OL Oncology Letters 1792-1074 1792-1082 D.A. Spandidos 10.3892/ol.2016.4216 OL-0-0-4216 Articles Clinical significance of pre-operative neutrophil lymphocyte ratio and platelet lymphocyte ratio as prognostic factors for patients with colorectal cancer ZOUZHEN-YU 1 LIUHAI-LIANG 2 NINGNING 3 LISONG-YAN 1 DUXIAO-HUI 1 4 LIRONG 1 Department of General Surgery, Chinese People's Liberation Army General Hospital, Beijing 100853, P.R. China Department of Oncological Surgery, Chinese People's Liberation Army General Hospital, Beijing 100853, P.R. China Department of Gastrointestinal Surgery, Peking University International Hospital, Beijing 102206, P.R. China Department of General Surgery, Hainan Branch of the Chinese People's Liberation Army General Hospital, Sanya, Hainan 572013, P.R. China Correspondence to: Professor Rong Li or Professor Xiao-Hui Du, Department of General Surgery, Chinese People's Liberation Army General Hospital, 28 Fuxing Road, Beijing 100853, P.R. China, E-mail: lirong@medmail.com.cn, E-mail: duxiaohui301@sina.com 03 2016 09 02 2016 11 3 2241 2248 12022015 08012016 Copyright © 2016, Spandidos Publications 2016

The present study aimed to investigate the independent prognostic values of the pre-operative neutrophil lymphocyte ratio (NLR) and platelet lymphocyte ratio (PLR) in patients with colorectal cancer (CRC). The present study retrospectively analyzed the data of 216 patients with CRC from a single hospital. The clinicopathological characteristics of the patients were compared and prognostic factors were evaluated. NLR and PLR were associated with tumor differentiation status and the tumor diameter, respectively, and PLR was also associated with the primary tumor classification (T classification). Furthermore, NLR and PLR were positively associated with each other (R2=0.5368; P<0.0001). Univariate analyses indicated that stage II and III patients with a high NLR (≥4.98; P<0.001) or PLR (≥246.36; P<0.001) possessed a significantly poorer 5-year OS rate compared with those with a low NLR or PLR. Post-operative adjuvant chemotherapy improved the 5-year OS rate in patients with a high NLR or PLR. Multivariate analyses indicated that NLR and PLR were independent prognostic factors [NLR, relative risk (RR)=4.074 and P<0.001; PLR, RR=2.029 and P=0.029] in patients with CRC, and were associated with the T classification, lymph node metastasis and post-operative adjuvant chemotherapy response of patients. Additionally, the area under the curve (AUC) was 0.748 for NLR (95% CI, 0.684–0.804; P<0.0001) and 0.690 for PLR (95% CI, 0.623–0.751; P<0.0001). The RR and AUC indicated that NLR was the superior predictive factor in patients with CRC. In conclusion, the pre-operative NLR and PLR were significant independent prognostic factors in patients with CRC, and NLR was more effective as a prognostic marker compared with PLR. Adjuvant chemotherapy appeared to be more effective in CRC patients with a higher NLR or PLR.

 neutrophil lymphocyte ratio platelet lymphocyte ratio colorectal cancer prognosis Introduction

Colorectal cancer (CRC) is the third most common cancer and the fourth leading cause of cancer mortality according to GLOBOCAN 2012 (1). High tumor stage and histological grade, in addition to the number of resected lymph nodes and intravascular invasion have all been identified as prognostic factors (2). Thus, investigation of the mechanisms underlying CRC etiology is of clinical importance.

The association between inflammation and cancer was identified in the 19th century by Rudolf Virchow (3). Since then, studies have confirmed the broad and significant effect of inflammation on tumor development, progression and response to therapy (4–6). The presence of inflammatory cells, growth factors, activated stroma and DNA-damage-promoting agents in the inflammatory environment function to sustain cell proliferation and increase neoplastic risk (5). Meanwhile, the tumor increases inflammatory process and promotes tumor proliferation and metastases development by decreasing apoptosis and increasing angiogenesis and DNA damage (4,5). Notably, the scope and effects of an inflammatory reaction have always been assessed according to a number of biochemical markers, including the neutrophil lymphocyte ratio (NLR) and platelet lymphocyte ratio (PLR), which are inexpensive markers of systemic inflammation (7). Previous studies have indicated that elevated NLR or PLR suggested a poor prognosis for various types of cancer, including ovarian (8), breast (9,10), non-small cell lung (11), esophageal (12,13), gastric (7,14), hepatocellular (15) and CRC (2,16–18). However, the current literature leaves certain questions unanswered. Firstly, it is unknown as to which parameter is superior for predicting the outcome of CRC. Secondly, to the best of our knowledge, only 2 studies have compared the prognostic value of NLR and PLR in patients with CRC (17,18). One study demonstrated that elevated NLR and PLR were identified as significant poor prognostic factors in metastatic CRC, and that NLR led to improved prognostic predictors (17). On the contrary, the other study indicated that PLR was a superior prognostic marker (18). However, the grouping of NLR and PLR in these studies was based on a cut-off value that was calculated in other studies, which did not accurately reflect the data. Therefore, the aim of the present study was to explore the clinical significance of NLR and PLR as independent prognostic factors in patients with CRC and to identify the factor that is more effective in this role.

 Patients and methods <sec> <title>Patients

A retrospective analysis was performed on data from 216 patients with CRC that underwent radical surgery at Chinese People's Liberation Army (PLA) General Hospital (Beijing, China) between July 2006 and June 2012. Patients were selected for the present study according to the following inclusion criteria: CRC confirmed by histopathology; radical resection with microscopically tumor-free resection margins; and complete blood count, clinicopathological and follow-up data. The exclusion criteria excluded patients for the following reasons: Underwent palliative surgery; complications of intestinal obstruction, hemorrhage or enterobrosis resulting in emergency surgery; clinical evidence of infection, systemic inflammation or autoimmune disorder; underwent or accepted neoadjuvant chemotherapy or radiotherapy; succumbed to CRC or other causes within 30 days of surgery; and a history of other malignancies. All enrolled CRC patients were staged according to the American Joint Committee on Cancer tumor-node-metastasis (TNM) classification system (19) and were treated according to the National Comprehensive Cancer Network clinical practice guidelines in oncology for colon (20) and rectal cancer (21). All the patients provided written informed consent prior to the present study, which was approved by the Ethics Committee of Chinese PLA General Hospital.

 Follow-up of patients

Letters and telephone interviews were used to follow-up each patient. The last follow-up date was July 1, 2013. The overall survival (OS) time was defined as the time between surgery and mortality from any cause or to the last date of follow-up.

 NLR and PLR grouping

All blood samples were taken 1 week prior to surgery. NLR was defined as the absolute neutrophil count divided by the absolute lymphocyte count. The patients were divided into two groups based on the NLR value, the NLR <4.98 and NLR ≥4.98 groups. PLR was defined as the absolute platelet count divided by the absolute lymphocyte count. The patients were divided into two groups based on the PLR value, the PLR <246.36 and PLR ≥246.36 groups.

 Statistical analysis

Statistical analysis was performed with IBM SPSS software version 20 (IBM SPSS, Armonk, NY, USA). Receiver operating characteristic (ROC) curves were plotted to calculate the area under the ROC curve (AUC). The Youden index (YI) was calculated to determine the optimal cutoff value for NLR and PLR. Linear regression was performed to evaluate the association between NLR and PLR. Continuous variables are presented as the mean ± standard error and categorical variables are presented as frequencies and percentages. The differences between clinicopathological characteristics grouped by NLR or PLR were compared using the Pearson χ2 test or Fisher's exact test for categorical variables and Student's t-test for continuous variables. Survival time curves and 5-year OS rates were calculated using the Kaplan-Meier method of univariate analysis, and the differences were compared using the log-rank test. Independent prognostic factors were evaluated using the Cox proportional hazard model of multivariate analysis. Variables with a univariate analysis value of P<0.05 were entered into multivariate analysis. Each test was two-tailed. P<0.05 was considered to indicate a statistically significant difference.

 Results <sec> <title>The ROC curve for optimal cutoff value and AUC

When the NLR was 4.98, YI was at its maximum (YI=0.4491), demonstrating that 4.98 was the optimal cutoff value for NLR. Therefore, patients were divided into low NLR (<4.98) and high NLR (≥4.98) groups. When the PLR was 246.36, YI was at its maximum (YI=0.3490). Therefore, patients were divided into low PLR (<246.36) and high PLR (≥246.36) groups.

The AUC for NLR was 0.748 (95% CI, 0.684–0.804; P<0.0001) and PLR was 0.690 (95% CI, 0.623–0.751; P<0.0001; Fig. 1).

 Association of NLR and PLR with clinicopathological characteristics

In total, 216 patients were enrolled in the present study. The median follow-up time was 38 months, with a range of 3–85 months. At the final follow-up date, 161 patients (74.5%) were alive. A comparison between the clinicopathological characteristics and the NLR and PLR are exhibited in Table I. High NLR and PLR were associated with poor tumor differentiation and a larger tumor diameter, respectively (P<0.05). A high PLR was also associated with a poor primary tumor classification (T classification) (P=0.006). In addition, there was a positive association between NLR and PLR. The regression equation was as follows: y=97.3626+19.7032× (R2=0.5368; P<0.0001; Fig. 2).

 Association of NLR and PLR with the 5-year OS rate

The 1, 3 and 5-year OS rates were 95.8, 76.0 and 70.2%, respectively. Univariate analyses demonstrated that the NLR, PLR, tumor location (P=0.003), tumor differentiation (P=0.014), T classification (P<0.001), lymph node (LN) metastasis (P<0.001), distant metastasis (P<0.001), TNM staging (P<0.001) and administration of post-operative adjuvant chemotherapy (P=0.047) were associated with the 5-year OS rate (Table II). Patients with a high NLR possessed a significantly poorer 5-year OS rate compared with patients with a low NLR (42.7 vs. 84.7%; P<0.001; Fig. 3). Patients with a high PLR possessed a significantly poorer 5-year OS rate compared with patients with a low PLR (34.0 vs. 79.2%; P<0.001; Fig. 4).

Patients with high values for NLR and PLR were allocated a score of 2, patients with a high NLR or PLR value were allocated a score of 1, and patients that did not possess high NLR or PLR values were allocated a score of 0. Univariate analysis revealed that patients with a score of 2 possessed a significantly poorer 5-year OS rate (27.2%) compared with patients with a score of 1 (60.0%) or 0 (85.5%; P<0.001). Patients with a score of 1 had a significantly poorer 5-year OS rate compared with patients with a score of 0 (P<0.001; Table II).

 Multivariate analyses of independent prognostic factors

Multivariate analyses using the Cox proportional hazards model identified NLR, PLR, T classification (P<0.001; 95% CI, 2.008–6.156), LN metastasis (P=0.030; 95% CI, 1.059–3.161) and post-operative adjuvant chemotherapy (P=0.021; 95% CI, 1.110–3.625) as independent prognostic factors (Table III). The risk of succumbing to CRC for patients with a high NLR was >4 times higher than patients with a low NLR (relative risk (RR)=4.074; P<0.001; 95% CI, 1.975–8.405). The risk of succumbing to CRC for patients with a high PLR was >2 times higher than patients with a low PLR (RR=2.029; P=0.029; 95% CI, 1.077–3.821).

 Association between the NLR and PLR and 5-year OS rate stratified by TNM staging

Patients in the NLR and PLR groups were stratified according to TNM staging. The results indicated that patients with TNM stage II or III disease and a high NLR or PLR possessed a significantly poorer 5-year OS rate compared with patients with a low NLR (stage II, P=0.002; stage III, P<0.001) or PLR (stage II, P<0.001; stage III, P<0.001; Table IV).

 Association between patients grouped by post-operative adjuvant chemotherapy and the 5-year OS rate stratified by NLR or PLR

The patients were divided into two groups according to post-operative adjuvant chemotherapy. Univariate analyses stratified by the NLR or PLR revealed that adjuvant chemotherapy did not affect the 5-year OS rate in patients with a low NLR (P=0.255) or PLR (P=0.259). However, adjuvant chemotherapy increased the 5-year OS rate from 29.2 to 49.1% in patients with a high NLR (P=0.015; Fig. 5) and from 21.4 to 42.7% in patients with a high PLR (P=0.019; Fig. 6; Table V).

 Discussion

CRC is the third most common cancer and the fourth leading cause of cancer-associated mortality, according to GLOBOCAN 2012 (1). In China, an increase in CRC risk factors, including an aging population and changes in eating habits (increased meat intake and reduced fiber intake), has rendered CRC the fifth most common cancer in the country, following lung, stomach, liver and esophageal cancers (22).

In 1863, Rudolf Virchow hypothesized that the origin of cancer was at sites of chronic inflammation, and this causal association between inflammation, innate immunity and cancer is more widely accepted at present (3,5). Inflammation is significant in tumor development, progression and response to therapy (4). The presence of inflammatory cells, growth factors, activated stroma and DNA-damage-promoting agents in the inflammatory environment act to sustain cell proliferation and increase neoplastic risk (5). In turn, the tumor increases the inflammatory process and promotes tumor proliferation and metastases development by decreasing apoptosis and increasing angiogenesis and DNA damage (4,5). The strongest association of chronic inflammation with malignancy has been reported in CRC arising from inflammatory bowel diseases (5,23). Therefore, the prognosis of CRC is not only associated with the biological behavior of the tumor, but also with the inflammatory reaction of the host.

Inflammatory reactions have always been assessed by a number of biochemical markers, in particular traditional hematological markers, including C-reactive protein (CRP) and differential leukocyte and platelet counts. CRP is an index of systemic inflammation and has been identified as a prognostic factor in patients with CRC and gastric cancer (24,25). However, serum CRP levels are not routinely assessed in the pre-operative assessment (12,14,18). Instead, NLR and PLR, calculated from leukocyte differential counts and platelet counts, respectively, are more readily available and inexpensive compared to CRP (7). Notably, numerous previous studies have already indicated that an elevated NLR and PLR is associated with a poorer survival in patients with ovarian (8), breast (9,10), non-small cell lung (11), esophageal (12,13), gastric (7,14) and hepatocellular cancers (15) and CRC (2,16–18).

NLR is the ratio of the absolute neutrophil count to the absolute lymphocyte count, and therefore the association between a high NLR and a poor prognosis, as revealed in the present study, is possibly indicative of the tumor-promoting activity associated with neutrophilia in the tumor environment. Tumors are known to produce myeloid growth factors, including granulocyte colony-stimulating factor, tumor necrosis factor-α, interleukin (IL)-1and IL-6, which may increase the number of neutrophilic granulocytes at the site of the tumor (13,18). Neutrophilia promotes tumor growth and metastasis by remodeling the extracellular matrix and releasing reactive oxygen species, nitric oxide and arginase, which suppress the T cell response and increases the rate of mutagenesis (10). Additionally, neutrophilia suppresses lymphocyte activity, therefore counteracting the antitumor immune response (7). An elevated NLR has been associated with a poor survival rate in breast (10), esophageal (12,13)and gastric cancers (7,14) and CRC (26). Chiang et al demonstrated that patients with an elevated NLR (>3) in colon cancer appeared to possess larger tumors and a more advanced tumor stage, and patients with stages I–III CRC possessed a poorer 5-year disease-free survival rate (26).

PLR is the ratio of the absolute platelet count to absolute lymphocyte count, and therefore, the association of a high PLR with a poor prognosis, as revealed in the present study, is possibly indicative of the tumor-promoting activity associated with platelets. Platelets are known to be important in hemostasis and thrombosis (27). In addition, platelets mediate tumor cell growth, dissemination and angiogenesis (28). In turn, tumor cells induce platelet aggregation, which is known to be the trigger for the development of cancer-associated thrombosis (28). Platelets recruited to the tumor microenvironment consequently release platelet-derived growth factor and transforming growth factor to promote tumor growth (7,29). However, platelets also regulate angiogenesis by releasing numerous proangiogenic proteins, including vascular endothelial growth factor, and aid the maintenance of vascular integrity, therefore facilitating tumor cell survival and growth (10,29). In addition, platelets shield tumor cells from host immune surveillance and direct cellular contact with natural killer cells by inducing platelet mimicry and constructing a mesh with fibrin that surrounds tumor cells within the vasculature during hematogenous dissemination (29). Tumor cells possess the ability to manipulate platelet activity to optimize tumor growth, proliferation, survival and metastasis (29). Several studies have identified the association between a poor survival rate and elevated PLR in solid tumors (2,8,9,11,16,30). Szkandera et al revealed that an elevated PLR was significantly associated with a decreased time to recurrence and demonstrated a trend towards a decreased OS time in patients with stage II and III colon cancer that underwent curative resection (2). Liu et al reported that patients with CRC and a higher PLR possessed a significantly lower 5-year OS rate compared with patients with a low PLR, and identified pre-operative PLR as a clinically significant factor for the assessment of the prognosis of resectable CRC (16).

An elevated NLR or PLR is always accompanied by lymphopenia, which is caused by systemic inflammation and leads to the release of a number of inhibitory immunological mediators, particularly IL-10 and transforming growth factor-β. These inhibitory immunological mediators may exert an immunosuppressive effect with an impaired lymphocyte function (31).

The present study demonstrated that CRC patients with a high NLR or PLR tended to possess more clinicopathological factors associated with advanced disease, including poor tumor differentiation, the presence of a large tumor and a higher T classification. Regarding post-operative outcomes, in the present study, CRC patients with a high NLR or PLR possessed a significantly poorer 5-year OS rate compared with patients with a low NLR or PLR, particularly in patients with TNM stage II and III disease, indicating that NLR and PLR were effective independent prognostic factors. In addition, the present study aimed to identify which prognostic factor was the more effective. In this respect, 2 previous studies presented notable data. Kwon et al analyzed 200 patients that underwent curative resection and revealed that NLR and PLR were good prognostic biomarkers of OS rate in a univariate analysis, but only PLR was an independent prognostic factor in multivariate Cox proportional hazards analysis (18). He et al demonstrated that an elevated NLR, PLR and carcinoembryonic antigen (CEA) level were significant predictors of a poorer OS rate and progression-free survival time following first-line chemotherapy in patients with metastatic CRC, but only NLR and CEA were validated as independent factors (17). These two studies selected cutoff values for NLR and PLR from previous studies (17,18). By contrast, the present study set the optimal cutoff value according to the maximal YI calculated from the ROC curve and grouped the patients accordingly, which is more suitable to the clinical data and more accurate for the specific study group. Additionally, the present study compared the predictive value of each factor using two methods.

Firstly, the present study compared NLR and PLR using their respective AUC values. According to the present results, the AUC for NLR was 0.748, which was greater compared with PLR (AUC=0.690). Secondly, the present study compared the risk of patients with a high NLR and PLR succumbing to CRC. The present results demonstrated that the risk of patients succumbing to CRC was increased in patients with a high NLR compared with patients with a high PLR (RR, 4.074 vs. 2.029). The AUC and RR data indicate that NLR is superior to PLR as a predictive factor for patients with CRC. Notably, Ishizuka et al investigated the prediction of cancer-specific survival time in patients with CRC using a parameter based on a combination of platelet count (COP) and NLR, and concluded that COP-NLR was a useful predictor of survival (32). Consequently, the present study also considered the combined effect of NLR and PLR on the prognostic significance. Accordingly, the present study allocated a score of 2, 1 or 0, according to the NLR and PLR, and performed a univariate analysis. The present results revealed that the combination of NLR and PLR was a valid prognostic factor.

The treatment history of the patients was another clinicopathological factor the present study investigated, although previous studies by Kwon et al and He et al did not consider the effect of an elevated NLR or PLR on adjuvant chemotherapy (17,18). According to the present results, patients with a high NLR or PLR that accepted adjuvant chemotherapy possessed a significantly improved 5-year OS rate compared with patients that did not possess an elevated NLR or PLR and did not accept adjuvant chemotherapy (P=0.015 and P=0.019, respectively). This difference was not observed in patients with a low NLR or PLR. Therefore, adjuvant chemotherapy appeared to be more effective in CRC patients with a high NLR or PLR.

In conclusion, the present study validates the use of pre-operative NLR and PLR as independent prognostic factors for CRC patients. Notably, NLR was observed to be more effective than PLR for predicting CRC. In addition, the present data suggests that neutrophils and platelets are important in promoting CRC progression, but neutrophils are more crucial. Furthermore, adjuvant chemotherapy appeared to be more effective in CRC patients with a high NLR or PLR. However, as an observational, single hospital, small-scale study, the present study is limited. Larger prospective studies are required to confirm these preliminary results.

 Acknowledgements

The present study was supported by the Natural Science Foundation of China (grant no. 61170123) and Natural Science Foundation of Hainan Province (grant no. 813226).

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ROC curves for NLR and PLR. The ROC curve for NLR is indicated by the black line, with an AUC of 0.748 (95% CI, 0.684–0.804; P<0.0001). The ROC curve for PLR is indicated by the gray line, with an AUC of 0.690 (95% CI, 0.623–0.751; P<0.0001). ROC, receiver operating characteristic; NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio; AUC, area under the ROC curve; CI, confidence interval.

Linear regression of NLR and PLR. NLR and PLR were positively associated with each other. Regression equation: y=97.3626+19.7032× (R2=0.5368; P<0.0001). NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio.

OS curve grouped by NLR. Patients with a high NLR (≥4.98) possessed a significantly poorer OS time compared with patients with a low NLR (<4.98; P<0.001). OS, overal survival; NLR, neutrophil lymphocyte ratio; Cum., cumulative.

OS curve grouped by PLR. Patients with a high PLR (≥246.36) possessed a significantly poorer OS time compared with patients with a low PLR (<246.36; P<0.001). OS, overal survival; PLR, platelet lymphocyte ratio; Cum., cumulative.

OS curve grouped by chemotherapy in patients with a high NLR. Adjuvant chemotherapy increased the 5-year OS rate from 29.2 to 49.1% in patients with a high NLR (≥4.98; P=0.015). OS, overall survival; NLR, neutrophil lymphocyte ratio; Cum., cumulative.

OS curve grouped by chemotherapy in patients with a high PLR. Adjuvant chemotherapy increased the 5-year OS rate from 21.4 to 42.7% in patients with a high PLR (≥246.36; P=0.019). OS, overall survival; PLR, platelet lymphocyte ratio; Cum., cumulative.

Clinicopathological characteristics of 216 patients with colorectal cancer, grouped by NLR and PLR.

NLR PLR
Characteristic NLR <4.98, n (%) NLR ≥4.98, n (%) P-value PLR <246.36, n (%) PLR ≥246.36, n (%) P-value
Total 141 (100.0)   75 (100.0)   172 (100.0)   44 (100.0)
Gender   0.659   0.114
  Male   91 (64.5) 46 (61.3) 114 (66.3) 23 (52.3)
  Female   50 (35.5) 29 (38.7)   58 (33.7) 21 (47.7)
Age, years   53.90±12.1 54.49±10.8   0.239 53.81±11.3   55.27±13.0   0.145
PLR 154.94±57.1 278.89±162.4 <0.001
NLR 3.81±2.8 10.19±6.0 <0.001
Tumor location 0.887   0.398
  Colon   73 (51.8) 40 (53.3)   87 (50.6) 26 (59.1)
  Rectum   68 (48.2) 35 (46.7)   85 (49.4) 18 (40.9)
Differentiation   0.019   0.019
  Well   26 (18.4) 5 (6.7)   28 (16.3) 3 (6.8)
  Moderate   83 (58.9) 43 (57.3) 104 (60.5) 22 (50.0)
  Poor   32 (22.7) 27 (36.0)   40 (23.3) 19 (43.2)
Tumor diameter, cm   4.54±1.9 5.73±3.1   0.007 4.58±2.0   6.40±3.4   0.001
T classification   0.187   0.006
  T1+T2   23 (16.3) 7 (9.3)   28 (16.3) 2 (4.5)
  T3   81 (57.4) 41 (54.7) 101 (58.7) 21 (47.7)
  T4   37 (26.2) 27 (36.0)   43 (25.0) 21 (47.7)
LN metastasis   0.070   0.058
  N0   77 (54.6) 36 (48.0)   93 (54.1) 20 (45.5)
  N1   50 (35.5) 23 (30.7)   60 (34.9) 13 (29.5)
  N2 14 (9.9) 16 (21.3)   19 (11.0) 11 (25.0)
Distant metastasis   0.053   0.122
  M0 128 (90.8) 61 (81.3) 154 (89.5) 35 (79.5)
  M1 13 (9.2) 14 (18.7)   18 (10.5)   9 (20.5)
TNM staging   0.062   0.082
  I   16 (11.3) 4 (5.3)   19 (11.0) 1 (2.3)
  II   61 (43.3) 28 (37.3)   71 (41.3) 18 (40.9)
  III   53 (37.6) 29 (38.7)   66 (38.4) 16 (36.4)
  IV 11 (7.8) 14 (18.7) 16 (9.3)   9 (20.5)

NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio; T, primary tumor; LN, lymph node; TNM, tumor-node-metastasis.

Univariate analyses in 216 patients with colorectal cancer.

Characteristic n 5-year OS rate, % P-value
Gender   0.724
  Male 137 72.4
  Female   79 65.4
Age, years   0.662
  <50   75 71.1
  ≥50 141 69.0
NLR <0.001
  <4.98 141 84.7
  ≥4.98   75 42.7
PLR <0.001
  <246.36 172 79.2
  ≥246.36   44 34.0
Tumor location   0.003
  Colon 113 62.9
  Rectum 103 77.4
Differentiation   0.014
  Well   31 71.0
  Moderate 126 76.8
  Poor   59 55.0
Tumor diameter, cm   0.967
  <5 104 68.9
  ≥5 112 71.0
T classification <0.001
  T1+T2   30 87.7
  T3 122 82.6
  T4   64 36.1
LN metastasis <0.001
  N0 113 86.3
  N1   73 63.5
  N2   30 22.2
Distant metastasis <0.001
  M0 189 76.2
  M1   27   9.6
TNM staging <0.001
  I   20 88.9
  II   89 88.2
  III   82 57.7
  IV   25   0.0
Chemotherapy   0.047
  Yes 149 73.6
  No   67 62.7
Score <0.001
  0 133 85.5
  1   47 60.0
  2   36 27.2

OS, overall survival; NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio; T, primary tumor; LN, lymph node; TNM, tumor-node-metastasis.

Multivariate analyses in 216 patients with colorectal cancer.

Feature P-value RR (95% CI)
NLR <0.001 4.074 (1.975–8.405)
PLR   0.029 2.029 (1.077–3.821)
Tumor location   0.362 0.741 (0.389–1.411)
Differentiation   0.755 0.918 (0.538–1.567)
T classification <0.001 3.516 (2.008–6.156)
LN metastasis   0.030 1.830 (1.059–3.161)
Distant metastasis   0.389 1.840 (0.459–7.375)
TNM staging   0.576 1.322 (0.497–3.516)
Chemotherapy   0.021 2.006 (1.110–3.625)

RR, relative risk; CI, confidence interval; NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio; T, primary tumor; LN, lymph node; TNM, tumor-node-metastasis.

The 5-year OS rate for NLR and PLR stratified by TNM staging.

TNM stage I TNM stage II TNM stage III TNM stage IV
Ratio n 5-year OS rate, % n 5-year OS rate, % n 5-year OS rate, % n 5-year OS rate, %
NLR
  <4.98 16   86.7 61 95.0 53 82.0 11   0.0
  ≥4.98   4 100.0 28 74.0 29 15.2 14   0.0
  P-value 0.514   0.002 <0.001 0.338
PLR
  <246.36 19   88.9 71 94.1 66 74.2 16   0.0
  ≥246.36   1 NA 18 65.5 16   7.5   9 16.7
  P-value NA <0.001 <0.001 0.256

OS, overall survival; NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio; TNM, tumor-node-metastasis; NA, not available.

The 5-year OS rate for adjuvant chemotherapy stratified by NLR or PLR.

NLR <4.98 NLR ≥4.98 PLR <246.36 PLR ≥246.36
Chemotherapy n 5-year OS rate, % n 5-year OS rate, % n 5-year OS rate, % n 5-year OS rate, %
Yes 96 87.2 53 49.1 119 81.5 30 42.7
No 45 79.7 22 29.2   53 74.1 14 21.4
P-value 0.255 0.015 0.259 0.019

OS, overall survival; NLR, neutrophil lymphocyte ratio; PLR, platelet lymphocyte ratio.