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. 2022 Apr 21;17(4):e0266346. doi: 10.1371/journal.pone.0266346

The cost of oral cancer: A systematic review

Rejane Faria Ribeiro-Rotta 1,*,#, Eduardo Antônio Rosa 1,#, Vanessa Milani 1,#, Nadielle Rodrigues Dias 1,#, Danielle Masterson 2,, Everton Nunes da Silva 3,, Ana Laura de Sene Amâncio Zara 1,#
Editor: Antoine Eskander4
PMCID: PMC9022815  PMID: 35446870

Abstract

Although clinical and epidemiological aspects of oral cancers (OC) are well-documented in the literature, there is a lack of evidence on the economic burden of OC. This study aims to provide a comprehensive systematic assessment on the economic burden of OC based on available evidence worldwide. A systematic review was conducted. The population was any individual, who were exposed to OC, considered here as lip (LC), oral cavity (OCC), or oropharynx (OPC) cancer. The outcome was information on direct (medical and non-medical) and indirect (productivity loss and early death) costs. The data sources included Scopus, Web of Science, Cochrane, BVS, and NHS EED. A search of grey literature (ISPOR and INAHTA proceedings) and a manual search in the reference lists of the included publications were performed (PROSPERO no. CRD42020172471). We identified 24 studies from 2001 to 2021, distributed by 15 countries, in 4 continents. In some developed western countries, the costs of LC, OCC, and OPC reached an average of Gross Domestic Product per capita of 18%, 75%, and 127%, respectively. Inpatient costs for OC and LC were 968% and 384% higher than those for outpatients, respectively. Advanced cancer staging was more costly (from ~22% to 373%) than the early cancer staging. The economic burden of oral cancer is substantial, though underestimated.

Introduction

Detection of oral cancer does not demand elaborate screening tests such as breast, prostate, and colon cancers. Oral cancer can be easily and effectively detected early with oral inspection during routine dental consultations and integrated in primary care [1]. To achieve this goal, current efforts must include target programs to educate high-risk persons and primary care providers about the main aspects of early detection [2]. Oral cancer staging plays an important role in survival rate, with early-stage (I and II) and advanced-stage (III and IV) lesions having a 5-year survival rate of 80% and 50% or less, respectively [3]. Additionally, advanced stages require more aggressive combined interventions, and consequently more expensive treatments. There are also equity concerns about oral cancers, since they asymmetrically affect different population groups and countries. Older, heavier male users of tobacco and alcohol, and people from low socioeconomic strata, as well as those who have a poor dietary intake are populations who are at a high risk of developing oral cancer [4]. Regarding geographical locations, the highest incidence rates occur in three low- and middle-income countries (Pakistan, Brazil, and India) [4]. There is also a growing incidence of oral and oropharynx cancer among young patients (<45 years), particularly in Africa, the Middle East, and Asia [5].

Although clinical and epidemiological aspects of oral cancers are well-documented in the literature, there is a lack of evidence on the economic burden of oral cancers worldwide. Cost-of-illness studies can provide information on the monetary consequences of a disease or condition, including healthcare costs and productivity losses, and its impact on societal or public health expenditure [6]. This information can be used to estimate avoidable costs if policies/programmes are implemented to reduce the prevalence of this disease. When available, it also can inform costs stratified by stages of the disease. In the United Kingdom, average treatment cost for oral cancer can range from I$ 3,343 in the early stages to I$24,890 in the advanced stages [7]. Cost-of-illness can also be used to inform priority setting, by providing estimates of how big a problem is in terms of costs [8]. Moreover, gathering information on costs may encourage decision makers to implement strategies for detecting and screening populations at high-risk of developing oral cancer, particularly by comparing costs at different stages of the disease. To the best of our knowledge, up to now there are no systematic reviews that synthesize evidence on the economic burden of oral cancer. The objective of this study is to provide a comprehensive systematic assessment of the economic burden of oral cancer based on available evidence worldwide.

Methods

A systematic review of studies revealing the costs of lip cancer (LC), oral cavity cancer (OCC), and oropharyngeal cancer (OPC) was conducted, taking into account any cost perspective (societal, third-party players, public systems). The method used was guided by the concepts of the Joanna Briggs Institute (JBI) [9] and in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines [10]. A systematic review protocol can be found as a preprint on Research Square (https://www.researchsquare.com/article/rs-34637/v1). This protocol was reformulated, and the final version can be found in Prospero (CRD42020172471).

Problem specification

What is the economic burden of oral cancer, including direct and indirect costs?

The question was framed using the acronym PEO (Population, Exposure, Outcome), which was used to define the search strategy. The population (P) considered for publication searching was any individual (human) or groups of individuals, without restriction of age, sex, race, or socioeconomic status, who were exposed (E) to oral cancer, considered here as LC, OCC, or OPC. The outcome (O) required from the publications was information on direct (medical and non-medical) and indirect (productivity loss and early death) costs.

Eligibility criteria

Original studies on the cost of oral cancer, which included direct and/or indirect costs, or that provided estimates per patient (average cost or by clinical stage) or economic burden as percentage of GDP or national healthcare expenditure were included in the review. No language or year of publication restriction was established.

Publications that met the following criteria were excluded:

  • Types of study such as: editorial, letters to the editor, systematic and non-systematic reviews of the literature, meta-analyses, case reports, case series, clinical trials.

  • Studies that estimated specific item components of oral cancer cost (e.g., only surgery or medication, etc).

  • Studies that addressed specific analyses, such as cost-effectiveness, cost-utility, cost-benefit, cost-minimization.

Information sources

A systematic literature search was carried out through a comprehensive search of databases in PubMed, Scopus, Web of Science, BVS (Biblioteca Virtual em Saúde) and NHS Economic Evaluation Database up to March 31, 2021. We also manually searched the references of the articles included for additional studies. Additionally, our search was supplemented by gray literature, with the search of abstracts of conference proceedings from annual meetings of the following societies: International Society for Pharmacoeconomics and Outcomes Research (ISPOR) and International Network of Agencies for Health Technology Assessment (INAHTA) [11] (accessed March 31, 2021).

Design of search strategy

To identify relevant cost-of-illness studies for LC, OCC, and OPC, appropriate disease-related MeSH terms were used (Additional file 1, available via https://figshare.com/s/f7eb4990efeb5021f131). To determine the search strategy, descriptors were selected by building a table (concept mapping). The table rows were allocated for each item of the acronym PEO and the columns for PubMed controlled vocabulary terms (Medical Subject Headings–MeSH), their subcategories (entry terms; see also), and uncontrolled vocabulary (free terms) usually obtained from titles and abstracts of the main publications, books, and gray literature on the research theme. After the PubMed MeSH controlled vocabulary tree was explored, terms were tested in the PubMed database and the most relevant descriptors were selected, and a search strategy was built (Additional file 2, available via https://figshare.com/s/f7eb4990efeb5021f131). The search strategy defined for PubMed was adapted for searches in the other databases.

All publications identified in the databases were exported to the Mendeley Reference Manager (Mendeley®, Elsevier, version 1.19.5/20019) for duplicate removal. After that, all publications were exported to Rayyan® software (Rayyan QCRI, Qatar Computing Research Institute–Data Analytics) [12] for the selection process.

Selection process

The stages of the selection process included at least one reviewer from each of the following fields of knowledge: oral cancer (EAR; VM; NRD; RFRR); epidemiology (ALSAZ); and / or health economics (ENS). Three reviewers (EAR; VM; NRD) read the title and abstract of publications using the software Rayyan (Rayyan QCRI). Kappa statistic was calculated to assess agreement between reviewers, in pairs, in the eligibility stage, with a significance level of 5% (p<0.05). The scale of Kappa value interpretation was as following: <0 no agreement; 0–0.20 slight; 0.21–0.40 fair; 0.41–0.60 moderate; 0.61–0.80 substantial and 0.81–1.0 perfect. All studies identified were screened based on the eligibility criteria and were forwarded for full-text review. Contact with the authors was established for the screened studies not available in full text. Two reviewers (EAR; ENS) independently read the full text for inclusion. Additional reviewers (RFRR; ALSAZ) were consulted for consensus in case of disagreement between the first two (EAR; ENS). Reviewers underwent training prior to the publication selection process, which was performed using 100 screened publications.

Data collection

An instrument was built to extract the relevant data on cost methodologies, designs, and approaches, using Research Electronic Data Capture (REDCap) [13]. This instrument included the following variables:

  1. Study identification: first author; country; journal and year of publication.

  2. Main study design characteristics: type of study (cost-of-illness study or another type of study that provides cost-of-illness information of oral cancer); epidemiological approach (longitudinal or cross-sectional or case control); sample (number, age, type of cancer, cancer anatomical site and stage); retrospective or prospective data gathering; data source; perspective of the analysis (societal, government, health insurance provider, hospital); time horizon; presence of a control group (patients not affected by oral cancer); location/setting (country, state, or city); cost-of-illness based approach (prevalence-based or incidence-based); estimation of resources and costs (single study-based or model-based); assumptions adopted (structural or other assumptions underpinning the study); year of cost estimation; currency; sensitivity analysis; use of discount rate; funding sources; conversion; data source (primary or secondary database). The perspective of studies was defined as: i) societal, which includes direct and indirect costs and/or out-of-pocket costs from patient point of view; ii) government (public payer), includes direct costs only; iii) health insurance provider (private payer), which includes direct costs reimbursed by the private health insurers; and iv) hospital, which includes direct cost charged by just one hospital, unless the authors explicitly reported the government or health insurer perspectives.

  3. Type of cost estimated: direct healthcare costs (hospitalization, surgery, chemotherapy, radiotherapy, intensive care unit, emergency room, physical therapists, speech therapists, medication, laboratory tests, imaging diagnosis and follow-up); direct non-healthcare costs (social services and transportation costs), indirect costs (productivity loss, early death).

  4. Primary study outcomes: costs related to oral cancer in patients, reported in monetary units or economic burden as a percentage of Gross Domestic Product (GDP) or national healthcare expenditure.

  5. Additional outcome: if the studies provided a specific breakdown of costs, this information was reported as a secondary outcome (outpatient and inpatient costs; cost by clinical stage; primary and recurrent tumor cost). We also calculated the economic burden of OC at individual level, by dividing the OC costs per patient by the GDP per capita of the country under investigation. This measure would indicate how catastrophic those costs could be for an average citizen (GDP per capita).

Data extraction was carried out by at least two of four reviewers (ALSAZ; EAR; ENS; RFRR), in a double-blind process, and disagreements were decided by consensus.

Data synthesis

All studies meeting the eligibility criteria were included in the study and critically appraised using the Larg & Moss’s guide [14] for assessing cost-of-illness. This checklist includes three domains: analytical framework; methodology and data; analysis and reporting. The method for assessing quality of individual studies was done at both the outcome and study level, independently, and in duplicate (EAR, ENS), and discrepancies were resolved by consensus. We provided a global score for the quality of each study by calculating the total number of points rated as “yes” and “not applicable (NA)”. Percentage intervals were established for meeting the items of the quality assessment instrument applied to the included studies: >80%; between 79% and 50%; and less than 50%. The average and standard deviation (SD) of the scores were calculated. The average of the scores were compared between study design groups (longitudinal studies, cross-sectional and case control studies, and cross-sectional studies based on information system data) and by domains, using a one-way analysis of variance (ANOVA) (p<0.05), by Open-Source Epidemiologic Statistics for Public Health (OpenEpi), version 3.01 [15]. In this section, this was considered the risk of bias information obtained from each study.

To calculate the percentage of the burden of the cost of oral cancer, GDP per capita of the countries where the studies were carried out was considered and converted to International Dollars (I$) by Purchasing Power Parity—PPP (2019) [16].

The results were presented in narrative form, using the Synthesis Without Meta-Analysis (SWiM) reporting guideline [17], and the main results were presented in tables.

Results

The search procedure is shown in the PRISMA flow diagram [10] (Fig 1). The systematic literature search identified 12,391 potentially relevant articles. After removal of duplicates, 6,864 studies were screened for inclusion (Fig 1). Following title and abstract review, full-text articles were assessed (n = 44) and excluded (n = 20) for the following reasons—they were not an oral cancer cost study, did not include a specific intervention cost, there was a head and neck cancer cost study that did not present oral cancer cost separately, only proceedings available and there were no abstracts. The author or co-authors were contacted by email for the nine studies which were unobtainable, and for which only the abstracts or the title was available. There was only one answer from all of these authors, stating that they had not published the full study. Overall, 24 studies met all the eligibility criteria and were included in the systematic review.

Fig 1. Data acquisition flowchart.

Fig 1

In the eligibility stage, Kappa coefficient was 0.83 (perfect) between the EAS and VM reviewers; 0.78 (substantial) between EAS and NRD and 0.78 (substantial) between VM and NRD.

Study characteristics

The study characteristics are summarized in Tables 1 and 2. The studies identified were published from 2001 to 2021 and distributed by continent as follows: Europe (n = 9), Asia (n = 7), America (n = 6), Oceania (n = 1), and 1 global study stratified by region and income of 195 countries. The study population size ranged from a minimum of 69 (Sri Lanka) [18] to a maximum of 62,265 (Korea) [19]. Four studies [2022] estimated costs by procedures and not per individual. The studies included investigated a wide variety of anatomical sites of the head and neck region, using a non-standardized terminology to identify them (Table 1).

Table 1. Summary of main characteristics of oral cancer cost studies from 2001 to 2020 (n = 24).

Study Country Sample (size, age, sex) Cancer anatomical sites
Longitudinal studies
1. Kim, 2011 [23] UK 11,403 (mean age 63.2 years old; female (30.2%); male (69.8%)) Lip; other and unspecified parts of tongue; oral cavity; pharynx; larynx
2. Polesel, 2019 [26] Italy 879 (18–54 (20.6%); 55–59 (18.8%); 60–64 (19.1%) 65–69 (22.4%); 70–75 (19.1%)); female (19.2%); male (80.8%) Oral cavity; oropharynx; hypopharynx; larynx
3. Jacobson, 2012 [24] USA 6,812 (mean age: commercial 53.42; medicare 74.51; medicaid 53.36 years old; male: commercial (68.7%); medicare (65.4%); medicaid (58.8%) Lip; base of tongue; gum; floor of mouth; other and unspecified parts of mouth; oral cavity; salivary gland cancer; major salivary gland; oropharynx
4. Pollaers, 2019 [25] Australia 113 (mean age 60 years old; female (39.0%); male (61.0%)) Other and unspecified parts of tongue; floor of mouth; retromolar trigone
5. Huang, 2020 [27] Taiwan 50,784 (mean age 55.0 years old; female (9.0%); male (91.0%)) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; tonsil; oropharynx; pyriform sinus; hypopharynx; other and ill-defined sites in the lip, oral cavity, and pharynx is a medical classification as listed by WHO under the range
Cross-sectional and case control studies
6. Rezapour, 2018 [29] Iran 3,024 (mean age 55.27 years old; female (37.8%); male (62.2%)) Lip; other and unspecified parts of tongue; floor of mouth; buccal
7. van Aghtoven, 2001 [35] The Netherlands 854 (not informed) Oral cavity; oropharynx; larynx
8. Fisher, 2018 [36] USA 462 (mean age 61.1 years old; female (19.3%); male (80.7%)) Oral cavity; oropharynx; hypopharynx/larynx; salivary glands; nasopharynx; other/unknown
9. Nijdam, 2005 [32] The Netherlands 344 (mean age 56 (34–87) years-old; male (62.5%) and female (37.5%)) Oropharynx
10. Amarasinghe, 2019 [18] Sri Lanka 69 (40–50 (24.6%); 50–60 (43.5%); 60–70 (17.4%); >70 (14.5%)) Lip; other and unspecified parts of tongue; floor of mouth; palate; other and unspecified parts of mouth
11. Goyal, 2014 [33] India 100 (mean age 50.17 years old; female (8.0%); male (92.0%)) Lip; other and unspecified parts of tongue; floor of mouth; buccal mucosa; retromolar trigone
12. Zavras, 2002 [37] Greece 95 (not informed) Upper lip, inner aspect; lower lip, inner aspect; lip, unspecified, inner aspect; commissure of lip; overlapping lesion of lip; lip, unspecified; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth
13. van der Linden, 2016 [38] The Netherlands 125 (72% <65 years old, 28% > 65 years old) Oral cavity; oropharynx; hypopharynx; nasopharynx; larynx
14. Epstein, 2008 [34] USA 695 (mean age 63.49 years old; female (53.7%); male (46.3%)) Lip; other and unspecified parts of tongue; gum; floor of mouth; other and unspecified parts of mouth; oropharynx; pharynx; nasopharynx; hypopharynx; Waldeyer’s ring
15. Lafuma, 2019 [30] France 267 (mean age 62 years old; female (15.0%); male (85.0%)) Base of tongue; gum; floor of mouth; palate; tonsil; oropharynx; nasopharynx; piriform sinus; hypopharynx; larynx
16. Patterson, 2020 [31] Global stratified by region and income 195 countries (data repositories) (not informed) Lip; palate; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; oral cavity; other and unspecified parts of mouth; tonsil; oropharynx; other pharynx; nasopharynx; larynx; thyroid
17. Han, 2010 [39] China 456 (mean age 54.63 years old; female (38.6%); male (61.4%)) Lip; other and unspecified parts of tongue; floor of mouth; palate; oral cavity; buccal mucosa, gingival tissues; retromolar trigon
18. Enomoto, 2015 [40] USA 7,383 (female (38.8%); male (61.2%)) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; tonsil; oropharynx; salivary gland; nasopharynx; hypopharynx
19. Lairson, 2017 [41] USA 934 (mean age 54 years old; female (18.2%); male (81.8%)) Base of tongue; soft palate; uvula; lingual tonsil; oropharynx; pharynx otherwise unspecific
20. Kim, 2020 [19] Korea 62,265 (not informed) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; tonsil; oropharynx; pyriform sinus; hypopharynx; other and ill-defined sites in the lip, oral cavity and pharynx is a medical classification as listed by WHO under the range
Cross-sectional studies based on information system data
21. Vatanasapt, 2012 [20] Thailand 207,439 visits (outpatient) and 8,360 admissions (inpatient) (not informed) Other and unspecified parts of mouth; oral cavity; oropharynx; nasopharynx; hypopharynx; pharynx; larynx; parathyroid gland; external and middle ear; malignant melanoma; non-melanoma skin cancer; benign neoplasms
22. Klussmann, 2013 [28] Germany 63,857 hospitalizations, 4,898 inpatient rehabilitations, and 17,494 sick leaves (age group: 15–80 years old; female (20.0%); male (80.0%)) Base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; oral cavity; tonsil; oropharynx; pharynx; nasopharynx; larynx
23. Keeping, 2018 [21] England 21,498 attendances (outpatient) and 27,326 hospital spells (inpatient) per year (not informed) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; oral cavity; other and unspecified parts of mouth; tonsil; oropharynx; larynx
24. Milani, 2021 [22] Brazil 117,317 admissions and 6,22,236 outpatient procedures (not informed) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; tonsil; oropharynx

Table 2. Methodological characteristics of oral cancer cost studies from 2001 to 2020.

Study Type of study* Study design Data source Cost-of-illness based approach Estimation of resources and cost Time horizon (years) Perspective
Longitudinal studies
1. Kim, 2011 [19] Cost-of-illness Retrospective longitudinal Secondary data Incidence Single study-based 5 Government
2. Polesel, 2019 [26] Cost-of-illness Prospective longitudinal Secondary data Incidence Single study-based 2 Unclear
3. Jacobson, 2012 [24] Cost analysis Retrospective longitudinal Secondary data Incidence Single study-based 1 Government and health insurance provider
4. Pollaers, 2019 [25] Cost analysis Retrospective longitudinal Secondary data Incidence Single study-based 5 Government
5. Huang, 2020 [27] Cost-of-illness Retrospective longitudinal Secondary data Incidence Single study-based 5 Societal and Government
Cross-sectional and case control studies
6. Rezapour, 2018 [29] Cost-of-illness Cross-sectional Primary and secondary data Prevalence Single study-based 1 Societal
7. van Aghtoven, 2001 [35] Cost analysis Cross-sectional Primary and secondary data Prevalence Model-based 10 Hospital
8. Fisher, 2018 [36] Cost analysis Cross-sectional Primary and secondary data Prevalence Single study-based 3 Government and health insurance provider
9. Nijdam, 2005 [32] Cost-of-illness Cross-sectional Primary data Prevalence Single study-based 4 Hospital
10. Amarasinghe, 2019 [18] Cost-of-illness Cross-sectional Primary data Prevalence Single study-based 1 Societal
11. Goyal, 2014 [33] Cost analysis Cross-sectional Primary data Prevalence Single study-based ~1 year 9 months Hospital
12. Zavras, 2002 [37] Cost analysis Cross-sectional Primary data Not clear Single study-based at least 6 months Hospital
13. van der Linden, 2016 [38] Cost analysis Cross-sectional Primary data Not clear Single study-based 1 Hospital
14. Epstein, 2008 [34] Cost analysis Cross-sectional Secondary data Prevalence Single study-based 1 Government
15. Lafuma, 2019 [30] Cost-of-illness Cross-sectional Secondary data Prevalence Single study-based 5 Societal
16. Patterson, 2020 [31] Cost-of-illness Cross-sectional Secondary data Incidence Model-based 1 Societal
17. Han, 2010 [39] Cost analysis Cross-sectional Secondary data Prevalence Single study-based 1 Hospital
18. Enomoto, 2015 [40] Cost analysis Cross-sectional Secondary data Prevalence Single study-based 1 Government
19. Lairson, 2017 [41] Cost-of-illness Case-control Secondary data Not clear Single study-based 2 Government and health insurance provider
20. Kim, 2020 [19] Cost-of-illness Cross-sectional Secondary data Prevalence Single study-based 5 Societal and Government
Cross-sectional studies based on information system data
21. Vatanasapt, 2012 [20] Cost-of-illness Cross-sectional Secondary data Incidence Single study-based 1 Government
22. Klussmann, 2013 [28] Cost-of-illness Cross-sectional Secondary data Prevalence Single study-based 1 Societal
23. Keeping, 2018 [21] Cost-of-illness Cross-sectional Secondary data Prevalence Single study-based 5 Hospital
24. Milani, 2021 [22] Cost-of-illness Cross-sectional Secondary data Prevalence Single study-based 9 Government

* We classified the type of study according to the comprehensiveness of the cost estimation. If the cost estimation was restricted to a small sample, the study was classified as cost analysis, generally a group of patients from one hospital; and if the cost estimation included a city, state or country, the study was classified as cost-of-illness.

The 24 included studies were stratified by study design, which revealed five longitudinal studies [2327] with a time horizon varying from one to five years. Of the 18 cross-sectional studies, 10 were cost-of-illness [1822, 2832], 8 cost analysis [3340] and one was a case control study [41]. The 24 studies used primary and/or secondary data sources, of which four were based on information system data [2022, 28]. The most frequent perspective of the studies was hospital (n = 7) [21, 32, 33, 35, 3739]. Two studies used estimation of resources and cost based on mathematical models [31, 35] (Table 2).

Quality assessment

The global quality score of the studies, considered as the percentage rate of compliance to the items of the quality evaluation instrument, was 47.8% (SD = 10.9). The quality score varied from 38% [20, 32] to 66% [19] (Table 3). Regarding the study designs, the average of quality scores was 49.1% (SD = 9.9) for longitudinal studies, 47.3% (SD = 5.8) for cross-sectional and case control studies, and 46.0% (SD = 7.2) for studies based on information system data. No statistically significant difference was found among the average scores by study design (p = 0.796). Considering all studies, the Analytical Framework domain had an average score of 68.8% (SD = 15.0), the Methodology and Data domain 42.9% (SD = 10.1), and the Analysis and Reporting domains 43.8% (SD = 16.1), presenting a statistically significant difference among the average scores (p<0.001). The average of the quality scores of cross-sectional studies and those studies based on system data differed among domains (respectively p<0.001 and p = 0.001). The Analytical Framework domain had the highest average score in each included publication, when compared to the other two domains.

Table 3. Assessment of quality of studies of oral cancer cost included in the systematic review, according to the critical guide of Larg & Moss, 2011 [14].

Domains Item Longitudinal studies Cross-sectional and case control studies Cross-sectional studies based on information system data
Kim (2011) Polesel (2019) Jacobson (2012) Pollaers (2019) Huang (2020) Rezapour (2018) van Agthoven (2001) Fisher (2018) Nijdam (2005) Amarasinghe (2019) Goyal (2014) Zavras (2002) van der Linden (2016) Epstein (2008) Lafuma (2019) Patterson (2020) Han (2010) Enomoto (2015) Lairson (2017) Kim (2020) Vatanasapt (2012) Klussmann (2013) Keeping (2018) Milani (2021)
Analytical framework 1A Cost—perspective
1B Cost—epidemiological approach
1CI Cost—societal
1CII Cost—timeframe
1CIII Cost—risk factor NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA NA
1CIV Cost—counterfactual population
Total number of positive and NA answers of the Analytical frame domain (%) 4 (67) 3 (50) 5 (83) 4 (67) 3 (50) 5 (83) 4 (67) 3 (50) 4 (67) 5 (83) 5 (83) 3 (50) 4 (67) 5 (83) 4 (67) 2 (33) 5 (83) 5 (83) 4 (67) 4 (67) 3 (50) 5 (83) 5 (83) 5 (83)
Positive and NA answers of the of the Analytical frame domain (average ± SD) (68.8±15.0) **p = 0.529 63.3 ± 13.9 68.9 ± 15.3 75.0 ± 16.7
Methodology and data 2AI Quantification—additional cost
2AII Quantification—confounders controlled
2AIII Quantification—important effects
2AIV Quantification—differences across subpopulations
2AV Quantification—required level of detail
2BI Resource quantification—population based (top-down)
2BII Resource quantification—person based (bottom-up)
2BIII Resource quantification—data representative
2BIV Resource quantification—other relevant issue (model-based)
2C Resource—healthcare
2D Productivity—losses and assumptions
2EI Intangible costs—mortality-related losses avoided
2EII Intangible costs—study’s perspective losses
Total number of positive and NA answers of the Methodology and data domain (%) 4 (31) 5 (38) 3 (23) 7 (54) 7 (54) 7 (54) 6 (46) 7 (54) 4 (31) 8 (62) 6 (46) 6 (46) 4 (31) 6 (46) 6 (46) 6 (46) 6 (46) 4 (31) 4 (31) 6 (46) 4 (31) 5 (38) 6 (46) 7 (54)
Positive and NA answers of the of the Methodology and data domain (average ± SD) (42.9±10.1) **p = 0.745 40.0 ± 13.8 44.1 ± 9.4 42.3 ± 9.9
Analysis and reporting 3A Study question answered
3B Range of estimates presented
3C No main uncertainties identified
3DI Sensitivity—analysis performed
3DII Sensitivity—key assumptions
3DIII Sensitivity—point estimates
3E Adequate documentation—cost components, data, sources, assumptions, and methods
3F Uncertainty—estimates discussed
3G Limitations
3H Results—appropriate level of detail
Total number of positive and NA answers of the Analysis and reporting domain (%) 4 (40) 10 (100) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 3 (30) 4 (40) 3 (30) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 4 (40) 9 (90) 4 (40) 4 (40) 4 (40) 4 (40)
Positive and NA answers of the of the Analysis and reporting domain (average ± SD) (43.8±16.1) **p = 0.443 52.0 ± 26.8 42.0 ± 13.7 40.0 ± 0.0
Total number of positive and NA answers (%) 12 (41) 18 (62) 12 (41) 15 (52) 14 (48) 16 (55) 14 (48) 14 (48) 11 (38) 17 (59) 13 (45) 12 (41) 12 (41) 15 (52) 14 (48) 12 (41) 16 (55) 13 (45) 12 (41) 19 (66) 11 (38) 14 (48) 15 (52) 16 (55)
Global score: 47.8% ± 10.9
Positive and NA answers per type of study groups (average ± SD)**p = 0.796 49.1 ± 9.9 47.3 ± 5.8 46.0 ± 7.2
ANOVA test per domain (p-value) 0.207 <0.001 0.001

SD: standard deviation.

**ANOVA test (p<0.05).

Cost components

Fourteen studies [18, 19, 2123, 2527, 32, 34, 35, 37, 39, 41] evaluated all components of direct medical costs (surgery, chemotherapy, radiotherapy, follow-up, medications, exams), and only six [18, 19, 22, 29, 30, 39] investigated non-medical costs. Regarding indirect costs, three studies [18, 28, 30] evaluated absenteeism costs, two evaluated both [19, 29] absenteeism and early death, and one investigated early death costs [31]. None of them estimated presenteeism costs (Table 4).

Table 4. Estimates of medical, non-medical, and indirect costs of oral cancer presented in the methods of studies from 2001 to 2020.

Study Direct costs Indirect cost
Medical costs Non-medical costs Absenteeism Early Death
Surgery Chemotherapy Radiotherapy Follow up Medications Exams
Longitudinal studies
1. Kim, 2011 [23]
2. Polesel, 2019 [26]
3. Jacobson, 2012 [24]
4. Pollaers, 2019 [25]
5. Huang, 2020 [27]
Cross-sectional and case control studies
6. Rezapour, 2018 [29]
7. van Aghtoven, 2001 [35]
8. Fisher, 2018 [36]
9. Nijdam, 2005 [32]
10. Amarasinghe, 2019 [18]
11. Goyal, 2014 [33]
12. Zavras, 2002 [37]
13. van der Linden, 2016 [38]
14. Epstein, 2008 [34]
15. Lafuma, 2019 [30]
16. Patterson, 2020 [31]
17. Han, 2010 [39]
18. Enomoto, 2015 [40]
19. Lairson, 2017 [41]
20. Kim, 2020 [19]
Cross-sectional studies based on information system data
21. Vatanasapt, 2012 [20]
22. Klussmann, 2013 [28]
23. Keeping, 2018 [21]
24. Milani, 2021 [22]

Studies that met the inclusion criteria presented the estimates of oral cancer cost according to a wide variety of aspects: cost per patient, monthly cost, total cost in a period, cost per treatment or procedure, from the payer’s perspective, cost components, outpatient and inpatient cost, services, by International Classification of Diseases, Tenth Revision (ICD-10) separately or in aggregate, by disease stage, follow-up, and disease recurrence (Table 5).

Table 5. Summary of costs estimates of included studies in the systematic review.

Study Year of cost Country Currency Cancer anatomical sites considered for cost Cost per patient (95% CI) Cost per patient by clinical stage Other measures of cost (95% CI)
Longitudinal studies
1. Kim, 2011 [23] 2009 United Kingdom Pounds (GBP) Lip; other and unspecified parts of tongue; oral cavity; pharynx; larynx Post-operative treatment for resected patients (average)– 5-year follow-up:
• Lip: 5,790
• Tongue: 19,493
• Oral cavity: 25,311
Not applicable Post-operative treatment for resected patients (average)– 5-year follow-up:
Inpatient care:
• Lip: 4,798
• Tongue: 17,910
• Oral cavity: 23,143
Outpatient care:
• Lip: 992
• Tongue: 1,583
• Oral cavity: 2,168
2. Polesel, 2019 [26] 2010 Italy Euros (EUR) Oral cavity (including lip and pharynx); oropharynx; hypopharynx; larynx Cost per patient (average– 95% CI)– 2-year follow-up:
• Oral cavity: 18,462 (17,720–19,205)
• Oropharynx: 24,253 (23,197–25,310)
Not applicable Cost per patient (average– 95%CI):
Oral cavity:
• Before treatment: 1,223 (1,103–1,343)
• 0–3 months treatment: 11,102 (10,702–11,503)
• 4–12 months treatment: 4,421 (3,838–5,004)
• 13–24 months treatment: 2,282 (2,071–2,493)
Oropharynx:
• Before treatment: 2,932 (2,640–3,223)
• 0–3 months treatment: 12,646 (12,123–13,170)
• 4–12 months treatment: 8,658 (7,562–9,754)
• 13–24 months treatment: 4,113 (3,696–4,531)
3. Jacobson, 2012 [24] 2009 United States of America US Dollars (USD) Lip; base of tongue; gum; floor of mouth; other and unspecified parts of mouth; oral cavity; salivary gland; major salivary gland; oropharynx Not reported Not applicable Oral cavity, oropharynx and salivary gland tumors (average ± standard deviation)– 1-year follow-up:
• Commercial insurance: 79,151 ± 86,170
• Medicare: 48,410 ± 61,599
• Medicaid: 59,404 ± 74,919
4. Pollaers, 2019 [25] 2016/2017 Australia Australian Dollars (AUD) Other and unspecified parts of tongue; floor of mouth; retromolar trigone Squamous cell carcinoma (average)– 2-year follow-up:
Floor of mouth: 103,832
• First year: 101,187
• Second year: 2,645
Tongue: 92,761
• First year: 86,391
• Second year: 6,279
Inpatients costs:
Stage I:
• 1-year: 33,985
• 2-year: 37,101
• 5-year: 43,661
Stage II:
• 1-year: 61,690
• 2-year: 45,376
• 5-year: 44,548
Stage III:
• 1-year: 79,684
• 2-year: 90,557
• 5-year: 88,976
Stage IVa:
• 1-year: 93,269
• 2-year: 104,257
• 5-year: 118,913
Squamous cell carcinoma of floor of the mouth, tongue, and alveolar trigone (average)– 2‐year follow‐up:
• Remained disease‐free: 65,012
• Cases with disease recurrence: 98,359
First year:
• Inpatient: 66,004
• Outpatient: 30,214
Second year:
• Inpatient: 72,208
• Outpatient: 35,590
5. Huang, 2020 [27] 2018 Taiwan US Dollars (USD) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; tonsil; oropharynx; piriform sinus; hypopharynx; ill-defined and unspecified sites of lips, oral cavity, and pharynx Average per patient– 2.3-years follow-up: 56,501
Mean ± standard deviation:
• Direct medical costs mean: 19,644 ± 15,305
• Indirect costs morbidity: 1,286 ± 1,386
• Indirect costs mortality: 35,570 ± 61,859
• All medication costs mean: 2,359
• Anticancer drug costs mean: 638
--- ---
Cross-sectional and case control studies
6. Rezapour, 2018 [29] 2014 Iran US Dollars (USD) Lip; other and unspecified parts of tongue; floor of mouth; buccal Floor of mouth, lip, tongue, buccal (average)– 1-year follow-up:
Direct costs:
• Diagnosis: 82
• Early stage (I/II): 2,225
• Advanced stage (III/IV): 10,532
• Recurrency: 1,485
• Follow-up: 291
Direct non-medical costs
• Traveling: 1,035
• Home care: 665
Indirect costs:
• Employed patients: 2,477
• Unemployed patients: 1,230
• Accompanied: 481
• Premature mortality: 106,257
Floor of mouth, lip, tongue, buccal (average)– 1-year follow-up:
• Stages I/II (surgery and radiotherapy): 2,225
• Stages III/IV (surgery, radiotherapy, and chemotherapy): 10,532
Total cost (Iran): 64,245,173
    Direct costs: 27,284,501
• Direct non-medical costs: 5,143,629
• Indirect costs: 31,817,043
7. van Agthoven, 2001 [35] 1996 The Netherlands Euros (EUR) Oral cavity; oropharynx; larynx Average per patient– 10-year follow-up:
• Oral cavity: 35,541
• Oropharynx: 35,642
Not applicable Oral cavity (per patient):
• Primary tumor: 25,425
• Recurrent tumor: 25,543
Oropharynx (per patient):
• Primary tumor: 25,679
• Recurrent tumor: 25,145
8. Fisher, 2018 [36] 2016 United States of America US Dollars (USD) Oral cavity; oropharynx; hypopharynx/larynx; salivary glands; nasopharynx; other/unknown Not reported Not applicable Monthly health care costs (average ± standard deviation):
Total costs: 14,391 ± 19,510
• Hospitalization: 8,136 ± 16,880
• Emergency visits: 433 ± 1,259
• Office visits: 123 ± 109
• Systemic anticancer therapy: 2,875 ± 5,259
• Medical oncology procedures: 2,415 ± 6,962
• Infused supportive care drugs: 232 ± 479
All other drugs delivered: 178 ± 242
9. Nijdam, 2005 [32] 2001 The Netherlands Euros (EUD) Oropharynx Oropharynx (average):
• BT group*: 18,001
• S group*: 28,130
• EBRT group*: 21,143
Not applicable Not available
10. Amarasinghe, 2019 [18] 2016 Sri Lanka US Dollars (USD) Lip; other and unspecified parts of tongue; floor of mouth; palate; other and unspecified parts of mouth Lip, tongue, and mouth (average)– 1-year follow-up:
Stage II:
    System cost:
• Recurrent costs: 381
• Capital cost: 13
Household:
• Direct costs: 256
• Indirect costs: 263
Stage III and IV:
System cost:
• Recurrent costs: 2,011
• Capital cost: 13
Household:
• Direct costs: 217
• Indirect costs: 263
Lip, tongue, and mouth per patient (average)– 1-year follow-up:
• Stage II: 912
• Stage III/IV: 2,507
Not available
11. Goyal, 2014 [33] 2011/2012 India Rupees (INR) Lip; other and unspecified parts of tongue; floor of mouth; buccal mucosa; retromolar trigone Hospitalization (average ± standard deviation): 1,46,092 ± 37,325 Hospitalization (average):
• Stage I: 1,49,995
• Stage II: 1,41,621
• Stage III: 1,82,859
Not available
12. Zavras, 2002 [37] 2001 Greece US Dollars (USD) Upper lip, inner aspect; lower lip, inner aspect; lip, unspecified, inner aspect; commissure of lip; overlapping lesion of lip; lip, unspecified; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth Average per patient: 7,450 Average:
• Stage I: 3,662
• Stage II: 5,867
• Stage III: 10,316
• Stage IV: 11,467
Not available
13. van der Linden, 2016 [38] 2013 The Netherlands Euros (EUR) Oral cavity; oropharynx; hypopharynx; nasopharynx; larynx Not reported Not applicable Cost per treatment group (average ± standard deviation):
• Cisplatin + 5-fluorouracil + cetuximab: 39,459 ± 21,149
• Other platinum-based combination therapy: 38,584 ± 26,065
• Methotrexate monotherapy: 10,075 ± 9,891
• Capecitabine monotherapy: 10,585 ± 14,544
• Other: 17,506 ± 16,634
14. Epstein, 2008 [34] 2002 United States of America US Dollars (USD) Lip; other and unspecified parts of tongue; gum; floor of mouth; other and unspecified parts of mouth; oropharynx; pharynx; nasopharynx; hypopharynx; Waldeyer’s ring Oral and pharyngeal squamous cell carcinoma (median– 95%CI)– 1-year follow-up: 25,319 (21,825–27,665) Oral and pharyngeal squamous cell carcinoma (median):
• No treatment 9,763 (IR: 3,520–24,439)
• Early-stage treatment: 22,658 (IR: 10,425–42,664)
• Late-stage treatment: 27,665 (IR: 19,335–52,547)
Not available
15. Lafuma, 2019 [30] 2018 France Euros (EUR) Base of tongue; gum; floor of mouth; palate; tonsil; oropharynx; nasopharynx; piriform sinus; hypopharynx; larynx Not reported Not applicable Squamous cell carcinomas of the head and neck (average– 95%CI):
Total costs: 52,943
Direct costs: 49,954
• Ambulatory care: 17,047 (14,941–19,152)
• Inpatient care 32,908 (29,525–36,290)
• Public hospitals: 26,015 (22,716–29,314)
• Private for-profit hospitals: 6,892 (4,809–8,976)
Indirect costs: 2,989
• Disability: 1,397 (624–2,171)
• Sick leave: 1,592 (888–2,297)
16. Patterson, 2020 [31] 2017 Global, stratified by region and income Purchasing Power Parity (PPP) Lip; palate; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; oral cavity; other and unspecified parts of mouth; tonsil; oropharynx; other pharynx; nasopharynx; larynx; thyroid Not reported Not applicable Projected global cumulative loss of 535 billion US dollars in economic output due to head and neck cancer between 2018 and 2030. Southeast Asia, East Asia, and Oceania will suffer the greatest GDP losses at 180 billion US Dollars, and South Asia will lose 133 billion US Dollars
17. Han, 2010 [39] 2007 China Chinese Yuans (CNY) Lip; other and unspecified parts of tongue; floor of mouth; palate; oral cavity; buccal mucosa; gingival tissues; retromolar trigon Squamous cell carcinoma (average ± standard deviation): 27,890 ± 11,032 Not applicable Squamous cell carcinoma (average ± standard deviation):
• Diagnosis: 3,465 ± 1,059
• Treatment: 19,995 ± 9,701
• Hospitalization: 4,429 ± 1,618
18. Enomoto, 2015 [40] 2009 United States of America US Dollars (USD) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; tonsil; oropharynx; salivary gland; nasopharynx; hypopharynx Not reported Not applicable Cost per patient ≤ 30 days before death (average):
Oral cavity:
• Hospice: 7,880
• Non hospice: 14,990
Oropharynx:
• Hospice: 8,790
• Non hospice: 16,390
19. Lairson, 2017 [41] 2015 United States of America US Dollars (USD) Base of tongue; soft palate; uvula; lingual tonsil; oropharynx; pharynx otherwise unspecified Oropharynx: 134,454 ± 108,635 Not applicable Cost per patient (average ± standard deviation) - 2-year follow-up:
Oropharynx:
• Inpatient: 24,341 ± 48,972
• Outpatient: 106,604 ± 82,221
• Outpatient prescription drugs: 3,550 ± 5,183
• Surgery: 8,320 ± 15,111
• Radiotherapy: 50,362 ± 28,928
• Chemotherapy: 3,277 ± 2,822
20. Kim, 2020 [19] 2015 Korea US Dollars (USD) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; tonsil; oropharynx; piriform sinus; hypopharynx; ill-defined and unspecified sites of lips, oral cavity, and pharynx *Average per patient: 20,107 --- Total cost: 1,248 billion
• Male: 1,057 billion
• Female: 190,9 million
Cross-sectional studies based on information system data
21. Vatanasapt 2012 [20] 2010 Thailand Baths (THB) Other and unspecified parts of mouth; oral cavity; oropharynx; nasopharynx; hypopharynx; pharynx; larynx; parathyroid gland; eternal and middle ear; malignant melanoma; non-melanoma skin cancer; benign neoplasms Average per hospitalization (95%CI):
• Oral cavity: 29,531 (28,316–30,745)
• Oropharynx: 26,331 (23,995–28,668)
• Ill-defined sites in oral cavity and pharynx: 19,356 (14,621–24,090)
Not applicable Total cost of hospitalization:
• Oral cavity: 191,685,473 (n = 6,491)
• Oropharynx: 37,258,803 (n = 1,415)
• Ill-defined sites in oral cavity and pharynx: 3,135,667 (n = 162)
22. Klussmann, 2013 [28] 2008 Germany Euros (EUR) Base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; other and unspecified parts of mouth; oral cavity; tonsil; oropharynx; pharynx; nasopharynx; larynx * Average per hospitalization:
Oral cavity:
Direct costs:
• Hospitalization: 6,482
• Inpatient rehabilitation: 2,713
Indirect costs:
• Sick leave: 3,669
Oropharynx:
Direct costs:
• Hospitalization: 4,• 268
Inpatient rehabilitation: 2,705
Indirect costs:
• Sick leave: 3,263
Not applicable *Total cost:
Oral cavity: 131,019,446
• Direct costs: 113,268,892
    ○ Hospitalization: 109,503,702
    ○ Inpatient rehabilitation: 3,765,190
• Indirect costs: 17,750,554
    ○ Sick leave: 17,750,554
Oropharynx: 99,404,580
• Direct costs: 83,029,501
    ○ Hospitalization: 78,983,397
    ○ Inpatient rehabilitation: 4,046,104
• Indirect costs: 16,375,079
    ○ Sick leave: 16,375,079
23. Keeping, 2018 [21] 2011 England Pounds (GBP) Lip; base of tongue; other and unspecified parts of tongue; gum; floor of mouth; palate; oral cavity; other and unspecified parts of mouth; tonsil; oropharynx; larynx Not applicable Not applicable Total cost– 5 years:
Oral cavity: 98,330,746
• Inpatient: 94,876,001
• Outpatient: 3,454,745
Oropharynx: 114,619,227
• Inpatient: 108,738,446
• Outpatient: 5,880,781
24. Milani, 2021 [22] 2018 Brazil International Dollar (I$) Lip, base of tongue, other and unspecified parts of tongue, gum floor of mouth, palate, other and unspecified parts of mouth, tonsil, and oropharynx * Average per hospitalization: 1,376
• Lip: 655
• Oral cavity: 1,640
• Oropharynx: 1,338
Not applicable Total cost– 9 years: 495.6 million
• Inpatient: 244.0 million
    ○ Professional: 117.9 million
    ○ Hospital service: 92.5 million
    ○ Intensive care unit:33.6 million
• Outpatient: 251.6 million
Lip: 22.7 million
• Inpatient: 18.1 million
    ○ Professional: 9.2 million
    ○ Hospital service: 7.9 million
    ○ Intensive care unit: 1.0 million
• Outpatient: 4.6 million
Oral cavity: 257.1 million
• Inpatient: 139.1 million
    ○ Professional: 69.6 million
    ○ Hospital service: 55.2 million
    ○ Intensive care unit: 14.3 million
• Outpatient: 118.0 million
Oropharynx: 215.8 million
• Inpatient: 86.8 million
    ○ Professional: 39.1 million
    ○ Hospital service: 29.4 million
    ○ Intensive care unit: 18.3 million
• Outpatient: 129.0 million

US, United States; GDP, Gross Domestic Product; 95% CI, 95% Confidence Interval; BT group, Brachytherapy group; S group, Surgery group; EBRT group, External beam radiotherapy group; IR, interquartile ranges 25%-75%; NR, Non reported; NA, Not applicable.

* Average cost estimate per event and total cost calculated by the authors of the present study according to the data reported for both sees.

The OC cost comparison among studies was not possible. The set of anatomical sites investigated varied widely, in addition to the different measurement and costing methods. Only one of the studies included presented costs, separately, related to the sites considered as oral cancer in this systematic review (lip, oral cavity, and oropharynx) [22]. Most of the studies investigated lip, oral cavity, and oropharynx cancers together with other types of cancers from head and neck region (Table 5).

Only two studies [22, 23] investigated the cost of lip cancer separately from other ICD-10. The cost of lip cancer was estimated at GBP5,790 pounds per patient, over a five-year follow-up in the UK. In Brazil, the total expenditure of lip cancer was I$22.7 million in the period of nine years, from which I$18.1 million for inpatient costs and I$4.6 million for outpatient costs [22] (Table 5).

Three studies [23, 26, 35] showed the cost of oral cavity cancer per patient, estimated at GBP25,311 pounds in five years of follow-up in the UK [23]; EUR18,462 in two years of follow-up [26] in Italy; and EUR35,541 in a mathematical model estimated for 10 years in the Netherlands [35]. Two studies [20, 30] estimated oral cavity cancer cost per hospitalization, by information system data, with an average of THB29,531 [20] for Thailand and EUR6,482 for Germany [28], both over a one-year follow-up. One Brazilian study presented the expenditure of oral cavity cancer, in 9 years, as I$257.1 million: on average I$139.1 million for inpatients and I$118.0 million for outpatients [22] (Table 5).

Three studies [26, 35, 41] showed the cost of oropharynx cancer per patient, estimated at EUR24,253 euros after two years of follow-up in Italy [26], EUR35,642 in a probabilistic mathematical model estimated for 10 years [35] in the Netherlands, which presented the health state after year 2, after year 4 and after years 5–10, calculated from the date of the primary diagnosis, and USD134,454 over a period of two years in the USA [41]. Three studies [20, 22, 28] estimated oropharynx cancer per hospitalization, by information system data, with an average of THB26,331 [20] in Thailand and EUR4,268 in Germany [28], both over a one-year follow-up, and I$1,338 in Brazil over nine years [22] (Table 5).

Only four studies showed the costs of OC by cost components (direct and indirect costs) [2830]. In France (2018) [30], the direct medical cost of head and neck cancer was EUR49,954 per patient, considering outpatient and inpatient care, public hospitals services, and private for-profit hospitals services. The indirect cost was EUR2,989 per patient for disability and sick leave. In Germany (2008) [28], the direct medical cost of oral cancer was approximately EUR113 million, and the indirect cost was EUR18 million (sick leave). The direct medical cost of oropharyngeal cancer was approximately EUR83 million, and the indirect cost was EUR16 million (sick leave) [28]. In Iran [29], the cost of lip cancer, and for other and unspecified parts of tongue, the floor of the mouth, and buccal cancers was approximately USD27 million, USD5 million, and USD32 million for direct and direct non-medical and indirect costs, respectively [29]. The direct medical costs in Taiwan (2018) [27] were USD19,644 per patient and indirect costs for morbidity and mortality were USD1,286 and USD35,570 per patient, respectively, in a follow-up over 2.3 years (Table 5).

The LC burden of cost was 18.3% of UK GDP per capita [23]. Regarding the OCC cost, the burden was 79.8%, 64.9%, and 79.8% of UK, Italian, and the Netherlands’ GDP per capita, respectively [23, 26, 35]. The OPC burden of cost was 85.2%, 80.3%, 215.0% of Italy, the Netherlands, and the USA GDP per capita, respectively [26, 35, 41] (Table 6).

Table 6. Burden of cost of lip, oral cavity, and oropharynx cancers according to Gross Domestic Product per capita.

Study Country (currency) PPP* conversion factor GDP** per capita (PPP 2019) Components Lip Oral cavity Oropharynx
1. Kim, 2011 [23] UK (GBP)   Cost per patient 5,790 25,311 ---
0.68 46,659 % GDP per capita 18.3% 79.8% ---
2. Polesel, 2019 [26] Italy (EUR)     Cost per patient --- 18,462 24,253
0.67 42,492 % GDP per capita --- 64.9% 85.2%
3. van Agthoven, 2001 [35] The Netherlands (EUR)     Cost per patient --- 35,541 35,642
0.78 56,935 % GDP per capita --- 79.8% 80.3%
4. Lairson, 2017 [41] EUA (USD)     Cost per patient --- --- 134,454
1.00 62,530 % GDP per capita --- --- 215.0%

*PPP: Purchasing Power Parity.

**GDP: Gross Domestic Product.

Five studies showed outpatient and inpatient costs [22, 23, 25, 30, 41]. In general, inpatient costs are higher than outpatient costs, with a coefficient of variation of 93% [30] to 967.5% [23]. Outpatient costs exceeded inpatient costs in those studies in which chemotherapy and radiotherapy procedures were performed as outpatient costs [22, 41] (Fig 2A).

Fig 2.

Fig 2

Oral cancer burden of cost and difference of costs (%) according to types of patient care (A) and clinical stage of the disease (B). Difference (%) = [(inpatient cost–outpatient cost)/outpatient cost x 100]. Currency: Kim,2011: Pounds; Lairson, 2017, Rezapour, 2018, Amarasinghe, 2019, Zavras, 2002, Epstein, 2008: US dollars; Pollaers, 2019: Australian dollars; Lafuma, 2019: Euros; Milani, 2021: International dollars (million); Goyal, 2014: rupees.

Regarding the resource quantification, most of the included studies used a top-down approach (18 studies), generally obtained by allocating portions of a known total expenditure to a specific disease stratified by type of cost. Only 6 studies relied on individual data (bottom-up approach), generally obtained by multiplying the unit costs by quantities.

Advanced staging was more expensive (from 21.9% to 373.3%) than early cancer staging [18, 25, 29, 34, 37], despite the lack of a clinical stage standard definition of the disease and the different sets of head and neck tumors studied (Fig 2B).

The treatment of recurrent squamous cell carcinoma of the floor of mouth, tongue, and alveolar trigone was 51% more expensive than the treatment of primary tumors, in a two-year follow-up study [25].

Discussion

Our systematic review highlights the economic impact of oral cancer as a rising burden from a worldwide perspective. In a resource‐scarce healthcare environment, with an aging population and an increasing number of new diagnoses of oral cancer, this new knowledge is imperative in guiding resource allocation for oral cancer care provision and research funding. Deployment of interventions to improve outcomes for patients should be measured not only in terms of clinical outcome, but also in terms of economic impact. Furthermore, the analysis uncovers the large heterogeneity of cost of illness studies (COI) focused on oral cancer.

In some western countries, the economic burden of OCC and OPC is more than 60% of GDP per capita [23, 26, 35], reaching 215% of US GDP per capita (OPC) [41]. Considering that the GDP per capita corresponds to the average income of families [16], it is a cost that the individual cannot, in most cases, bear alone, and which requires the support of governments. Governments and health insurance providers are supposed to be the organizations supplying support to the population in order to face the high cost of chronic diseases. Nevertheless, oral cancer has a 90% chance of being cured, if detected early [42, 43].

The development of effective public policies is crucial for reducing these health expenditures. Oral cancer is confirmed as a public health problem and was a concern of at least 17 countries on 4 continents, based on the studies included in this review.

The main characteristics that qualify a COI study are expressed in its methodological definition. These include, among other aspects, the epidemiological approach, costing method and data collection. Incidence-based COI studies should include both direct and indirect costs throughout the life course to outcome. Prevalence-based COIs also include direct and indirect costs over a given period from any stage of the disease. For an acute illness, these two approaches would estimate similar costs. However, for a chronic disease, such as oral cancer, longitudinal incidence-based studies would provide more accurate estimates of the costs of this disease overt time. Considering the costing method for identifying and measuring resources, the COI approach can be micro (bottom up) or macro costing (top down). Using the micro-costing method, costing components and items are measured at the most detailed level possible, with estimated costs per individual, and the selection of a representative sample is recommended to allow external validity or generalizability of the results to a broader population. In macro costing, the total aggregate cost is divided by the number of individuals and can be expressed as an average value. Generally, COI studies that use micro-costing are more accurate, but less generalizable. Regarding data collection, retrospective studies represent a challenge because the data are secondary, generally intended for other purposes (epidemiological or surveillance) and may not be sufficient for a COI study. Most of the studies included in this systematic review did not meet all the items of the instrument used for quality assessment.

Although the economic burden of oral cancer was substantial, this systematic review showed that the costs may be underestimated, and only one [19] of the 24 studies considered all components of cost-of-illness simultaneously. In addition, from the six studies that analyzed indirect costs [18, 19, 2831], only three studies [19, 29, 31] included costs of early death related to the disease, which is one of the most expensive items for society [44]. Further longitudinal studies with higher quality are needed, not only methodologically, but in their data analysis and reporting of results. These studies should include, not only direct medical costs, but also direct non-medical and indirect costs, so that more accurate estimates can contribute to cost evaluation of health promotion and disease management programs.

The wide heterogeneity of COI studies was identified in both the aspects related to disease characterization and those related to economic issues. Regarding the disease, the main sources of heterogeneity were the characteristics of the samples; the lack of standardization in the definition of the clinical stage of the disease, and the different sets of head and neck tumors studied. The heterogeneity related to economic issues of the studies were found in their design, perspective, time horizon, sources of information, components and costing items, the health system of each country, currency, and reporting of cost results. The World Health Organization (WHO) recommendation is that the results of COI studies be reported in international dollars according to the PPP, to better support country-to-country comparisons of costs [45]. The development of protocols for the cost evaluation of oral cancer should be encouraged, as it has been by the Pan American Health Organization (PAHO) with the protocol for calculating the cost of hospital infections [46], since these analyses are complex and depend on the objectives of the studies. Protocols may contribute to the reduction of heterogeneity, favoring the comparison between different regions and health systems, in order to obtain a more accurate calculation of oral cancer cost.

In general, inpatient costs are higher than outpatient costs. However, this depends on the provision of health resources in each healthcare unit of the health system in each country. For example, in the USA [41], outpatient costs were higher than inpatient costs because most patients were treated with radiotherapy in outpatient care, which is one of the most expensive treatments for oral cancer management.

The costs of oral cancer in advanced clinical staging were higher than those at early stages, which occurred regardless of the heterogeneous characteristics of the studies. Most cases of oral cancer have been diagnosed in advanced staging for almost two decades [47] which in addition to compromising patient survival, determines high-cost treatments and suggests flaws in policies to promote preventive measures/strategies and early detection and diagnosis. This reinforces the importance of public policies that prioritize actions in the context of primary care, including health education for the population, qualification of professionals for the early detection of the disease, and the monitoring of the population at risk through opportunistic screening [7, 48].

The main limitation of this review was the difficulty of finding average cost results per patient from cancer sites, defined here as oral cancer (ICD-10 C01-C06, C09, and C10). These difficulties are possibly associated with the presentation of study results as aggregate costs of head and neck cancer and, also as a result of the absence of an international standardization defining which anatomical sites should characterize oral cancer. The heterogeneity of studies in other aspects of the disease characteristics, method, and economic issues may also have impacted on our findings, which did not allow a meta-analysis.

Decision makers increasingly require economic evidence to inform health policies [49, 50] and systematic reviews of economic evaluations (COI and cost-effectiveness) have grown accordingly [5155]. This study provides a comprehensive and critical overview of the COI analyses conducted around the world, which highlights the magnitude of the financial impact of oral cancer on societal or public health expenditure. This evidence can contribute to priority setting, particularly in the context of scarce resources. Our results can also be used by several other key stakeholders, such as international organizations (WHO and World Bank), health insurance companies, and health providers (health facilities and health workers).

This systematic review can also provide relevant insights for the health technology assessment field, particularly for economic evaluation studies. COI studies represent the first step towards complete economic analysis (e.g., cost-effectiveness analysis) and can also support budgetary impact analysis, by identifying, measuring, and valuing costs related to a specific disease or health condition [56].

Conclusion

This systematic review shows that the economic burden of oral cancer is substantial and underestimated. The cost of LC, OCC, and OPC reach an average of 18%, 75%, and 127% of GDP per capita, respectively, in some western countries. Further high-quality COI studies are needed, especially with robust methodological design and those that include, in addition to direct medical costs, the direct non-medical and indirect costs. Standardization of the terminology of the types of cancer and clarity in reporting the sources of cost information are crucial to consider in the COI studies. Also, if COI studies present international dollars as the unit price to reflect the economic cost of goods, and allow inter-country comparison of costs, this could support policy makers to identify major cost drivers of oral cancer and to make decisions regarding a more effective public policy for the prevention of oral cancer.

Supporting information

S1 Checklist. PRISMA 2020 checklist.

(PDF)

Data Availability

All data files are available from the Figshare database (accession number https://figshare.com/s/f7eb4990efeb5021f131).

Funding Statement

The authors received no specific funding for this work.

References

Decision Letter 0

Antoine Eskander

22 Nov 2021

PONE-D-21-31795The cost of oral cancer: a systematic reviewPLOS ONE

Dear Dr. ROTTA,

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Reviewers' comments:

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Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

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2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: N/A

Reviewer #2: N/A

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Reviewer #1: No

Reviewer #2: Yes

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Reviewer #1: Yes

Reviewer #2: Yes

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5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: I thank the authors for their submission. This is a nice systematic review of the economic burden of oral cancer. From a methodologic perspective, this work is rigorous and adheres to many best practices including a completed PRISMA checklist as well as an a priori protocol, available and registered on PROSPERO.

My main reservation is with the concept of cost of illness studies more broadly. Cost of illness studies are frequently criticized for not being grounded in welfare theory. They are descriptive and felt to have limited utility in informing resource allocation, particularly in comparison to other forms health economic evaluation (eg. cost-effectiveness analyses). Nonetheless, by comprehensively outlining direct and indirect cost components across various countries, I do think this review may assist with future cost-effectiveness studies in oral cancer. The authors touch on some of these issues briefly in the limitations section, though I do think the limitations of COI should be discussed more explicitly.

The quality of included studies was poor. On pages 31 and 32 the authors very briefly outline what constitutes a high-quality COI study in oral cancer. This should be further elaborated on. I think many of these concepts might not be well known to the head and neck oncology audience. A concise but explicit discussion of prevalence vs. incidence approaches, top-down vs bottom up, prospective vs. retrospective etc. might be helpful to the reader.

Minor Comments:

-I appreciate the explicit use of ‘PICO’ in the development of the research question, though do not think that an abbreviation for population (P) , exposure (E), and outcome (O) are needed in the abstract.

-Could the authors explain why other health economic evaluation studies (CEA, CUA etc…) were explicitly excluded? Presumably some of these studies would have tabulated the direct and indirect costs of oral cancer and could potentially have been included?

-For the Larg and Moss checklist, how did the authors define the threshold of >80% points as ‘high quality’ and 50-79% as ‘medium quality’? Is that an accepted approach?

-Do the authors have any statistical measures of agreement during the article screening phase?

-In the results section “€35,642 in a mathematical model estimated for 10 years”. Could you briefly explain what the ‘mathematical model’ was?

-Table 2 – How did the authors categorize the study as a ‘cost-analysis’ vs ‘cost-of-illness’ study? Could the authors clarify either in the body of the manuscript or as a footnote in the table?

-Additional files 1 and 2 appear to be missing, though I was able to piece together the search strategy and MESH terms from the published protocol. The only additional file included is the completed PRISMA checklist.

Reviewer #2: Thank you for inviting me to review this article. This systematic review study identified 24 studies (2001-2021) published around the world on the cost of oral cancer. Both direct and indirect costs were considered. Grey literature and non-English papers were also searched. The included studies mostly followed the standard cost-of-illness approach and adopted a provider (hospital) perspective. Direct medical costs were examined by most studies, while direct non-medical costs and indirect costs associated with premature mortality and work absence were seldom assessed. Four studies have estimated burden of illness using cost per patient over per-capita GDP. These studies found the cost burden of lip, oral cavity, and oropharynx cancers to amount to 18.3%, 74.8%, and 126.8% of the per-capita GDP of various developed nations.

This is a well-conducted systematic review with meaningful economic outputs to inform resource allocation in cancer care. I have a few major concerns about the review methodology and other minor suggestions that the authors may want to consider in their revisions.

Major comments:

1. It is unclear how the cost items in Table 4 and lines 151-154 were defined. If the authors want to survey all types of costs associated with oral cancer (i.e., in order to understand the economic burden of oral cancer), why use an a priorly defined list of cost items to deliberately limit the scope of cost? Are these cost items derived from an established costing framework for oral cancers from the literature? If not, the authors should include a section that outlines how they determined and refined a costing framework and cost components which by itself should be a contribution of this review.

The authors might want to consult this systematic review on the methodology of defining a costing framework: Clarke K, Klarenbach S, Vlaicu S et al. The direct and indirect economic costs incurred by living kidney donors—a systematic review. Doi: 10.1093/ndt/gfl069

In particular, the authors only considered two types of indirect costs (work absenteeism and premature mortality). What about the indirect loss due to disability or the extra expense of senior care/childcare due to the patient being hospitalized and unable to provide such care? All these questions beg for a costing framework that exhaustively identifies and categorizes all potential cost components of oral cancer before the literature search.

2. The authors can enhance this study significantly by formally defining the key elements of an economic analysis before the literature search. For example, in what way does a cost-of-illness study differ from a cost study (Table 2)? Why is Patterson (2020) a cost-of-illness study (Table 2) if it has only assessed the indirect costs of premature mortality resulted from oral cancers (Table 4)? Another key concept that begs for clarification is perspective (Table 2). I find it unconventional to categorize “perspectives” into hospital, government, payer, and society. It appears the authors are mixing up two concepts: 1) the provider of care or the setting in which the care occurs, such as hospital; 2) the payer who affords the cost of care, such as the government (public payer) or the society. I would make 2 columns in Table 2 to distinguish these entities and add a formal definition for perspective in the methods section. Furthermore, if Milani (2021) used a government (public payer) perspective, it should not have included any direct non-medical costs (unless the government reimburses for these costs). Same with Han (2010) and Amarasinghe (2019).

3. It is absolutely essential that a common currency & year (such as 2019 USD) is used throughout the manuscript (and Table 5) to make between-study comparisons and summarization of costs meaningful. Could the authors convert all currencies (and explain how it is converted) to a common currency & year and present both the initial and converted currency? One way to do this is to first inflate the initial currency to 2019 constant values using the national annual CPI and then adjusted to 2019 USD (or another currency) using PPP from OECD. A minor point is to please remove the currency symbols and replace them with the ISO codes for currencies.

Minor comments:

Methods

Lines 98-99: why explicitly excluding cost-effectiveness/cost-utility studies since they also assessed cost? Studies might not examine costs as their primary objective but nonetheless present useful data. Perhaps the authors want to state that they only included studies whose primary objective was to assess the cost of oral cancer.

Results

In Table 1, the authors might want to report more information of cohort from each study (age, sex composition etc) beyond the size of cohort. Difference of the study cohort contributes to the high between-study heterogeneity as well.

Page 19 (Table 4): please revise Table 4 to reflect two major categories of costs (direct vs. indirect costs), and under direct costs the authors can further define direct medical costs and direct non-medical costs.

Page 30 (Table 6): since only 4 studies reported the economic burden of oral cancer as a percentage of per-capita GDP, and all studies were based in developed western countries, I would not state these results as a general finding in the abstract.

Furthermore, only one of these 4 studies (Kim 2020) has examined all cost components as defined in Table 4. Then, why is the cost-per-patient estimate from the remaining 3 studies reliable if the authors have already identified them to represent an underestimation?

Alternatively, the authors might want to use the estimate of Rezapour (2018) to manually compute the burden of disease as a percentage of total cost in per-capita GDP.

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Decision Letter 1

Antoine Eskander

21 Mar 2022

The cost of oral cancer: a systematic review

PONE-D-21-31795R1

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

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Kind regards,

Antoine Eskander, MD, ScM, FRCSC

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Thank you for addressing all concerns.

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

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2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: (No Response)

Reviewer #2: (No Response)

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Reviewer #2: Yes: Rui Fu

Acceptance letter

Antoine Eskander

30 Mar 2022

PONE-D-21-31795R1

The cost of oral cancer: a systematic review

Dear Dr. ROTTA:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

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on behalf of

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Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Checklist. PRISMA 2020 checklist.

    (PDF)

    Attachment

    Submitted filename: response to reviewer_07022022.pdf

    Data Availability Statement

    All data files are available from the Figshare database (accession number https://figshare.com/s/f7eb4990efeb5021f131).


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