Neutrophil-to-lymphocyte ratio as a prognostic biomarker for patients with locally advanced esophageal squamous cell carcinoma treated with definitive chemoradiotherapy

Abstract

The present study evaluated the clinical and prognostic value of neutrophil-to-lymphocyte ratio (NLR) in patients with locally advanced esophageal squamous cell carcinoma (ESCC) treated with definitive chemoradiotherapy (dCRT). A total of 517 patients with ESCC were enrolled and analysed retrospectively. The NLR was calculated at three time points: baseline, post-treatment, and at the time of tumor progression. Elevated NLR was defined as a ratio ≥5. High NLR at baseline was present in 204 (39%) patients and was significantly correlated with larger tumour size, advanced TNM stage, worse ECOG performance status, and dCRT response (p < 0.05). At a median follow-up of 17 months, patients with higher NLR at baseline had poorer progression-free survival (PFS) and overall survival (OS). On multivariate analysis, elevated NLR at baseline was independently associated with PFS and OS (HR = 1.529, p < 0.001 for PFS; HR = 1.856, p < 0.001 for OS). In addition, patients with high pre- and post-treatment NLR demonstrated worse clinical outcomes than other groups. Our results suggest that NLR is an independent prognostic indicator for patients with ESCC undergoing dCRT and changes in NLR level with treatment may indicate therapeutic benefit.

Introduction

The prognosis of esophageal squamous cell carcinoma (ESCC) remains extremely poor in spite of improvements in surgical techniques, with a 5-year survival rate ranging from 15% to 25%1. Most patients are diagnosed at locally advanced stages (T3N1), and the concurrent chemoradiotherapy (CCRT) with or without surgery are widely accepted alternatives for curative treatment of these patients2,3. The clinical outcomes with this treatment have been comparable to those achieved with surgery alone4. However, the treatment failure rate after dCRT is high; approximately 56% of patients do not achieve complete response (CR) to dCRT5. Improved survival is more often observed in patients who achieve primary CR to dCRT compared with patients showing an incomplete response6. In addition, ineffective therapy for a resistant tumor could potentially reduce the quality of life in these patients. Therefore, the determination of molecular markers that can predict patients who would benefit from dCRT has important clinical implications.

Recently, several studies have revealed that the presence of an ongoing systemic inflammatory response is associated with adverse outcomes in variety of solid organ malignancies, including ESCC7,8. Such response may lead to tumor invasion, progression, and metastasis through recruitment of T lymphocytes, chemokines, aberrant activation of cytokines, suppression of apoptosis, DNA damage, and subversion of the adaptive immune system9. There are a number of parameters that can be used to measure systemic inflammation response, such as cytokine levels, modified Glasgow Prognostic Score (mGPS, which combines C-reactive protein and albumin), platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), and neutrophil-to-lymphocyte ratio (NLR)10,11,12. Among these parameters, NLR is an easily calculated, reproducible, and inexpensive marker of systemic inflammation response, and has been widely investigated as a predictive or prognostic factor in advanced stages of various kinds of cancer including ESCCC, renal cell carcinoma, gastric cancer, and prostate cancer13,14,15,16. Recently, Yao et al.17 reported that pre-treatment NLR was an independent prognostic factor for patients with non-small cell lung cancer; and that patients with high pretreatment NLR were resistant to platinum-based chemotherapy, indicating a role of NLR in chemotherapy resistance. However, the prognostic value of NLR in locally advanced ESCC treated with dCRT has not been studied previously. We hypothesised that ESCC patients with elevated NLR would show resistance to dCRT and poor survival.

Therefore, the aim of the present study was to examine the association of pretreatment NLR with treatment response rate, progression-free survival (PFS), and overall survival (OS) in patients with locally advanced ESCC treated with dCRT. We also analysed the impact of change of NLR with treatment to investigate its role as a response indicator.

Methods

Criteria for reporting recommendations for tumor markers in prognosis study (REMARK) were followed wherever possible.

Study population

The study protocol was approved by the Institutional Review Board for human studies of Huai’an First People’s Hospital, Huai’an, China; and informed written consent was obtained from all subjects. The study was performed in accordance with the approved guidelines. Patients with locally advanced ESCC treated with dCRT at the Nanjing Medical University Huai’an First Hospital between January 2006 and May 2010 were identified and retrospectively analysed. The inclusion criteria were as follows: (a) histologically confirmed primary ESCC by available biopsy specimens; (b) previously untreated; (c) Karnofsky score ≥70; (d) age ≤75 years; (e) no other significant medical disease. Patients with any evidence of active infection or presence of a chronic inflammatory condition were ineligible. Patients with hematology disease were excluded. Tumor were staged according to the conventional tumor-node-metastasis (TNM) classification for esophageal carcinoma (UICC, 6th edition), and the pretreatment clinical staging was based on the results of barium swallow, esophagogastroduodenoscopy (EGD), neck, chest, or abdominal CT examination, and bone scan.

Data collection and definitions

Clinicopathologic characteristics including age, gender, Eastern Cooperative Oncology Group performance status (ECOG PS), tumor length, tumor differentiation, smoking status, and TNM stage were extracted from patients medial records. The laboratory data collected included hemoglobin concentration, absolute WBC count, absolute neutrophil count, and absolute lymphocyte count. At diagnosis, data on serum carcinoembryonic antigen (CEA) and squamous cell carcinoma antigen (SCCA) levels were also collected. The NLR was defined by dividing the number of absolute neutrophil count by the number of absolute lymphocyte count. A NLR of 5 or greater was considered elevated in accordance with previous studies18,19,20, and the cut-off point of ≥5 provided the strongest prognostic significance in our preplanned analysis. The values of NLR were calculated at three time points: baseline (pretreatment), post-treatment (within three days after dCRT), and at the time of progression.

Definitive chemoradiotherapy

Chemotherapy

For patients with adequate bone marrow, renal, and hepatic function, chemotherapy was performed with a PF-based regimen (cisplatin/fluorouracil). Chemotherapy started on day 1, concurrent with initiation of radiotherapy. Cisplatin (80 mg per square metre of body surface area) was administered intravenously on Day 1, and fluorouracil (1 g per square metre of body surface area) was administered as a continuous infusion from Day 1 to Day 4. Two courses of chemotherapy were administered at a 4-week interval during radiotherapy.

Radiotherapy

All patients were treated with external-beam radiation using 6 or 15 MV LINAC (Siemens ONCOR). The radiation treatment was delivered as three-dimensional conformal radiation therapy or intensity-modulated radiation treatment to ensure tumour coverage and spare adjacent normal organs. Information from EGD examination and CT scan was studied in detail before delineation of target tumour volume. A total radiation dose of 50–60 Gy (1.8–2.0 Gy/fraction, 5 days per week) was given to the target of the gross oesophageal mass and enlarged lymph nodes.

Clinical response evaluation and follow-up

To evaluate the treatment response, esophagogram, EGD and CT scan were performed 4 weeks after completion of dCRT. The response to treatment was assessed basically according to the following criteria. CR was defined as complete regression of all assessable lesions; partial response (PR) was defined as more than 50% reduction in primary tumor size or more of the sum of the lesions and no progression of assessable lesions; stable disease (SD) was defined as a reduction of <50% or increase <25% in tumor size; progressive disease (PD) was defined as an increase ≥25% in primary tumor volume or appearance of new lesions. We divided these categories into two groups: the effective group consisted o CR and PR, the resistant group consisted of SD and PD.

Follow-up evaluation was performed every 3 months for the first year, every 6 months for an additional 2 years, and then at the end of each year to study end or until death. During the follow-up period, diagnostic examinations were performed when recurrence and/or metastasis was suspected. Follow-up data were obtained from patients’ medical records and/or telephone interviews.

Statistical analysis

The primary endpoints were OS and PFS. OS was defined as the time from diagnosis to death (event), or last follow-up (censored), and PFS was calculated from the date of therapy initiation to the time of disease progression (event), or last date of follow up (censored).

Continuous data were expressed as the median (range), and categorical variables were reported as frequencies and percentages. Continuous data were analysed using Mann-Whitney U test or Kruskal-Wallis test. Categorical variables were compared using Fisher’s exact test or chi-square test. Survival curves were plotted with Kaplan–Meier method, and the differences were compared using a log-rank test. Univariate and multivariate Cox regression analyses were performed to evaluate potential prognostic factors for survival, and only variables that showed statistical significance in univariate analysis were subsequently entered into multivariate analysis. All statistical analyses were conducted using SPSS Statistics version 20.0 (IBM, Inc.). A two-sided p value less than 0.05 was considered statistically significant.

Results

Patient characteristics and treatment outcomes

A total of 517 patients met the inclusion criteria and were selected for this study. Most of the patients were male (n = 407, 79%), and the median age at diagnosis was 65 years (range, 36 to 74 years). There were 83 (16%) cases with stage II disease, 377 (73%) cases with stage III disease, and 57 (11%) cases with stage IV disease. Median tumour length was 4 cm (range, 2 to 12 cm) and 224 primary tumours (43%) were longer than 5 cm. Detailed patient characteristics at baseline are shown in Table 1.

Table 1 Characteristics of patients.

All 517 patients underwent concurrent dCRT with two cycles of PF. After treatment, CR, PR, SD, and PD were observed in 88 (17%), 203 (39%), 211 (41%), and 15 patients (3%), respectively. After dCRT, 17 patients (3%) underwent esophagectomy and 160 patients (31%) received adjuvant chemotherapy. With a median follow-up of 17 months (range, 2 to 76 months), 431 (83%) of the 517 patients died. Of these, the cause of death was progression of recurrent disease in 396 (92%) patients, treatment-related esophagoaortic fistula in 3 (1%) patients, and other causes in the remaining 32 (7%) patients. The median PFS and OS for the whole cohort of patients were 12 months and17 months, respectively.

For all patients, the median values for baseline serum WBC count, neutrophil count, lymphocyte count, and NLR were 5.86 × 109/L (range, 2.87 to 16.00), 4.06 × 109/L (range, 1.39 to 12.80), 1.12 × 109/L (range, 0.28 to 3.47), and 3.24 (range, 0.85 to 19.28), respectively.

Correlation between baseline NLR and clinicopathologic characteristics

At baseline, 204 (39%) patients had a high baseline NLR ≥ 5 and 313 (61%) patients had NLR < 5. The relationships between clinicopathologic variables and pretreatment NLR are shown in Table 2.

Table 2 Relationships between clinicopathological characteristics and pre-treatment NLR.

High NLR at baseline was significantly associated with worse ECOG PS (p = 0.033), larger tumor size (p < 0.001), distant lymph node metastasis (p < 0.001), advanced TNM stage (p < 0.001), and low response rate to dCRT (p < 0.001, Table 2). However, age, gender, tumor location, tumor differentiation, smoking status, hemoglobin concentration, CEA level, and SCCA level were not significantly different between the two groups (p > 0.05, Table 2).

Baseline NLR and response to dCRT

Tumour responses to dCRT for the 517 patients are shown in Table 3. The objective response rate was significantly lower in patients with baseline NLR ≥ 5 than in patients with NLR < 5 (33 vs. 72%, p < 0.001, Table 3), indicating that NLR might be a predictive factor for dCRT in ESCC before treatment. However, there was no significant difference in dCRT response between post-treatment NLR ≥ 5 or <5 (52 vs 58%, p = 0.256, Table 3). The sensitivity of a low baseline NLR for predicting dCRT response was 72% (224/313) and the specificity was 67% (137/204). Unexpectedly, no significant correlations were observed between dCRT response and clinicopathologic parameters such as age, gender, tumor length, tumor location, tumor differentiation, and radiotherapy dose (Supplementary Table S1, P > 0.05).

Table 3 Relationship between NLR categories and response to definitive chemoradiotherapy.

Prognostic significance of baseline NLR and other parameters

To further examine whether pretreatment NLR was associated with outcomes of ESCC patients after dCRT, Kaplan–Meier survival analysis was used to compare the low (n = 313) and high (n = 204) NLR subgroups Fig. 1. Patients with high pretreatment NLR had worse PFS (NLR ≥ 5 vs. NLR < 5, median PFS 9 vs. 15 months, p < 0.001, Fig. 1A) and OS (NLR ≥ 5 vs. NLR < 5, median OS 12 vs. 20 months, p < 0.001, Fig. 1B).

Figure 1
figure1

Association of baseline NLR (≥5 versus <5) with overall survival (A) and progression free survival (B).

Results of univariate analysis indicated that ECOG PS (≥2), tumor length (≥5), lymph node metastasis (positive), tumor stage (III/IV), dCRT response (SD + PD), SCCA level (≥1.5), and baseline NLR radio (≥5) were significantly correlated with decreased PFS or OS (p < 0.05, Table 4). All 8 clinicopathologic characteristics were therefore entered into subsequent multivariate analysis. The results of multivariate analysis revealed that pretreatment NLR, tumor stage, and dCRT response were independently prognostic factors of PFS and OS (Table 5).

Table 4 Univariate analysis of factors associated with progression free survival and overall survival.
Table 5 Multivariate analysis of factors associated with progression free survival and overall survival.

Changes in NLR and clinical outcomes

We also examined changes in NLR values according to disease and treatment status. After dCRT, NLR decreased significantly (mean ± SD: baseline, 4.48 ± 3.05 vs. post-treatment, 3.87 ± 2.17, p < 0.001, Fig. 2) because of the effect of the treatment. However, NLR subsequently increased significantly to 5.04 ± 2.34 at tumour progression (p < 0.001 compared with the ratio after completion of dCRT, Fig. 2).

Figure 2: Change of NLR at baseline (pre-treatment, n = 517), after the completion of dCRT (post-treatment, n = 517), and at tumor progression (n = 436).
figure2

Horizontal lines inside the box plots represent the median, boxes represent the interquartile range, and whiskers represent 97.5th and 2.5th percentiles.

Patients were divided into four groups based on changes in NLR before and after dCRT (Table 6). (1) NLR ≥ 5 at baseline and after dCRT (n = 64, high-high group); (2) NLR ≥ 5 before dCRT and <5 after dCRT (n = 140, high-low group); (3) NLR < 5 at baseline and after dCRT (n = 251, low-low group); (4) NLR < 5 at baseline and ≥5 after dCRT (n = 62, low-high group). Patients in group 1 had significantly shorter PFS (median, 6 vs. 10 months, p < 0.001) and OS (median, 10 vs. 14 months, p < 0.001, Table 6) than those in group 2. However, patients in group 3 showed no significant differences from those in group 4 for PFS (median, 15 vs. 14 months, p = 0.720) and OS (median, 20 vs. 20.5 months, p = 0.793, Table 6).

Table 6 Change in NLR and benefit from dCRT.

Discussion

The results of the present study supported our hypothesis and indicated that pretreatment NLR may be correlated with treatment response rate, PFS, and OS in patients with locally advanced ESCC treated with dCRT. In this retrospective study, patients with high pretreatment NLR (≥5) had a worse dCRT response rate and poorer PFS and OS. Although several studies have shown an association between NLR and prognosis of patients with ESCC, they mainly reported results for patients treated with surgery21,22. Moreover, our results also showed that patients with normalised post-treatment NLR (at 4 weeks after treatment) had a better PFS and OS than those with sustained high NLR. To our knowledge, this study is the first to assess clinical significance of NLR in patients with local advanced ESCC treated with dCRT.

As a biomarker of inflammation and immunology, increased NLR was previously correlated with advanced stage in endometrial cancer, small-cell lung cancer, and colorectal cancer23,24,25. Consistent with these reports, elevated NLR was also associated with advanced clinical stage and lymph node metastasis in the present study of ESCC. However, Sharaiha et al. examined a cohort of 295 esophageal cancer patients treated with esophagectomy and found no association between pretreatment NLR and tumor stage8. At present, it was difficult to explain such phenomena. The different pathological types could contribute to the different results.

Currently, definitive chemoradiotherapy with a PF regimen is an important component of the treatment of locally advanced ESCC, and the clinical CR to dCRT is widely accepted as the most important predictor of patient outcome26,27. However, chemoradiotherapy resistance and development of distant metastasis are major challenges in the management of ESCC28. Thus, in the present study, we focused markers related to systemic inflammation response that are known to be associated with chemotherapeutic efficacy. The role of NLR as a biomarker for evaluation of treatment response has been reported in several cancers treated with chemotherapy or radiotherapy, such as lung cancer, urothelial cancer, hepatocellular carcinoma, and prostate cancer29,30,31,32. In line with previous studies, a significant association between pretreatment NLR and dCRT response was observed in the current study. NLR was the only factor that showed a significant association with the dCRT response in ESCC. Consequently, the results of the present study provide important information to help physicians and patients make a more informed selection about the appropriateness of definitive chemoradiotherapy in ESCC.

Recently, mounting evidence indicates that the existence of systemic inflammation response, as evidenced by NLR, mGPS, CRP, and PLR, is correlated with a worse prognosis in patients with cancers33,34,35,36. The prognostic value of NLR has been demonstrated in many solid organ malignancies included in a recently published meta-analysis of 49 articles containing 14282 patients. These studies showed a broad prognostic impact of NLR across different cancer types, cancer stages, and treatments9. These findings have been replicated in the present study. In multivariate survival analysis, pretreatment NLR was an independent factor correlated with PFS and OS. The role of inflammation in carcinogenesis and tumor progression has been established during the past decade37, but the mechanisms connecting elevated NLR and poor outcomes remain elusive. Recent studies revealed that the presence of a systemic inflammation response could result in relative neutrophilia and lymphocytopenia. On one hand, neutrophils are able to secrete circulating vascular endothelial growth factors, which stimulate tumor angiogenesis, and release IL-1, IL-6, and TNF-alpha, which contribute to tumor progression38,39. Furthermore, relative neutrophilia could activate immunosuppression through inhibition of the activity of lymphocytes and other immune cells40. On the other hand, lymphocytes, usually CD4+ helper T and natural killers cells form the major component of the cell-mediated immune response to tumor infiltration and can attack tumor cells and eliminate nascent cancer cells16. A low lymphocyte count may be responsible for an inadequate host-to-tumor immunologic reaction with reduced response against tumor, leading to a worse clinical prognosis25,41. As NLR is calculated simply from the peripheral neutrophil count and lymphocyte count, a high NLR reflects enhanced neutrophil-dependent inflammatory response and/or a decreased lymphocyte-mediated anti tumor immune response, both of which contribute to tumor initiation, invasion, and metastasis. Baseline neutrophil and lymphocyte counts alone may provide limited reflection on the inflammatory response in tumor progression and are not independent prognostic factors for patients prognosis. Our findings indicated that the combination of neutrophil and lymphocyte provided more prognosis information than either component alone.

A previous study demonstrated the prognostic significance of pre- and post-treatment NLR in prostate cancer patients who received second-line chemotherapy42. The author observed that conversion from high to low NLR was associated with improved survival. In malignant mesothelioma, patients whose NLR normalised after 1 cycle of systemic therapy were found to have better prognosis compared with those whose NLR remained abnormal43. In our study, NLR values increased with tumor progression, and patients whose NLR remained ≥5 after dCRT had shorter PFS and OS than those whose NLR decreased to <5. These findings indicated that NLR might reflect the efficacy of treatment and help in monitoring progression of ESCC.

The present study provides the first clinical evidence supporting NLR as a biomarker for prognosis of patients with locally advanced ESCC. However, research limitations exist in our study. First, the retrospective design of the study may lead to bias, and the results must be validated in prospective study. Second, the total number of patients included is relatively small. In addition, unknown physiological factors that potential affecting the NLR might influence our results.

In conclusion, our results demonstrated that pretreatment NLR ≥ 5 was an independent prognostic factor for poor survival in patients with locally advanced ESCC treated with dCRT. Moreover, changes in NLR level with treatment may indicate therapeutic benefit.

Additional Information

How to cite this article: Zhou, X.-L. et al. Neutrophil-to-lymphocyte ratio as a prognostic biomarker for patients with locally advanced esophageal squamous cell carcinoma treated with definitive chemoradiotherapy. Sci. Rep. 7, 42581; doi: 10.1038/srep42581 (2017).

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

References

  1. 1

    Pennathur, A., Gibson, M. K., Jobe, B. A. & Luketich, J. D. Oesophageal carcinoma. Lancet 381, 400–412, doi: 10.1016/s0140-6736(12)60643-6 (2013).

    Article  Google Scholar 

  2. 2

    Stahl, M. Chemoradiation With and Without Surgery in Patients With Locally Advanced Squamous Cell Carcinoma of the Esophagus. J Clin Oncol 23, 2310–2317, doi: 10.1200/jco.2005.00.034 (2005).

    Article  Google Scholar 

  3. 3

    Rustgi, A. K. & El-Serag, H. B. Esophageal carcinoma. N Engl J Med 371, 2499–2509, doi: 10.1056/NEJMra1314530 (2014).

    Article  CAS  PubMed  Google Scholar 

  4. 4

    Matsuda, S. et al. Comparison of transthoracic esophagectomy with definitive chemoradiotherapy as initial treatment for patients with esophageal squamous cell carcinoma who could tolerate transthoracic esophagectomy. Ann Surg Oncol 22, 1866–1873, doi: 10.1245/s10434-014-4337-7 (2015).

    Article  PubMed  Google Scholar 

  5. 5

    Ishikura, S. et al. Long-term toxicity after definitive chemoradiotherapy for squamous cell carcinoma of the thoracic esophagus. J Clin Oncol 21, 2697–2702, doi: 10.1200/JCO.2003.03.055 (2003).

    Article  CAS  PubMed  Google Scholar 

  6. 6

    Zhou, X. L. et al. High expression of long non-coding RNA AFAP1-AS1 predicts chemoradioresistance and poor prognosis in patients with esophageal squamous cell carcinoma treated with definitive chemoradiotherapy. Mol Carcinog, doi: 10.1002/mc.22454 (2016).

  7. 7

    Gu, X. B., Tian, T., Tian, X. J. & Zhang, X. J. Prognostic significance of neutrophil-to-lymphocyte ratio in non-small cell lung cancer: a meta-analysis. Sci Rep 5, 12493, doi: 10.1038/srep12493 (2015).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

  8. 8

    Sharaiha, R. Z. et al. Elevated preoperative neutrophil:lymphocyte ratio as a predictor of postoperative disease recurrence in esophageal cancer. Ann Surg Oncol 18, 3362–3369, doi: 10.1245/s10434-011-1754-8 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9

    Paramanathan, A., Saxena, A. & Morris, D. L. A systematic review and meta-analysis on the impact of pre-operative neutrophil lymphocyte ratio on long term outcomes after curative intent resection of solid tumours. Surg Oncol 23, 31–39, doi: 10.1016/j.suronc.2013.12.001 (2014).

    Article  PubMed  Google Scholar 

  10. 10

    McMillan, D. C. The systemic inflammation-based Glasgow Prognostic Score: A decade of experience in patients with cancer. Cancer Treat Rev 39, 534–540, doi: 10.1016/j.ctrv.2012.08.003 (2013).

    Article  PubMed  Google Scholar 

  11. 11

    Deng, Q. et al. Prognostic value of pre-operative inflammatory response biomarkers in gastric cancer patients and the construction of a predictive model. J Transl Med 13, 66, doi: 10.1186/s12967-015-0409-0 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. 12

    Del Prete, M. et al. Prognostic clinical factors in pretreated colorectal cancer patients receiving regorafenib implications for clinical management. Oncotarget 6, 33982–92, doi: 10.18632/oncotarget.5053 (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  13. 13

    Keizman, D. et al. The association of pre-treatment neutrophil to lymphocyte ratio with response rate, progression free survival and overall survival of patients treated with sunitinib for metastatic renal cell carcinoma. Eur J Cancer 48, 202–208, doi: 10.1016/j.ejca.2011.09.001 (2012).

    Article  CAS  PubMed  Google Scholar 

  14. 14

    Cho, I. R. et al. Pre-treatment neutrophil to lymphocyte ratio as a prognostic marker to predict chemotherapeutic response and survival outcomes in metastatic advanced gastric cancer. Gastric cancer 17, 703–710, doi: 10.1007/s10120-013-0330-2 (2014).

    Article  CAS  PubMed  Google Scholar 

  15. 15

    Yodying, H. et al. Prognostic Significance of Neutrophil-to-Lymphocyte Ratio and Platelet-to-Lymphocyte Ratio in Oncologic Outcomes of Esophageal Cancer: A Systematic Review and Meta-analysis. Ann Surg Oncol 23, 646–654, doi: 10.1245/s10434-015-4869-5 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  16. 16

    Keizman, D. et al. Pretreatment neutrophil-to-lymphocyte ratio in metastatic castration-resistant prostate cancer patients treated with ketoconazole: association with outcome and predictive nomogram. Oncologist 17, 1508–1514, doi: 10.1634/theoncologist.2012-0125 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. 17

    Yao, Y., Yuan, D., Liu, H., Gu, X. & Song, Y. Pretreatment neutrophil to lymphocyte ratio is associated with response to therapy and prognosis of advanced non-small cell lung cancer patients treated with first-line platinum-based chemotherapy. Cancer Immunol Immunother 62, 471–479, doi: 10.1007/s00262-012-1347-9 (2013).

    Article  CAS  PubMed  Google Scholar 

  18. 18

    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, doi: 10.1002/jso.20329 (2005).

    Article  CAS  PubMed  Google Scholar 

  19. 19

    Halazun, K. J. et al. Elevated preoperative neutrophil to lymphocyte ratio predicts survival following hepatic resection for colorectal liver metastases. Eur J Surg Oncol 34, 55–60, doi: 10.1016/j.ejso.2007.02.014 (2008).

    Article  CAS  PubMed  Google Scholar 

  20. 20

    Kishi, Y. et al. Blood Neutrophil-to-Lymphocyte Ratio Predicts Survival in Patients with Colorectal Liver Metastases Treated with Systemic Chemotherapy. Ann Surg Oncol 16, 614–622, doi: 10.1245/s10434-008-0267-6 (2009).

    Article  PubMed  Google Scholar 

  21. 21

    Chen, P. C. & Feng, J. F. A Novel Inflammation-Based Stage (I Stage) in Patients with Resectable Esophageal Squamous Cell Carcinoma. Mediators Inflamm 2016, 5396747, doi: 10.1155/2016/5396747 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. 22

    Feng, J. F., Huang, Y. & Chen, Q. X. The combination of platelet count and neutrophil lymphocyte ratio is a predictive factor in patients with esophageal squamous cell carcinoma. Transl Oncol 7, 632–637, doi: 10.1016/j.tranon.2014.07.009 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  23. 23

    Cummings, M. et al. Preoperative neutrophil:lymphocyte and platelet:lymphocyte ratios predict endometrial cancer survival. Br J Cancer 113, 311–320, doi: 10.1038/bjc.2015.200 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. 24

    Kang, M. H. et al. The prognostic impact of the neutrophil-to-lymphocyte ratio in patients with small-cell lung cancer. Br J Cancer 111, 452–460, doi: 10.1038/bjc.2014.317 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. 25

    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, doi: 10.1038/bjc.2015.87 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. 26

    He, L.-R. et al. High expression of EZH2 is associated with tumor aggressiveness and poor prognosis in patients with esophageal squamous cell carcinoma treated with definitive chemoradiotherapy. Int J Cancer 127, 138–147, doi: 10.1002/ijc.25031 (2010).

    Article  CAS  PubMed  Google Scholar 

  27. 27

    Zhang, J. X. et al. PITX2: a promising predictive biomarker of patients’ prognosis and chemoradioresistance in esophageal squamous cell carcinoma. Int J cancer 132, 2567–2577, doi: 10.1002/ijc.27930 (2013).

    Article  CAS  PubMed  Google Scholar 

  28. 28

    Hamano, R. et al. Overexpression of miR-200c induces chemoresistance in esophageal cancers mediated through activation of the Akt signaling pathway. Clin Cancer Res 17, 3029–3038, doi: 10.1158/1078-0432.CCR-10-2532 (2011).

    Article  CAS  PubMed  Google Scholar 

  29. 29

    Rossi, L. et al. High neutrophil-to-lymphocyte ratio persistent during first-line chemotherapy predicts poor clinical outcome in patients with advanced urothelial cancer. Ann Surg Oncol 22, 1377–1384, doi: 10.1245/s10434-014-4097-4 (2015).

    Article  PubMed  Google Scholar 

  30. 30

    Shaverdian, N. et al. Pretreatment Immune Parameters Predict for Overall Survival and Toxicity in Early-Stage Non–Small-Cell Lung Cancer Patients Treated With Stereotactic Body Radiation Therapy. Clin Lung Cancer 17, 39–46, doi: 10.1016/j.cllc.2015.07.007 (2016).

    Article  PubMed  Google Scholar 

  31. 31

    Terashima, T. et al. Blood neutrophil to lymphocyte ratio as a predictor in patients with advanced hepatocellular carcinoma treated with hepatic arterial infusion chemotherapy. Hepatol Res 45, 949–959, doi: 10.1111/hepr.12436 (2015).

    Article  CAS  PubMed  Google Scholar 

  32. 32

    van Soest, R. J. et al. Neutrophil-to-lymphocyte ratio as a prognostic biomarker for men with metastatic castration-resistant prostate cancer receiving first-line chemotherapy: data from two randomized phase III trials. Ann Oncol 26, 743–749, doi: 10.1093/annonc/mdu569 (2015).

    Article  CAS  PubMed  Google Scholar 

  33. 33

    Santoni, M. et al. Pre-treatment neutrophil-to-lymphocyte ratio may be associated with the outcome in patients treated with everolimus for metastatic renal cell carcinoma. Br J Cancer 109, 1755–1759, doi: 10.1038/bjc.2013.522 (2013).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. 34

    Zhang, P. et al. The modified glasgow prognostic score is an independent prognostic factor in patients with inoperable thoracic esophageal squamous cell carcinoma undergoing chemoradiotherapy. J Cancer 5, 689–695, doi: 10.7150/jca.9569 (2014).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. 35

    Szkandera, J. et al. Validation of C-reactive protein levels as a prognostic indicator for survival in a large cohort of pancreatic cancer patients. Br J Cancer 110, 183–188, doi: 10.1038/bjc.2013.701 (2014).

    Article  CAS  PubMed  Google Scholar 

  36. 36

    Zhang, W. W., Liu, K. J., Hu, G. L. & Liang, W. J. Preoperative platelet/lymphocyte ratio is a superior prognostic factor compared to other systemic inflammatory response markers in ovarian cancer patients. Tumour Biol 36, 8831–8837, doi: 10.1007/s13277-015-3533-9 (2015).

    Article  CAS  PubMed  Google Scholar 

  37. 37

    Balkwill, F. & Mantovani, A. Inflammation and cancer: back to Virchow? Lancet 357, 539–545, doi: 10.1016/s0140-6736(00)04046-0 (2001).

    Article  CAS  PubMed  Google Scholar 

  38. 38

    Shen, L. et al. Baseline neutrophil-lymphocyte ratio (&gt;/=2.8) as a prognostic factor for patients with locally advanced rectal cancer undergoing neoadjuvant chemoradiation. Radiat Oncol 9, 295, doi: 10.1186/s13014-014-0295-2 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  39. 39

    Kang, M., Jeong, C. W., Kwak, C., Kim, H. H. & Ku, J. H. The Prognostic Significance of the Early Postoperative Neutrophil-to-Lymphocyte Ratio in Patients with Urothelial Carcinoma of the Bladder Undergoing Radical Cystectomy. Ann Surg Oncol 23, 335–342, doi: 10.1245/s10434-015-4708-8 (2016).

    Article  PubMed  Google Scholar 

  40. 40

    Han, S. et al. Pre-treatment neutrophil-to-lymphocyte ratio is associated with neutrophil and T-cell infiltration and predicts clinical outcome in patients with glioblastoma. BMC Cancer 15, 617, doi: 10.1186/s12885-015-1629-7 (2015).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. 41

    An, X. et al. Elevated neutrophil to lymphocyte ratio predicts survival in advanced pancreatic cancer. Biomarkers 15, 516–522, doi: 10.3109/1354750X.2010.491557 (2010).

    Article  CAS  PubMed  Google Scholar 

  42. 42

    Lorente, D. et al. Baseline neutrophil-lymphocyte ratio (NLR) is associated with survival and response to treatment with second-line chemotherapy for advanced prostate cancer independent of baseline steroid use. Ann Oncol 26, 750–755, doi: 10.1093/annonc/mdu587 (2015).

    Article  CAS  PubMed  Google Scholar 

  43. 43

    Kao, S. C. et al. High blood neutrophil-to-lymphocyte ratio is an indicator of poor prognosis in malignant mesothelioma patients undergoing systemic therapy. Clin Cancer Res 16, 5805–5813, doi: 10.1158/1078-0432.CCR-10-2245 (2010).

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We would like to thank all of the study participants for agreeing to participate in medical research.

Author information

Affiliations

Authors

Contributions

Y.S.T., X.L.Z., and Y.Q.L. conceived and designed the experiments and were responsible for writing the manuscript. W.G.Z. and C.H.Y. were responsible for data analysis. Y.Q.S., W.W.W., D.C.H., and G.Z.T. recruited the patients and collected their clinical data. All authors reviewed the final manuscript.

Corresponding author

Correspondence to Yu-Suo Tong.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Supplementary information

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Zhou, X., Li, Y., Zhu, W. et al. Neutrophil-to-lymphocyte ratio as a prognostic biomarker for patients with locally advanced esophageal squamous cell carcinoma treated with definitive chemoradiotherapy. Sci Rep 7, 42581 (2017). https://doi.org/10.1038/srep42581

Download citation

Comments

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.

Search

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing