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Prognostic factors in oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil: 10-year follow-up

Abstract

Objective:

To descriptively analyze the epidemiological data, clinical stage, and outcomes of oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, and to estimate the influence of clinical stage and treatment type on overall and disease-free survival.

Methods:

We retrospectively analyzed epidemiological data from the São Paulo Cancer Center Foundation database relative to patients with oropharyngeal squamous cell carcinoma diagnosed between 2004 and 2014 in the state of São Paulo. Univariate and multivariate Cox regression analyses were performed to assess factors associated with the outcomes. A forward stepwise selection procedure was used. Survival curves were estimated by the Kaplan-Meier method and compared by the Gehan-Breslow-Wilcoxon test.

Results:

A total of 8075 individuals with oropharyngeal squamous cell carcinoma were identified. Of these, 86.3% were diagnosed at an advanced stage and 13.7% at an early stage. Only 27.2% of patients were treated surgically, whereas 57.5% were treated medically. Patients undergoing surgery had longer overall survival than those receiving medical treatment in both early- and advanced-stage oropharyngeal squamous cell carcinoma. However, there was no significant difference in disease-free survival between surgical and medical treatment.

Conclusion:

No significant difference in disease-free survival between medical and surgical treatment suggests similar complete remission rates with both approaches. Patients receiving medical treatment had shorter overall survival, which may be due to complications from chemotherapy and radiotherapy. However, we cannot confirm this relationship based on the data provided by the São Paulo Cancer Center Foundation. Prospective studies are warranted to assess whether the lower overall survival rate in patients receiving medical treatment is secondary to complications from chemotherapy and radiotherapy.

Level of evidence:

2C.

KEYWORDS
Squamous cell carcinoma; Oropharynx; Survival

HIGHLIGHTS

Among patients with oropharyngeal squamous cell carcinoma, 86.3% had advanced-stage disease and 13.7% had early-stage disease at diagnosis.

Disease-free survival did not differ significantly between patients receiving medical and surgical treatment among patients with the same staging.

Patients receiving medical treatment had shorter overall survival in both early and advanced stages of the disease compared with those undergoing surgery.

Introduction

Head and neck neoplasms are the sixth most common type of cancer worldwide with approximately 630,000 new cases annually, resulting in more than 350,000 deaths every year. Considering geographical variations due to sociocultural differences, approximately 10% of these neoplasms are Oropharyngeal Squamous Cell Carcinoma (OPSCC).11 Ramqvist T, Dalianis T. Oropharyngeal cancer epidemic and human papillomavirus. Emerg Infect Dis. 2010;16:1671–7.,22 Vigneswaran N, Williams MD. Epidemiologic trends in head and neck cancer and aids in diagnosis. Oral Maxillofac Surg Clin North Am. 2014;26:123–41. Squamous Cell Carcinoma (SSC) accounts for more than 90% of all neoplasms of the oral cavity and pharynx.33 Mayne ST, Morse DE, Winn DM. Cancers of the oral cavity and pharynx. In: Schottenfeld D, Fraumeni JF, editors. Cancer Epidemiology and Prevention. New York: Oxford University Press; 2006. p. 674–96. OPSCC is more common in men than in women,33 Mayne ST, Morse DE, Winn DM. Cancers of the oral cavity and pharynx. In: Schottenfeld D, Fraumeni JF, editors. Cancer Epidemiology and Prevention. New York: Oxford University Press; 2006. p. 674–96.,44 Curado MP, Johnson NW, Kerr AR, Silva DRM, Lanfranchi H, Pereira DL, et al. Oral and oropharynx cancer in South America: incidence, mortality trends and gaps in public databases as presented to the Global Oral Cancer Forum. Transl Res Oral Oncol. 2016, http://dx.doi.org/10.1177/2057178X16653761.
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Patients with HPV-negative OPSCC have an important history of tobacco use and alcohol consumption, unlike patients with HPV-positive OPSCC who tend to be younger, male, white, and from high-income countries.44 Curado MP, Johnson NW, Kerr AR, Silva DRM, Lanfranchi H, Pereira DL, et al. Oral and oropharynx cancer in South America: incidence, mortality trends and gaps in public databases as presented to the Global Oral Cancer Forum. Transl Res Oral Oncol. 2016, http://dx.doi.org/10.1177/2057178X16653761.
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and there is no consensus on the best management of these cases. Different cancer centers use surgery, RT, and Chemotherapy (CT) in a variety of combinations.77 Licitra L, Bernier J, Grandi C, Merlano M, Bruzzi P, Lefebvre JL. Cancer of the oropharynx. Crit Rev Oncol Hematol. 2002;41:107–22, http://dx.doi.org/10.1016/s1040- 8428(01)00129-9.
http://dx.doi.org/10.1016/s1040- 8428(01...
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http://dx.doi.org/10.1016/j.otorri.2012....
,3030 Soo KC, Tan EH, Wee J, Lim D, Tai BC, Khoo ML, et al. Surgery and adjuvant radiotherapy vs concurrent chemoradiotherapy in stage III/IV nonmetastatic squamous cell head and neck cancer: a randomised comparison. Br J Cancer. 2005;93:279–86, http://dx.doi.org/10.1038/sj.bjc.6602696.
http://dx.doi.org/10.1038/sj.bjc.6602696...
,3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...

Many issues remain unresolved concerning OPSCC, especially regarding the optimal treatment strategy. Therefore, the aim of the present study was to analyze epidemiological data from patients with OPSCC and compare the outcomes of surgical and medical treatment according to OPSCC stage at diagnosis in the cancer network of the state of São Paulo, Brazil.

Methods

We retrospectively analyzed epidemiological data obtained from the São Paulo Cancer Center Foundation (Fundação Oncocentro de São Paulo, or FOSP for short, in Portuguese) database relative to patients with OPSCC diagnosed between 2004 and 2014 in the state of São Paulo. The following variables were analyzed: sex; age; clinical stage, divided into early (stage I or II) and advanced (stage III or IV); and type of treatment, divided into surgical (surgery alone, surgery and RT, surgery and CT, surgery with RT and CT, surgery with RT, CT, and hormone therapy), medical (RT alone, CT alone, RT and CT), other combinations, and no treatment performed.

The database is available on the FOSP official website at http://www.fosp.saude.sp.gov.br/publicacoes/rhc. The data are in the public domain and not nominal. In accordance with the policy of the Brazilian National Research Ethics Committee (CEP/PRP No. 068/202), studies using publicly available datasets are exempt from institutional research ethics committee approval as they do not involve human subjects.

For inclusion of patients, we selected the anatomic sites for oropharyngeal cancer development based on topographic diagnosis according to the International Classification of Diseases for Oncology (ICD-O) second edition until the end of 2005, and ICD-O third edition from 2006 onward. Initially, all patients listed in the FOSP database with an ICD-O code corresponding to a neoplasm in an anatomic site related to the oropharynx were eligible for inclusion. Subsequently, patients without a diagnosis of OPSCC were excluded.

For descriptive statistics, categorical variables were expressed as numbers (n) and percentages (%), and numerical variables as mean (SD) or median (minimum and maximum values). Univariate and multivariate Cox regression analyses were performed to assess factors associated with the outcomes. A forward stepwise selection procedure was used. Survival curves were estimated by the Kaplan-Meier method and compared by the Gehan-Breslow-Wilcoxon test. The level of significance was set at 5% for all analyses.

Results

A total of 8075 patients with OPSCC were identified in the state of São Paulo, with an increasing incidence from 2004 to 2014; 7181 were men (88.9%) and 894 were women (11.1%) (Fig. 1). The mean patient age was 57.96 (SD, ± 10.14) years. Patients aged 50–59 years were the most affected (n = 3181, 39.4%), followed by patients aged 60–69 years (n = 2210, 27.4%) and those aged 40–49 years (n = 1424, 17.6%). Therefore, patients aged 40–69 years accounted for 84.4% of cases, whereas those below 40 years of age accounted for only 2.2% of cases.

Figure 1
Incidence of oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014.

Patients were divided into 2 groups according to OPSCC stage at diagnosis: early (stage I or II) and advanced (stage III or IV). However, there was no record of this information for 290/8075 patients. Among the remaining 7785 patients, 86.3% were diagnosed at an advanced stage and 13.7% at an early stage. The mean time from diagnosis to initiation of treatment was 69.21 days. This indicates a delay in treatment initiation even after a diagnosis has been reached.

Data on OPSCC type of treatment and reason for untreated patients are shown in Table 1. Only 27.2% of patients were treated surgically, whereas 57.5% were treated medically. In 416 cases (5.2%), patients received other treatment combinations, but it was not recorded whether or not surgery was performed.

Table 1
Number of cases of oropharyngeal squamous cell carcinoma according to type of treatment and reasons for untreated patients in the state of São Paulo, Brazil, 2004–2014.

No treatment was performed to 819 patients (10.1%). In 483 cases (5.9%), patient died before treatment, 448 (5.5%) from cancer and 35 (0.4%) for other causes; 112 (1.4%) did not undergo treatment due to advanced disease or lack of clinical conditions; 11 (0.1%) due to other comorbities; 17 (0.2%) dropped out and 12 (0.1%) refused treatment. There was no information in 44 (0.5%) cases; and 147 (1.8%) were classified as other causes.

The results of univariate and multivariate Cox regression analyses performed to identify factors related to death and overall recurrence are shown in Tables 2 and 3, respectively.

Table 2
Results of Cox regression analysis to estimate the factors associated with death in patients with oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014.
Table 3
Results of Cox regression analysis to estimate the factors associated with overall recurrence in patients with oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014.

Univariate analysis showed that age, sex, clinical stage at diagnosis, type of treatment, and overall recurrence were significantly associated with death as an outcome. Clinical stage at diagnosis was the most relevant variable, with a Hazard Ratio (HR) of 2.062. The comparison of types of treatment showed an HR of 1.737 for death among patients receiving medical treatment compared with those receiving surgical treatment. Men and patients with recurrence were also more likely to die, with an HRs of 1.296 and 1.298, respectively. The results of the multivariate analysis supported the findings of the univariate analysis. Advanced-stage OPSCC had an HR of 1.822 in relation to early-stage disease. Patients receiving medical treatment were more likely to die than those undergoing surgery, with an HR of 1.614. Men and patients with recurrence were also more likely to die, with an HRs of 1.253 and 1.132, respectively.

Regarding disease-free survival, univariate analysis showed no statistically significant differences for the variables sex, age, time from diagnosis to initiation of treatment, or type of treatment. However, patients with advanced-stage OPSCC were more likely to have overall recurrence than those with early-stage disease in both univariate and multivariate analyses, with an HRs of 1.522 and 1.513, respectively (p < 0.0001).

Kaplan-Meier curves of overall survival and disease-free survival are shown in Figs. 2 and 3. Overall survival was 60.6% at 1-year, 23.7% at 5-years, and 13.4% at 10-years. Disease-free survival was 91.1%, 67.7%, and 59.0% at 1, 5 and 10-years, respectively.

Figure 2
Kaplan-Meier curve of overall survival (all-cause mortality) for patients with oropharyngeal squamous cell carcinoma in the state of Sao Paulo, Brazil, 2004–2014. Cumulative survival (standard error): 1-year: 60.6% (0.5%); 5-years: 23.7% (0.5%); 10 years: 13.4% (0.6%).

Figure 3
Kaplan-Meier curve of disease-free survival (all-cause mortality) for patients with oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014. Cumulative survival (standard error): 1-year: 91.1% (0.4%); 5-years: 67.7% (0.8%); 10-years: 59.0% (1.3%).

Kaplan-Meier curves of death and overall recurrence according to clinical stage and treatment were used to determine the influence of these factors on overall survival and disease-free survival. Patients were stratified into 4 groups according to clinical stage and treatment as follows: early and non-surgical; early and surgical; advanced and non-surgical; and advanced and surgical. There was a significant difference between the groups in overall survival (Fig. 4). Patients with early-stage OPSCC had better results than those with advanced-stage disease, regardless of treatment type. Patients treated medically had shorter overall survival in both early and advanced stages. Fig. 5 shows the results of the comparison of the same 4 groups for disease-free survival. There was a statistically significant difference between clinical stages, where patients with early-stage OPSCC had better results than those with advanced-stage disease, regardless of treatment type. However, there was no significant difference between the groups with the same clinical stage at diagnosis when comparing surgical vs. medical treatment.

Figure 4
Kaplan-Meier curve of death according to clinical stage and treatment for patients with oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014.

Figure 5
Kaplan-Meier curve of disease-free survival according to clinical stage and treatment for patients with oropharyngeal squamous cell carcinoma in the state of São Paulo, Brazil, 2004–2014.

Discussion

The treatment of OPSCC is historically controversial and there is no universally consolidated protocol to guide treatment decision-making.2828 Preuss SF, Dinh V, Klussmann JP, Semrau R, Mueller RP, Guntinas-Lichius O. Outcome of multimodal treatment for oropharyngeal carcinoma: a single institution experience. Oral Oncol. 2007;43:402–7, http://dx.doi.org/10.1016/j.oraloncology.2006.04.015.
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,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
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,4242 Chi AC, Day TA, Neville BW. Oral cavity and oropharyngeal squamous cell carcinoma–an update. CA Cancer J Clin. 2015;65:401–21, http://dx.doi.org/10.3322/caac.21293.
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Several approaches have been described using different combinations, such as RT alone, surgery alone, and adjuvant or neoadjuvant RT, combined or not with CT, in addition to neck dissection, which can be radical, selective, or even elective.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
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,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
,4141 Kraus DH, Vastola AP, Huvos AG, Spiro RH. Surgical management of squamous cell carcinoma of the base of the tongue. Am J Surg. 1993;166:384–8, http://dx.doi.org/10.1016/s0002-9610(05)80338-1.
http://dx.doi.org/10.1016/s0002-9610(05)...
The National Head and Neck Cancer Audit recognizes the variation in treatment strategies for OPSCC across cancer networks in England and Wales.3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
Surgical techniques are also a matter of debate due to the different morbidities that might result from them.3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
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,4343 Leonhardt FD, Quon H, Abrahão M, O’Malley BW Jr, Weinstein GS. Transoral robotic surgery for oropharyngeal carcinoma and its impact on patient-reported quality of life and function. Head Neck. 2012;34:146–54, http://dx.doi.org/10.1002/hed.21688.
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The ultimate goal of treatment is cure with minimal functional and aesthetic morbidity.11 Ramqvist T, Dalianis T. Oropharyngeal cancer epidemic and human papillomavirus. Emerg Infect Dis. 2010;16:1671–7.,77 Licitra L, Bernier J, Grandi C, Merlano M, Bruzzi P, Lefebvre JL. Cancer of the oropharynx. Crit Rev Oncol Hematol. 2002;41:107–22, http://dx.doi.org/10.1016/s1040- 8428(01)00129-9.
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Until the 1990s, open surgery was the primary treatment for OPSCC because of limited access to this complex anatomic site. After the 1990s, concurrent CT and RT gained popularity because of the potential morbidity involved in open surgery.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
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,3535 Parsons JT, Mendenhall WM, Stringer SP, Amdur RJ, Hinerman RW, Villaret DB, et al. Squamous cell carcinoma of the oropharynx: surgery, radiation therapy, or both. Cancer. 2002;94:2967-80, http://dx.doi.org/10.1002/cncr.10567.
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,4444 Zafereo ME, Weber RS, Lewin JS, Roberts DB, Hanasono MM. Complications, and functional outcomes following complex oropharyngeal reconstruction. Head Neck. 2010;32:1003–11, http://dx.doi.org/10.1002/hed.21290.
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,4545 Baskin RM, Boyce BJ, Amdur R, Mendenhall WM, Hitchcock K, Silver N, et al. Transoral robotic surgery for oropharyngeal cancer: patient selection and special considerations. Cancer Manag Res. 2018;10:839–46, http://dx.doi.org/10.2147/CMAR.S118891. Published 2018 Apr 20.
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However, if salvage surgery is required after RT, it will be a more technically challenging procedure due to tissue edema and fibrosis, with an increased risk of postoperative complications and poor wound healing.4646 Hamoir M, Schmitz S, Suarez C, Strojan P, Hutcheson KA, Rodrigo JP, et al. The current role of salvage surgery in recurrent head and neck squamous cell carcinoma. Cancers (Basel). 2018;10:267, http://dx.doi.org/10.3390/cancers10080267. Published 2018 Aug 10.
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,4747 Hasan Z, Dwivedi RC, Gunaratne DA, Virk SA, Palme CE, Riffat F. Systematic review and meta-analysis of the complications of salvage total laryngectomy. Eur J Surg Oncol. 2017;43:42–51, http://dx.doi.org/10.1016/j.ejso.2016.05.017.
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,4848 Sassler AM, Esclamado RM, Wolf GT. Surgery after organ preservation therapy. Analysis of wound complications. Arch Otolaryngol Head Neck Surg. 1995;121:162–5, http://dx.doi.org/10.1001/archotol.1995.01890020024006.
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Sassler et al.4848 Sassler AM, Esclamado RM, Wolf GT. Surgery after organ preservation therapy. Analysis of wound complications. Arch Otolaryngol Head Neck Surg. 1995;121:162–5, http://dx.doi.org/10.1001/archotol.1995.01890020024006.
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found major wound complications in 61% of patients undergoing salvage surgery after completing CT and RT. Complications of Chemoradiotherapy (CRT) include mucositis, fibrosis, xerostomia, dermatitis, osteoradionecrosis, neutropenia, and dysphagia.4949 Hutcheson KA, Lewin JS, Barringer DA, Lisec A, Gunn GB, Moore MW, et al. Late dysphagia after radiotherapy-based treatment of head and neck cancer. Cancer. 2012;118:5793–9, http://dx.doi.org/10.1002/cncr.27631.
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,5050 Caudell JJ, Schaner PE, Meredith RF, Locher JL, Nabell LM, Carroll WR, et al. Factors associated with long-term dysphagia after definitive radiotherapy for locally advanced head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2009;73:410–5, http://dx.doi.org/10.1016/j.ijrobp.2008.04.048.
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,5151 Tschudi D, Stoeckli S, Schmid S. Quality of life after different treatment modalities for carcinoma of the oropharynx. Laryngoscope. 2003;113:1949–54, http://dx.doi.org/10.1097/00005537-200311000-00018.
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,5252 Lim GC, Holsinger FC, Li RJ. Transoral endoscopic head and neck surgery: the contemporary treatment of head and neck cancer. Hematol Oncol Clin North Am. 2015;29:1075–92, http://dx.doi.org/10.1016/j.hoc.2015.08.001.
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,5353 Yeh DH, Tarn S, Fung K, MacNeil SD, Yoo J, Winquist E, et al. Transoral robotic surgery vs. radiotherapy for management of oropharyngeal squamous cell carcinoma–a systematic review of the literature. Eur J Surg Oncol. 2015;41:1603–14, http://dx.doi.org/10.1016/j.ejso.2015.09.007.
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Studies have also demonstrated severe late toxicity5454 Yeh DH, Tarn S, Fung K, MacNeil SD, Yoo J, Winquist E, et al. Factors associated with severe late toxicity after concurrent chemoradiation for locally advanced head and neck cancer: an RTOG analysis. J Clin Oncol. 2008;26:3582–9, http://dx.doi.org/10.1016/j.ejso.2015.09.007.
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and high rates of gastrostomy tube dependence in patients treated with CRT4949 Hutcheson KA, Lewin JS, Barringer DA, Lisec A, Gunn GB, Moore MW, et al. Late dysphagia after radiotherapy-based treatment of head and neck cancer. Cancer. 2012;118:5793–9, http://dx.doi.org/10.1002/cncr.27631.
http://dx.doi.org/10.1002/cncr.27631...

Primary RT and surgery have been shown to be equally effective in patients with early-stage OPSCC3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
,3636 Caudell JJ, Gillison ML, Maghami E, Spencer S, Pfister DG, Adkins D, et al. NCCN Guidelines® Insights: Head and Neck Cancers, Version 1.2022. J Natl Compr Canc Netw. 2022;20:224–34, http://dx.doi.org/10.6004/jnccn.2022.0016.
http://dx.doi.org/10.6004/jnccn.2022.001...
,3838 Morisod B, Simon C. Meta-analysis on survival of patients treated with transoral surgery versus radiotherapy for early-stage squamous cell carcinoma of the oropharynx. Head Neck. 2016;38:E2143-50, http://dx.doi.org/10.1002/hed. 23995.
http://dx.doi.org/10.1002/hed. 23995...
,3939 Baliga S, Kabarriti R, Jiang J, Mehta V, Guha C, Kalnicki S, et al. Utilization of Transoral Robotic Surgery (TORS) in patients with Oropharyngeal Squamous Cell Carcinoma and its impact on survival and use of chemotherapy. Oral Oncol. 2018;86:75–80, http://dx.doi.org/10.1016/j.oraloncology.2018.06.009.
http://dx.doi.org/10.1016/j.oraloncology...
and are recommended by the U.S. National Comprehensive Cancer Network (NCCN).3636 Caudell JJ, Gillison ML, Maghami E, Spencer S, Pfister DG, Adkins D, et al. NCCN Guidelines® Insights: Head and Neck Cancers, Version 1.2022. J Natl Compr Canc Netw. 2022;20:224–34, http://dx.doi.org/10.6004/jnccn.2022.0016.
http://dx.doi.org/10.6004/jnccn.2022.001...
In view of similar oncologic outcomes, the complications and functional outcomes associated with each modality gain importance in the choice of treatment. Many centers have opted for organ preservation protocols using RT due to complications secondary to surgery.3131 Mendenhall WM, Morris CG, Amdur RJ, Hinerman RW, Malyapa RS, Werning JW, et al. Definitive radiotherapy for tonsillar squamous cell carcinoma. Am J Clin Oncol. 2006;29:290–7, http://dx.doi.org/10.1097/01.coc.0000209510.19360.f9.
http://dx.doi.org/10.1097/01.coc.0000209...
,3535 Parsons JT, Mendenhall WM, Stringer SP, Amdur RJ, Hinerman RW, Villaret DB, et al. Squamous cell carcinoma of the oropharynx: surgery, radiation therapy, or both. Cancer. 2002;94:2967-80, http://dx.doi.org/10.1002/cncr.10567.
http://dx.doi.org/10.1002/cncr.10567...
However, postoperative adverse effects are mainly caused by access to the oropharynx through a transmandibular or transfacial approach.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
,5050 Caudell JJ, Schaner PE, Meredith RF, Locher JL, Nabell LM, Carroll WR, et al. Factors associated with long-term dysphagia after definitive radiotherapy for locally advanced head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2009;73:410–5, http://dx.doi.org/10.1016/j.ijrobp.2008.04.048.
http://dx.doi.org/10.1016/j.ijrobp.2008....
Transoral Surgery (TORS) have been developed to reduce surgical morbidity, with 5-year survival rates similar to those of RT in patients with early-stage OPSCC.3838 Morisod B, Simon C. Meta-analysis on survival of patients treated with transoral surgery versus radiotherapy for early-stage squamous cell carcinoma of the oropharynx. Head Neck. 2016;38:E2143-50, http://dx.doi.org/10.1002/hed. 23995.
http://dx.doi.org/10.1002/hed. 23995...
,3939 Baliga S, Kabarriti R, Jiang J, Mehta V, Guha C, Kalnicki S, et al. Utilization of Transoral Robotic Surgery (TORS) in patients with Oropharyngeal Squamous Cell Carcinoma and its impact on survival and use of chemotherapy. Oral Oncol. 2018;86:75–80, http://dx.doi.org/10.1016/j.oraloncology.2018.06.009.
http://dx.doi.org/10.1016/j.oraloncology...
Althoug some studies suggest superior functional outcomes with TORS compared to CRT or RT,5555 Chen AM, Daly ME, Luu Q, Donald PJ, Farwell DG. Comparison of functional outcomes and quality of life between transoral surgery and definitive chemoradiother-apy for oropharyngeal cancer. Head Neck. 2015;37:381–5, http://dx.doi.org/10.1002/hed.23610.
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,5656 Ling DC, Chapman BV, Kim J, Choby GW, Kabolizadeh P, Clump DA, et al. Oncologic outcomes and patient-reported quality of life in patients with oropharyngeal squamous cell carcinoma treated with definitive transoral robotic surgery versus definitive chemoradiation. Oral Oncol. 2016;61:41–6, http://dx.doi.org/10.1016/j.oraloncology.2016.08.004.
http://dx.doi.org/10.1016/j.oraloncology...
a more recently published randomize trial compared swallow-related outcomes in patients with T1-T2 N0-N2 (LN ≤4cm) treated with primary RT versus those treated with TORS and showed that RT arm had better outcomes. Nevertheless, this difference was not clinically meaningful and became less pronounced with the passage of time.5757 Nichols AC, Theurer J, Prisman E, Read N, Berthelet E, Tran E, et al. Randomized trial of radiotherapy versus transoral robotic surgery for oropharyngeal squamous cell carcinoma: long-term results of the ORATOR trial. J Clin Oncol. 2022;40:866–75, http://dx.doi.org/10.1200/JCO.21.01961.
http://dx.doi.org/10.1200/JCO.21.01961...

Single modality therapy is recommended for patients with early-stage OPSCC to avoid the adverse effects of combined modality therapy.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
,3636 Caudell JJ, Gillison ML, Maghami E, Spencer S, Pfister DG, Adkins D, et al. NCCN Guidelines® Insights: Head and Neck Cancers, Version 1.2022. J Natl Compr Canc Netw. 2022;20:224–34, http://dx.doi.org/10.6004/jnccn.2022.0016.
http://dx.doi.org/10.6004/jnccn.2022.001...
In this context, given the potential late adverse effects of RT, TORS is highly promising. Furthermore, surgical resection of the tumor allows for adequate histopathologic staging of the neoplasm and identification of patients who would benefit from adjuvant therapy.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
If pathologic analysis of the resected tumor shows extracapsular spread with positive margins unsuitable for reapproach, adjuvant CRT is recommended.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
,3636 Caudell JJ, Gillison ML, Maghami E, Spencer S, Pfister DG, Adkins D, et al. NCCN Guidelines® Insights: Head and Neck Cancers, Version 1.2022. J Natl Compr Canc Netw. 2022;20:224–34, http://dx.doi.org/10.6004/jnccn.2022.0016.
http://dx.doi.org/10.6004/jnccn.2022.001...

Approximately 75%–81% of patients with OPSCC are diagnosed in stages III or IV,4040 Zhen W, Karnell LH, Hoffman HT, Funk GF, Buatti JM, Menck HR. The National Cancer Data Base report on squamous cell carcinoma of the base of tongue. Head Neck. 2004;26:660-74, http://dx.doi.org/10.1002/hed.20064.
http://dx.doi.org/10.1002/hed.20064...
,4141 Kraus DH, Vastola AP, Huvos AG, Spiro RH. Surgical management of squamous cell carcinoma of the base of the tongue. Am J Surg. 1993;166:384–8, http://dx.doi.org/10.1016/s0002-9610(05)80338-1.
http://dx.doi.org/10.1016/s0002-9610(05)...
in which the treatment strategy is challenging due to the greater extent of disease. For adequate exposure of the tumor for resection, different techniques are used based on the size and anatomic site of the neoplasm.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
,3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...
Macroscopic tumor-free margins of 1.5–2.0cm are recommended in combination with frozen section analysis, which requires extensive surgery, but few centers have the expertise to perform it.3232 Golusi´nski W, Golusin´ska-Kardach E. Current role of surgery in the management of oropharyngeal cancer. Front Oncol. 2019;9:388, http://dx.doi.org/10.3389/fonc.2019.00388. Published 2019 May 24.
http://dx.doi.org/10.3389/fonc.2019.0038...
Therefore, different cancer centers use surgery, RT, and CT in a variety of combinations for patients with advanced-stage OPSCC.3333 Mehanna H, Evans M, Beasley M, Chatterjee S, Dilkes M, Homer J, et al. Oropharyngeal cancer: United Kingdom National Multidisciplinary Guidelines. J Laryngol Otol. 2016;130:S90–6, http://dx.doi.org/10.1017/S0022215116000505.
http://dx.doi.org/10.1017/S0022215116000...

Studies comparing the outcomes of surgical and medical treatment of patients with advanced-stage OPSCC have produced conflicting results.2727 O’Connell D, Seikaly H, Murphy R, Fung C, Cooper T, Knox A, et al. Primary surgery versus chemoradiotherapy for advanced oropharyngeal cancers: a longitudinal population study. J Otolaryngol Head Neck Surg. 2013;42:31, http://dx.doi.org/10.1186/1916-0216-42-31. Published 2013 Apr 22.
http://dx.doi.org/10.1186/1916-0216-42-3...
,2929 Díaz-Molina JP, Rodrigo JP, Alvarez-Marcos C, Blay P, de la Rúa A, Estrada E, et al. Functional and oncological results of non-surgical vs surgical treatment in squamous cell carcinomas of the oropharynx. Acta Otorrinolaringol Esp. 2012;63:348–54, http://dx.doi.org/10.1016/j.otorri.2012.02.005.
http://dx.doi.org/10.1016/j.otorri.2012....
,3030 Soo KC, Tan EH, Wee J, Lim D, Tai BC, Khoo ML, et al. Surgery and adjuvant radiotherapy vs concurrent chemoradiotherapy in stage III/IV nonmetastatic squamous cell head and neck cancer: a randomised comparison. Br J Cancer. 2005;93:279–86, http://dx.doi.org/10.1038/sj.bjc.6602696.
http://dx.doi.org/10.1038/sj.bjc.6602696...
O’Connell et al.2727 O’Connell D, Seikaly H, Murphy R, Fung C, Cooper T, Knox A, et al. Primary surgery versus chemoradiotherapy for advanced oropharyngeal cancers: a longitudinal population study. J Otolaryngol Head Neck Surg. 2013;42:31, http://dx.doi.org/10.1186/1916-0216-42-31. Published 2013 Apr 22.
http://dx.doi.org/10.1186/1916-0216-42-3...
showed better 5-year survival rates with surgery followed by adjuvant combined CRT (71.1%) than with CRT (48.6%) or surgery followed by adjuvant RT (53.9%) for patients with advanced-stage disease. Díaz-Molina et al.2929 Díaz-Molina JP, Rodrigo JP, Alvarez-Marcos C, Blay P, de la Rúa A, Estrada E, et al. Functional and oncological results of non-surgical vs surgical treatment in squamous cell carcinomas of the oropharynx. Acta Otorrinolaringol Esp. 2012;63:348–54, http://dx.doi.org/10.1016/j.otorri.2012.02.005.
http://dx.doi.org/10.1016/j.otorri.2012....
compared oncologic and functional outcomes in patients with OPSCC treated with RT vs. surgery. In advanced stages, surgery was associated with a better prognosis than RT, with a 5-year disease- specific survival rates of 47% and 17%, respectively. Although the rate of successful return to oral food intake was higher in the surgical group, overall functional outcomes were similar in both groups.2929 Díaz-Molina JP, Rodrigo JP, Alvarez-Marcos C, Blay P, de la Rúa A, Estrada E, et al. Functional and oncological results of non-surgical vs surgical treatment in squamous cell carcinomas of the oropharynx. Acta Otorrinolaringol Esp. 2012;63:348–54, http://dx.doi.org/10.1016/j.otorri.2012.02.005.
http://dx.doi.org/10.1016/j.otorri.2012....
Kamran et al.5858 Kamran SC, Qureshi MM, Jalisi S, Salama A, Grillone G, Truong MT. Primary surgery versus primary radiation-based treatment for locally advanced oropharyngeal cancer. Laryngoscope. 2018;128:1353–64, http://dx.doi.org/10.1002/lary.26903.
http://dx.doi.org/10.1002/lary.26903...
found improved survival in primary surgery with RT±CT for locally advanced OPC has an compared to primary radiation-based treatment, with a 3-year survival rates of 85.4% and 72.6%, respectively. In contrast, Soo et al.3030 Soo KC, Tan EH, Wee J, Lim D, Tai BC, Khoo ML, et al. Surgery and adjuvant radiotherapy vs concurrent chemoradiotherapy in stage III/IV nonmetastatic squamous cell head and neck cancer: a randomised comparison. Br J Cancer. 2005;93:279–86, http://dx.doi.org/10.1038/sj.bjc.6602696.
http://dx.doi.org/10.1038/sj.bjc.6602696...
found no statistically significant difference in overall survival and 3-year disease-free survival rates when comparing surgery followed by adjuvant RT vs. CRT in patients with advanced-stage OPSCC, despite the significantly higher incidence of toxicity among patients receiving medical treatment. The heterogeneity of the results of studies comparing surgical vs. medical treatment may reflect a treatment selection bias in relation to the time when the study was performed. Until the 1990s, patients were predominantly treated with open surgery. CRT gained popularity in the 2000s, with TORS being introduced around 2010. TORS as a primary treatment for advanced oropharyngeal malignancy confers excellent survival and swallowing outcomes as Haughey et al.5959 Haughey BH, Hinni ML, Salassa JR, Hayden RE, Grant DG, Rich JT, et al. Transoral laser microsurgery as primary treatment for advanced-stage oropharyngeal cancer: a United States multicenter study. Head Neck. 2011;33:1683–94, http://dx.doi.org/10.1002/hed.21669.
http://dx.doi.org/10.1002/hed.21669...
showed. The authors found 3-year overall survival, disease-specific survival, and disease-free survival were 86%, 88% and 82%, respectively. Local control was 97% and 87% of patients had normal swallowing or episodic dysphagia.

The present study showed no significant difference in disease-free survival between patients receiving medical and surgical treatment, regardless of OPSCC stage, which suggests similar complete remission rates with both approaches. However, patients who were not treated with surgery had shorter overall survival in both early and advanced stages of the disease. A possible explanation for this result may be the higher rate of deaths due to complications secondary to CT and RT compared with surgery. In this context, surgery would be the most suitable treatment for patients with OPSCC. However, the overall survival rate considers all-cause mortality, which includes deaths from cancer, treatment complications, or any other noncancer-related circumstances, and the FOSP data do not allow us to determine the proportion of deaths associated with the adverse effects of CT and RT. Therefore, we could not directly relate the lower overall survival of patients to treatment complications.

Our study has limitations inherent in a retrospective analysis. Comparison of nonrandomized data is associated with several problems including patient selection, incomplete medical records, and application of different staging systems. The FOSP has used different staging systems over the years: TNM fifth edition until 2005, TNM sixth edition from 2006 to 2013, and TNM seventh edition from 2014 onward. Therefore, patients with the same diagnosis could be classified into different stages depending on the year of diagnosis registration. Since the study used cases previous to the last TNM edition and does not differentiate positive or negative of HPV we cannot use this important prognostic factor trying to understand differences in treatment methods. Another limitation is the lack of information on comorbidities, type of surgery performed, and reason for medical treatment. The choice of nonsurgical treatment because of tumor unresectability or impaired functional status may determine selection bias, since patients within this profile are more likely to have adverse outcomes, regardless of treatment type. Additionally, we could not collect data on functional outcomes and quality of life, which are relevant factors in the comparison of treatment modalities.

The strengths of our study include a set of results that provide data on the population of patients with OPSCC in the state of São Paulo, with a sample representative of the demographic profile of the disease described in the literature. We identified a total of 8075 patients with OPSCC, with an increased OPSCC incidence in recent years and a higher prevalence in men (88.9%), in patients aged 50–70 years (66.0%), and of advanced-stage disease at diagnosis (86.3%). The mean time from diagnosis to initiation of treatment was 69.21 days, which might reflect the work overload of cancer centers in Brazil. It is important to note that 5.9% of patients died before treatment; and 1.5% did not start treatment due to advanced disease, lack of clinical conditions or other comorbities. Most patients received medical treatment (57.5%), which also may be a consequence of the delay in treatment initiation, with patients already presenting with unresectable tumors at the time of treatment decision- making. Our study also raises issues to be investigated in future research, such as the proportion of deaths related to the complications of each treatment modality.

Prospective randomized controlled trials that differentiate HPV-related and non-HPV-related tumors are warranted to provide consistent data on the best approach for patients with OPSCC.

Conclusion

Within the limitations of the present study, our results provide epidemiological data on patients with OPSCC in the state of São Paulo, Brazil. There was no significant difference in disease-free survival between surgical and medical treatment, but patients who were not treated surgically had shorter overall survival. Prospective studies are warranted to assess whether these results are secondary to complications from the use of CT and RT.

Acknowledgments

We are grateful to the Department of Otolaryngology & Head and Neck Surgery of Universidade Estadual de Campinas (Unicamp), to Unicamp Professors, staff, and residents, and to the Statistics Department of Unicamp School of Medical Sciences for assistance with statistical calculations. This study received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

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Publication Dates

  • Publication in this collection
    16 Jan 2023
  • Date of issue
    2022

History

  • Received
    19 Apr 2022
  • Accepted
    22 July 2022
  • Published
    05 Aug 2022
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial. Sede da Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico Facial, Av. Indianópolia, 1287, 04063-002 São Paulo/SP Brasil, Tel.: (0xx11) 5053-7500, Fax: (0xx11) 5053-7512 - São Paulo - SP - Brazil
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