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Neutrophil/lymphocyte ratio has a prognostic value for patients with terminal cancer

  • 1, 2Email author,
  • 2,
  • 2,
  • 2,
  • 2,
  • 2,
  • 2,
  • 2,
  • 2,
  • 2 and
  • 2
World Journal of Surgical Oncology201614:148

https://doi.org/10.1186/s12957-016-0904-7

  • Received: 16 November 2015
  • Accepted: 10 May 2016
  • Published:

Abstract

Background

Determining prognosis in advanced cancer is of key importance. Various prognostic scores have been developed. However, they are often very complex. In this study, we evaluated the feasibility of neutrophil/lymphocyte ratio (NLR) as an index to estimate survival in terminal cancer patients.

Methods

NLR was calculated retrospectively based on blood tests performed at 3 months, 2 months, 4 weeks, 3 weeks, 2 weeks, 1 week, and within 3 days before death in 160 cancer patients (82 men, 78 women; age range, 33–99 years; mean age, 69.8 years).

Results

NLR increased significantly with time (P < 0.0001). Mean NLR was significantly higher in patients who died within 4 weeks (29.82) than in those who lived more than 4 weeks (6.15). The NLR cutoff point was set at 9.21 according to receiver operating characteristic curve analysis (area under the curve, 0.82; 95 % confidence interval, 0.79–0.85). We inferred that life expectancy would be <4 weeks when NLR >9.21. The sensitivity, specificity, positive predictive value, and negative predictive value were 65.6, 84.1, 90.6, and 51.1 %, respectively. The positive and negative likelihood ratios were 4.125 and 0.409, respectively.

Conclusions

NLR appears to be a useful and simple parameter to predict the clinical outcomes of patients with terminal cancer.

Keywords

  • Blood cells
  • Inflammation
  • Neoplasms
  • Palliative care
  • Prognosis

Background

Determining prognosis in patients with advanced cancer is of key importance. Previous studies have shown that physicians do not accurately estimate survival time [1, 2]. A systematic review of the accuracy of clinical predictions of survival in terminally ill cancer patients has shown that physicians consistently overestimate survival; however, their predictions are highly correlated with actual survival [3].

Various prognostic scores have been developed. The palliative prognostic score (PPS) [4] and the palliative prognostic index (PPI) [5] are frequently used for prognostic estimates in patients with terminal-stage cancer, but these methods are not simple and often include subjective factors. These scores are widely used by palliative care physicians to make the remaining time that patients have left to live more meaningful. However, oncologists regard them as complex predictive formula. The inability to make accurate forecasts about a patient’s prognosis is a reason why treatment often runs counter to the patient’s expectations. Therefore, we consider it important to have an index that enables doctors to easily predict the prognosis of cancer patients.

Neutrophil/lymphocyte ratio (NLR) is an immunological index commonly used in cancer therapy and diagnosis [612]. In this study, we evaluated the feasibility of NLR as an index to estimate survival in terminal cancer patients.

Methods

This retrospective study included data from 160 consecutive patients who received palliative care and died in the Toho University Ohashi Medical Center between May 2011 and November 2013. The inclusion criteria were (i) histologically or clinically confirmed malignant tumor and (ii) death after hospitalization. We implemented a comprehensive agreement method to obtain consent from the patients regarding the study. The study was approved by the ethical review board of Toho University Ohashi Medical Center.

Data on white blood cell (WBC) counts and neutrophil and lymphocyte fractions (%) were extracted retrospectively from electronic records of blood tests performed at 3 months, 2 months, 4 weeks, 3 weeks, 2 weeks, 1 week, and within 3 days before death of the cancer patients. NLR was calculated by dividing the absolute count of band and segmented neutrophils by the number of lymphocytes in the complete blood count.

All statistical analyses were performed with EZR (Saitama Medical Center, Jichi Medical University, Saitama, Japan), the graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria). More precisely, EZR is a modified version of R commander designed to add statistical functions frequently used in biostatistics [13]. Continuous variables were expressed as mean ± standard deviation. Comparisons between time points were performed using the Friedman rank sum test. Comparisons between groups were performed using the t test. The receiver operating characteristic (ROC) curve was generated by plotting the sensitivity value against the false-positive rate (1-specificity). We assessed the predictive value of life expectancy <4 weeks by calculating the area under the curve (AUC) and estimated the optimal cutoff value based on maximum sensitivity and specificity. Differences were considered statistically significant if the null hypothesis could be rejected with >95 % confidence (P < 0.05).

Results

The average age of the patients (82 men, 78 women) was 69.8 years (age range, 33–99 years). Patient characteristics and primary tumor sites are shown in Table 1. The feasibility of using NLR was evaluated from 735 data points.
Table 1

Patient characteristics (n = 160)

Age, mean (range)

69.8 (33–99) years

Sex, male/female

82:78

Site of primary tumor

Lung

33

CUP

7

Colon/rectum

32

Esophagus

5

Stomach

25

Cervix

5

Breast

13

Uterine body

4

Pancreas

11

Ovary

3

Biliary tract

7

Ureter

2

Bladder

7

Other

6

CUP cancer of unknown primary

The median NLR values were 3.83 at 3 months before death, 5.38 at 2 months, 8.53 at 4 weeks, 10.22 at 3 weeks, 11.48 at 2 weeks, 21.16 at 1 week, and 37.40 within 3 days (Table 2). NLR values increased significantly with time (P < 0.0001) (Fig. 1).
Table 2

NLR values at various times before death

Time before death

Numbers of patients

Neutrophils × 109/L, mean ± standard deviation

Lymphocytes × 109/L, mean ± standard deviation

NLR, mean ± standard deviation (median)

3 months

109

4.84 ± 3.99

1.07 ± 0.54

5.64 ± 6.30 (3.83)

2 months

111

5.62 ± 3.45

0.99 ± 0.52

6.65 ± 5.36 (5.38)

4 weeks

112

7.93 ± 5.02

0.87 ± 0.49

12.28 ± 11.25 (8.53)

3 weeks

99

7.90 ± 4.23

0.78 ± 0.50

13.91 ± 13.83 (10.22)

2 weeks

110

9.10 ± 5.71

0.84 ± 1.03

25.15 ± 36.93 (11.48)

1 week

100

11.53 ± 7.48

0.55 ± 0.41

44.28 ± 56.62 (21.16)

3 days

96

13.50 ± 11.25

0.52 ± 0.71

57.74 ± 61.41 (37.40)

Fig. 1
Fig. 1

The time course of the NLR value. NLR values increased significantly with time

The mean NLR value of patients who lived more than 4 weeks was 6.15 ± 5.86, while that of those who died within 4 weeks was 29.82 ± 44.19; a significant difference was observed between the two groups (P < 0.00000001) (Table 3).
Table 3

Mean NLR of the patients who lived more than or up to 4 weeks

 

More than 4 weeks

Up to 4 weeks

P value

NLR, mean ± standard deviation

6.15 ± 5.86

29.82 ± 44.19

P < 0.00000001

In ROC analysis, the area under the curve was 0.82 (95 % confidence interval (CI), 0.79–0.85) (Fig. 2). Using a cutoff point of NLR of 9.21, life expectancy was assumed to be <4 weeks yielded a sensitivity of 65.6 %, (95 % CI, 61.4–69.7 %), specificity of 84.1 % (95 % CI, 78.6–88.7 %), positive predictive value (PPV) of 90.6 % (95 % CI, 87.2–93.4 %), negative predictive value (NPV) of 51.1 % (95 % CI, 45.8–56.4 %), positive likelihood ratio of 4.125 (95 % CI, 3.025–5.626), and negative likelihood ratio of 0.409 (95 % CI, 0.358–0.467).
Fig. 2
Fig. 2

The ROC curve of NLR (lived more than or up 4 weeks). Receiver operating characteristic curve analysis of NLR in the patients who lived more than or up to 4 weeks. The cutoff point was set to 9.21. Area under the curve, 0.82; 95 % confidence interval, 0.79–0.85

Discussion

Prognostic scoring tools are applied to predict the life expectancy of terminal cancer patients. In daily clinical practice, tools such as PPS and PPI are used by palliative care physicians [4, 5]. Here, we suggest the use of NLR as a simple tool to estimate survival in terminal cancer patients.

PPS grades the clinical prediction of survival, anorexia, Karnofsky’s performance status, dyspnea, WBC count, and lymphocyte count. A lower grade means a lower life expectancy (within 30 days). One disadvantage of this tool is that it considers the clinical prediction of survival, which is a subjective parameter [4].

PPI includes various parameters such as the existence of edema, dyspnea at rest, delirium, PPS grade, and the amount of oral intake. However, some of these parameters are also subjective. In patients with PPI grade 6 or higher, life expectancy is <3 weeks with a sensitivity of 83 %, specificity of 85 %, PPV of 80 %, and NPV of 87 %. In patients with PPI grade 4 or higher, the sensitivity is 79 %, specificity is 77 %, PPV is 83 %, and NPV is 71 % [5].

Besides their subjectivity, PPS and PPI are complex. Therefore, they are not commonly used by specialists other than palliative care physicians (e.g., oncologists and general practitioners). Accurately predicting life expectancy would enable clinicians to provide more appropriate end-of-life care for terminally ill patients, who would like to think how they wish to spend their remaining time. However, unreliable predictions could lead clinicians to administer unnecessary body-rending chemotherapy and mislead the patients’ preferences. These problems are more likely to occur in cases in which palliative care physicians are not involved.

According to Glare et al. [3], physicians tend to interpret the prognosis more optimistically. Therefore, easy-to-use, objective prognostic tools are needed. The development of such tools could be useful for oncologists and healthcare providers in daily clinical and home-based care.

In our earlier studies, we discussed about the prognostic nutritional index (Onodera’s PNI), which depends only on objective data such as serum albumin level and peripheral lymphocyte count [14]. This was originally used in digestive surgery to evaluate the patients’ preoperative nutritional condition, and anastomosis of digestive tract was considered contraindicated in cases of grades of 40 and under [15]. It was also considered to be a prognosis index in stage IV cancer of the digestive tract. It was used as a vague predictive formula that estimated the possibility of death within 60 days when the patient was graded 35 and under. PNI showed lower value as time proceeded, and therefore, it was considered a feasible factor to estimate the prognosis of patients with terminal cancer.

In this study, we evaluated NLR as a simple prognostic index of survival in terminal cancer patients. This method requires minimal blood test items, and thus, it would be a least invasive approach to the patient. The prognosis prediction by NLR is believed to have moderate accuracy, with 0.81 area under the curve according to ROC analysis and a 4.125 positive likelihood ratio.

It has been reported that critically ill cancer patients in the intensive care unit exhibit high NLR values [16]. Other studies have shown that pre-treatment NLR could serve as a feasible prognosis factor in cases of non-small-cell lung cancer [6], ureteral cancer [7], esophageal squamous cell cancer [8], biliary tract cancer [9], unresectable gastric cancer [10], liver cancer [11], and pancreatic cancer [12].

NLR is an inflammation marker. There is a strong relationship between inflammation and cancer. But the mechanism of neutrophilia in cancer patients is not fully understood, and it is believed to be the result of a combination of factors. One obvious cause of neutrophilia is paraneoplastic production of myeloid growth factors, such as granulocyte colony-stimulating factor, by cancer cells themselves. Other possible factors that cause neutrophilia are coexistent infection and cancer-related inflammation [17]. Lymphocytes play a critical role in tumor defense, inducing cytotoxic cell death through the immune response. Lymphopenia is frequently observed in patients with advanced cancer, reflecting cancer-related immunosuppression [18]. Therefore, neutrophilia and lymphopenia worsen with the progression of cancer. NLR increases with time in patient with terminal cancer.

This study also has some limitations. First, it was performed on a relatively small population, but our major aim in this pilot study was merely to assess the feasibility of using the NLR as an index to estimate survival in patients with terminal cancer, using our consecutive patients. Second, this study had a retrospective, single-center design, and a potential bias in the selection of patients. Finally, this study analyzed patients with various cancer, and it is not known whether the significance of the NLR for predicting life expectancy is consistent irrespective of the type of cancer. To improve the prediction of prognosis of terminal cancer, it may be necessary to combine other indices together with the NLR. Thus, larger, prospective studies will need to be performed to confirm these preliminary results.

Conclusions

In the present study, the NLR has emerged as a feasible factor for prognosis prediction in terminal-stage cancer. NLR is easy to determine based on blood test results and could be applied by cancer clinicians as well as healthcare providers who do not specialize in palliative medicine.

Availability of data and material section

Raw data https://zenodo.org/record/50485.

Abbreviations

CI: 

confidence interval

CUP: 

cancer of the unknown primary

NLR: 

neutrophil/lymphocyte ratio

NPV: 

negative predictive value

PNI: 

prognostic nutritional index

PPI: 

palliative prognostic index

PPS: 

palliative prognostic score

PPV: 

positive predictive value

ROC: 

receiver operating characteristic

WBC: 

white blood cell

Declarations

Acknowledgements

This manuscript has been edited and proofread by Editage Cactus Communications.

Funding

The authors declare that they had no funding source for this study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Palliative Care Team, Toho University Ohashi Medical Center, 2-17-6 Ohashi, Meguroku, Tokyo 1538515, Japan
(2)
Department of Surgery, Toho University Ohashi Medical Center, Meguroku, Tokyo, Japan

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Copyright

© Nakamura et al. 2016

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