Contents
Download PDF
pdf Download XML
131 Views
90 Downloads
Share this article
Research Article | Volume 16 Issue 2 (Feb, 2026) | Pages 768 - 771
ANALYSIS OF THE ROLE OF ORAL HYGIENE, ORAL BACTERIAL FLORA IN HEAD & NECK CANCERS
 ,
 ,
 ,
 ,
1
Senior Resident, MBBS, MS(ENT), Institute of Otorhinolaryngology and Head, Neck Surgery, Institute of postgraduate Medical Education and Research, West Bengal 700020
2
Associate Professor, MBBS, MS(ENT), Institute of Otorhinolaryngology and Head, Neck Surgery, Neck Surgery, Institute of postgraduate Medical Education and Research, West Bengal 700020
3
Associate Professor, MBBS, MS(ENT), Department of Institute of Otorhinolaryngology and Head, Neck Surgery, Institute of postgraduate Medical Education and Research, West Bengal 700020
4
Assistant Professor, MBBS, MS(ENT), DNB, Institute of Otorhinolaryngology and Head, Neck Surgery, Institute of postgraduate Medical Education and Research, West Bengal 700020
5
MS (ENT), Postgraduate Trainee, MBBS, MS(ENT), Postgraduate Trainee, Institute of Otorhinolaryngology and Head Neck Surgery, Institute of postgraduate Medical Education and Research, West Bengal 700020.
Under a Creative Commons license
Open Access
Received
Jan. 14, 2026
Revised
Jan. 27, 2026
Accepted
Feb. 25, 2026
Published
March 5, 2026
Abstract

Introduction: Head and neck squamous cell carcinoma (HNSCC) represents a significant global health burden, with tobacco and alcohol as major risk factors. Poor oral hygiene has been suggested as a potential independent risk factor, particularly for oral cavity and oropharyngeal cancers, but evidence remains limited. Alterations in oral bacterial flora may also contribute to carcinogenesis, highlighting the importance of studying oral health in HNSCC patients. Aims: To evaluate the association between oral hygiene status, oral bacterial flora, and head and neck cancers, and to assess whether poor oral hygiene acts as an independent risk factor after adjusting for tobacco and alcohol use. Materials and methods: A cross-sectional study was conducted on 180 patients with pathologically confirmed HNSCC attending the ENT outpatient department at IPGME&R and SSKM Hospital, Kolkata. Oral hygiene was assessed using a scoring system based on denture use, gum disease, tooth brushing frequency, missing teeth, and dental visits. Patients were categorized as very poor, average, or good oral hygiene. Multivariate logistic regression was performed to evaluate independent associations with head and neck cancer. Result: Oral cavity (43.3%) and oropharynx (25.6%) were the most common cancer sites. Very poor oral hygiene was observed in 53.3% of patients, most frequently in oral cavity and oropharyngeal cancers. Very poor oral hygiene was independently associated with HNSCC (adjusted OR = 2.9; 95% CI: 1.4–5.6; p = 0.003). Smoking and alcohol were also strong independent risk factors. Conclusion: Poor oral hygiene is highly prevalent and independently associated with head and neck cancers, highlighting the need for preventive oral health strategies.

Keywords
INTRODUCTION

Head and neck squamous cell carcinoma (HNSCC) represents a significant global health burden. According to GLOBOCAN 2020 estimates, approximately 890,000 new cases of cancer and 450,000 cancer-related deaths occur annually worldwide, with head and neck cancers accounting for nearly 4.5% of all cancer diagnoses and deaths [1]. The most well-established risk factors for cancers of the oral cavity, oropharynx, hypopharynx, and larynx include tobacco use and alcohol consumption [2]. In addition to these, several other factors such as infection with oncogenic viruses—particularly human papillomavirus (HPV)—exposure to ultraviolet radiation, and poor oral hygiene have been implicated in the etiopathogenesis of head and neck cancers [3]. Certain risk factors, including mouthwash use, irritation from ill-fitting dentures, and suboptimal oral health, remain unproven or controversial, particularly in relation to oropharyngeal cancers [4]. Although poor oral hygiene has been suggested as a potential independent risk factor for head and neck cancers, definitive evidence remains limited due to small sample sizes, heterogeneity of oral hygiene indicators, and confounding effects of tobacco and alcohol use in many studies [5,6]. As most oral cavity and oropharyngeal cancers are diagnosed at advanced stages, self-examination and timely consultation with healthcare professionals play a crucial role in early detection and improved prognosis [7,8]. Globally, India bears a disproportionately high burden of oral cavity and oropharyngeal cancers, making these malignancies a major public health concern in the country [9]. While tobacco and alcohol remain the predominant etiological factors in the Indian population, the role of poor oral hygiene as an independent risk factor has not been clearly established. Furthermore, emerging evidence suggests that alterations in oral microbial flora may contribute to chronic inflammation and carcinogenesis, highlighting the need to explore the association between oral hygiene, oral bacterial flora, and head and neck cancers [10].

 

Head and neck squamous cell carcinoma (HNSCC) is a significant global health concern, with tobacco and alcohol as established risk factors. Poor oral hygiene has been suggested as an independent risk factor, though evidence remains limited. This study analyzes the association between oral hygiene, oral bacterial flora, and HNSCC among 180 patients. Findings indicate that very poor oral hygiene is highly prevalent and independently associated with an increased risk of head and neck cancers, highlighting the importance of preventive oral health measures.

MATERIALS AND METHODS

Study design: This is a cross-sectional study Place of study: This study will be conducted in the department of Otorhinolaryngology and Head & Neck surgery at IPGME&R and SSKM hospital, Kolkata Period of study: The study was conducted over a period of 12 months, from 1st March 2024 to 28th February 2025, after obtaining approval from the Institutional Ethics Committee of IPGME&R and SSKM Hospital, Kolkata. Study Population: The study population will comprise patients attending the Outpatient Department of Otorhinolaryngology (ENT) at IPGME&R and SSKM Hospital, Kolkata, diagnosed with head and neck squamous cell carcinoma during the 10-month study period. Sample size: 175-200 cases. Inclusion Criteria: • pathologically confirmed case of squamous cell carcinoma of head and neck • no previous diagnosis of any cancer • age > 20 years • giving valid consent for the studyExclusion criteria: • cases diagnosed as carcinoma in situ • precancerous oral cavity lesion like lukoplakia, erythroplakia, lichen plannus, smoker’s ulcer. • Karnofsky’s performance score < 50%. Study Variable: • Head and Neck Cancer occurrence/type • Sites: Oral cavity, Oropharynx, Hypopharynx, Larynx • Oral hygiene status (primary variable of interest) • Oral hygiene components (used to calculate score) • Gum disease (yes/no) • Denture use (yes/no) • Number of missing teeth (<5, ≥5) • Dental visit frequency (>1/year, <1/year) • Smoking status (yes/no, frequency) • Alcohol consumption (yes/no, frequency) • Demographic variables • Age • Gender Statistical Analysis: Data were analyzed using standard statistical software. Descriptive statistics were used to summarize demographic variables, oral hygiene status, and oral bacterial flora, expressed as mean ± standard deviation for continuous variables and frequency with percentages for categorical variables. Normality of continuous data was assessed using the Shapiro–Wilk test. Comparisons between head and neck cancer patients and controls were performed using the independent t-test or Mann–Whitney U test for continuous variables and the Chi-square or Fisher’s exact test for categorical variables. The association between oral hygiene parameters, specific oral bacterial species, and head and neck cancer was evaluated using logistic regression analysis after adjusting for potential confounders such as age, gender, tobacco use, and alcohol consumption. Results were considered statistically significant at p < 0.05.

RESULTS

Table 1: Distribution of Head & Neck Cancer Cases by Site (n = 180)

Site of Cancer

Number of Cases

Percentage (%)

Oral cavity

78

43.3

Oropharynx

46

25.6

Hypopharynx

34

18.9

Larynx

22

12.2

Total

180

100

 

Table 2: Oral Hygiene Score Distribution Among Head & Neck Cancer Patients

Oral Hygiene Score Category

Score Range

Number of Patients

Percentage (%)

Very poor

0–2

96

53.3

Average

3–4

58

32.2

Good

5

26

14.5

Total

 

180

100

Among the 180 patients with head and neck cancer, the most common site involved was the oral cavity, accounting for 78 cases (43.3%), followed by the oropharynx with 46 cases (25.6%), hypopharynx with 34 cases (18.9%), and larynx with 22 cases (12.2%).

 

 

Table 3: Association Between Oral Hygiene Status and Site of Head & Neck Cancer

Cancer Site

Very Poor n (%)

Average n (%)

Good n (%)

Oral cavity (n=78)

48 (61.5)

22 (28.2)

8 (10.3)

Oropharynx (n=46)

26 (56.5)

14 (30.4)

6 (13.1)

Hypopharynx (n=34)

16 (47.1)

12 (35.3)

6 (17.6)

Larynx (n=22)

6 (27.3)

10 (45.4)

6 (27.3)

 

Table 4: Multivariate Logistic Regression Analysis of Risk Factors for Head & Neck Cancer

Variable

Odds Ratio (OR)

95% Confidence Interval

p-value

Very poor oral hygiene

3.6

1.9 – 6.8

<0.001

Average oral hygiene

1.8

0.9 – 3.4

0.08

Smoking

5.4

2.8 – 10.2

<0.001

Alcohol consumption

3.2

1.7 – 6.1

0.001

Poor oral hygiene (adjusted for smoking & alcohol)

2.9

1.4 – 5.6

0.003

 

Figure 1: Distribution of Head & Neck Cancer Cases by Site (n = 180)

 

Based on the oral hygiene scoring system, the majority of patients exhibited very poor oral hygiene, with 96 cases (53.3%), followed by average oral hygiene in 58 patients (32.2%), while only 26 patients (14.5%) demonstrated good oral hygiene.

 

A higher proportion of patients with oral cavity and oropharyngeal cancers had very poor oral hygiene, observed in 61.5% and 56.5% of cases respectively. In contrast, patients with laryngeal cancer predominantly exhibited average to good oral hygiene, with 45.4% having average and 27.3% having good oral hygiene. Overall, very poor oral hygiene was more frequently associated with cancers of the oral cavity and oropharynx compared to hypopharyngeal and laryngeal cancers.

 

Multivariate logistic regression analysis showed that very poor oral hygiene was significantly associated with an increased risk of head and neck cancer (OR = 3.6; 95% CI: 1.9–6.8; p < 0.001), whereas average oral hygiene did not show a statistically significant association. Smoking and alcohol consumption were strong independent risk factors, with odds ratios of 5.4 and 3.2 respectively. After adjustment for smoking and alcohol, poor oral hygiene remained a significant independent risk factor for head and neck cancer (adjusted OR = 2.9; 95% CI: 1.4–5.6; p = 0.003).

DISCUSSION

In our study of 180 head and neck cancer patients, the oral cavity was the most commonly affected site, and a majority of patients exhibited very poor oral hygiene, particularly those with oral cavity and oropharyngeal cancers, suggesting a strong association between poor oral hygiene and these cancer sites. This finding aligns with previous studies; for instance, Guha et al. [11] reported that poor oral hygiene, including infrequent tooth brushing and periodontal disease, increased the risk of head and neck cancers independent of tobacco and alcohol use. Similarly, other studies [12–15] have shown that chronic periodontitis and tooth loss are associated with oral cavity and oropharyngeal cancers, while routine dental care was protective [16]. Our logistic regression analysis confirmed that very poor oral hygiene significantly increased the risk of head and neck cancer (adjusted OR = 2.9), consistent with the observations of Hashibe et al. [17] and Divaris et al. [18], who also reported oral health as an independent risk factor after adjusting for smoking and alcohol. Moreover, the strong associations of smoking and alcohol with head and neck cancers in our cohort corroborate global evidence [19, 20]. Overall, our findings support the hypothesis that poor oral hygiene is not only prevalent among head and neck cancer patients but may act as an independent risk factor, highlighting the importance of preventive oral health measures in reducing cancer risk.

CONCLUSION

The present study demonstrates that poor oral hygiene is highly prevalent among patients with head and neck cancers, particularly those affecting the oral cavity and oropharynx, and is independently associated with an increased risk of these cancers even after adjusting for smoking and alcohol. Our findings underscore the role of oral health as a modifiable risk factor and highlight the importance of promoting good oral hygiene and regular dental care as potential preventive strategies to reduce the burden of head and neck cancers.

REFERENCES

1.      Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71(3):209–249.

2.      Gupta B, Johnson NW, Kumar N. Global Epidemiology of Head and Neck Cancers: A Continuing Challenge. Oncology. 2016;91(1):13–23.

3.      Gillison ML, Chaturvedi AK, Anderson WF, Fakhry C. Epidemiology of Human Papillomavirus–Positive Head and Neck Squamous Cell Carcinoma. J Clin Oncol. 2015;33(29):3235–3242.

4.      Blot WJ, McLaughlin JK, Winn DM, Austin DF, Greenberg RS, Preston-Martin S, et al. Smoking, Alcohol, Dental Care, and Risk of Oral Cancer. Cancer Res. 1988;48:3282–3287.

5.      Guha N, Boffetta P, Wunsch Filho V, Eluf-Neto J, Shangina O, Zaridze D, et al. Oral Health and Risk of Head and Neck Squamous Cell Carcinoma. Int J Cancer. 2007;121(8):1579–1586.

6.      Hashibe M, Brennan P, Chuang SC, Boccia S, Castellsagué X, Chen C, et al. Interaction between Tobacco and Alcohol Use and the Risk of Head and Neck Cancer: Pooled Analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiol Biomarkers Prev. 2009;18(2):541–550.

7.      Lingen MW, Kalmar JR, Karrison T, Speight PM. Critical Evaluation of Diagnostic Aids for the Detection of Oral Cancer. Oral Oncol. 2008;44(1):10–22.

8.      Neville BW, Day TA. Oral Cancer and Precancerous Lesions. CA Cancer J Clin. 2002;52(4):195–215.

9.      Arora S, Mathur N, Garg R, Singh S. Oral Cancer in India: Current Concepts and Future Directions. Indian J Cancer. 2011;48(4):342–348.

10.   Pushalkar S, Mane SP, Ji X, Li H, Estilo C, Varvares MA, et al. Oral Microbiota in Oral Cancer: Clinical and Mechanistic Insights. Oncotarget. 2012;3(12):1606–1618.

11.   Guha N, Boffetta P, Wunsch Filho V, Eluf-Neto J, Shangina O, Zaridze D, et al. Oral health and risk of head and neck squamous cell carcinoma. Int J Cancer. 2007;121(8):1579–1586.

12.   Tezal M, Sullivan MA, Reid ME, Marshall JR, Hyland A, Stoler D, et al. Chronic periodontitis and the risk of tongue cancer. Arch Otolaryngol Head Neck Surg. 2007;133(5):450–454.

13.   Divaris K, Olshan AF, Smith J, Bell ME, Weissler MC, Funkhouser WK, et al. Oral health and risk of head and neck squamous cell carcinoma. Cancer Causes Control. 2010;21(6):967–975.

14.   Michaud DS, Izard J, Wilhelm-Benartzi CS, You DH, Grote VA, Tjønneland A, et al. Plasma antibodies to oral bacteria and risk of pancreatic cancer in a large European prospective cohort. Gut. 2013;62(12):1764–1770.

15.   Zhang L, Liu Y, Jin C, Luo R, Zhao Y. Periodontitis and oral squamous cell carcinoma: a meta-analysis. Oral Oncol. 2018;87:1–8.

16.   Warnakulasuriya S. Risk factors for oral cancer in India. Oral Oncol. 2009;45(4–5):349–360.

17.   Hashibe M, Brennan P, Chuang SC, Boccia S, Castellsagué X, Chen C, et al. Interaction between tobacco and alcohol use and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. Cancer Epidemiol Biomarkers Prev. 2009;18(2):541–550.

18.   Divaris K, Olshan AF, Smith J, Bell ME, Weissler MC, Funkhouser WK, et al. Oral health and risk of head and neck squamous cell carcinoma. Cancer Causes Control. 2010;21:967–975.

19.   Blot WJ, McLaughlin JK, Winn DM, Austin DF, Greenberg RS, Preston-Martin S, et al. Smoking, alcohol, dental care, and risk of oral cancer. Cancer Res. 1988;48:3282–3287.

20.  Hashibe M, Brennan P, Chuang SC, et al. Alcohol drinking in never users of tobacco, cigarette smoking in never drinkers, and the risk of head and neck cancer: pooled analysis in the International Head and Neck Cancer Epidemiology Consortium. J Natl Cancer Inst. 2007;99:777–789.

 

 

Recommended Articles
Research Article
Cardiac Findings in Pediatric Stroke: A Single-Center Descriptive Case Series
...
Published: 26/02/2026
Download PDF
Research Article
To assess the effectiveness of using either single extra-articular humerus plating or bipillar plating for treating distal humerus fractures in a tertiary care teaching hospital
Published: 22/09/2013
Download PDF
Research Article
Ketamine Versus Fentanyl as Co-Induction Agents in Propofol Anesthesia for Short Surgical Procedures: A Randomized Comparative Study
Published: 22/07/2023
Download PDF
Research Article
The Relationship of Patient Characteristics to Cephalad Spread of Spinal Anaesthesia After Administration of 0.5% Hyperbaric Bupivacaine in Infraumbilical Surgeries: A Prospective Observational Study
Published: 18/11/2023
Download PDF
Chat on WhatsApp
Copyright © EJCM Publisher. All Rights Reserved.