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Article

Derived Neutrophils to Lymphocyte Ratio Predicts Survival Benefit from TPF Induction Chemotherapy in Local Advanced Oral Squamous Cellular Carcinoma

by
Fangxing Zhu
1,2,3,4,5,6,†,
Xinyu Zhou
1,2,3,4,5,6,†,
Yiyi Zhang
1,2,3,4,5,6,
Zhihang Zhou
1,2,3,4,5,6,
Yingying Huang
1,2,3,4,5,6,
Laiping Zhong
7,8,
Tongchao Zhao
7,8,* and
Wenjun Yang
1,2,3,4,5,6,*
1
Department of Oral & Maxillofacial-Head & Neck Oncology, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, No. 639, Zhizaoju Road, Shanghai 200011, China
2
College of Stomatology, Shanghai Jiao Tong University, No. 639, Zhizaoju Road, Shanghai 200011, China
3
National Center for Stomatology, Shanghai 200011, China
4
National Clinical Research Center for Oral Diseases, No. 639, Zhizaoju Road, Shanghai 200011, China
5
Shanghai Key Laboratory of Stomatology, Shanghai 200011, China
6
Shanghai Research Institute of Stomatology, No. 639, Zhizaoju Road, Shanghai 200011, China
7
Department of Stomatology, Huashan Hospital, Fudan University, Shanghai 200040, China
8
Huangpu Branch, Shanghai Ninth People’s Hospital, Shanghai JiaoTong University School of Medicine, No. 58, Pu Yu Dong Road, Shanghai 200011, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work and are co-first authors.
Cancers 2024, 16(15), 2707; https://doi.org/10.3390/cancers16152707
Submission received: 3 July 2024 / Revised: 20 July 2024 / Accepted: 29 July 2024 / Published: 30 July 2024
(This article belongs to the Special Issue Advancements in Head and Neck Cancer Surgery)
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Versions Notes

Abstract

:

Simple Summary

This study aimed to evaluate the derived neutrophil to lymphocyte ratio (dNLR) in predicting the prognosis of patients with locally advanced oral squamous cell carcinoma, as well as the survival benefits from induction chemotherapy with docetaxel, cisplatin, and 5-fluorouracil (5-FU). The dNLR is an independent negative predictive factor for the disease. Patients with cTNM stage III disease and a low dNLR may benefit from induction chemotherapy.

Abstract

Background: This study aimed to evaluate the derived neutrophil to lymphocyte ratio (dNLR) in predicting the prognosis of patients with locally advanced oral squamous cell carcinoma (LAOSCC) and to assess the survival benefits from docetaxel, cisplatin, and 5-fluorouracil (5-FU) (TPF) induction chemotherapy (IC). Methods: Patients from a phase III trial involving TPF IC in stage III/IVA OSCC patients (NCT01542931) were enrolled. Receiver operating characteristic curves were constructed, and the area under the curve was computed to determine dNLR cutoff points. Kaplan–Meier survival estimates and Cox proportional hazards models were used for longitudinal analysis. Results: A total of 224 patients were identified (median age: 55.4 years; range: 26 to 75 years; median follow-up: 90 months; range: 3.2 to 93 months). The cutoff point for the dNLR was 1.555. Multivariate analysis showed that the dNLR was an independent negative predictive factor for survival (overall survival (OS): hazard ratio (HR) = 1.154, 95% confidence interval (CI): 1.018–1.309, p = 0.025; disease-free survival (DFS): HR = 1.123, 95% CI: 1.000–1.260, p = 0.050; local recurrence-free survival (LRFS): HR = 1.134, 95% CI: 1.002–1.283, p = 0.047; distant metastasis-free survival (DMFS): HR = 1.146, 95% CI: 1.010–1.300, p = 0.035). A low dNLR combined with cTNM stage III disease predicted benefit from TPF IC for the patients [OS (χ2 = 4.674, p = 0.031), DFS (χ2 = 7.134, p = 0.008), LRFS (χ2 = 5.937, p = 0.015), and DMFS (χ2 = 4.832, p = 0.028)]. Conclusions: The dNLR is an independent negative predictive factor in LAOSCC patients. Patients with cTNM stage III disease and a low dNLR can benefit from TPF IC.

1. Introduction

Oral squamous cell carcinoma (OSCC) is the most common tumor in the oral and maxillofacial region, accounting for 90% of lip and oral cavity cancer [1] and ranking as the 16th most common malignancy worldwide [2]. The global annual estimated incidence of lip and oral cavity cancer was 389,485 incident cases in 2022 [2]. According to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines Version 1.2022 [3], the mainstream management of OSCC remains radical surgery combined with sequential therapy. This approach, however, compromises patients’ quality of life due to the extensive excision and neck dissection, followed by postoperative radiation. Such treatments can impair critical functions of the oral and maxillofacial region, including eating, drinking, swallowing, and speaking, as well as alter appearance, posing significant threats to patients’ lives. In most countries, the five-year survival rates for cancers of the tongue, oral cavity, and oropharynx are around 50% [4], with a total of 188,230 deaths from cancer of the lip and oral cavity reported in 2022 [2]. Therefore, it is urgent to identify the most effective treatment strategy for the appropriate patients.
Although various neoadjuvant therapies have been tested in clinical trials, challenging the traditional standard therapy (radical surgery and postoperative radiation), no single treatment strategy has been universally beneficial. In our previous phase III clinical trial, docetaxel, cisplatin, and 5-fluorouracil (5-FU) (TPF) were used as induction chemotherapy in patients with locally advanced oral squamous cell carcinoma (LAOSCC) (registration ID: NCT01542931). However, only a portion of pathologic responders benefited from this approach [5]. Other phase III clinical trials have shown varying survival benefits from additional TPF induction chemotherapy [6,7,8]. In the NCT00095875 trial, TPF induction chemotherapy did not provide extra survival benefits beyond concurrent chemoradiotherapy in locally advanced head and neck cancer [6]. Conversely, the NCT01245959 trial demonstrated that adding TPF induction chemotherapy to concurrent chemoradiotherapy significantly improved failure-free survival in locoregionally advanced nasopharyngeal carcinoma with acceptable toxicity [7]. Similarly, the NCT01086826 trial showed that TPF induction chemotherapy significantly improved radiological complete responses, progression-free survival, and overall survival without compromising compliance with concomitant platinum-based chemoradiotherapy in locally advanced head and neck squamous cell carcinoma [8]. These findings highlight the potential value of neoadjuvant therapy, suggesting that only a subset of patients benefit from TPF induction chemotherapy [5]. This underscores the need for a personalized treatment strategy to identify specific patients who will benefit. The rise of personalized medicine and the increasing importance of biomarkers in tailoring treatment strategies have led to numerous clinical trials exploring different approaches. In our previous studies, growth differentiation factor 15 (GDF15) was identified as a potential predictive biomarker, with patients exhibiting cN- and high expression of GDF15 benefiting from TPF induction chemotherapy in LAOSCC [9]. Additionally, normal body mass index (BMI) was found to predict survival benefits from TPF induction chemotherapy in patients with stage IVA cancer within the same cohort [10].
The derived neutrophil to lymphocyte ratio (dNLR) is an index easily obtained from a routine complete blood count (CBC) test. It is calculated as the ratio of neutrophils to the difference between leukocytes and neutrophils, reflecting the relative quantity of tumor-immune-related cells in leukocytes. A smaller dNLR indicates more tumor-immune-related cell infiltration [11]. The prognostic value of the dNLR has been demonstrated in various cancers, including pancreatic ductal adenocarcinoma [12], breast cancer [13], non-small cell lung cancer [14,15], advanced or metastatic melanoma [16,17], metastatic prostate cancer [18,19], metastatic renal cell carcinoma [20], advanced or metastatic colorectal cancer [21,22], intrahepatic cholangiocarcinoma [15], and upper tract urothelial carcinoma [23]. However, in the field of head and neck squamous cell carcinoma (HNSCC), there is no clear evidence supporting the dNLR as a prognostic biomarker [24,25]. It has been suggested that the slightly decreased prognostic value might be due to a smaller area under the curve-receiver operating characteristic (AUC-ROC) for predicting overall survival (OS) [24]. Additionally, no literature has reported on the relationship between the dNLR and survival benefits from TPF induction chemotherapy. Despite this, TPF induction chemotherapy has shown benefits in previous trials (NCT01542931, NCT01245959, and NCT01086826) [5,7,8]. Therefore, it is crucial to identify the exact patient population that will benefit from TPF induction chemotherapy. In summary, this study aimed to demonstrate our findings on the predictive value of the dNLR for survival benefits from TPF induction chemotherapy in patients with LAOSCC.

2. Patients and Methods

2.1. Patients

OSCC patients diagnosed with TNM clinical stage III or IVA, treated in the Department of Oral and Maxillofacial-Head and Neck Oncology at Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, were enrolled in this study. The cohort participated in a prospective, randomized, phase III trial (NCT01542931) to investigate the potential benefits of TPF induction chemotherapy [5]. Patients were randomly allocated to either the experimental group (TPF induction chemotherapy, surgery, and postoperative radiotherapy) or the control group (surgery and postoperative radiotherapy). Clinical data from the control group were used to evaluate the prognostic value of the following biomarkers: derived neutrophil to lymphocyte ratio (dNLR), neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR), lymphocyte to monocyte ratio (LMR), and pan-immune inflammation value (PIV).

2.2. Ethical Approval

The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013) and approved by the Shanghai Ninth People’s Hospital institutional review board. Signed informed consent forms were obtained from all patients.

2.3. Baseline Characteristics

All clinical baseline characteristics and data were measured and recorded when patients were first referred to our department. This information was extracted from electronic medical records, independently recorded, and verified by the researchers. The biomarkers were calculated from the baseline CBC. dNLR is defined as the absolute neutrophil count divided by the white cell count minus the absolute neutrophil count; NLR is defined as the absolute neutrophil count divided by the absolute lymphocyte count; PLR is defined as the platelet count divided by the absolute lymphocyte count; LMR is defined as the absolute lymphocyte count divided by the absolute monocyte count; and PIV is defined as the absolute neutrophil count multiplied by the platelet count multiplied by the absolute monocyte count divided by the absolute lymphocyte count. Positive alcohol use and smoking status were defined as previously described [5].

2.4. TPF Induction Chemotherapy and Standard Treatment

The treatment strategy was reported previously [5]. In brief, the palpable edges of the primary lesion (both the longest and shortest axes) were marked 0.5 cm away from the lesion before induction chemotherapy. Chemotherapy consisted of docetaxel 75 mg/m2 intravenously on day 1, followed by cisplatin 75 mg/m2 intravenously on day 1, and fluorouracil 750 mg/m2 per day as a 120-hour continuous intravenous infusion on days 1 through 5. TPF induction chemotherapy was administered every 3 weeks for two cycles, unless there was disease progression or unacceptable toxicity. For the surgical component, radical resection of the primary lesion and full neck dissection (functional or radical) with appropriate reconstruction (pedicle or free flap) were performed. Radiotherapy was initiated 4 to 6 weeks after surgery. Standard conformal or intensity-modulated radiotherapy was administered at a dose of 1.8 to 2 Gy per day, 5 days per week, for 6 weeks (totaling 54 to 60 Gy). No concurrent chemotherapy was given with postoperative radiotherapy.

2.5. Follow-Up Visit and Clinical End-Point Assessment

Patients were followed every three months for the first two years, every six months for the next three to five years, and once a year thereafter until death or data censorship. The primary outcome of this study was overall survival (OS), calculated from the day of random assignment to death. The secondary outcomes included disease-free survival (DFS), locoregional recurrence-free survival (LRFS), and distant metastasis-free survival (DMFS), calculated from the day of random assignment to cancer recurrence, locoregional recurrence, distant metastasis, or death from any cause.

2.6. Statistical Analysis

Continuous variables were presented as the mean ± SD. For comparing clinical and histologic data, χ2 tests were used for categorical variables, and the Student’s t-test or Mann–Whitney U test were used for continuous variables. ROC curves were constructed, and AUC values were computed. The Youden index was used to determine the optimal cutoff points for the dNLR. A prognostic multivariate model was built using Cox regression analysis to investigate the hazard ratio (HR). To validate the assumptions of the Cox proportional hazards model, we tested for the proportionality of hazards using Schoenfeld residuals. The Schoenfeld residuals were plotted and statistically assessed to ensure no significant deviations from the proportional hazards assumption. Additionally, model fit was evaluated using the Akaike Information Criterion (AIC) to ensure the robustness and reliability of our results, as previously indicated [26,27]. The variables included in the multivariate model were determined by univariate Cox regression analysis and clinical evaluation. The Kaplan–Meier method and log-rank test were used for survival analysis. Two-sided tests with a significance level of 0.05 were adopted for all hypothesis-generating tests. The data were analyzed using IBM SPSS Statistics 25, IBM Corporation (Armonk, NY, USA).

3. Results

3.1. Patients

There were 256 patients [179 (69.9%) males and 77 (30.1%) females, with an average age of 55.4 years (range 26 to 75 years), and 168 (66.4%) patients older than 60 years] enrolled in the previous trial. Of these, 224 patients completed the treatment, 29 patients did not complete the treatment, and 3 patients declined any treatment. In the experimental group (TPF induction chemotherapy, surgery, and postoperative radiotherapy), there were 109 patients who completed the treatment. In the control group (surgery and postoperative radiotherapy), there were 115 patients who completed the treatment (including 2 patients who declined TPF induction chemotherapy). The median follow-up time was 80 months (range: 3.2 to 93 months).
Regarding the dNLR, the mean value in the control group was 1.89 ± 1.45, while in the TPF chemotherapy induction group, it was 1.81 ± 1.59. There was no statistically significant difference between the two groups in the baseline dNLR (U = 7411, p = 0.187). The most common primary tumor site was the tongue (113 [44.1%]), followed by the buccal mucosa (45 [17.6%]), gingiva (39 [15.6%]), floor of the oral cavity (30 [11.7%]), palate (18 [7.0%]), and the retromolar trigone (10 [3.9%]). The clinical TNM stages were distributed as follows: III (177 [69.1%]) and IVA (79 [30.9%]). Detailed clinical characteristics and treatments are shown in Table 1.

3.2. The dNLR Predicts Survival Outcomes in LAOSCC Patients Treated by Surgery and Postoperative Radiation (the Control Group)

According to the baseline CBC, the continuous variable dNLR had an average value of 1.89, ranging from 0.20 to 10.75. A cutoff point of 1.555 was identified to predict OS, calculated based on the ROC curves and the Youden’s index (p < 0.001, AUC = 0.681, Figure 1A, Supplementary Table S1). This same cutoff point was confirmed for DFS (p = 0.003, AUC = 0.651, Figure 1B, Supplementary Table S2), LRFS (p = 0.004, AUC = 0.649, Figure 1C, Supplementary Table S3), and DMFS (p < 0.001, AUC = 0.681, Figure 1D, Supplementary Table S4). Subsequently, patients in both the control and experimental groups were categorized into high dNLR (>1.555) and low dNLR (≤1.555) groups. In the control group, 66 patients were allocated to the high dNLR group and 62 to the low dNLR group. In the experimental group, 73 patients were allocated to the high dNLR group and 55 to the low dNLR group. It was found that in the control group, there was a statistical correlation between clinical stage and dNLR, with stage IVA disease being more associated with a high dNLR (χ2 = 3.863, p = 0.049, Table 1).
To further verify the effectiveness of the dNLR cutoff point of ≤1.555 in predicting a good prognosis in the control group, survival analysis was performed, comparing patients with a high dNLR and a low dNLR. The Kaplan–Meier analysis showed that patients with a low dNLR had significantly longer OS, DFS, LRFS, and DMFS compared to patients with a high dNLR. According to the log-rank test, patients with a low dNLR had significantly longer OS (χ2 = 12.791, p < 0.001), DFS (χ2 = 12.067, p = 0.001), LRFS (χ2 = 11.598, p = 0.001), and DMFS (χ2 = 12.394, p < 0.001) compared to those with a high dNLR in the control group (Figure 2). In the control group, patients with a high dNLR had a lower 5-year survival rate. The 5-year survival rates for OS, DFS, LRFS, and DMFS were 40.4%, 34.4%, 35.9%, and 40.4%, respectively, for high dNLR patients, whereas the rates were 69.4%, 59.7%, 62.9%, and 67.7%, respectively, for low dNLR patients (Table 2).
Univariate Cox model analyses were conducted in the control group. The BMI at diagnosis, cTNM stage (vs. stage III), and dNLR were found to have significant correlations with OS, DFS, LRFS, and DMFS (Table 3). The underweight group had worse survival outcomes compared to the normoweight group (OS: HR = 2.145, 95% CI: 1.065–4.321, p = 0.033; LRFS: HR = 2.106, 95% CI: 1.053–4.210, p = 0.035; DMFS: HR = 2.067, 95% CI: 1.027–4.162, p = 0.042). The overweight and obese groups had better clinical survival outcomes than the normoweight group, but this did not show statistical significance. Additionally, the cTNM stage showed statistical significance with survival outcomes (stage IVA vs. III: OS: HR = 1.993, 95% CI: 1.184–3.354, p = 0.009; DFS: HR = 1.792, 95% CI: 1.088–2.952, p = 0.022; LRFS: HR = 1.939, 95% CI: 1.173–3.207, p = 0.010; DMFS: HR = 1.603, 95% CI: 1.127–3.190, p = 0.016). In terms of the dNLR, statistically significant differences were found in survival outcomes (OS: HR = 1.227, 95% CI: 1.099–1.369, p < 0.001; DFS: HR = 1.186, 95% CI: 1.063–1.324, p = 0.002; LRFS: HR = 1.200, 95% CI: 1.073–1.341, p = 0.001; DMFS: HR = 1.218, 95% CI: 1.091–1.361, p < 0.001). The PLR also showed slightly but statistically significant differences in survival outcomes (DFS: HR = 1.004, 95% CI: 1.000–1.008, p = 0.044; LRFS: HR = 1.005, 95% CI: 1.000–1.009, p = 0.030). The proportionality of hazards was assessed using Schoenfeld residuals, which confirmed no significant deviations from the proportional hazards assumption (Supplementary Figure S4). The model fit was evaluated using the Akaike Information Criterion (AIC), and the results indicated a well-fitting model with AIC values supporting the robustness of the Cox regression analyses performed (Supplementary Table S5).
To investigate the applicability of the aforementioned prognostic factors, a multivariate analysis was adjusted for potentially confounding clinical variables. Both the cTNM stage (stage IVA vs. III, OS: HR = 1.911, 95% CI: 1.098–3.328, p = 0.022; LRFS: HR = 1.756, 95% CI: 1.029–2.996, p = 0.039; DMFS: HR = 1.797, 95% CI: 1.003–3.125, p = 0.038) and the dNLR (OS: HR = 1.154, 95% CI: 1.018–1.309, p = 0.025; DFS: HR = 1.123, 95% CI: 1.260–1.000, p = 0.050; LRFS: HR = 1.134, 95% CI: 1.002–1.283, p = 0.047; DMFS: HR = 1.146, 95% CI: 1.010–1.300, p = 0.035) were found to be independent predictive factors in the control group (Table 4). The PLR showed no statistical significance in the multivariate analysis.

3.3. The dNLR Predicts Survival Outcomes in LAOSCC Patients Treated by TPF Induction Chemotherapy, Surgery, and Postoperative Radiation (the Experimental Group)

In the experimental group, patients were further allocated into two subgroups based on their baseline dNLR, using the cutoff point of 1.555 from the control group. The five-year OS, DFS, LRFS, and DMFS were 35.7%, 30.3%, 32.1%, and 35.7%, respectively, in patients with a high dNLR, compared to 80.8%, 74.0%, 74.0%, and 80.8%, respectively, in the low dNLR group (Table 2). According to the log-rank test, patients in the low dNLR group had significantly longer OS (χ2 = 28.333, p < 0.001), DFS (χ2 = 26.935, p < 0.001), LRFS (χ2 = 24.822, p < 0.001), and DMFS (χ2 = 28.818, p < 0.001).
Univariate Cox model analyses revealed that the cTNM stage (stage IVA vs. III, OS: HR = 1.588, 95% CI: 1.015–2.755, p = 0.022; DFS: HR = 2.461, 95% CI: 1.398–4.331, p = 0.002; LRFS: HR = 2.493, 95% CI: 1.413–4.399, p = 0.009; DMFS: HR = 1.603, 95% CI: 1.060–3.500, p = 0.031), the dNLR (OS: HR = 1.154, 95% CI: 1.035–1.285, p = 0.010; DFS: HR = 1.141, 95% CI: 1.029–1.266, p = 0.013; LRFS: HR = 1.139, 95% CI: 1.024–1.268, p = 0.016; DMFS: HR = 1.152, 95% CI: 1.034–1.282, p = 0.010), the NLR (DFS: HR = 1.326, 95% CI:1.015–1.731, p = 0.038; LRFS: HR = 1.315, 95% CI: 1.005–1.722, p = 0.046), and the PLR (DFS: HR = 1.009, 95% CI: 1.002–1.017, p = 0.017; LRFS: HR = 1.008, 95% CI: 1.000–1.016, p = 0.040) had statistically significant correlations with the survival outcomes (Table 5).
A multivariate Cox model analysis further confirmed that the cTNM stage was an independent predictive factor for some survival outcomes (OS: HR = 1.924, 95% CI: 1.057–3.499, p = 0.032; DFS: HR = 1.926, 95% CI: 1.154–3.215, p = 0.012; LRFS: HR = 1.991, 95% CI: 1.188–3.337, p = 0.024; DMFS: HR = 1.926, 95% CI: 1.014–2.782, p = 0.033). Additionally, the dNLR was identified as an independent predictive factor for all survival outcomes (OS: HR = 1.160, 95% CI: 1.031–1.276, p = 0.011; DFS: HR = 1.239, 95% CI: 1.019–1.250, p = 0.021; LRFS: HR = 1.125, 95% CI: 1.014–1.249, p = 0.027; DMFS: HR = 1.145, 95% CI: 1.030–1.272, p = 0.012) (Table 6).

3.4. Combining the cTNM Stage and dNLR to Predict the Benefit of TPF Induction Chemotherapy for LAOSCC Patients

After grouping patients based on management methods (control group or experimental group) and combining the independent predictive factors previously verified, different subgroups were created according to the cTNM stage and dNLR level. The Kaplan–Meier method and log-rank test were used for survival analysis (Figure 3).
When comparing the survival rates of the experimental group and control group, as reported in our previous publications, no statistical significance was found between the two treatment groups (Supplement Figure S1). Surprisingly, in the subgroup of patients with cTNM stage III disease and a low dNLR (dNLR ≤ 1.555), the log-rank test indicated that patients in the experimental group had significantly longer OS (χ2 = 4.674, p = 0.031), DFS (χ2 = 7.134, p = 0.008), LRFS (χ2 = 5.937, p = 0.015), and DMFS (χ2 = 4.832, p = 0.028) compared to the control group (Figure 3). This suggests that patients with cTNM stage III disease and a low dNLR (dNLR ≤ 1.555) can benefit from TPF induction chemotherapy. In other subgroups, divided solely by cTNM stage or dNLR level, no statistically significant survival benefit from TPF induction chemotherapy was observed (Supplement Figures S2 and S3).

4. Discussion

In this study, the CBC, clinical characteristics, and survival outcomes of LAOSCC patients were retrospectively analyzed. In the control group, through univariate and multivariate Cox model analyses, the baseline dNLR (as a continuous variable) was confirmed as an independent prognostic factor for survival outcomes (Table 3 and Table 4). Using the ROC curve and Youden’s index (Figure 1), a dNLR cutoff point of 1.555 was established for all survival outcomes (OS, DFS, LRFS, and DMFS). Based on this cutoff point, patients were categorized into two subgroups: low dNLR and high dNLR. Patients with a low baseline dNLR had better survival outcomes (Figure 2), and this finding was consistent in the experimental group (Table 5 and Table 6). Concurrently, the cTNM stage (as a categorical variable) was confirmed as an independent prognostic factor for survival outcomes. When combining the two variables—cTNM stage III disease and low dNLR (dNLR ≤ 1.555)—this specific patient population showed significant benefit from TPF induction chemotherapy (Figure 3).
In recent years, many immune biomarkers easily acquired from a CBC have been introduced into the field of tumor therapy as prognostic factors. These include the neutrophil to lymphocyte ratio (NLR) [28,29,30], the derived neutrophil to lymphocyte ratio (dNLR) [11,14,18,31], the platelet to lymphocyte ratio (PLR) [32,33,34], the lymphocyte to monocyte ratio (LMR) [20,35], and the pan-immune inflammation value (PIV) [36,37]. In OSCC, the NLR has been reported as a significant independent predictor of disease-specific survival (DSS) [38,39] and is significantly correlated with stromal infiltration of CD8+, CD4+, and CD20+ lymphocytes [40]. The dNLR has been correlated with the occurrence of complications [41]. The PLR has shown a stronger association with DSS and progression-free survival (PFS) in patients who are male, have stage III/IV OSCC, or have lymph node metastasis [42]. The NLR and dNLR appear similar and have comparable effects on cancer-specific mortality [43], and a positive correlation between the dNLR and NLR has been found [44]. However, the calculation method for the dNLR includes not only lymphocytes but also monocytes and other subtypes of immune-related cells. In this study, dNLR, NLR, PLR, LMR, and PIV were analyzed using univariate and multivariate Cox regression analyses. Only the dNLR demonstrated an independent negative effect on survival prognosis (Table 3, Table 4, Table 5 and Table 6). We believe the complexity of the tumor immune microenvironment and the neutrophil heterogeneity among OSCC patients contribute to these results.
To our knowledge, this is the first time that the dNLR has been confirmed as an independent prognostic factor for the survival of OSCC patients through multivariate analysis. These patients were treated either with surgery and postoperative radiation or with TPF induction chemotherapy, surgery, and postoperative radiation. Additionally, this is the first time that the dNLR level and cTNM stage have been confirmed as criteria for identifying patient populations that can benefit from TPF induction chemotherapy (Figure 3). In our previous phase III clinical trial (registration ID: NCT01542931), TPF induction chemotherapy did not improve survival compared with upfront surgery [5]. However, patients with cN2 disease appeared to have improved OS (HR, 0.418; 95% CI, 0.179 to 0.974; p = 0.043) and DMFS (HR, 0.418; 95% CI, 0.179 to 0.974; p = 0.043) when treated with TPF induction chemotherapy compared to those who were not [5]. Thus, efforts were made to identify clinically valuable biomarkers to screen appropriate OSCC patient populations for TPF induction chemotherapy. Lymph node ratio (LNR), the ratio of pathologically confirmed positive lymph nodes to the total number of surgically removed lymph nodes, was found to be connected to prognosis and could be an independent prognostic factor. OSCC patients with high-risk LNR (>7.6%) or positive extranodal extension (ENE) had significantly worse clinical outcomes than patients with low-risk LNR (≤7.6%) or negative ENE [45]. In another of our previous studies, BMI was also found to be an independent prognostic factor. Compared to normoweight patients, overweight and obese patients had better clinical outcomes, while underweight status was associated with poor survival [10]. Furthermore, normoweight patients with cTNM stage IVA disease benefited from TPF induction chemotherapy followed by surgery and postoperative radiation, compared to surgery and postoperative radiation alone, in terms of OS and DMFS. In this study, the dNLR was found to be an independent prognostic factor for assessing the survival of OSCC patients, even after adjusting for other important variables. This finding is consistent with many other clinical trials that reported a significant relationship between low dNLR values and a good prognosis or favorable clinical or pathological responses [11,14,18,31,43,46,47].
In the present study, to account for the potential influence of TPF induction chemotherapy on inflammation biomarkers, hematology and survival data from the control group were used to form the ROC curve and calculate the AUC for the dNLR cutoff point. All four survival rates pointed to the same dNLR cutoff point of 1.555. This demonstrated that the dNLR can be an independent prognostic factor for the survival of OSCC patients based on multivariate analysis. There have been other reported dNLR cutoff points for different types of tumors. For instance, a dNLR cutoff point of 1.775 was found useful in predicting metastatic disease in testicular germ-cell tumors [47]. Another study on breast cancer reported a baseline dNLR cutoff point of less than 1.715 in predicting pathological complete response [46]. In patients treated with the immune checkpoint inhibitor pembrolizumab for non-small cell lung cancer, those with a dNLR cutoff < 2.6 had significantly higher objective response rates (ORRs), longer median progression-free survival, and higher numbers of tumor-associated CD8+, FOXP3+, PD-1+ immune cells, and PD-1+ CD8+ T cells [11]. In the Lung Immune Prognostic Index (LIPI), a dNLR cutoff of 3 was used to determine the prognosis of non-small cell carcinoma [14]. Various factors, such as tumor type, TNM stage, systemic inflammation, and population differences, contribute to these differing cutoff points. This may indicate the more malignant biological behavior of OSCC compared to other tumor types.
It was reported that a lower baseline dNLR level is associated with a higher number of tumor-associated immune cells [11]. In this study, a statistically significant correlation between the dNLR and cTNM stage (Table 1) was found in the control group, suggesting a mutual relationship where cTNM stage IVA disease often coincides with a high dNLR. Similar results have been reported for colorectal cancer, renal cell carcinoma, and gastric cancer [48,49,50], where TNM stage is positively related to dNLR. A low dNLR is associated with significantly increased tumor-associated CD8+, FOXP3+, and PD-1+ immune cells and favorable outcomes [11]. Stage III and stage IVA are all considered local advanced diseases in OSCC; thus, this difference was neglected in the following analysis.
A high baseline dNLR level indicates a relatively higher number of neutrophils. Neutrophils exhibit diversity, heterogeneity, and plasticity in cancer [51,52,53]. Different subgroups of neutrophils, each involved in distinct biological processes, have been reported [52,54]. In mouse and human lung cancer models, seven populations of neutrophils were identified, and CD40 agonist antibody treatment increased immune response by more than 10-fold in both N1a (Sellhi Ngphi) and N2 (Sellhi Cxcl10hi) neutrophil populations, characterized by high expression of interferon-stimulated genes (ISGs) [54]. This suggests that individuals with high baseline dNLR levels may lack the capacity for neutrophil differentiation into ISG-high expression subtypes, leading to an unfavorable prognosis. Furthermore, in the tumor immune microenvironment, tumors can modulate neutrophil extracellular traps (NETosis), causing NET-associated complications like thrombosis. NETosis captures tumors, promotes their growth, and leads to subsequent metastasis [55]. In breast cancer, the tumor-secreted protease cathepsin C promotes breast-to-lung metastasis by regulating the recruitment of neutrophils and the formation of neutrophil extracellular traps [56].
A high baseline dNLR level can also be due to low levels of leukocytes other than neutrophils, primarily lymphocytes. Lymphocytes play a crucial role in tumor immunity. However, the functional state of T lymphocytes is also critical to tumor immunity. T cell dysfunction in human cancer is associated with changes in T cell functionality rather than inactivity [57]. Although low dNLR levels predict a better prognosis in this study, the state of lymphocytes should still be considered.
There were some limitations to this study. Typically, patients with LAOSCC diagnosed as cTNM stage IVA have worse survival outcomes, which could lead to potential bias. Fortunately, this was not observed in the TPF induction chemotherapy group. This issue could be addressed in another clinical trial with a larger sample size to verify the possible connection between TNM stage and baseline dNLR in LAOSCC. Additionally, the retrospective nature of the study may include unnecessary confounding factors, and another clinical trial is needed to confirm whether the dNLR cutoff point is a suitable boundary for other survival rates or OSCC patients with different systemic conditions or TNM stages.

5. Conclusions

The dNLR can be considered an independent negative prognostic factor for the prognosis of OSCC patients. Patients with a baseline dNLR ≤ 1.555 have a better prognosis. Patients with stage III disease and a dNLR ≤ 1.555 can benefit from TPF induction chemotherapy, but further studies are needed to explain the biological association.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/cancers16152707/s1, Figure S1. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival between the control group and the experimental group. TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU). Figure S2. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in the low-dNLR patient group. Survival analysis of (E) overall survival, (F) disease-free survival, (G) locoregional recurrence-free survival, and (H) distant metastasis-free survival in the high-dNLR patient group. dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU). Figure S3. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in the patient group with cTNM stage III disease. Survival analysis of (E) overall survival, (F) disease-free survival, (G) locoregional recurrence-free survival, and (H) distant metastasis-free survival in the patients with cTNM stage IVA disease. dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU). Figure S4. Schoenfeld residuals for proportinoal hazards derived neutrophil to lymphocyte ratio in (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival and platelet to lymphocyte ratio in (E) overall survival, (F) disease-free survival, (G) locoregional recurrence-free survival, and (H) distant metastasis-free survival. Table S1. Sensitivity analysis of overall survival in patients treated with surgery and postoperative radiation. Table S2. Sensitivity analysis of disease-free survival in patients treated with surgery and postoperative radiation. Table S3. Sensitivity analysis of locoregional recurrence-free survival in patients treated with surgery and postoperative radiation. Table S4. Sensitivity analysis of distant metastasis-free survival in patients treated with surgery and postoperative radiation. Table S5. Model fit using Akaike Information Criterion (AIC).

Author Contributions

Conceptualization, L.Z., T.Z. and W.Y.; methodology, F.Z. and X.Z.; software, X.Z.; writing—original draft preparation, F.Z.; writing—review and editing, Y.Z.; visualization, Z.Z.; supervision, Y.H.; project administration, T.Z.; funding acquisition, L.Z., T.Z. and W.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Science and Technology Commission of Shanghai Municipality, grant number: 22YF1421700 (T.Z.) and 21Y21900300 (L.Z.); the National Natural Science Foundation of China, grant numbers: 81972525 and 82172734 (L.Z.); the Shanghai Huangpu District Science and Technology Commission, grant number: HLQ202304 (L.Z.); and The Biobank Project of Shanghai Ninth People’s Hospital, grant number: YBKB202214 (W.Y.).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Ethics Committee, Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine (SH9H-2021-TK558-1, 11 November 2021).

Informed Consent Statement

Written informed consent has been obtained from the patients to publish this paper.

Data Availability Statement

The data presented in this study are available in this article and Supplementary Material.

Acknowledgments

We are extremely grateful to all of our study participants for allowing their (anonymized) data to be published.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Miranda-Filho, A.; Bray, F. Global patterns and trends in cancers of the lip, tongue and mouth. Oral Oncol. 2020, 102, 104551. [Google Scholar] [CrossRef] [PubMed]
  2. Bray, F.; Laversanne, M.; Sung, H.; Ferlay, J.; Siegel, R.L.; Soerjomataram, I.; Jemal, A. Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2024, 74, 229–263. [Google Scholar] [CrossRef] [PubMed]
  3. Caudell, J.J.; Gillison, M.L.; Maghami, E.; Spencer, S.; Pfister, D.G.; Adkins, D.; Birkeland, A.C.; Brizel, D.M.; Busse, P.M.; Cmelak, A.J.; et al. NCCN Guidelines® Insights: Head and Neck Cancers, Version 1.2022. J. Natl. Compr. Cancer Netw. 2022, 20, 224–234. [Google Scholar] [CrossRef] [PubMed]
  4. Warnakulasuriya, S. Global epidemiology of oral and oropharyngeal cancer. Oral Oncol. 2009, 45, 309–316. [Google Scholar] [CrossRef] [PubMed]
  5. Zhong, L.-P.; Zhang, C.-P.; Ren, G.-X.; Guo, W.; William, W.N.; Sun, J.; Zhu, H.-G.; Tu, W.-Y.; Li, J.; Cai, Y.-L.; et al. Randomized phase III trial of induction chemotherapy with docetaxel, cisplatin, and fluorouracil followed by surgery versus up-front surgery in locally advanced resectable oral squamous cell carcinoma. J. Clin. Oncol. 2013, 31, 744–751. [Google Scholar] [CrossRef]
  6. Haddad, R.; O’Neill, A.; Rabinowits, G.; Tishler, R.; Khuri, F.; Adkins, D.; Clark, J.; Sarlis, N.; Lorch, J.; Beitler, J.J.; et al. Induction chemotherapy followed by concurrent chemoradiotherapy (sequential chemoradiotherapy) versus concurrent chemoradiotherapy alone in locally advanced head and neck cancer (PARADIGM): A randomised phase 3 trial. Lancet Oncol. 2013, 14, 257–264. [Google Scholar] [CrossRef]
  7. Sun, Y.; Li, W.-F.; Chen, N.-Y.; Zhang, N.; Hu, G.-Q.; Xie, F.-Y.; Sun, Y.; Chen, X.-Z.; Li, J.-G.; Zhu, X.-D.; et al. Induction chemotherapy plus concurrent chemoradiotherapy versus concurrent chemoradiotherapy alone in locoregionally advanced nasopharyngeal carcinoma: A phase 3, multicentre, randomised controlled trial. Lancet Oncol. 2016, 17, 1509–1520. [Google Scholar] [CrossRef]
  8. Ghi, M.G.; Paccagnella, A.; Ferrari, D.; Foa, P.; Alterio, D.; Codecà, C.; Nolè, F.; Verri, E.; Orecchia, R.; Morelli, F.; et al. Induction TPF followed by concomitant treatment versus concomitant treatment alone in locally advanced head and neck cancer. A phase II-III trial. Ann. Oncol. 2017, 28, 2206–2212. [Google Scholar] [CrossRef] [PubMed]
  9. Yang, C.Z.; Ma, J.; Zhu, D.W.; Liu, Y.; Montgomery, B.; Wang, L.Z.; Li, J.; Zhang, Z.Y.; Zhang, C.P.; Zhong, L.P. GDF15 is a potential predictive biomarker for TPF induction chemotherapy and promotes tumorigenesis and progression in oral squamous cell carcinoma. Ann. Oncol. 2014, 25, 1215–1222. [Google Scholar] [CrossRef]
  10. Zhao, T.-C.; Liang, S.-Y.; Ju, W.-T.; Liu, Y.; Tan, Y.-R.; Zhu, D.-W.; Zhang, C.-P.; Zhang, Z.-Y.; Zhong, L.-P. Normal BMI predicts the survival benefits of inductive docetaxel, cisplatin, and 5-fluorouracil in patients with locally advanced oral squamous cell carcinoma. Clin. Nutr. 2020, 39, 2751–2758. [Google Scholar] [CrossRef]
  11. Alessi, J.V.; Ricciuti, B.; Alden, S.L.; A Bertram, A.; Lin, J.J.; Sakhi, M.; Nishino, M.; Vaz, V.R.; Lindsay, J.; Turner, M.M.; et al. Low peripheral blood derived neutrophil-to-lymphocyte ratio (dNLR) is associated with increased tumor T-cell infiltration and favorable outcomes to first-line pembrolizumab in non-small cell lung cancer. J. Immunother. Cancer 2021, 9, e003536. [Google Scholar] [CrossRef] [PubMed]
  12. Caputo, D.; Quagliarini, E.; Coppola, A.; La Vaccara, V.; Marmiroli, B.; Sartori, B.; Caracciolo, G.; Pozzi, D. Inflammatory biomarkers and nanotechnology: New insights in pancreatic cancer early detection. Int. J. Surg. 2023, 109, 2934–2940. [Google Scholar] [CrossRef] [PubMed]
  13. Kim, C.G.; Kim, M.H.; Kim, J.H.; Kim, S.-G.; Kim, G.M.; Kim, T.Y.; Ryu, W.-J.; Park, H.S.; Park, S.; Cho, Y.U.; et al. On-treatment derived neutrophil-to-lymphocyte ratio and survival with palbociclib and endocrine treatment: Analysis of a multicenter retrospective cohort and the PALOMA-2/3 study with immune correlates. Breast Cancer Res. 2023, 25, 4. [Google Scholar] [CrossRef] [PubMed]
  14. Kazandjian, D.; Gong, Y.; Keegan, P.; Pazdur, R.; Blumenthal, G.M. Prognostic Value of the Lung Immune Prognostic Index for Patients Treated for Metastatic Non-Small Cell Lung Cancer. JAMA Oncol. 2019, 5, 1481–1485. [Google Scholar] [CrossRef] [PubMed]
  15. Li, C.; Wu, J.; Jiang, L.; Zhang, L.; Huang, J.; Tian, Y.; Zhao, Y.; Liu, X.; Xia, L.; E, H.; et al. The predictive value of inflammatory biomarkers for major pathological response in non-small cell lung cancer patients receiving neoadjuvant chemoimmunotherapy and its association with the immune-related tumor microenvironment: A multi-center study. Cancer Immunol. Immunother. 2023, 72, 783–794. [Google Scholar] [CrossRef]
  16. Capone, M.; Giannarelli, D.; Mallardo, D.; Madonna, G.; Festino, L.; Grimaldi, A.M.; Vanella, V.; Simeone, E.; Paone, M.; Palmieri, G.; et al. Baseline neutrophil-to-lymphocyte ratio (NLR) and derived NLR could predict overall survival in patients with advanced melanoma treated with nivolumab. J. Immunother. Cancer 2018, 6, 74. [Google Scholar] [CrossRef]
  17. Ferrucci, P.F.; Ascierto, P.A.; Pigozzo, J.; Del Vecchio, M.; Maio, M.; Cappellini, G.C.A.; Guidoboni, M.; Queirolo, P.; Savoia, P.; Mandalà, M.; et al. Baseline neutrophils and derived neutrophil-to-lymphocyte ratio: Prognostic relevance in metastatic melanoma patients receiving ipilimumab. Ann. Oncol. 2016, 27, 732–738. [Google Scholar] [CrossRef]
  18. Bauckneht, M.; Rebuzzi, S.E.; Signori, A.; Frantellizzi, V.; Murianni, V.; Rizzini, E.L.; Mascia, M.; Lavelli, V.; Donegani, M.I.; Ponzano, M.; et al. The prognostic power of inflammatory indices and clinical factors in metastatic castration-resistant prostate cancer patients treated with radium-223 (BIO-Ra study). Eur. J. Nucl. Med. Mol. Imaging 2022, 49, 1063–1074. [Google Scholar] [CrossRef]
  19. van Soest, R.J.; Templeton, A.J.; Vera-Badillo, F.E.; Mercier, F.; Sonpavde, G.; Amir, E.; Tombal, B.; Rosenthal, M.; Eisenberger, M.A.; Tannock, I.F.; 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. 2015, 26, 743–749. [Google Scholar] [CrossRef]
  20. Rebuzzi, S.E.; Signori, A.; Banna, G.L.; Maruzzo, M.; De Giorgi, U.; Pedrazzoli, P.; Sbrana, A.; Zucali, P.A.; Masini, C.; Naglieri, E.; et al. Inflammatory indices and clinical factors in metastatic renal cell carcinoma patients treated with nivolumab: The development of a novel prognostic score (Meet-URO 15 study). Ther. Adv. Med. Oncol. 2021, 13, 17588359211019642. [Google Scholar] [CrossRef]
  21. Colloca, G.A.; Venturino, A.; Guarneri, D. Reduction of derived neutrophil-to-lymphocyte ratio after four weeks predicts the outcome of patients receiving second-line chemotherapy for metastatic colorectal cancer. Cancer Immunol. Immunother. 2021, 70, 1115–1125. [Google Scholar] [CrossRef]
  22. Grenader, T.; Nash, S.; Adams, R.; Kaplan, R.; Fisher, D.; Maughan, T.; Bridgewater, J. Derived neutrophil lymphocyte ratio is predictive of survival from intermittent therapy in advanced colorectal cancer: A post hoc analysis of the MRC COIN study. Br. J. Cancer 2016, 114, 612–615. [Google Scholar] [CrossRef]
  23. Dalpiaz, O.; Pichler, M.; Mannweiler, S.; Hernández, J.M.M.; Stojakovic, T.; Pummer, K.; Zigeuner, R.; Hutterer, G.C. Validation of the pretreatment derived neutrophil-lymphocyte ratio as a prognostic factor in a European cohort of patients with upper tract urothelial carcinoma. Br. J. Cancer 2014, 110, 2531–2536. [Google Scholar] [CrossRef] [PubMed]
  24. Jariod-Ferrer, M.; Arbones-Mainar, J.M.; Gavin-Clavero, M.A.; Simón-Sanz, M.V.; Moral-Saez, I.; Cisneros-Gimeno, A.I.; Martinez-Trufero, J. Are Comorbidities Associated with Overall Survival in Patients with Oral Squamous Cell Carcinoma? J. Oral Maxillofac. Surg. 2019, 77, 1906–1914. [Google Scholar] [CrossRef] [PubMed]
  25. Kwon, H.R.; Cho, J.; Park, S.; Lee, S.-H.; Ahn, M.-J.; Choi, J.Y.; Lee, K.-H.; Jung, H.A.; Moon, S.H. Metabolic parameters on baseline (18)F-FDG PET/CT are potential predictive biomarkers for immunotherapy in patients with head and neck squamous cell carcinoma. Front. Med. 2022, 9, 896494. [Google Scholar] [CrossRef] [PubMed]
  26. Stoppa, G.; Mensi, C.; Fazzo, L.; Minelli, G.; Manno, V.; Consonni, D.; Biggeri, A.; Catelan, D. Spatial Analysis of Shared Risk Factors between Pleural and Ovarian Cancer Mortality in Lombardy (Italy). Int. J. Environ. Res. Public Health 2022, 19, 3467. [Google Scholar] [CrossRef] [PubMed]
  27. Marami Milani, M.R.; Hense, A.; Rahmani, E.; Ploeger, A. Applying Least Absolute Shrinkage Selection Operator and Akaike Information Criterion Analysis to Find the Best Multiple Linear Regression Models between Climate Indices and Components of Cow’s Milk. Foods 2016, 5, 52. [Google Scholar] [CrossRef] [PubMed]
  28. Casadei-Gardini, A.; Rimini, M.; Kudo, M.; Shimose, S.; Tada, T.; Suda, G.; Goh, M.J.; Jefremow, A.; Scartozzi, M.; Cabibbo, G.; et al. Real Life Study of Lenvatinib Therapy for Hepatocellular Carcinoma: RELEVANT Study. Liver Cancer 2022, 11, 527–539. [Google Scholar] [CrossRef]
  29. Fiore, M.; Ljevar, S.; Pasquali, S.; Morelli, D.; Callegaro, D.; Sanfilippo, R.; Barisella, M.; Sangalli, C.; Miceli, R.; Gronchi, A. Preoperative Neutrophil-To-Lymphocyte Ratio and A New Inflammatory Biomarkers Prognostic Index For Primary Retroperitoneal Sarcomas. Clin. Cancer Res. 2022, 29, 614–620. [Google Scholar] [CrossRef]
  30. Sui, Q.; Zhang, X.; Chen, C.; Tang, J.; Yu, J.; Li, W.; Han, K.; Jiang, W.; Liao, L.; Kong, L.; et al. Inflammation promotes resistance to immune checkpoint inhibitors in high microsatellite instability colorectal cancer. Nat. Commun. 2022, 13, 7316. [Google Scholar] [CrossRef]
  31. Mezquita, L.; Preeshagul, I.; Auclin, E.; Saravia, D.; Hendriks, L.; Rizvi, H.; Park, W.; Nadal, E.; Martin-Romano, P.; Ruffinelli, J.C.; et al. Predicting immunotherapy outcomes under therapy in patients with advanced NSCLC using dNLR and its early dynamics. Eur. J. Cancer 2021, 151, 211–220. [Google Scholar] [CrossRef]
  32. Abbate, V.; Barone, S.; Troise, S.; Laface, C.; Bonavolontà, P.; Pacella, D.; Salzano, G.; Iaconetta, G.; Califano, L.; Orabona, G.D. The Combination of Inflammatory Biomarkers as Prognostic Indicator in Salivary Gland Malignancy. Cancers 2022, 14, 5934. [Google Scholar] [CrossRef] [PubMed]
  33. Li, X.; Sun, W.; Ding, X.; Li, W.; Chen, J. Prognostic model of immune checkpoint inhibitors combined with anti-angiogenic agents in unresectable hepatocellular carcinoma. Front. Immunol. 2022, 13, 1060051. [Google Scholar] [CrossRef]
  34. Minici, R.; Siciliano, M.A.; Ammendola, M.; Santoro, R.C.; Barbieri, V.; Ranieri, G.; Laganà, D. Prognostic Role of Neutrophil-to-Lymphocyte Ratio (NLR), Lymphocyte-to-Monocyte Ratio (LMR), Platelet-to-Lymphocyte Ratio (PLR) and Lymphocyte-to-C Reactive Protein Ratio (LCR) in Patients with Hepatocellular Carcinoma (HCC) undergoing Chemoembolizations (TACE) of the Liver: The Unexplored Corner Linking Tumor Microenvironment, Biomarkers and Interventional Radiology. Cancers 2022, 15, 257. [Google Scholar] [CrossRef] [PubMed]
  35. Kachuri, L.; Jeon, S.; DeWan, A.T.; Metayer, C.; Ma, X.; Witte, J.S.; Chiang, C.W.; Wiemels, J.L.; de Smith, A.J. Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Am. J. Hum. Genet. 2021, 108, 1823–1835. [Google Scholar] [CrossRef]
  36. Russo, P.; Palermo, G.; Iacovelli, R.; Ragonese, M.; Ciccarese, C.; Maioriello, G.; Fantasia, F.; Bizzarri, F.P.; Marino, F.; Moosavi, K.; et al. Comparison of PIV and Other Immune Inflammation Markers of Oncological and Survival Outcomes in Patients Undergoing Radical Cystectomy. Cancers 2024, 16, 651. [Google Scholar] [CrossRef] [PubMed]
  37. Feng, J.; Wang, L.; Yang, X.; Chen, Q.; Cheng, X. Pretreatment Pan-Immune-Inflammation Value (PIV) in Predicting Therapeutic Response and Clinical Outcomes of Neoadjuvant Immunochemotherapy for Esophageal Squamous Cell Carcinoma. Ann. Surg. Oncol. 2024, 31, 272–283. [Google Scholar] [CrossRef]
  38. Sano, Y.; Kogashiwa, Y.; Araki, R.; Enoki, Y.; Ikeda, T.; Yoda, T.; Nakahira, M.; Sugasawa, M. Correlation of Inflammatory Markers, Survival, and COX2 Expression in Oral Cancer and Implications for Prognosis. Otolaryngol.-Head Neck Surg. 2018, 158, 667–676. [Google Scholar] [CrossRef]
  39. Zubair, F.; McMahon, J.; Kryklyas, G.; Wicks, C. Systemic inflammatory response in predicting outcomes of patients undergoing curative resection for oral squamous cell carcinoma. Br. J. Oral Maxillofac. Surg. 2022, 60, 589–595. [Google Scholar] [CrossRef]
  40. Ruiz-Ranz, M.; Lequerica-Fernández, P.; Rodríguez-Santamarta, T.; Suárez-Sánchez, F.J.; López-Pintor, R.M.; García-Pedrero, J.M.; de Vicente, J.C. Prognostic implications of preoperative systemic inflammatory markers in oral squamous cell carcinoma, and correlations with the local immune tumor microenvironment. Front. Immunol. 2022, 13, 941351. [Google Scholar] [CrossRef]
  41. Košec, A.; Solter, D.; Ribić, A.; Knežević, M.; Vagić, D.; Pegan, A. Systemic Inflammatory Markers as Predictors of Postoperative Complications and Survival in Patients with Advanced Head and Neck Squamous Cell Carcinoma Undergoing Free-Flap Reconstruction. J. Oral Maxillofac. Surg. 2022, 80, 744–755. [Google Scholar] [CrossRef] [PubMed]
  42. Cho, U.; Sung, Y.E.; Kim, M.S.; Lee, Y.S. Prognostic Role of Systemic Inflammatory Markers in Patients Undergoing Surgical Resection for Oral Squamous Cell Carcinoma. Biomedicines 2022, 10, 1268. [Google Scholar] [CrossRef]
  43. Xiong, Y.; Zhao, N.; Zheng, Y.; Wang, J.; Wei, F.; Ren, X. Prognostic value of pretreatment inflammatory biomarkers in advanced lung adenocarcinoma patients receiving first-line pemetrexed/platinum doublet. Tumour Biol. 2017, 39, 1010428317701639. [Google Scholar] [CrossRef] [PubMed]
  44. Winarto, H.; Habiburrahman, M.; Anggraeni, T.D.; Nuryanto, K.H.; Julianti, R.A.; Purwoto, G.; Andrijono, A. The Utility of Pre-Treatment Inflammation Markers as Associative Factors to the Adverse Outcomes of Vulvar Cancer: A Study on Staging, Nodal Involvement, and Metastasis Models. J. Clin. Med. 2022, 12, 96. [Google Scholar] [CrossRef]
  45. Zhao, T.; Liang, S.; Ju, W.; Fu, Y.; Zhou, Z.; Wang, L.; Li, J.; Zhang, C.; Zhang, Z.; Zhong, L. High-risk lymph node ratio predicts worse prognosis in patients with locally advanced oral cancer. J. Oral Pathol. Med. 2020, 49, 787–795. [Google Scholar] [CrossRef] [PubMed]
  46. Ocaña, A.; Chacón, J.I.; Calvo, L.; Antón, A.; Mansutti, M.; Albanell, J.; Martínez, M.T.; Lahuerta, A.; Bisagni, G.; Bermejo, B.; et al. Derived Neutrophil-to-Lymphocyte Ratio Predicts Pathological Complete Response to Neoadjuvant Chemotherapy in Breast Cancer. Front. Oncol. 2021, 11, 827625. [Google Scholar] [CrossRef] [PubMed]
  47. Bumbasirevic, U.; Bojanic, N.; Simic, T.; Milojevic, B.; Zivkovic, M.; Kosanovic, T.; Kajmakovic, B.; Janicic, A.; Durutovic, O.; Radovanovic, M.; et al. Interplay between Comprehensive Inflammation Indices and Redox Biomarkers in Testicular Germ-Cell Tumors. J. Pers. Med. 2022, 12, 833. [Google Scholar] [CrossRef] [PubMed]
  48. Song, S.; Li, C.; Li, S.; Gao, H.; Lan, X.; Xue, Y. Derived neutrophil to lymphocyte ratio and monocyte to lymphocyte ratio may be better biomarkers for predicting overall survival of patients with advanced gastric cancer. OncoTargets Ther. 2017, 10, 3145–3154. [Google Scholar] [CrossRef] [PubMed]
  49. Rajwa, P.; Życzkowski, M.; Paradysz, A.; Slabon-Turska, M.; Suliga, K.; Bujak, K.; Bryniarski, P. Novel hematological biomarkers predict survival in renal cell carcinoma patients treated with nephrectomy. Arch. Med. Sci. 2020, 16, 1062–1071. [Google Scholar] [CrossRef]
  50. Liu, X.C.; Dai, Y.L.; Huang, F.; Zhong, Z.J.; Liu, X.F. Diagnostic Value of Carcinoembryonic Antigen Combined with Multi-Inflammatory Cell Ratios in Colorectal Cancer. Dis. Markers 2022, 2022, 4889616. [Google Scholar] [CrossRef]
  51. Jaillon, S.; Ponzetta, A.; Di Mitri, D.; Santoni, A.; Bonecchi, R.; Mantovani, A. Neutrophil diversity and plasticity in tumour progression and therapy. Nat. Rev. Cancer 2020, 20, 485–503. [Google Scholar] [CrossRef] [PubMed]
  52. Xue, R.; Zhang, Q.; Cao, Q.; Kong, R.; Xiang, X.; Liu, H.; Feng, M.; Wang, F.; Cheng, J.; Li, Z.; et al. Liver tumour immune microenvironment subtypes and neutrophil heterogeneity. Nature 2022, 612, 141–147. [Google Scholar] [CrossRef]
  53. Hedrick, C.C.; Malanchi, I. Neutrophils in cancer: Heterogeneous and multifaceted. Nat. Rev. Immunol. 2022, 22, 173–187. [Google Scholar] [CrossRef] [PubMed]
  54. Gungabeesoon, J.; Gort-Freitas, N.A.; Kiss, M.; Bolli, E.; Messemaker, M.; Siwicki, M.; Hicham, M.; Bill, R.; Koch, P.; Cianciaruso, C.; et al. A neutrophil response linked to tumor control in immunotherapy. Cell 2023, 186, 1448–1464.e20. [Google Scholar] [CrossRef] [PubMed]
  55. Papayannopoulos, V. Neutrophil extracellular traps in immunity and disease. Nat. Rev. Immunol. 2018, 18, 134–147. [Google Scholar] [CrossRef]
  56. Xiao, Y.; Cong, M.; Li, J.; He, D.; Wu, Q.; Tian, P.; Wang, Y.; Yang, S.; Liang, C.; Liang, Y.; et al. Cathepsin C promotes breast cancer lung metastasis by modulating neutrophil infiltration and neutrophil extracellular trap formation. Cancer Cell 2021, 39, 423–437.e7. [Google Scholar] [CrossRef]
  57. van der Leun, A.M.; Thommen, D.S.; Schumacher, T.N. CD8+ T cell states in human cancer: Insights from single-cell analysis. Nat. Rev. Cancer 2020, 20, 218–232. [Google Scholar] [CrossRef]
Cancers 16 02707 g001
Figure 1. Receiver operating characteristic curve for (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in patients treated with surgery and postoperative radiation (the control group). AUC, area under the curve.
Figure 1. Receiver operating characteristic curve for (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in patients treated with surgery and postoperative radiation (the control group). AUC, area under the curve.
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Cancers 16 02707 g002
Figure 2. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival between patients with a low derived neutrophils to lymphocyte ratio and a high derived neutrophils to lymphocyte ratio in patients treated with surgery and postoperative radiation (the control group). Survival analysis of (E) overall survival, (F) disease-free survival, (G) locoregional recurrence-free survival, and (H) distant metastasis-free survival in patients treated with TPF induction chemotherapy, surgery, and postoperative radiation (the experimental group). dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU).
Figure 2. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival between patients with a low derived neutrophils to lymphocyte ratio and a high derived neutrophils to lymphocyte ratio in patients treated with surgery and postoperative radiation (the control group). Survival analysis of (E) overall survival, (F) disease-free survival, (G) locoregional recurrence-free survival, and (H) distant metastasis-free survival in patients treated with TPF induction chemotherapy, surgery, and postoperative radiation (the experimental group). dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU).
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Figure 3. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in the patient group with a low dNLR combined with cTNM stage III disease between the control group and the experimental group. dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU).
Figure 3. Survival analysis of (A) overall survival, (B) disease-free survival, (C) locoregional recurrence-free survival, and (D) distant metastasis-free survival in the patient group with a low dNLR combined with cTNM stage III disease between the control group and the experimental group. dNLR, derived neutrophils to lymphocyte ratio; TPF, docetaxel, cisplatin, and 5-fluorouracil (5-FU).
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Table 1. Demographic and clinical data of the OSCC patients.
Table 1. Demographic and clinical data of the OSCC patients.
TotalControl Group TPF Chemotherapy Induction
dNLR ≤ 1.555dNLR > 1.555t/χ2/Fisher Exact Test dNLR ≤ 1.555dNLR > 1.555t/χ2/Fisher Exact Test
N%N%N%pN%N%p
Age (years)
Average55.4 54.8 56.1 56 56.2
Range26, 75 26, 75 29, 74 32, 73 29, 74
<6016866457340612.0550.152496734620.3870.534
≥60883417272639 24332138
Gender
Female7730203220300.0570.812212916290.0020.968
Male1797042684670 52713971
Smoking status
Negative12649396332482.6910.101364923420.710 0.400
Positive1305123373452 37513258
Alcohol status
Negative9838426840610.7070.400456231560.3630.547
Positive1586220322639 28382444
Tumor site
Tongue11344315029442.5680.766344719354.3520.500
Buccal45189151117 13181222
Gingiva40169151015 1216916
Floor of the mouth30126101218 68611
Palate1873535 57713
Retromolar triangle1044612 3424
BMI
Underweight20858691.1370.25857480.5010.617
Normal1325234553959 35492445
Overweight722816261726 24331528
Obese291171146 8111019
cT stage
T19400231.6370.74945350.9110.937
T2572212191320 20271222
T31495840654061 38523156
T4411610161117 1115916
cN stage
N011043315030453.5160.172294020360.3970.820
N1943723371929 30412240
N252208131726 14191324
Clinical TNM stage
III17769508143653.8630.049496735640.1690.681
IVa793112192335 24332036
OSCC: oral squamous cell carcinoma; TPF: docetaxel, cisplatin, and 5-fluorouracil (5-FU); dNLR: derived neutrophil to lymphocyte ratio; BMI: body mass index.
Table 2. The 5-year survival outcomes of the patients with different treatments and different baseline dNLR levels.
Table 2. The 5-year survival outcomes of the patients with different treatments and different baseline dNLR levels.
Control Group (N = 115)Experimental Group (N = 109)
Low dNLRHigh dNLRLow dNLRHigh dNLR
(n = 56)(n = 59)(n = 63)(n = 46)
Overall survival69.4%40.4%77.4%35.7%
Disease-free survival57.8%30.4%74.0%28.1%
Locoregional recurrence-free survival62.9%35.9%74.0%32.1%
Distant metastasis-free survival67.7%40.4%80.8%35.7%
TPF: docetaxel, cisplatin, and 5-fluorouracil (5-FU); dNLR: derived neutrophil to lymphocyte ratio.
Table 3. Univariate analysis of clinical prognostic factors for clinical outcomes in the control group (surgery and postoperative radiation).
Table 3. Univariate analysis of clinical prognostic factors for clinical outcomes in the control group (surgery and postoperative radiation).
VariableOSDFSLRFSDMFS
HR95% CIpHR95% CIpHR95% CIpHR95% CIp
Sex (vs. Female)0.9650.568–1.6420.8970.7360.452–1.1990.2190.7440.453–1.2220.2420.9850.580–1.6760.957
Age (vs. < 60 years)1.1990.716–2.0090.4901.0660.654–1.7380.7961.0750.654–1.7680.7751.1660.697–1.9520.559
Smoking status (vs. non-smoker)1.2190.743–2.0000.4331.0210.639–1.6300.9321.0130.630–1.6300.9561.2250.747–2.0090.421
Alcohol status (vs. non-alcohol abuser)1.3850.807–2.3760.2371.4410.867–2.3940.1581.3390.799–2.2450.2861.4320.834–2.4560.193
BMI at diagnosis 0.005 0.009 0.007 0.008
NormalRef. Ref. Ref. Ref.
Underweight2.1451.065–4.3210.0331.9150.961–3.8140.0652.1061.053–4.2100.0352.0671.027–4.1620.042
Overweight0.5270.270–1.0290.0600.5810.319–1.0620.0770.1130.334–1.1220.6120.5380.276–1.0510.070
Obese0.3980.123–1.2870.1240.3320.103–1.0690.0640.3450.107–1.1140.0750.3990.123–1.2920.125
cTNM (vs. III)1.9931.184–3.3540.0091.7921.088–2.9520.0221.9391.173–3.2070.0101.6031.127–3.1900.016
dNLR1.2271.099–1.369<0.0011.1861.063–1.3240.0021.2001.073–1.3410.0011.2181.091–1.361<0.001
NLR1.0730.936–1.2300.3111.0980.979–1.2310.1091.1130.995–1.2450.0611.0740.935–1.2320.313
PLR1.0020.997–1.0070.3911.0041.000–1.0080.0441.0051.000–1.0090.0301.0020.997–1.0070.399
LMR0.9590.828–1.1110.5770.9330.811–1.0750.3380.9130.788–1.0570.2220.9580.828–1.1090.568
PIV1.0000.999–1.0010.9911.0000.999–1.0010.9851.0000.999–1.0010.9251.0000.999–1.0010.991
OS: overall survival; DFS: disease-free survival; LRFS: locoregional recurrence-free survival; DMFS: distant metastasis-free survival; HR: hazard ratio; BMI: body mass index; dNLR: derived neutrophil to lymphocyte ratio; NLR: neutrophil to lymphocyte ratio; PLR: platelet to lymphocyte ratio; LMR: lymphocyte to monocyte ratio; PIV: pan-immune inflammation value.
Table 4. Multivariate analysis of clinical prognostic factors for clinical outcomes in the control group (surgery and postoperative radiation).
Table 4. Multivariate analysis of clinical prognostic factors for clinical outcomes in the control group (surgery and postoperative radiation).
VariableOSDFSLRFSDMFS
HR95% CIpHR95% CIpHR95% CIpHR95% CIp
BMI at diagnosis 0.067 0.063 0.062 0.083
NormalRef. Ref. Ref. Ref.
Underweight1.5570.708–3.4250.2711.4950.700–3.1910.2991.6620.777–3.5540.1901.5150.689–3.3350.302
Overweight0.5100.995–1.2680.0610.5740.313–1.0500.0710.6050.329–1.1110.1050.5230.267–1.0240.059
Obese0.4770.146–1.5570.2200.3850.118–1.2500.1120.4000.123–1.3010.1280.4750.146–1.5520.218
cTNM (vs. III)1.9111.098–3.3280.0221.6280.959–2.7630.0711.7561.029–2.9960.0391.7971.003–3.1250.038
dNLR1.1541.018–1.3090.0251.1231.001–1.2820.0501.1341.002–1.2830.0471.1461.010–1.3000.035
PLR1.0020.996–1.0080.5051.0050.999–1.0110.0921.0050.999–1.0100.1071.0020.996–1.0080.498
OS: overall survival; DFS: disease-free survival; LRFS: locoregional recurrence-free survival; DMFS: distant metastasis-free survival; HR: hazard ratio; BMI: body mass index; dNLR: derived neutrophil to lymphocyte ratio; PLR: platelet to lymphocyte ratio.
Table 5. Univariate analysis of clinical prognostic factors for clinical outcomes in the experimental group (TPF induction chemotherapy, surgery, and postoperative radiation).
Table 5. Univariate analysis of clinical prognostic factors for clinical outcomes in the experimental group (TPF induction chemotherapy, surgery, and postoperative radiation).
VariableOS DFS LRFS DMFS
HR95% CIpHR95% CIpHR95% CIpHR95% CIp
Sex (vs. Female)1.2120.657–2.2370.5391.2190.687–2.1600.4991.1890.670–2.1110.5551.2070.654–2.2280.548
Age (vs. < 60 years)1.1930.682–2.0870.5351.1860.704–1.9960.5211.2130.719–2.0470.4701.1830.676–2.0680.556
Smoking status (vs. non-smoker)1.3660.785–2.3780.2701.2660.757–2.1160.3691.2210.728–2.0480.4481.3740.789–2.3930.261
Alcohol status (vs. non-alcohol abuser)1.1440.661–1.9780.6311.1750.706–1.9550.5341.1240.672–1.8800.6561.1350.656–1.9630.650
BMI at diagnosis 0.550 0.504 0.511 0.567
NormalRef. Ref. Ref. Ref.
Underweight1.5490.593–4.0510.3721.2560.488–3.2360.6371.3140.509–3.3930.5731.5640.598–4.0880.362
Overweight0.7430.380–1.4530.3860.6590.351–1.2400.1960.6760.358–1.2760.2270.7570.387–1.4800.415
Obese1.0650.480–2.3610.8771.0190.485–2.1400.9611.0540.500–2.2200.8901.0650.480–2.3620.876
cTNM (vs. III)1.5881.015–2.7550.0222.4611.398–4.3310.0022.4931.413–4.3990.0091.6031.060–3.5000.031
dNLR1.1541.035–1.2850.0101.1411.029–1.2660.0131.1391.024–1.2680.0161.1521.034–1.2820.010
NLR1.2860.953–1.7370.1001.3261.015–1.7310.0381.3151.005–1.7220.0461.3090.967–1.7720.082
PLR1.0091.000–1.0170.0511.0091.002–1.0170.0171.0081.000–1.0160.0401.0091.000–1.0170.054
LMR1.0920.921–1.2950.3121.0380.879–1.2250.6621.0390.879–1.2290.6521.0900.920–1.2930.320
PIV1.0000.999–1.0010.9911.0000.999–1.0010.9851.0011.000–1.0020.1161.0000.999–1.0010.991
TPF: docetaxel, cisplatin, and 5-fluorouracil (5-FU); OS: overall survival; DFS: disease-free survival; LRFS: locoregional recurrence-free survival; DMFS: distant metastasis-free survival; HR: hazard ratio; BMI: body mass index; dNLR: derived neutrophil to lymphocyte ratio.
Table 6. Multivariate analysis of clinical prognostic factors for clinical outcomes in the experimental group (TPF induction chemotherapy, surgery, and postoperative radiation).
Table 6. Multivariate analysis of clinical prognostic factors for clinical outcomes in the experimental group (TPF induction chemotherapy, surgery, and postoperative radiation).
VariableOSDFSLRFSDMFS
HR95% CIpHR95% CIpHR95% CIpHR95% CIp
cTNM (vs. III)1.9241.057–3.4990.0321.9261.154–3.2150.0121.9911.188–3.3370.0241.9261.014–2.7820.033
dNLR1.1601.031, 1.2760.0111.2391.019, 1.2500.0211.1251.014, 1.2490.0271.1451.030, 1.2720.012
PLR1.0080.998–1.0190.1251.0091.000–1.0190.0521.0080.998–1.0170.1451.0080.997–1.0180.154
TPF: docetaxel, cisplatin, and 5-fluorouracil (5-FU); OS: overall survival; DFS: disease-free survival; LRFS: locoregional recurrence-free survival; DMFS: distant metastasis-free survival; HR: hazard ratio; dNLR: derived neutrophil to lymphocyte ratio; PLR: platelet to lymphocyte ratio.
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MDPI and ACS Style

Zhu, F.; Zhou, X.; Zhang, Y.; Zhou, Z.; Huang, Y.; Zhong, L.; Zhao, T.; Yang, W. Derived Neutrophils to Lymphocyte Ratio Predicts Survival Benefit from TPF Induction Chemotherapy in Local Advanced Oral Squamous Cellular Carcinoma. Cancers 2024, 16, 2707. https://doi.org/10.3390/cancers16152707

AMA Style

Zhu F, Zhou X, Zhang Y, Zhou Z, Huang Y, Zhong L, Zhao T, Yang W. Derived Neutrophils to Lymphocyte Ratio Predicts Survival Benefit from TPF Induction Chemotherapy in Local Advanced Oral Squamous Cellular Carcinoma. Cancers. 2024; 16(15):2707. https://doi.org/10.3390/cancers16152707

Chicago/Turabian Style

Zhu, Fangxing, Xinyu Zhou, Yiyi Zhang, Zhihang Zhou, Yingying Huang, Laiping Zhong, Tongchao Zhao, and Wenjun Yang. 2024. "Derived Neutrophils to Lymphocyte Ratio Predicts Survival Benefit from TPF Induction Chemotherapy in Local Advanced Oral Squamous Cellular Carcinoma" Cancers 16, no. 15: 2707. https://doi.org/10.3390/cancers16152707

APA Style

Zhu, F., Zhou, X., Zhang, Y., Zhou, Z., Huang, Y., Zhong, L., Zhao, T., & Yang, W. (2024). Derived Neutrophils to Lymphocyte Ratio Predicts Survival Benefit from TPF Induction Chemotherapy in Local Advanced Oral Squamous Cellular Carcinoma. Cancers, 16(15), 2707. https://doi.org/10.3390/cancers16152707

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