metricas
covid
Buscar en
Clinics
Toda la web
Inicio Clinics Survival trends of patients with oral and oropharyngeal cancer treated at a canc...
Journal Information
Vol. 75.
(January 2020)
Share
Share
Download PDF
More article options
Visits
1405
Vol. 75.
(January 2020)
ORIGINAL ARTICLE
Open Access
Survival trends of patients with oral and oropharyngeal cancer treated at a cancer center in São Paulo, Brazil
Visits
1405
Luiz Paulo KowalskiI, Max Moura de OliveiraII, Rossana Veronica Mendoza LopezII,III, Diego Rodrigues Mendonça e SilvaII, Mauro Kazuo IkedaI, Maria Paula CuradoII,
Corresponding author
mp.curado@accamargo.org.br

Corresponding author.
I Departamento de Cirurgia de Cabeca e Pescoco e Otorrinolaringologia, A.C. Camargo Cancer Center, Sao Paulo, SP, BR
II Grupo de Epidemiologia e Estatistica em Cancer, Centro Internacional de Pesquisa, A.C. Camargo Cancer Center, Sao Paulo, SP, BR
III Centro de Investigacao Translacional em Oncologia, Institute of Cancer do Estado de Sao Paulo, Sao Paulo, SP, BR
This item has received

Under a Creative Commons license
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (3)
Show moreShow less
OBJECTIVE:

We aimed to estimate the overall survival (OS) and conditional survival (CS) in patients diagnosed with oral and oropharyngeal squamous cell carcinoma (SCC) and to determine their survival trends.

METHODS:

The study included all consecutive patients treated at the A.C. Camargo Cancer Center for oral or oropharyngeal SCC between 2001 and 2012. Data were obtained from the Hospital Cancer Registry. OS and CS were analyzed using the Kaplan-Meier method to evaluate the probability of survival with Cox predictor models.

RESULTS:

Data of 505 oral and 380 oropharyngeal SCC patients obtained in 2001–2006 and 2007–2012 were analyzed. Most of the oral SCC (59%) and oropharyngeal SCC (90%) patients had stages III–IV SCC. The 5-year OS for patients with oral SCC was 51.7%, with no significant difference between the first and second periods. The CS rates in 2007–2012 were 65% after the first year and 86% up to the fifth year. For oropharyngeal SCC, the 5-year OS rate was 45.0% in the first period. The survival rate increased to 49.1% from 2007 to 2012, with a reduction in the risk of death (HR=0.69;0.52–09.2). The CS estimates from 2007 to 2012 were 59% after the first year and 75% up to the fifth year.

CONCLUSION:

Survival across the two time periods remained stable for oral SCC but showed a significant increase for oropharyngeal SCC, possibly because of improvements in the patients' response to radiotherapy, such as intensity-modulated radiation therapy, and the use of more accurate diagnostic imaging approaches.

KEYWORDS:
Survival Analysis
Prognosis
Oral Cavity
Oropharynx
Cancer
Full Text
INTRODUCTION

In 2018, 354,864 new cases of lip and oral cancer (OC) and 92,877 new cases of oropharyngeal cancer were reported worldwide. The number of deaths from lip cancer and OC was 51,005, whereas that from oropharyngeal cancer was 51,005 1. In 2018, 19,898 new cases of lip cancer and OC were reported in Latin America and Caribbean countries 1, whereas 14,700 new cases were reported in Brazil 2. A total of 9,180 individuals from Latin America and Caribbean countries and 4,629 from Brazil developed oropharyngeal cancer 1. Therefore, the number of individuals diagnosed with oral and oropharyngeal squamous cell carcinoma (SCC) in Brazil is almost half the number of those diagnosed with oral and oropharyngeal SCC in Latin America and Caribbean countries.

Cancers in the oral cavity and oropharynx are classified as head and neck cancers, and 90% of them are SCC 3,4. Tobacco and alcohol use are the main risk factors for OC. For oropharyngeal cancer, human papilloma virus (HPV) infection has also been considered a risk factor and prognostic biomarker 5–7.

The survival rates for head and neck cancer vary depending on the site involved 7. Previous European and American population-based studies reported that the 5-year relative survival of German people with OC diagnosed in 2002–2006 was 54.6% 8, whereas that of Danish people with head and neck cancer was 62.4% (2010–2014) 9. For American individuals with cancer in the oral cavity, oropharynx, and subsites (base of tongue, hard palate, tonsil, etc.), SEER reported a 5-year relative survival of 62.9% 4.

In the United States (US), the 5-year relative survival of oropharyngeal cancer patients increased from 33.3% in 1992–1996 to 42.2% in 2002–2006 4.

On the basis of the hospital data, there were differences in overall survival (OS) rates between public and private institutions. In Argentina, the survival estimate for OC was 39% in public hospitals 10. In Chile, the survival estimate for OC was 46% in private hospitals 11. In Brazil, Santa Catarina reported a 5-year OS for OC and pharyngeal cancer of 33.3% 12. In Maceio, northeast of Brazil, the 5-year OS for oropharyngeal cancer was 27.8% 12,13. In Santa Maria, south of Brazil, the 5-year OS for OC and oropharyngeal cancer was 42%; however, patients with oropharyngeal cancer had the worst survival rates 14.

Retrospective studies have shown survival differences according to tumor site and subsite (base of tongue, hard palate, and tonsil) for oropharyngeal cancer and sex and age for OC 15.

Conditional survival (CS) provides an estimate of the chances of surviving in the second to the fifth year after diagnosis, after surviving for at least a year; it is a dynamic survival indicator wherein the prognosis is based on the number of years survived after treatment 16,17. Thus, we evaluated the survival of patients with OC and oropharyngeal cancer by assessing their OS and CS rates in order to provide prognostic information. CS analysis provide prognostic information for cancer survivors; it was performed to estimate the probability of survival after 1 to 5 years 17. In the US, a marked improvement in the CS of oropharyngeal cancer patients (26.6%–60.0%) was observed during the period 1997–1998 18.

The present study aimed to estimate the OS and CS in patients diagnosed with oral and oropharyngeal SCC at the A.C. Camargo Cancer Center (ACCCC) in Sao Paulo, Brazil, to determine the progress in patients' survival. The study was conducted in H&N patients treated at a specialized treatment center between 2001 and 2012.

METHODS

Data of patients diagnosed with oral SCC (C02, C05 except C051-C052, and C06) and oropharyngeal SCC (C01, C051-C052, C09, and C10) according ICD-O3 between 2001 and 2012 were extracted from the Hospital Cancer Registry of ACCCC 19; the morphological codes (8050/3, 8070/3, 8074/3, 8076/3, and 8083/3) 19 for oral and oropharyngeal SCC were registered at the ACCCC with follow-up until December 31, 2017. The Ethics Committee approved the study (n° 2462/17 on Dec 5, 2017). The patients were stratified by age group (≤50 years, 51–60 years, and >60 years); sex (male and female), diagnostic period (2001–2006 and 2007–2012), clinical stage (I–II and III–IV) 20,21 and treatment procedure (surgery alone, surgery with chemoradiation, and other/palliative care). The absolute and relative frequencies were described.

OS was calculated from the date of diagnosis to the date of death (of any cause) or the date on which the latest information was available. Survival curves were calculated using the Kaplan-Meier method; the probabilities for survival at 1 year, 3 years, and 5 years were described using independent variables. The differences in survival curves were compared using a log-rank test. The hazard ratio (HR) as its corresponding 95% confidence interval (CI) were determined using a Cox regression model.

We calculated the CS, which is the dynamic probability of the patient surviving t years, given that a patient has already survived for s years after diagnosis 22. Thus, we were able to estimate the patient's chance of surviving an additional t years after surviving for s years (with the total being t+s years). CS was calculated on the basis of survival probability data accumulated using the Kaplan-Meier method according to the following formula:

CS rates were plotted for 1–5 years after diagnosis. The level of significance was 5% for all hypotheses. All analyses were performed using SPSS v.25 for Windows.

RESULTS

Between 2001 and 2012, 885 patients with oral and oropharyngeal SCC were treated at ACCCC. Of them, 505 had OC, whereas 380 had oropharyngeal cancer. In relation to age distribution, 50% of patients with OC were aged >60 years, whereas 42% of those with oropharyngeal cancer were aged. With regard to sex, OC (2:1) and oropharyngeal cancer (6:1) were more common in men. The majority of patients had advanced-stage (stage III–IV) cancer (OC: 59% (290/505), oropharyngeal cancer: 90% (339/380); Table 1). The proportions of patients with missing 5-year clinical follow-up data were 6.4% (OC) and 3.9% (oropharyngeal cancer).

Table 1.

Characteristics of patients with oral and oropharyngeal SCC treated at the A.C. Camargo Cancer Center during the diagnostic period, HCR, 2001–2012.

Oral cavity  Oropharynx  Total 
N=505  N=380  N=885 
Characteristics  n (%)  n (%)  n (%) 
Age group (yrs)       
≤50  118 (23.4)  82 (21.6)  200 (22.6) 
51-60  139 (27.5)  138 (36.3)  277 (31.3) 
>60  248 (49.1)  160 (42.1)  408 (46.1) 
Gender       
Male  335 (66.3)  324 (85.3)  659 (74.5) 
Female  170 (33.7)  56 (14.7)  226 (25.5) 
Period of diagnosis       
2001-2006  197 (39.0)  129 (33.9)  326 (36.8) 
2007-2012  308 (61.0)  251 (66.1)  559 (63.2) 
Clinical stage       
I-II  203 (41.2)  37 (9.8)  240 (27.6) 
III-IV  290 (58.8)  339 (90.2)  629 (72.4) 

SCC, squamous cell carcinoma; HCR, Hospital Cancer Registry.

Oral SCC

There was an improvement in the treatment (combining surgery and chemoradiotherapy) response of stage III–IV patients, which increased from 48.7% in 2001–2006 to 63.2% in 2007–2012 (p<0.006) (Table 2).

Table 2.

Treatment adopted for patients with oral and oropharyngeal squamous cell carcinoma at the A.C. Camargo Cancer Center, according to period of diagnosis and clinical stage, HCR, 2001–2012.

    Period of diagnosis   
Clinical stage  Treatment  2001-2006  2007-2012  Total  p 
Oral cavity
I-IISurgery only  60 (80)  100 (78.1)  160 (78.8)  0.494 
Surgery with (C)RT  13 (17.3)  24 (18.8)  37 (18.2)   
(C)RT  1 (1.3)  4 (3.1)  5 (2.5)   
Palliative  1 (1.3)  0 (0)  1 (0.5)   
Subtotal  75 (100)  128 (100)  203 (100)   
III-IVSurgery only  45 (37.8)  34 (19.9)  79 (27.2)  0.006 
Surgery with (C)RT  58 (48.7)  108 (63.2)  166 (57.2)   
(C)RT  11 (9.2)  24 (14)  35 (12.1)   
Palliative  5 (4.2)  5 (2.9)  10 (3.4)   
Subtotal  119 (100)  171 (100)  290 (100)   
TotalSurgery only  107 (54.3)  139 (45.1)  246 (48.7)  0.087 
Surgery with (C)RT  71 (36)  134 (43.5)  205 (40.6)   
(C)RT  12 (6.1)  29 (9.4)  41 (8.1)   
Palliative  7 (3.6)  6 (1.9)  13 (2.6)   
  Total  197 (100)  308 (100)  505 (100)   
Oropharynx
I-IISurgery with or without (C)RT  10 (83.3)  18 (72.0)  28 (75.7)  0.452 
(C)RT  2 (16.7)  7 (28.0)  9 (24.3)   
Subtotal  12 (100)  25 (100.0)  37 (100.0)   
III-IVSurgery with or without (C)RT  71 (61.2)  57 (25.6)  128 (37.8)  <0.001 
(C)RT  36 (31.0)  160 (71.7)  196 (57.8)   
Palliative  9 (7.8)  6 (2.7)  15 (4.4)   
Subtotal  116 (100.0)  223 (100.0)  339 (100.0)   
TotalSurgery with or without (C)RT  81 (62.8)  77 (30.7)  158 (41.6)  <0.001 
(C)RT  39 (30.2)  167 (66.5)  206 (54.2)   
Palliative  9 (7.0)  7 (2.8)  16 (4.2)   
Total  129 (100.0)  251 (100.0)  380 (100.0)   

(C)RT, (chemo)radiotherapy; HCR, Hospital Cancer Registry.

The OS rates for OC were 79.0%, 58.4%, and 51.7% in the first, third, and fifth years after diagnosis, respectively. The OS for oral SCC in 2001–2006 was 49.7% and that in 2007–2012 was 53.1% (p=0.440) (Figure 1a). The 5-year OS was higher in patients aged ≤50 years (61.8%) and in those with stage I–II cancer (74.0%) (Table 3). The risk of death was 1.42 times higher in patients with oral SCC aged >60 years and 3.58 higher in those with clinical stage III–IV SCC (Table 4).

Figure 1.

Overall survival of patients with oral and oropharyngeal squamous cell carcinoma treated at the A. C. Camargo Cancer Center, Hospital Cancer Registry, 2001–2012, by period of diagnosis.

(0.1MB).
Table 3.

Survival probabilities at 1, 3, and 5 years in patients with oral and oropharyngeal squamous cell carcinoma treated at the A.C. Camargo Cancer Center, HCR, 2001–2012.

    Oral cavity  Oropharynx 
      Probability of survival    Probability of survival 
Variable  Group  Deaths/total  1 year  3 years  5 years  p  Deaths/total  1 years  3 years  5 years  p 
Overall    240/505  79.0%  58.4%  51.7%    207/380  76.3%  50.4%  45.0%   
Period  2001-2006  99/197  79.7%  56.3%  49.7%  0.440  81/129  69.8%  44.2%  37.2%  0.010 
  2007-2012  141/308  78.6%  59.7%  53.1%    126/251  79.6%  53.7%  49.1%   
Gender  Male  166/335  79.5%  55.9%  49.6%  0.185  178/324  76.5%  50.4%  44.7%  0.894 
  Female  74/170  78.1%  63.3%  56.0%    29/56  75.0%  51.1%  47.2%   
Age group (yrs)  ≤50  45/118  85.6%  65.3%  61.8%  0.017  34/82  82.9%  61.9%  58.1%  0.007 
  51-60  64/139  84.1%  60.1%  53.2%    72/138  72.5%  52.9%  47.7%   
  >60  131/248  73.1%  54.1%  46.0%    101/160  76.1%  42.4%  35.9%   
Clinical stage  I-II  51/203  93.5%  83.9%  74.0%  <0.001  9/37  94.6%  78.0%  75.2%  <0.001 
  III-IV  184/290  69.6%  40.8%  36.2%    195/339  74.6%  47.8%  42.0%   

HCR, Hospital Cancer Registry.

Table 4.

Hazard ratio associated with 5-year survival in patients with oral and oropharyngeal squamous cell carcinomas treated at the A.C. Camargo Cancer Center, Hospital Cancer Registry, 2001–2012.

    Oral cavityOropharynx
Variable  Group  HRunadjusted (95%CI)  p value  HRadjusted (95%CI)  p value  HRunadjusted (95%CI)  p value  HRadjusted (95%CI)  p value 
Period  2001-2006  1.00    1.00    1.00    1.00   
  2007-2012  0.90 (0.70-1.17)  0.443  0.91 (0.70-1.18)  0.487  0.70 (0.53-0.92)  0.012  0.69 (0.52-0.92)  0.012 
Gender  Female  1.00    1.00    1.00    1.00   
  Male  1.20 (0.91-1.58)  0.189  1.14 (0.86-1.51)  0.360  1.03 (0.69-1.52)  0.885  0.94 (0.63-1.39)  0.747 
Age group (yrs)  ≤50  1.00    1.00    1.00    1.00   
  51-60  1.27 (0.87-1.87)  0.213  1.05 (0.71-1.55)  0.807  1.36 (0.91-2.05)  0.136  1.46 (0.97-2.20)  0.073 
  >60  1.60 (1.14-2.24)  0.007  1.42 (1.01-2.01)  0.044  1.80 (1.22-2.65)  0.003  1.88 (1.27-2.78)  0.002 
Clinical stage  I-II  1.00    1.00    1.00    1.00   
  III-IV  3.66 (2.68-5.00)  <0.001  3.58 (2.61-4.89)  <0.001  3.10 (1.59-6.04)  0.001  3.23 (1.65-6.30)  0.001 

*HR, hazard ratio.

CS of patients with oral SCC increased from 65% after the first year to 86% in the fifth year after diagnosis, demonstrating an improvement in survival in the most recent period (Figure 2b). With the passage of time, the chances of survival increase. However, the risk of death from oral SCC remained unchanged in the two study periods.

Figure 2.

Five-year probability conditional survival of patients with oral and oropharyngeal squamous cell carcinoma treated at the A. C. Camargo Cancer Center, Hospital Cancer Registry 2001–2012, according period of diagnosis. Oro, oropharynx; OC, oral cavity.

(0.16MB).
Oropharyngeal SCC

Approximately 75.7% of patients with oropharyngeal SCC were treated with chemoradiation, with differences noted between the first and second period (p<0.001). Of the patients with stage III–IV cancer treated between 2001 and 2006, 31% received chemoradiation; between 2007 and 2012, 71.7% of the patients received chemoradiation (Table 2). OS probabilities for oropharyngeal SCC were 76.3% and 45.0% in the first and fifth years after diagnosis, respectively. The 5-year OS was higher in patients diagnosed between 2007 and 2012 (49.1%; p=0.010) (Figure 1b), those aged ≤50 years (58.1%; p=0.007), and those with stage I–II cancer (75.2%; p<0.001) (Table 3). The HR in the adjusted analysis and risk of death were higher in patients aged >60 years (HR 1.88) and those with stage III–IV disease (HR: 3.23) (Table 4).

The 5-year CS after having survived for 1 year was 48% for those diagnosed between 2001 and 2006 and 59% for those diagnosed between 2007 and 2012 (Figure 2b). Therefore, the survival rate of oropharyngeal SCC increased in the more recent period.

DISCUSSION

The 5-year OS rates were 52% for oral SCC and 45% for oropharyngeal cancer in the period 2001–2012. However, the 5-year survival of patients with oral SCC remained unchanged (49.7%–53.1%), whereas that of patients with oropharyngeal SCC increased from 37.2% to 49.1%. By contrast, Ridder et al. reported a 5-year survival rate of 60% 15, whereas Du et al. 23 reported 5-year survival rates of 69% and 56% for OC and oropharyngeal cancer, respectively.

The majority of patients with oral SCC in our study were aged 60 years, whereas those with oropharyngeal SCC tended to be younger, which is similar to the findings in the literature 24. A previous study conducted in ACCCC identified that comorbidities are prognostic factors for older adults with head and neck cancer 25. A review by VanderWale et al. 26 described that the treatment toxicity can be quite morbid for older adults as they are often excluded from clinical trials that provide definitions on the standards of care.

In both OC and oropharyngeal cancer, we observed an increase in mortality risk for patients aged >60 years and those with stage III/IV SCC, which is similar to the findings reported by Ridder et al. 15. Although a greater mortality risk was reported in men 15,21,23,24, this study did not find a survival difference between sexes.

The 5-year OS for stage I–II patients with OC and oropharyngeal cancer was around 74%, although the proportion of patients with early-stage (I–II) OC was 41% and that of patients with early-stage (I–II) oropharyngeal cancer was 9.8%. Zanoni et al. 27 reported an OS rate of 64.4% (1985–2015) for OC patients admitted at the Memorial Sloan Kettering Cancer Center, a rate higher than that observed in this study; however, 58% of the patients treated had stage I–II SCC, whereas 39% had stage III–IV SCC. In 11 hospitals in Europe, 45% of the OC patients had stage III–IV SCC 15. Du et al. 23 observed that 38% of OC patients had stage III–IV SCC, whereas 59% had stage III–IV SCC. Amit et al. 28, in a multicentric international study conducted in seven international institutions including ACCCC in two decades (1990 to 2011), reported an improvement (from 59% to 70%) in the survival of patients with OC in the most recent period.

The multicenter CHANCE study (USA) reported a 54% 5-year OS for OC 21, which is similar to our data. In Portugal, Monteiro et al. 29 observed that 71% of their patients with OC were diagnosed at stage III–IV, with a survival rate of 41%, without significant improvements over time (38% for 2000–2004 and 42% for 2005–2009). In a university hospital in Santa Maria, Brazil, the OS was 42% in 2004–2014 14. Thus, the OS rate for patients with OC has been around 55% at most treatment centers.

Survival for oropharyngeal cancer improved significantly between 2001 and 2012 (from 37.2% to 49.1%), although around 90% of the treated patients had stage III–IV cancers. The presence of HPV in the oropharynx and its role as a prognostic factor affected the therapeutic planning in these cases and had an influence on the improvement in survival 5. Brazilian studies showed that the majority of patients diagnosed with oropharyngeal cancer are not HPV-positive (i.e., low prevalence, 3%–9%) 30,31.

A review on the treatment of older patients with head and neck cancer indicated that oropharyngeal cancer patients aged 65 years and older have survival outcomes similar to those of younger patients with head and neck cancer; however, they may experience worse toxicity 26. Sandulache et al. 32 reported a 40% 5-year OS for oropharyngeal cancer and indicated that 30% of the patients were unable to complete the treatment.

For locally advanced oropharyngeal cancer, chemotherapy combined with radiation treatment has been reported to significantly improve OS 33,34. Du et al. 23 observed that 84% of oropharyngeal cancer patients had stage III–IV cancers, which is the same as the finding of this study (90%). Monteiro et al. 29 reported a 27% 5-year OS rate for oropharyngeal cancer, with a significant reduction in mortality from 2000–2004 (28%) to 2005–2009 (24%) in Northern Portugal. Patients with advanced stages have worst survival 35. Although 90% of the patients with oropharyngeal cancer treated at the ACCCC had clinical stage III–IV cancers, the survival among these patients increased from the previous period to the more current period, likely because of the changes in therapeutic planning, such as the use of IMRT and new target therapies 36.

For oropharyngeal cancer, there was a difference in terms of the period of diagnosis, with a lower risk of death observed in patients treated in the more recent period (2007–2012), similar to the findings of Monteiro et al. 29.

With regard to the 5-year CS of OC patients, CS increased to 17% in patients who survived 1 year and to 13% in those who survived 5 years after the diagnosis (2007–2012 versus 2001–2006); similar results were observed in a single institution in the same period 37.

For oropharyngeal cancer, a similar increase in CS was observed in 2007–2012 and 2001-2006; the probability of CS at the first year was 11%, and it increased to 14% after 5 years. The CS of oral cancer patients 5 years after diagnosis had increased, whereas that of patients with oropharyngeal cancer had decreased. The decrease in oropharyngeal cancer survival after 5 years remains unclear.

The lack of progress in CS among older adults with oral and oropharyngeal SCC could be related to the presence of comorbidities and other competitive causes of death. In this article, because of the number of patients, we were not able to stratify patients by age, stage, and period to estimate the CS as Yang et al. 17 described.

The OS of patients with OC and oropharyngeal cancer increased from 2007 to 2012; however, the majority of patients who underwent treatment had advanced-stage cancer. The OS of patients with stage I and II oral SCC was 74%, whereas that of oropharyngeal SCC patients was 75.2%, which is two times higher than the rates observed among those with stage III and IV cancers with these topographies.

Hospital Cancer Registries are database that were created under the law 38 in Brazil, but the use of these registries has limitations: they cannot provide comprehensive clinical information and data on patients' outcomes. At ACCCC, the Hospital Cancer Registry is in collaboration with Fundação Oncocentro de São Paulo; from 2000 to 2012, the registry had 36,343 registered cancer cases 39.

The limitation of this study is the lack of information on the p16 status for oropharyngeal SCC because this biomarker had not yet been routinely adopted during the study period and the cause of death was not described in the Hospital Cancer Registry.

Therefore, early diagnosis of OC and oropharyngeal cancer is likely to increase the chances of cure and survival among these patients.

AUTHOR CONTRIBUTIONS

Kowalski LP and Curado MP contributed to the conception and design. Oliveira MM and Lopez RVM contributed to the analysis and interpretation of data, and manuscript drafting. Silva DRM extracted the data and drafted the manuscript. Kowalski LP and Ikeda MK critically reviewed the manuscript. Curado MP discussed and critically reviewed the manuscript and supervised the research. All authors approved the final version of the manuscript to be published.

REFERENCES
[1]
J Ferlay , M Ervik , F Lam .
Global Cancer Observatory: Cancer Today.
[2]
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) .
Estimativa 2018 - Incidência de câncer no Brasil.
[3]
D Chin , GM Boyle , S Porceddu , DR Theile , PG Parsons , WB Coman .
Head and neck cancer: past, present and future.
[4]
D Pulte , H Brenner .
Changes in survival in head and neck cancers in the late 20th and early 21st century: a period analysis.
[5]
ML Gillison , WM Koch , RB Capone , M Spafford , WH Westra , L Wu , et al.
Evidence for a causal association between human papillomavirus and a subset of head and neck cancers.
[6]
S Marur , AA Forastiere .
Head and Neck Squamous Cell Carcinoma: Update on Epidemiology, Diagnosis, and Treatment.
[7]
AL Carvalho , IN Nishimoto , JA Califano , LP Kowalski .
Trends in incidence and prognosis for head and neck cancer in the United States: a site-specific analysis of the SEER database.
[8]
S Listl , L Jansen , A Stenzinger , K Freier , K Emrich , B Holleczek , et al.
Survival of patients with oral cavity cancer in Germany.
[9]
KK Jakobsen , C Grønhøj , DH Jensen , KKS Karnov , TK Agander , L Specht , et al.
Increasing incidence and survival of head and neck cancers in Denmark: a nationwide study from 1980 to 2014.
[10]
D Brandizzi , M Gandolfo , ML Velazco , RL Cabrini , HE Lanfranchi .
Clinical features and evolution of oral cancer: A study of 274 cases in Buenos Aires, Argentina.
Med Oral Patol Oral Cir Bucal, 13 (2008), pp. E544-E548
[11]
DB Momares , CG Contreras , RB Martínez , JN Ávalos , RL Carmona .
Sobrevida en Carcinoma Espinocelular de Mucosa Oral: Análisis de 161 pacientes.
Rev Chil Cir, 66 (2014), pp. 568-576
[12]
IJ Schneider , ME Flores , DA Nickel , LG Martins , J Traebert .
Survival rates of patients with cancer of the lip, mouth and pharynx: a cohort study of 10 years.
[13]
ACOV Le Campion , CMB Ribeiro , RR Luiz , FF da Silva Júnior , HCS Barros , KCB Dos Santos , et al.
Low Survival Rates of Oral and Oropharyngeal Squamous Cell Carcinoma.
Int J Dent, 2017 (2017),
[14]
JDS Moro , MC Maroneze , TM Ardenghi , LM Barin , CC Danesi .
Oral and oropharyngeal cancer: epidemiology and survival analysis.
[15]
M de Ridder , AJM Balm , RJ Baatenburg de Jong , CHJ Terhaard , RP Takes , M Slingerland , et al.
Variation in head and neck cancer care in the Netherlands: A retrospective cohort evaluation of incidence, treatment and outcome.
[16]
S Hieke , M Kleber , C Köning , M Engelhardt , M Schumacher .
Conditional Survival: A Useful Concept to Provide Information on How Prognosis Evolves over Time.
[17]
YH Yang , SH Liu , PS Ho , IY Huang , CH Chen , TY Shieh .
Conditional survival rates of buccal and tongue cancer patients: how far does the benefit go?.
[18]
CD Fuller , SJ Wang , CR Thomas Jr , HT Hoffman , RS Weber , DI Rosenthal .
Conditional survival in head and neck squamous cell carcinoma: results from the SEER dataset 1973-1998.
[19]
International Classification of Diseases for Oncology.
Third Edition, First Revision, World Health Organization, (2013),
[20]
Brasil .
Ministério da Saúde. Secretaria de Atenção è Saúde. Instituto Nacional de Câncer. TNM: classificação de tumores malignos. 6. ed.
INCA, (2004),
[21]
Brasil .
Ministério da Saúde. Instituto Nacional de Câncer José Alencar Gomes da Silva. Coordenação-Geral de Prevenção e Vigilância. 7. ed.
INCA, (2012),
[22]
SH Jung , HY Lee , SC Chow .
Statistical Methods for Conditional Survival Analysis.
[23]
E Du , AL Mazul , D Farquhar , P Brennan , D Anantharaman , B Abedi-Ardekani , et al.
Long-term Survival in Head and Neck Cancer: Impact of Site, Stage, Smoking, and Human Papillomavirus Status.
[24]
AK Chaturvedi , WF Anderson , J Lortet-Tieulent , MP Curado , J Ferlay , S Franceschi , et al.
Worldwide trends in incidence rates for oral cavity and oropharyngeal cancers.
[25]
A Sanabria , AL Carvalho , JG Vartanian , J Magrin , MK Ikeda , LP Kowalski .
Comorbidity is a prognostic factor in elderly patients with head and neck cancer.
[26]
NA VanderWalde , M Fleming , J Weiss , BS Chera .
Treatment of older patients with head and neck cancer: a review.
[27]
DK Zanoni , PH Montero , JC Migliacci , JP Shah , RJ Wong , I Ganly , et al.
Survival outcomes after treatment of cancer of the oral cavity (1985-2015).
[28]
M Amit , TC Yen , CT Liao , Y Binenbaum , P Chaturvedi , JP Agarwal , et al.
Clinical nodal stage is a significant predictor of outcome in patients with oral cavity squamous cell carcinoma and pathologically negative neck metastases: results of the international consortium for outcome research.
[29]
LS Monteiro , L Antunes , LL Santos , MJ Bento , S Warnakulasuriya .
Survival probabilities and trends for lip, oral cavity and oropharynx cancers in Northern Portugal in the period 2000-2009.
Ecancermedicalscience, 12 (2018), pp. 855
[30]
KB Ribeiro , JE Levi , M Pawlita , S Koifman , E Matos , J Eluf-Neto , et al.
Low human papillomavirus prevalence in head and neck cancer: results from two large case-control studies in high-incidence regions.
[31]
RV López , JE Levi , J Eluf-Neto , RJ Koifman , S Koifman , MP Curado , et al.
Human papillomavirus (HPV) 16 and the prognosis of head and neck cancer in a geographical region with a low prevalence of HPV infection.
[32]
VC Sandulache , J Hamblin , S Lai , T Pezzi , HD Skinner , NA Khan , et al.
Oropharyngeal squamous cell carcinoma in the veteran population: Association with traditional carcinogen exposure and poor clinical outcomes.
[33]
G Calais , E Bardet , C Sire , M Alfonsi , J Bourhis , B Rhein , et al.
Radiotherapy with concomitant weekly docetaxel for Stages III/IV oropharynx carcinoma. Results of the 98-02 GORTEC Phase II trial.
[34]
F Denis , P Garaud , E Bardet , M Alfonsi , C Sire , T Germain , et al.
Final results of the 94-01 French Head and Neck Oncology and Radiotherapy Group randomized trial comparing radiotherapy alone with concomitant radiochemotherapy in advanced-stage oropharynx carcinoma.
[35]
LP Kowalski , AL Carvalho .
Influence of time delay and clinical upstaging in the prognosis of head and neck cancer.
[36]
AK Chan , SH Huang , LW Le , E Yu , LA Dawson , JJ Kim , et al.
Postoperative intensity-modulated radiotherapy following surgery for oral cavity squamous cell carcinoma: patterns of failure.
[37]
SW Chen , Q Zhang , ZM Guo , WK Chen , WW Liu , YF Chen , et al.
Trends in clinical features and survival of oral cavity cancer: fifty years of experience with 3,362 consecutive cases from a single institution.
[38]
Ministério da Saúde .
Brasil. Portaria N°. 3.662, 24 de novembro de 2010.
[39]
São Paulo .
Secretaria de Estado da Saúde de São Paulo. Fundação Oncocentro de São Paulo. Banco de dados RHC.
Fundação Oncocentro de São Paulo, (2019),

No potential conflict of interest was reported.

Copyright © 2020. CLINICS
Download PDF
Article options
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos

Quizás le interese:
10.6061/clinics/2021/e2836
No mostrar más