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DOI: 10.1055/s-0045-1809906
Cost Analysis of Sentinel Lymph Node Biopsy for Oral Tongue Squamous Cell Carcinoma: Institutional Cohort and Population-Based Simulation
Authors
Funding The author(s) received no financial support for the research.
Abstract
Introduction
In oral carcinoma patients classified as cN0, selective neck dissection (SND) and sentinel lymph node biopsy (SLNB) may be used to stage the neck with equivalent oncological results.
Objective
Compare the costs of SLNB and SND for oral squamous cell carcinoma.
Methods
Analysis of institutional cohort and Markov chain model simulation using populational data.
Results
We included 84 patients submitted to transoral resection and SLNB or SND and patients submitted only to SND. The mean cost was R$4,943,67 for SLNB and R$ 11,005.49 for SND with significant differences in length of stay (one versus three days, p < 0.001), operative time (92 versus 177 minutes, p < 0.001) and postoperative hospital visits in 60 days (two versus eight, p < 0.001). For the simulation model, the probability of not finding the SLN ranged from 0.0% to 5.7% with 0.5% increments and the probability of occult neck metastasis ranged from 9.0% to 100.0% with 1% increments. The costs of SLNB increase progressively as the rate of occult neck metastasis increases. When this rate reaches 56%, the cost difference becomes not significant. With rates above 72%, SLNB becomes significantly more expensive than SND. Using a public database, we calculate a cost decrease ranging from 27.93% to 66.54% with SLNB adoption.
Conclusion
SLNB adoption may significantly decrease the costs associated with early-stage oral cancer treatment. It would allow more patients to be treated with the same number of resources now available.
Introduction
According to the International Agency on Cancer Research (IARC) in its report on cancer incidence, 377.713 new cases of oral and lip carcinoma will be diagnosed in 2021 accounting for 177.757 deaths.[1] The Brazilian Cancer Institute (INCA) considers oral squamous cell carcinoma (OSCC) the sixth most frequent cancer in Brazilian males with a significant impact on mortality.[2] Multiple international guidelines suggest upfront surgery as the treatment of choice for patients with stage I and II. It consists of the removal of the primary tumor with adequate surgical margins and treatment of the neck lymph nodes by observation, selective neck dissection (SND), or sentinel lymph node biopsy (SLNB).[3]
Neck treatment is directed by the estimated risk of occult lymph node metastasis with a 20% threshold conventionally accepted for elective surgery indication.[4] Recently, two prospective randomized clinical trials compared SND to observation and demonstrated a significant survival advantage of the former.[5] [6] But SND also has significant morbidity with shoulder function impairment and shoulder and neck pain at arm exertion.[7] To minimize these risks, the concept of SLNB was applied to OSCC.[8]
A European prospective cohort evaluated the diagnostic profile of SLNB when compared to SND and demonstrated an 86% sensitivity with a negative predictive value (NPV) of 95% with minimal morbidity and considered the procedure oncologically sound.[9] In an American multicentric prospective study, the NPV was 94% with routine pathological evaluation and increased to 96% with the addition of immunohistochemistry.[10] Two meta-analyses compared the NPV of SLNB and END in OSCC. Liu et al synthesized the results of 66 articles including 3,566 patients. The sentinel node was found in 96.3% of patients with an NPV of 94%.[11] The meta-analysis by Yang et al encompassed 35 articles with 1,084 patients with a successful SLNB in 98% of patients and NPV of 96%.[12] Finally, two prospective randomized trials compared SLNB versus SND regarding survival outcomes and quality of life (QoL). A French study demonstrated the equivalence of oncologic results in overall and recurrence-free survival. QoL outcomes were significantly better in the SLNB group after six months but equivalent at 12 months.[13] A Japanese study with a similar design had a similar result regarding oncologic outcomes but a sustained significant improvement in QoL after 12 months.[14] The financial costs of SLNB were compared to SND in two retrospective studies. Using the cost parameters and methodology of the Japanese health system, SLNB caused a significant cost reduction when compared to SND.[15] A Dutch study found similar results favoring SLNB.[16]
Although SLNB is already in use in Brazil,[17] [18] the costs associated with this treatment modality were not evaluated. Our objective is to evaluate the cost of SLNB in the Brazilian reality using data from a single institution to generate the monetary data and public information about the stage at diagnosis distribution of patients with OSCC to simulate an estimation of cost change with the adoption of SLNB.
Methods
We analyzed patients treated at a single tertiary institution. Three patient cohorts were included: patients submitted to transoral OSCC resection and SLNB with prospective collection of clinical, pathological, and cost data; patients submitted to transoral OSCC resection and SND with prospective collection of clinical and pathological data and retrospective collection of cost data and patients submitted to metachronous SND after transoral resection with prospective collection of clinical and pathological data and retrospective collection of cost data. The purpose of this third cohort is to provide cost data on patients treated SLNB and afterward submitted to SND due to a metastatic lymph node.
Inclusion criteria were primary oral tongue tumors classified as cT1 and cT2 and no evidence of metastatic cervical lymph node after clinical and radiological evaluation by computer tomography or nuclear magnetic resonance. Patients with a history of previous malignant neoplasms in the head and neck area, previous treatment of the index tumor, or submitted to SND by alternative access routes were excluded from analysis. Patients were paired in the 1:3 proportion regarding neck treatment based on age, gender, comorbidities, and CT stage.
We used a bottom-up cost analysis with the creation of itemized lists of material and personal resources used during treatment, including preoperative staging and preoperative exams, medical and paramedical costs, structural costs, and rehabilitation. The price attributed to each item was retrieved from the Electronic Auction Site (Bolsa Eletrônica de Compras do Estado de São Paulo, www.bec.sp.gov.br). If the item was not found, the Health Ministerium price information was used. Hospital costs were extracted from the DataSUS (www2.datasus.gov.br). Since adjuvant treatment depends on the pathological data but not on the surgical procedure, we chose not to include it in this analysis. We used a time horizon of 60 days after surgery. All costs are expressed in Brazilian real (R$) and when the item price was not published in the current year, we used the General Price Index (Índice Geral de Preços, IPCA-E) for value correction since this index incorporates the health sector in its composition. [Fig. 1] demonstrates the costs that were included or excluded in this analysis.


All data analysis was performed using the R software (www.cran.org). Continuous variables are described by median and range or mean and standard deviation (SD). Student t-test was used for mean comparison while the Mann-Whitney test was used for median comparison. A Markov model was designed to compare multiple possible situations. In this model, the probability of not finding the sentinel lymph node and the probability of a metastatic sentinel lymph node were independently varied to evaluate and compare the cost of each strategy. For each model change, 1,000 individual patients were simulated. Based on the prospective trials by Garrel et al[13] and Hasegawa et al,[14] oncologic results of both treatments were considered equivalent. All analyses were performed based on the intention to treat, therefore patients allocated to SLNB but submitted to SND were computed in the SLNB arm.
This study was submitted to the Institutional Review Board (Protocol Number 3633/24).
Results
We analyzed 84 patients in this study, 12 consecutive patients in the SLNB group, 36 consecutive patients in the simultaneous transoral resection SND group, and 36 patients in the delayed SND group. Demographic, clinical, and pathological data of patients included in this analysis are shown in [Table 1]. Depth of invasion (DOI) distribution is shown in [Fig. 2] for the entire cohort and each treatment group. Cost distribution according to treatment modality is shown in [Fig. 3]. The mean cost in the SLNB group was R$ 4.943.67 and in the SND group was R$ 11,005.49 (p < 0.001). Treatment costs of the primary tumor are included in these values. Variables with a significant difference between groups were hospital length of stay (one versus three days, p < 0.001), surgical theatre use (92 minutes versus 177 minutes, p < 0.001), and number of hospital visits in 60 days (two versus eight, p < 0.001).
SD: standard deviation; SLNB: sentinel lymph node biopsy; SND: selective neck dissection;




Transition probabilities to different states were defined based on literature data to allow the modeling of a wide range of scenarios. The probability of not finding the sentinel node ranged from 0%[14] to 5.7%.[13] The probability of metastatic SLNB was estimated from public data from the Oncocentro Foundation (Fundação Oncocentro, http://www.fosp.saude.sp.gov.br). From 8,802 patients with OSCC staged as cT1-2, pathological neck staging was present in 3,427 patients with 316 cases of cervical metastasis (9.2%). Based on this data, we modeled the probability of metastatic SLNB ranging from 9.0% to 100.0%. The probability of not finding the sentinel node varied in 0.5% increments while the probability of metastatic lymph nodes at pathological report in 1.0% increments. For each probability variation, the cost of each strategy was simulated in 1,000 patients and the mean was compared. A progressive increase in the cost of SLNB is observed as more patients are submitted to SND ([Fig. 4]). In this simulation, the difference in cost of the two strategies becomes non-significant when the transition probability reaches the 56% mark and SLNB becomes more expensive than SND after the 72% mark. It occurs due to the addition of costs from a second in-hospital treatment and increased medical and paramedical postoperative visits and rehabilitation costs.


If this data is applied to the Oncocentro Foundation series, SLNB as initial neck treatment will incur a reduction ranging from 27.93% to 66.54% if we compute the lower cost threshold and upper-cost threshold when compared to SND.
Discussion
Cancer treatment consumes a significant parcel of healthcare resources due to increasing incidence and raising costs.[19] Therefore, optimization of resource allocation is a major priority and may significantly impact on the number of treated patients.
The impact of SLNB adoption on OSCC treatment costs remains an open question in the literature. An initial analysis in Japan using the Japanese Health Ministerium data shows a significant reduction in costs and patient morbidity with its adoption. In a similar manner to our analysis, the cost of SLNB increases as the incidence of micrometastasis rises.[15] Analyzing data from the European Sentinel Node Trial and using an initial probability of 25% for occult neck metastasis, SLNB caused a significant cost reduction even when all patients were staged as pN + . For cost quantification, data from the British Health System was used.[20] Both simulations share similarities with our model, but significant distinctions may be highlighted. Our model has an outcome comparable to the one found by Kosuda et al,[15] emphasizing the need for rigorous preoperative staging. Gover et al compared five different neck treatment strategies using a public health system payer perspective. In this simulation, SLNB was the most cost-effective strategy.[16] A different model considered fine needle cytologic evaluation of the neck as the first step for neck treatment definition. This simulation considered SLNB as the most cost-effective strategy considering a five-year horizon, but SND when a lifetime horizon was considered.[21] A major difference from other models, including ours, is their use of a Markov model with fixed transition probabilities. Since the risk of neck recurrence is time-dependent,[22] the use of a model not accounting for this information may not be useful in clinical practice.
A significant limitation of this study is the participation of a single center. Therefore, the costs reported reflect the surgical and anesthetic practices of a single institution and do not capture the heterogeneity existing among different practices. This is a finding reported by the SENT trial regarding hospital length of stay.[9] The use of public auction prices means that the calculated price is not that of an institution, but a theoretical construct with greater generality. It also allows to leverage of costs from different institutions by focusing on the items expended and not the price put upon them by health providers.
Conclusion
The replacement of the SND by SLNB has the potential to significantly decrease the costs associated with the treatment of OSCC patients without sacrificing oncological safety. Considering its incidence and financial impact, more patients could be treated with the same financial and structural resources.
Conflict of Interest
The Authors Declare No Conflicts Of Interest.
Authors' Contributions
HFK: conceptualization, data curation, data analysis, writing – original draft; GBC: data curation, analysis review, writing – review & editing; JGV: data analysis, writing – review & editing; LPK: analysis review, writing – review & editing.
Data Availability Statement
Data supporting the results of this study are available upon a reasonable request from the corresponding author.
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            References
- 1 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021; 71 (03) 209-249
- 2 https://www.inca.gov.br/estimativa/sintese-de-resultados-e-comentarios . Acessado em 03 de setembro de 2021.
- 3 Köhler HF, Mehanna H, Shah JP. et al. Comparison of different guidelines for oral cancer. Eur Arch Otorhinolaryngol 2021; 278 (08) 2961-2973
- 4 Weiss MH, Harrison LB, Isaacs RS. Use of decision analysis in planning a management strategy for the stage N0 neck. Arch Otolaryngol Head Neck Surg 1994; 120 (07) 699-702
- 5 D'Cruz AK, Vaish R, Kapre N. et al; Head and Neck Disease Management Group. Elective versus Therapeutic Neck Dissection in Node-Negative Oral Cancer. N Engl J Med 2015; 373 (06) 521-529
- 6 Hutchison IL, Ridout F, Cheung SMY. et al. Nationwide randomised trial evaluating elective neck dissection for early stage oral cancer (SEND study) with meta-analysis and concurrent real-world cohort. Br J Cancer 2019; 121 (10) 827-836
- 7 de Bree R, Takes RP, Shah JP. et al. Elective neck dissection in oral squamous cell carcinoma: Past, present and future. Oral Oncol 2019; 90: 87-93
- 8 Calabrese L, Bruschini R, Ansarin M. et al. Role of sentinel lymph node biopsy in oral cancer. Acta Otorhinolaryngol Ital 2006; 26 (06) 345-349
- 9 Schilling C, Stoeckli SJ, Haerle SK. et al. Sentinel European Node Trial (SENT): 3-year results of sentinel node biopsy in oral cancer. Eur J Cancer 2015; 51 (18) 2777-2784
- 10 Civantos FJ, Zitsch RP, Schuller DE. et al. Sentinel lymph node biopsy accurately stages the regional lymph nodes for T1-T2 oral squamous cell carcinomas: results of a prospective multi-institutional trial. J Clin Oncol 2010; 28 (08) 1395-1400
- 11 Liu M, Wang SJ, Yang X, Peng H. Diagnostic Efficacy of Sentinel Lymph Node Biopsy in Early Oral Squamous Cell Carcinoma: A Meta-Analysis of 66 Studies. PLoS One 2017; 12 (01) e0170322
- 12 Yang Y, Zhou J, Wu H. Diagnostic value of sentinel lymph node biopsy for cT1/T2N0 tongue squamous cell carcinoma: a meta-analysis. Eur Arch Otorhinolaryngol 2017; 274 (11) 3843-3852
- 13 Garrel R, Poissonnet G, Moyà Plana A. et al. Equivalence Randomized Trial to Compare Treatment on the Basis of Sentinel Node Biopsy Versus Neck Node Dissection in Operable T1-T2N0 Oral and Oropharyngeal Cancer. J Clin Oncol 2020; 38 (34) 4010-4018
- 14 Hasegawa Y, Tsukahara K, Yoshimoto S. et al; HNCMM Research Group. Neck Dissections Based on Sentinel Lymph Node Navigation Versus Elective Neck Dissections in Early Oral Cancers: A Randomized, Multicenter, and Noninferiority Trial. J Clin Oncol 2021; 39 (18) 2025-2036
- 15 Kosuda S, Kusano S, Kohno N. et al. Feasibility and cost-effectiveness of sentinel lymph node radiolocalization in stage N0 head and neck cancer. Arch Otolaryngol Head Neck Surg 2003; 129 (10) 1105-1109
- 16 Govers TM, Takes RP, Baris Karakullukcu M. et al. Management of the N0 neck in early stage oral squamous cell cancer: a modeling study of the cost-effectiveness. Oral Oncol 2013; 49 (08) 771-777
- 17 Chone CT, Magalhes RS, Etchehebere E, Camargo E, Altemani A, Crespo AN. Predictive value of sentinel node biopsy in head and neck cancer. Acta Otolaryngol 2008; 128 (08) 920-924
- 18 Seferin MR, Pinto FR, Lin CS. et al. Sentinel lymph node biopsy in early oral cavity tumors: evaluation of the oncologic efficacy compared to elective neck dissection. Arch Head Neck Surg. 2018; 47: e0876
- 19 Lana AP, Perelman J, Gurgel Andrade EI, Acúrcio F, Guerra Jr AA, Cherchiglia ML. Cost analysis of cancer in Brazil: a population-based study of patients treated by public health system from 2001-2015. Value Health Reg Issues 2020; 23: 137-147
- 20 O'Connor R, Pezier T, Schilling C, McGurk M. The relative cost of sentinel lymph node biopsy in early oral cancer. J Craniomaxillofac Surg 2013; 41 (08) 721-727
- 21 van der Linden N, Flach GB, de Bree R, Uyl-de Groot CA. Cost-utility of sentinel lymph node biopsy in cT1-T2N0 oral cancer. Oral Oncol 2016; 53: 20-26
- 22 Mizrachi A, Migliacci JC, Montero PH. et al. Neck recurrence in clinically node-negative oral cancer: 27-year experience at a single institution. Oral Oncol 2018; 78: 94-101
Address for correspondence
Publication History
Received: 27 November 2022
Accepted: 02 April 2023
Article published online:
16 October 2025
© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
Thieme Revinter Publicações Ltda.
Rua Rego Freitas, 175, loja 1, República, São Paulo, SP, CEP 01220-010, Brazil
Hugo Fontan Köhler, Genival Barbosa de Carvalho, José Guilherme Vartanian, Luiz Paulo Kowalski. Cost Analysis of Sentinel Lymph Node Biopsy for Oral Tongue Squamous Cell Carcinoma: Institutional Cohort and Population-Based Simulation. Int Arch Otorhinolaryngol 2025; 29: s00451809906.
DOI: 10.1055/s-0045-1809906
- 
            References
- 1 Sung H, Ferlay J, Siegel RL. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2021; 71 (03) 209-249
- 2 https://www.inca.gov.br/estimativa/sintese-de-resultados-e-comentarios . Acessado em 03 de setembro de 2021.
- 3 Köhler HF, Mehanna H, Shah JP. et al. Comparison of different guidelines for oral cancer. Eur Arch Otorhinolaryngol 2021; 278 (08) 2961-2973
- 4 Weiss MH, Harrison LB, Isaacs RS. Use of decision analysis in planning a management strategy for the stage N0 neck. Arch Otolaryngol Head Neck Surg 1994; 120 (07) 699-702
- 5 D'Cruz AK, Vaish R, Kapre N. et al; Head and Neck Disease Management Group. Elective versus Therapeutic Neck Dissection in Node-Negative Oral Cancer. N Engl J Med 2015; 373 (06) 521-529
- 6 Hutchison IL, Ridout F, Cheung SMY. et al. Nationwide randomised trial evaluating elective neck dissection for early stage oral cancer (SEND study) with meta-analysis and concurrent real-world cohort. Br J Cancer 2019; 121 (10) 827-836
- 7 de Bree R, Takes RP, Shah JP. et al. Elective neck dissection in oral squamous cell carcinoma: Past, present and future. Oral Oncol 2019; 90: 87-93
- 8 Calabrese L, Bruschini R, Ansarin M. et al. Role of sentinel lymph node biopsy in oral cancer. Acta Otorhinolaryngol Ital 2006; 26 (06) 345-349
- 9 Schilling C, Stoeckli SJ, Haerle SK. et al. Sentinel European Node Trial (SENT): 3-year results of sentinel node biopsy in oral cancer. Eur J Cancer 2015; 51 (18) 2777-2784
- 10 Civantos FJ, Zitsch RP, Schuller DE. et al. Sentinel lymph node biopsy accurately stages the regional lymph nodes for T1-T2 oral squamous cell carcinomas: results of a prospective multi-institutional trial. J Clin Oncol 2010; 28 (08) 1395-1400
- 11 Liu M, Wang SJ, Yang X, Peng H. Diagnostic Efficacy of Sentinel Lymph Node Biopsy in Early Oral Squamous Cell Carcinoma: A Meta-Analysis of 66 Studies. PLoS One 2017; 12 (01) e0170322
- 12 Yang Y, Zhou J, Wu H. Diagnostic value of sentinel lymph node biopsy for cT1/T2N0 tongue squamous cell carcinoma: a meta-analysis. Eur Arch Otorhinolaryngol 2017; 274 (11) 3843-3852
- 13 Garrel R, Poissonnet G, Moyà Plana A. et al. Equivalence Randomized Trial to Compare Treatment on the Basis of Sentinel Node Biopsy Versus Neck Node Dissection in Operable T1-T2N0 Oral and Oropharyngeal Cancer. J Clin Oncol 2020; 38 (34) 4010-4018
- 14 Hasegawa Y, Tsukahara K, Yoshimoto S. et al; HNCMM Research Group. Neck Dissections Based on Sentinel Lymph Node Navigation Versus Elective Neck Dissections in Early Oral Cancers: A Randomized, Multicenter, and Noninferiority Trial. J Clin Oncol 2021; 39 (18) 2025-2036
- 15 Kosuda S, Kusano S, Kohno N. et al. Feasibility and cost-effectiveness of sentinel lymph node radiolocalization in stage N0 head and neck cancer. Arch Otolaryngol Head Neck Surg 2003; 129 (10) 1105-1109
- 16 Govers TM, Takes RP, Baris Karakullukcu M. et al. Management of the N0 neck in early stage oral squamous cell cancer: a modeling study of the cost-effectiveness. Oral Oncol 2013; 49 (08) 771-777
- 17 Chone CT, Magalhes RS, Etchehebere E, Camargo E, Altemani A, Crespo AN. Predictive value of sentinel node biopsy in head and neck cancer. Acta Otolaryngol 2008; 128 (08) 920-924
- 18 Seferin MR, Pinto FR, Lin CS. et al. Sentinel lymph node biopsy in early oral cavity tumors: evaluation of the oncologic efficacy compared to elective neck dissection. Arch Head Neck Surg. 2018; 47: e0876
- 19 Lana AP, Perelman J, Gurgel Andrade EI, Acúrcio F, Guerra Jr AA, Cherchiglia ML. Cost analysis of cancer in Brazil: a population-based study of patients treated by public health system from 2001-2015. Value Health Reg Issues 2020; 23: 137-147
- 20 O'Connor R, Pezier T, Schilling C, McGurk M. The relative cost of sentinel lymph node biopsy in early oral cancer. J Craniomaxillofac Surg 2013; 41 (08) 721-727
- 21 van der Linden N, Flach GB, de Bree R, Uyl-de Groot CA. Cost-utility of sentinel lymph node biopsy in cT1-T2N0 oral cancer. Oral Oncol 2016; 53: 20-26
- 22 Mizrachi A, Migliacci JC, Montero PH. et al. Neck recurrence in clinically node-negative oral cancer: 27-year experience at a single institution. Oral Oncol 2018; 78: 94-101








 
     
      
         
      
    
