Clinical significance of tumor-infiltrating lymphocytes and neutrophil-to-lymphocyte ratio in patients with stage III colon cancer who underwent surgery followed by FOLFOX chemotherapy

Article metrics

  • 698 Accesses

  • 1 Citations


Local tumor immune response and host immunity have been suggested as important prognosticators respectively in colorectal cancer. However, the utility of combination of these parameters remains inconclusive. The aim of this study was to investigate the combinational impact of local and host tumor immune response, as determined by tumor-infiltrating lymphocytes (TILs) and neutrophil-to-lymphocyte ratio (NLR), in patients with stage III colon cancer. Patients with stage III colon cancer homogeneously treated with surgery followed by FOLFOX chemotherapy between Jan 2007 and Aug 2013 were included retrospectively. Hematoxylin and eosin (H&E) stained tumor sections of local inflammatory infiltrate (TILs) were classified as 0–3 by the Klintrup-Mäkinen grading method. NLR was measured within 1 month of surgery. The association of NLR and TILs with survival, alone or combined, were measured using multivariate Cox proportional hazard regression analysis. Among 137 patients, 75 (54.7%) were identified as the high TIL group (TILs 2 and 3) and 97 (70.8%) as the low NLR group (NLR < 3). Of the patients with high TILs, 51 (68%) had a low NLR. In univariate analysis, operation time, complications, lymph node ratio (LNR), stage, TILs, and high TILs with low NLR were significantly associated with overall survival(OS). Multivariate Cox regression identified operation time, stage, and TILs as independent risk factors for OS. When high TILs with low NLR vs. others was entered into multivariate analysis, this also proved to be a significant predictor of OS (HR 4.1, 95% CI 1.1–14.2, P = 0.025), with an increased C-index and lower AIC value compared to TILs. Measuring TILs using H&E stained sections could stratify the prognosis of stage III colon cancer. Considering host immunity, using the combination of TILs and NLR, allowed the prognosis to be stratified in more detail.


Colon cancer management includes curative surgical resection and adjuvant chemotherapy if indicated. In stage III colon cancer, adjuvant chemotherapy using the FOLFOX (folinic acid, 5-fluorouracil, and oxaliplatin) regimen is regarded as a standard of care1. In a pooled analysis published recently, which tried to compare the noninferiority of 3 months and 6 months adjuvant therapy with either FOLFOX or CAPOX (capecitabine and oxaliplatin), the noninferiority was not confirmed in the overall stage III colon cancer cohort2. However, in a lower-risk group, which was defined as T1, T2, or T3 and N1 cancers, it was shown that 3 months of therapy was as effective as 6 months, especially in patients treated with CAPOX. Thus, risk stratification could identify the patients most likely to benefit from more or less chemotherapy treatment and enable clinicians to balance expected survival gain against common therapeutic toxicities such as oxaliplatin-induced neuropathy in patients with stage III colon cancer3.

Tumor-infiltrating lymphocytes (TILs) are thought to be an important indicator reflecting the local immune-related tumor microenvironment4. An immunoscore has been suggested, which is designed to count tumor-infiltrating T-cells using a combination of both CD3+ and CD8+ densities measured in the invasive margin and tumor center of colon cancer5. A recent international validation study has demonstrated that TNM staging and immunoscore remained significant parameters for survival and immunoscore gave the highest relative contribution to the risk of all clinical variables, even including TNM stages in patients with stage I–III colon cancer6. However, measuring immunoscore is often time and effort consuming due to additional immunohistochemistry (IHC) staining and equipment requirements. This might be a hurdle in achieving the widespread clinical use of this score. Previously, TILs have been measured using hematoxylin and eosin (H&E) stained tumor sections. Local inflammatory infiltrate was classified as 0–3 using H&E stained tumor sections by the method described by Klintrup-Mäkinen (K-M grading)7. It was reported that TILs measured by K-M grading can be used as an important prognostic marker in colorectal cancer8,9,10. Nevertheless, TIL-based stratification when measured by the K-M grading system, has not been thoroughly investigated especially for stage III colon cancer patients who underwent surgery followed by adjuvant FOLFOX chemotherapy.

The role of cellular-mediated inflammatory response in carcinogenesis, which can be represented as lymphocytes, neutrophils, and monocytes in the complete blood cell count, is known to be important11,12. The neutrophil-to-lymphocyte ratio (NLR) is a widely used prognostic marker of various tumors including colorectal cancer13,14,15. The relative convenience and non-invasiveness in obtaining NLR is advantageous. Nevertheless, there are still several obstacles on applying NLR in the management of colorectal cancer patients. A very early study investigating the impact of NLR in patients with colorectal cancer revealed that NLR might be dependent on tumor stage and a prognostic impact was not demonstrated in a multivariable analysis16. The lack of a generally applicable cut-off value is a main limitation17. Although the explanation for the discordance of the results across studies in colorectal cancer is multifactorial, part of the reason may be attributed to the different treatment options especially in the administration of chemotherapy regimens13 or simultaneous inclusion of colon and rectal cancer patients. The prognostic impact of NLR on rectal cancer measured before surgery might differ from that of colon cancer because preoperative chemoradiotherapy for indicated rectal cancer patients could change the densities of peripheral inflammatory cells18. For these reasons, the prognostic impact of NLR in stage III colon cancer who underwent curative surgery followed by FOLFOX chemotherapy deserves to be investigated, in that the impact of NLR might be analyzed on a cohort who underwent relatively uniform treatments.

Current evidence shows that local immune-related tumor response as well as the host immunity have prognostic value, respectively. As far as we know, few studies considered local and systemic inflammatory response of tumor simultaneously to evaluate their prognostic value9,19. Furthermore, whether combination of these two separate immune reactions, although affect each patient’s prognosis at the same time, provide useful prognostic information in stage III colon cancer is unclear. Thus, the aim of this study was to investigate the prognostic impact of TILs and NLR, alone or combined, in patients with stage III colon cancer who underwent surgery followed by FOLFOX chemotherapy.

Materials and Methods


From January 2007 to August 2013, patients who underwent surgery followed by adjuvant FOLFOX chemotherapy for stage III colon cancer at Gangnam Severance Hospital, Yonsei University College of Medicine were initially selected. Patients were included if a slide was available for pathology review and they had undergone a complete blood test within 4 weeks of surgery. Patients who underwent an emergency surgery or palliative surgery (n = 11), who underwent surgery after diagnosed or treated for intestinal obstruction (n = 5), who had inflammatory bowel disease history (n = 2), and who had preoperative chemotherapy (n = 3) were excluded from this study because these factors might influence the systemic or local inflammatory status. Finally, 137 patients were included in our study. All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This study was approved by the institutional review board (IRB) of Gangnam Severance Hospital. Informed consent was waived for this retrospective study by the IRB.

Treatments and follow-up

All included patients underwent standard colectomy with regional lymphadenectomy according to the standard surgical principle20. All tumor staging was evaluated and classified according to the definition of the 7th American Joint Committee on Cancer and Union for International Cancer Control TNM classification system21. Microsatellite instability (MSI) and KRAS status were evaluated according to the techniques described in detail previously22,23. However, not all of the patients underwent these two molecular examinations completely. All patients who underwent surgery visited our hospital every 3 months for 3 years and then every 6 months until 5 years. At each follow-up visit, serum carcinoembryonic antigen (CEA) level was measured. Abdominopelvic computed tomography (CT) scans were performed with an average interval of 6 months. Chest CT was done at either 6 or 12-month schedules depending on the discretion of the physician. 18-Fludeoxyglucose (FDG) positron emission tomography (PET) scan was performed on suspicion of recurrence as indicated by the surgeon. Colonoscopy was performed usually 1, 3, and 5 years after surgery. Patient follow-up lasted until the cut-off date (Dec 2017) or the death of the patient. The median follow-up period was 67.8 months (range, 7.5–129.6 months).

Measurement of TILs and NLR

The patients’ slides were reviewed by an experienced pathologist, who had no information on the clinical outcomes of the patients. TILs were evaluated using slides of H&E stained sections and were scored according to the K-M grading7. As described in detail in other studies8,24, the deepest area of the invasive margin of the tumor area was assessed by using a 4-degree scale. A score of 0 was given when there was no increase in lymphocytes, 1 denoted a mild and patchy increase in lymphocytes, 2 denoted a moderate and band like lymphocytic infiltrate with some destruction of cancer cell islands, and 3 denoted a marked and florid cuplike lymphocytic infiltrate with frequent destruction of cancer cell islands. Macrophages and granulocytes could be identified under microscope with H&E staining and excluded in TILs measurements. Area of acute inflammation and necrosis was also excluded in measuring TILs. Subsequently, we designated scores 0 and 1 as the low TIL group and scores 2 and 3 as the high TIL group in further analysis.

NLR was measured as the ratio of neutrophils divided by lymphocytes. All included patients underwent a baseline blood test within 30 days of definite surgery. The median number of days from the measurement of NLR to surgery was 6 days (range 1–30 days). The NLR was dichotomized as NLR < 3 (low NLR) and NLR ≥ 3 (high NLR). The cut-off value 3 was derived from previous studies measuring its clinical impact25,26.

Statistical analysis

All statistical analyses were performed using the SPSS software, version 23.0 (IBM SPSS, Chicago, IL, USA) and R package version 3.4.4 (R-project, Institute for Statistics and Mathematics). Differences between groups were analyzed using the chi-square test or Fisher’s exact test for dichotomous parameters. Continuous variables were presented as the mean ± standard deviation and were analyzed using the Student’s t test. Overall survival (OS) was determined using the data from the date of surgery until death or last follow-up. Survival curves were constructed using the Kaplan-Meier method and the log-rank test was used to compare survival rates between the groups. In analyses where OS was the outcome, we cross classified TILs and NLR of 3 or greater into four categories (high TILs with low NLR, high TILs with high NLR, low TILs with high NLR, or low TILs with low NLR) and calculated the Kaplan-Meier curves. According to the survival outcomes, the groups were dichotomized as high TILs with low NLR and others, and we used this classification in further statistical analysis.

All variables P < 0.1 on univariate analysis were initially entered into the multivariate analysis. Using multivariable-adjusted Cox proportional hazards regression analysis done by a backward stepwise selection of variables, we evaluated differences in OS by category of TILs and other biomarkers. Models were adjusted for operation time, complications, lymph node ratio (LNR), and stage. Next, we examined NLR and TILs in combination as independent predictors of survival in multivariable-adjusted Cox proportional hazards models. Harrell’s concordance index (C-index) and Akaike information criterion (AIC) were calculated for the comparison of different predictive models. A higher C-index value would indicate better concordance of survival times and a smaller AIC value indicated a more goodness-of-fit for predicting outcomes27,28. P < 0.05 was considered to be statistically significant.


Of 137 stage III colon cancer patients who underwent surgery followed by adjuvant FOLFOX chemotherapy, 13 (9.5%), 49 (35.8%), 44 (32.1%), and 31 (22.6%) patients were classified as K-M grade 0, 1, 2, and 3, respectively. Thus, 75 patients (54.7%) were grouped as high TILs and 62 patients (45.2%) were grouped as low TILs. With regard to NLR, 97 patients (70.8%) and 40 patients (29.1%) showed low NLR (NLR < 3) and high NLR (NLR ≥ 3), respectively. There was greater female predominance in the high TIL group than in the low TIL group (48% in high TILs vs. 25.8% in low TILs, P = 0.008). Tumors larger than 5 cm were significantly more common in the high NLR group than in the low NLR group (P = 0.017). Among patients with high TILs, 51 patients (68%) showed low NLR whereas, 24 patients showed high NLR (P = 0.456) (Table 1, Supplementary data).

Table 1 Comparison of patient characteristics and pathologic outcomes according to the TILs and NLR respectively.

In univariate analysis, there was a significant difference in 5-year OS between the high TILs and the low TILs (Hazard Ratio, HR: 2.6; confidence interval, CI: 1.1–6.2; P = 0.021). In contrast, there was no survival difference between the low NLR group and the high NLR group (HR: 1.4, CI: 0.6–3.3, P = 0.331). In addition, LNR (P = 0.025), and stage (P = 0.018) were significantly associated with OS. Operation time, complications showed trends for association with OS, but these did not reach statistical significance (Table 2).

Table 2 Univariate analysis for overall survival.

When we classified patients using the combination of TILs and NLR, there was a significant difference in the 5-year OS between the groups (5-year OS: 93.8% in high TILs with low NLR, 83.3% in high TILs with high NLR, 78.3% in low TILs with low NLR and 75% in low TILs with high NLR, P = 0.04) (Fig. 1A). Thus, we dichotomized patients into two groups: the high TILs with low NLR group versus others. There was also a significant difference in 5-year OS between the newly defined classifications (high TILs with low NLR: 93.8% vs. others: 79.1%, P = 0.005) (Fig. 1B).

Figure 1

Overall survival according to the combination of TILS and NLR. (A) 4 groups comparison (B) 2 group comparison.

Factors with a p-value less than 0.1 in univariate analysis such as operation time, complications, LNR, stage, and TILs were entered into a multivariable analysis in the first stage. Operation time (HR: 2.4, CI: 1–5.6, P = 0.043), stage (IIIC vs. IIIB, HR: 0.3, CI: 0.1–0.7, P = 0.009), and TILs (HR: 2.5, CI: 1–5.9, P = 0.032) were proved to be independent risk factors for OS (Model 1). In the second stage, we entered high TILs with low NLR versus others, instead of TILs, into a multivariable model (Model 2). The results showed that stage (IIIC vs. IIIB, HR: 0.3, CI: 0.1–0.7, P = 0.007), and high TILs with low NLR (HR: 4.1, CI: 1.1–4.2, P = 0.025) were independently associated with OS. Model 2 showed higher fitness in terms of Akaike information criterion (AIC) (226.289 in Model 2 vs. 229.221 in Model 1) and higher predictive power in terms of C-index [0.737, 95% CI (0.623–0.850) in Model 2 vs. 0.717, 95% CI (0.604–0.831) in Model 1] than Model 1 (Table 3).

Table 3 Multivariate analysis using different parameters.

In subgroup analysis according to each stage, 11, 88, and 38 patients were classified into stage IIIA, IIIB, and IIIC, respectively. Patients with high TILs with low NLR showed better 5-year OS in the stage IIIB group (100% in high TILs with low NLR group vs. 86% in others, P = 0.011). In contrast, there was no difference between the two groups in stage IIIA (P = 0.617) and stage IIIC (P = 0.16), respectively (Fig. 2).

Figure 2

Overall survival according to the combination of TILs and NLR in each stage. (A) Stage IIIA (n = 11), (B) Stage IIIB (n = 88), (C) Stage IIIC (n = 38).


This study has demonstrated that TILs measured by H&E staining could stratify the prognosis of patients with stage III colon cancer who underwent surgery followed by FOLFOX chemotherapy. Although NLR per se could not predict prognosis in our cohort, a combination of TILs and NLR could allow us to distinguish the survival outcomes of patients in more detail. Thus, considering local tumor response and systemic immunity by TILs measured by H&E staining and NLR might be an affordable and effective option for risk stratification in patient with stage III colon cancer.

The clinical impact of IHC-based measurements of TILs such as CD3, CD8, CD45, and FOXP3 have been widely investigated in colorectal cancer29,30,31,32,33,34. According to a recent international validation study, immunoscore, measuring total tumor-infiltrating and cytotoxic tumor-infiltrating T-cells, can stratify patients’ outcomes more definitely than TNM stage6. However, one concern of this approach is that a considerable number of patients (858/3539, 24%) in the retrospective study were filtered by quality control and could not be included in their multinational study6. Among them, 41.6% (357/858) of the excluded patients were associated with the failure of obtaining proper IHC results. The IHC-based measurement may not be always successful in some environments with scarce resources, which prevents the widespread adoption of IHC. Many studies have evaluated the impact of TILs measured by the H&E staining of sections from colorectal cancer patients. Huh et al. analyzed 546 colorectal cancer patients and concluded that TILs have a prognostic impact8. Interestingly, the impact of TILs was demonstrated only in stage III colorectal cancer, and not in stage I and II colorectal cancer patients. In that study, however, various chemotherapy agents were used, and FOLFOX chemotherapy, which is regarded as the standard chemotherapy for stage III colon cancer in current practice, was used for only 6 patients (1%). Another study measured the TILs of colorectal cancer patients according to the recommendation of the International TILs Working Group in breast cancer10. The patients were composed of stage II and stage III colon and rectal cancer patients with or without adjuvant chemotherapy10. In their study, the density of TILs, where high TIL level was defined as more than 42%, was independently associated with OS in multivariate analysis. Although TILs were proven to be a significant predictor of survival, the results were derived from a heterogeneous cohort, which included stage II and III rectal cancer patients who did not receive radiation therapy. In addition, TILs measured by H&E staining in colorectal cancer have been thoroughly investigated by the one group and these studies demonstrated that local tumor infiltrate was associated with survival24,35,36. Nevertheless, one concern might be that their studies showed a relatively low incidence of 12 or more lymph nodes examined24,35,36. Thus, it was difficult to completely exclude the possibility that surgical quality affected the survival outcomes. Therefore, these previous studies cannot definitively inform us that the TILs defined by H&E stain may have an impact on the prognosis of patients with stage III colon cancer who underwent FOLFOX chemotherapy. Our study demonstrated that TILs can be used as an independent prognostic factor for patients with stage III colon cancer. The strength of the present study is that our group included relatively homogeneously treated patients with a high proportion of adequately retrieved lymph nodes (95%) and all patients had undergone adjuvant FOLFOX chemotherapy. Our result can be applied relatively easily in clinical practice because an H&E examination is a routine procedure for the evaluation of tumor staging.

The clinical impact of NLR per se was not demonstrated in our study. Although many studies concluded that NLR is an important inflammatory biomarker in colorectal cancer, there are several issues to be mentioned. As depicted in one of the earlier studies, which investigated the impact of NLR in colorectal cancer, Walsh and colleagues showed that an NLR greater than 5 correlated with OS only in univariate analysis16. Because NLR was dependent on Dukes stage, the significance was lost in multivariate analysis16. According to a study by Li and colleagues, which included 5,336 patients and is one of the largest scale studies dealing with this issue for colorectal cancer, NLR dichotomized as 2.72 can predict patients’ OS37. However, in that study, the clinical impact of inflammatory markers including NLR was not evident in patients who did not undergo adjuvant chemotherapy. The authors explained that the significance of NLR might not be demonstrated due to the overall good survival outcome of this subgroup. Malietzis and colleagues analyzed the impact of NLR in 506 colorectal cancer patients who did not undergo adjuvant chemotherapy25. They showed that an NLR of more than 3 was identified as an independent prognostic factor for disease-free survival. Interestingly, this correlation did not last when OS was evaluated. Although we could not elucidate the reason of the negative impact of NLR per se in our group, it is worth mentioning that most of the previous studies evaluating the impact of NLR in colorectal cancer include heterogeneous groups of patients. Most of the studies included colon cancer and rectal cancer patients simultaneously and patients who either underwent adjuvant chemotherapy or did not. In addition, the chemotherapeutic agents and regimens were diverse and included 5FU, capecitabine, FOLFOX, etc. As we already know, rectal cancer patients usually underwent preoperative or postoperative radiation therapies, thus the radiation effect cannot be ignored in the statistical analysis. In node-positive colon cancer patients, the benefit of adjuvant chemotherapy is well established. Thus, the real effects of NLR might be more fairly evaluated in environments where chemotherapy was considered as a treatment option. Nevertheless, considering our relatively small number of patients, whether NLR has an impact on patients with stage III colon cancer remains undetermined.

Pine et al. analyzed the correlation of TILs and NLR and its impact on survival using 358 colorectal cancer patients19. In their study, TILs (expressed as a lymphocytic reaction at the invasive margin in their paper) were correlated with the NLR, which was divided using a cut-off value of 5. There was a significantly lower rate of patients with more than 5 NLR in the high TIL group (15.3% in the high TIL group vs. 29.2% in the low TIL group, P = 0.005). NLR dichotomized as 5 was proven to be an independent prognostic factor for OS, however, TILs were not an independent factor in multivariate analysis. The authors did not include the combination of these two parameters in statistical analysis. Contrary to their study, our study showed no direct correlation between TILs and NLR, however, TILs have an impact on OS and NLR did not. Again, we want to point out there were some differences in the inclusion criteria and OS outcomes might differ between the two studies because of the difference of included study periods.

One of the interesting findings in our study is that the combination of TILs with NLR had a higher relative contribution to the risk stratification of patients’ survival than TILs alone. Patients with high TILs showed different prognosis according to the NLR group (5-year OS; high TILs with low NLR, 93.8%, vs. high TILs with high NLR, 83.3%, P = 0.038). In contrast, this kind of discrimination was not demonstrated in patients in the low TIL group (5-year OS; low TILs with low NLR, 78.3%, vs. low TILs with high NLR, 75%, P = 0.892). Although the underlying reason for this association is not evident, it has been speculated that the NLR might have a partial effect on patient survival. One step further, our study showed that even among the same sub-staging, risk stratification may be possible according to the combination of local tumor immune response and host immunity defined as TILs and NLR. In patients with stage IIIB, the OS was significantly better in patients with high TILs with low NLR than in others (P = 0.011), although this correlation was not demonstrated in patients with stage IIIA or IIIC. Considering the distinct difference between groups of 5-year OS in stage IIIC (83.3% vs. 61.5%, P = 0.16) and the low number of included patients with stage IIIA (n = 11), these results might be derived from a type II error, which might be a limitation of this retrospective study. Further study is warranted to validate our findings.

This study has several limitations, which deserve to be mentioned. The small number of patients included in this retrospective study might be a main limitation. The TIL measurement was performed by one single pathologist, which might be a source of bias. However, previous studies evaluating inter-observer agreement on this subject showed good agreement (kappa value: 0.81 in each study)24,35. The cut-off value to discriminate between the high or low group using NLR is not strongly established. According to a recent review13, the cut-off value ranged from 2 to 5 and the proportion of the high NLR group might be different between the studies or may be diverse between races. This might be a critical limitation in the general application of this value17. Although our group used 3 as a reference value for dichotomization, if we applied the cut-off value as 5 or 2.72 (which was recommended by Li and colleagues37), there was no difference of OS between the two subgroups divided by NLR, respectively. There are several reports on the clinical impact of MSI, KRAS, NRAS, and BRAF mutations in the prognosis of colorectal cancer38,39,40. The effect of these genomic alterations in colorectal cancer may enter into the multivariable analysis; however, due to the retrospective study design, it was not possible to include all these variables in the analysis. Finally, the H&E-based K-M grading of inflammatory infiltrate has some inherent limitations compared to the IHC-based measurements. As explained in several previous studies6,36, the K-M grade provides a measure of the overall, generalized inflammatory cell infiltrate, in contrast, immunoscore measured the host adaptive T-lymphocyte. Consequently, the K-M grade can be elevated by not only the increasing tumor-infiltrating T lymphocytes, but also by increasing the density of the innate immune infiltrate such as neutrophils and macrophages6,36. Improvement of prognostic power by the combination of TILs and NLR in our study might suggest one possibility to overcome this limitation of K-M based tumor infiltrate measurements, although these results should be validated in other cohorts. In fact, Turner and colleagues have already demonstrated that the combination of two markers, such as intratumoral immune infiltrate and NLR, could further stratify the prognosis independent of standard high-risk criteria. Patients with prominent systemic and local inflammatory response (low chronic inflammatory cell density with high NLR) showed the worst outcome (5-year OS 55.8%) in stage II colon cancer9.

In conclusion, our study demonstrated that TILs measured by H&E staining and a combination of TILs and NLR could stratify patients’ survival in stage III colon cancers. These parameters can be obtained during clinical practice without any additional effort or equipment. Thus, we believe this approach is worth considering in view of cost-effectiveness and convenience. Evaluation of chemotherapy efficacy according to risk stratification using these easily obtained biomarkers may be required to select patients who may benefit from reduced chemotherapy in stage III colon cancer.


  1. 1.

    Andre, T. et al. Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer. N Engl J Med 350, 2343–2351, (2004).

  2. 2.

    Grothey, A. et al. Duration of Adjuvant Chemotherapy for Stage III Colon Cancer. N Engl J Med 378, 1177–1188, (2018).

  3. 3.

    Gebremedhn, E. G., Shortland, P. J. & Mahns, D. A. The incidence of acute oxaliplatin-induced neuropathy and its impact on treatment in the first cycle: a systematic review. BMC Cancer 18, 410, (2018).

  4. 4.

    Binnewies, M. et al. Understanding the tumor immune microenvironment (TIME) for effective therapy. Nat Med 24, 541–550, (2018).

  5. 5.

    Galon, J. et al. Towards the introduction of the ‘Immunoscore’ in the classification of malignant tumours. J Pathol 232, 199–209, (2014).

  6. 6.

    Pages, F. et al. International validation of the consensus Immunoscore for the classification of colon cancer: a prognostic and accuracy study. Lancet 391, 2128–2139, (2018).

  7. 7.

    Klintrup, K. et al. Inflammation and prognosis in colorectal cancer. Eur J Cancer 41, 2645–2654, (2005).

  8. 8.

    Huh, J. W., Lee, J. H. & Kim, H. R. Prognostic significance of tumor-infiltrating lymphocytes for patients with colorectal cancer. Arch Surg 147, 366–372, (2012).

  9. 9.

    Turner, N. et al. Analysis of local chronic inflammatory cell infiltrate combined with systemic inflammation improves prognostication in stage II colon cancer independent of standard clinicopathologic criteria. Int J Cancer 138, 671–678, (2016).

  10. 10.

    Iseki, Y. et al. A new method for evaluating tumor-infiltrating lymphocytes (TILs) in colorectal cancer using hematoxylin and eosin (H-E)-stained tumor sections. PLoS One 13, e0192744, (2018).

  11. 11.

    Lee, M. Y. & Lottsfeldt, J. L. Augmentation of neutrophilic granulocyte progenitors in the bone marrow of mice with tumor-induced neutrophilia: cytochemical study of in vitro colonies. Blood 64, 499–506 (1984).

  12. 12.

    Kelsey, K. T. & Wiencke, J. K. Immunomethylomics: A Novel Cancer Risk Prediction Tool. Ann Am Thorac Soc 15, S76–s80, (2018).

  13. 13.

    Haram, A. et al. The prognostic value of neutrophil-to-lymphocyte ratio in colorectal cancer: A systematic review. J Surg Oncol 115, 470–479, (2017).

  14. 14.

    Li, M. X. et al. Prognostic role of neutrophil-to-lymphocyte ratio in colorectal cancer: a systematic review and meta-analysis. Int J Cancer 134, 2403–2413, (2014).

  15. 15.

    Templeton, A. J. et al. Prognostic role of neutrophil-to-lymphocyte ratio in solid tumors: a systematic review and meta-analysis. J Natl Cancer Inst 106, dju124, (2014).

  16. 16.

    Walsh, S. R., Cook, E. J., Goulder, F., Justin, T. A. & Keeling, N. J. Neutrophil-lymphocyte ratio as a prognostic factor in colorectal cancer. J Surg Oncol 91, 181–184, (2005).

  17. 17.

    Dupre, A. & Malik, H. Z. Inflammation and cancer: What a surgical oncologist should know. Eur J Surg Oncol 44, 566–570, (2018).

  18. 18.

    Cha, Y. J., Park, E. J., Baik, S. H., Lee, K. Y. & Kang, J. Prognostic impact of persistent lower neutrophil-to-lymphocyte ratio during preoperative chemoradiotherapy in locally advanced rectal cancer patients: A propensity score matching analysis. PLoS One 14, e0214415, (2019).

  19. 19.

    Pine, J. K. et al. Systemic neutrophil-to-lymphocyte ratio in colorectal cancer: the relationship to patient survival, tumour biology and local lymphocytic response to tumour. Br J Cancer 113, 204–211, (2015).

  20. 20.

    Jung, Y. B., Kang, J., Park, E. J., Baik, S. H. & Lee, K. Y. Time to Initiation of Adjuvant Chemotherapy in Colon Cancer: Comparison of Open, Laparoscopic, and Robotic Surgery. J Laparoendosc Adv Surg Tech A 26, 799–805, (2016).

  21. 21.

    Edge, S. B. & Compton, C. C. The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol 17, 1471–1474, (2010).

  22. 22.

    Kang, J. et al. Clinical implications of microsatellite instability in T1 colorectal cancer. Yonsei Med J 56, 175–181, (2015).

  23. 23.

    Lee, J. H. et al. Relationship Between 18F-Fluorodeoxyglucose Uptake and V-Ki-Ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog Mutation in Colorectal Cancer Patients: Variability Depending on C-Reactive Protein Level. Medicine (Baltimore) 95, e2236, (2016).

  24. 24.

    Roxburgh, C. S., Salmond, J. M., Horgan, P. G., Oien, K. A. & McMillan, D. C. Comparison of the prognostic value of inflammation-based pathologic and biochemical criteria in patients undergoing potentially curative resection for colorectal cancer. Ann Surg 249, 788–793, (2009).

  25. 25.

    Malietzis, G. et al. A preoperative neutrophil to lymphocyte ratio of 3 predicts disease-free survival after curative elective colorectal cancer surgery. Ann Surg 260, 287–292, (2014).

  26. 26.

    Feliciano, E. M. C. et al. Association of Systemic Inflammation and Sarcopenia With Survival in Nonmetastatic Colorectal Cancer: Results From the C SCANS Study. JAMA Oncol 3, e172319, (2017).

  27. 27.

    Harrell, F. E. Jr., Lee, K. L. & Mark, D. B. Multivariable prognostic models: issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors. Stat Med 15, 361–387,<361::Aid-sim168>3.0.Co;2-4 (1996).

  28. 28.

    Akaike, H. Information theory and an extension of the maximum likelihood principle in Selected papers of hirotugu akaike 199–213 (Springer, 1998).

  29. 29.

    Lee, W. S., Park, S., Lee, W. Y., Yun, S. H. & Chun, H. K. Clinical impact of tumor-infiltrating lymphocytes for survival in stage II colon cancer. Cancer 116, 5188–5199, (2010).

  30. 30.

    Emile, J. F. et al. Prospective validation of a lymphocyte infiltration prognostic test in stage III colon cancer patients treated with adjuvant FOLFOX. Eur J Cancer 82, 16–24, (2017).

  31. 31.

    Galon, J. et al. Type, density, and location of immune cells within human colorectal tumors predict clinical outcome. Science 313, 1960–1964, (2006).

  32. 32.

    Pages, F. et al. In situ cytotoxic and memory T cells predict outcome in patients with early-stage colorectal cancer. J Clin Oncol 27, 5944–5951, (2009).

  33. 33.

    Richards, C. H. et al. The clinical utility of the local inflammatory response in colorectal cancer. Eur J Cancer 50, 309–319, (2014).

  34. 34.

    Kim, Y., Bae, J. M., Li, G., Cho, N. Y. & Kang, G. H. Image analyzer-based assessment of tumor-infiltrating T cell subsets and their prognostic values in colorectal carcinomas. PLoS One 10, e0122183, (2015).

  35. 35.

    Roxburgh, C. S., Salmond, J. M., Horgan, P. G., Oien, K. A. & McMillan, D. C. Tumour inflammatory infiltrate predicts survival following curative resection for node-negative colorectal cancer. Eur J Cancer 45, 2138–2145, (2009).

  36. 36.

    Park, J. H., McMillan, D. C., Edwards, J., Horgan, P. G. & Roxburgh, C. S. Comparison of the prognostic value of measures of the tumor inflammatory cell infiltrate and tumor-associated stroma in patients with primary operable colorectal cancer. Oncoimmunology 5, e1098801, (2016).

  37. 37.

    Li, Y. et al. Nomograms for predicting prognostic value of inflammatory biomarkers in colorectal cancer patients after radical resection. Int J Cancer 139, 220–231, (2016).

  38. 38.

    Modest, D. P. et al. Outcome according to KRAS-, NRAS- and BRAF-mutation as well as KRAS mutation variants: pooled analysis of five randomized trials in metastatic colorectal cancer by the AIO colorectal cancer study group. Ann Oncol 27, 1746–1753, (2016).

  39. 39.

    Peeters, M. et al. Prevalence of RAS mutations and individual variation patterns among patients with metastatic colorectal cancer: A pooled analysis of randomised controlled trials. Eur J Cancer 51, 1704–1713, (2015).

  40. 40.

    Domingo, E. et al. Mutation burden and other molecular markers of prognosis in colorectal cancer treated with curative intent: results from the QUASAR 2 clinical trial and an Australian community-based series. Lancet Gastroenterol Hepatol 3, 635–643, (2018).

Download references

Author information

J. Kang designed this study. Y.J. Cha, E.J. Park, S.H. Baik and K.Y. Lee contributed to gather clinical data. J. Kang and Y.J. Cha wrote the main manuscript text. All authors reviewed the manuscript.

Correspondence to Jeonghyun Kang.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Cha, Y.J., Park, E.J., Baik, S.H. et al. Clinical significance of tumor-infiltrating lymphocytes and neutrophil-to-lymphocyte ratio in patients with stage III colon cancer who underwent surgery followed by FOLFOX chemotherapy. Sci Rep 9, 11617 (2019) doi:10.1038/s41598-019-48140-1

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.