer.

Authors:  Wei-Feng Zheng; Ting-Ting Ji; Yong Lin; Rong-Zhou Li
Journal:  Oncotarget       Date:  2016-07-12

2.  Comparison of different lymph node staging systems in prognosis of gastric cancer: a bi-institutional study from Hungary.

Authors:  Dezső Tóth; Adrienn Bíró; Zsolt Varga; Miklós Török; Péter Árkosy
Journal:  Chin J Cancer Res       Date:  2017-08       Impact factor: 5.087

3.  The prognostic value of negative lymph node count for patients with gastric cancer who received preoperative radiotherapy.

Authors:  Xinxing Li; Weigang Zhang; Xianwen Zhang; Haolu Wang; Kai Xu; Houshan Yao; Jun Yao; Xiaowen Liang; Zhiqian Hu
Journal:  Oncotarget       Date:  2017-07-18

4.  Prognostic value of the number of negative lymph nodes in esophageal carcinoma without lymphatic metastasis.

Authors:  HanRan Wu; ChangQing Liu; MeiQing Xu; MingFa Guo; ShiBin Xu; MingRan Xie
Journal:  Thorac Cancer       Date:  2018-06-28       Impact factor: 3.500

5.  Isolation of circulating tumor cells in patients undergoing surgery for esophageal cancer and a specific confirmation method.

Authors:  Yunpeng Zhao; Shukang Zhao; Yingjie Chen; Xiaopeng Dong; Chuanliang Peng; Qifeng Sun; Lei Shan; Zhendan Wang; Xiaogang Zhao
Journal:  Oncol Lett       Date:  2019-02-06       Impact factor: 2.967

6.  Anatomical location-based nodal staging system is superior to the 7th edition of the American Joint Committee on Cancer staging system among patients with surgically resected, histologically low-grade gastric cancer: A single institutional experience.

Authors:  Mei-Wen Chen; Chien-Pin Chan; Yih-Jeng Lin; Hsu-Heng Yen
Journal:  PLoS One       Date:  2019-02-05       Impact factor: 3.240

7.  Construction of a nomogram for the prediction of prognosis in patients with resectable gastric cancer undergoing fewer than sixteen lymph node biopsies.

Authors:  Zhe Li; Hong Cen
Journal:  Onco Targets Ther       Date:  2019-09-11       Impact factor: 4.147

8.  Lymph Node Yield Following Packet Submission After Isolation By Surgeon During Gastrectomy.

Authors:  Pengpeng Wang; Kecheng Zhang; Hongqing Xi; Wenquan Liang; Tianyu Xie; Yunhe Gao; Bo Wei; Lin Chen
Journal:  Cancer Manag Res       Date:  2019-11-19       Impact factor: 3.989

9.  Increased number of negative lymph nodes is associated with improved survival outcome in node positive gastric cancer following radical gastrectomy.

Authors:  Rong-Liang Shi; Qian Chen; Jun Bing Ding; Zhen Yang; Gaofeng Pan; Daowen Jiang; Weiyan Liu
Journal:  Oncotarget       Date:  2016-06-07

10.  Nodal staging score and adequacy of nodal staging.

Authors:  Hui-Min Chen; Ge Feng
Journal:  Onco Targets Ther       Date:  2019-01-08       Impact factor: 4.147

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