Prognostic effects of surgery or radiotherapy on adenoid cystic carcinoma of the head and neck: a retrospective cohort study
Introduction
Adenoid cystic carcinoma (ACC) is a kind of rare tumor with an incidence of 5–10 cases per million people annually (1). ACC is a major pathological subtype accounting for approximately 1% of all head and neck malignancies and comprising approximately 25% of all salivary gland cancer cases (2,3). The incidence of ACC is increasing slowly, and ACC is associated with a high recurrence rate, perineural invasion, the delayed onset of distant metastasis, and poor long-term survival (4). The overall survival rates of ACC patients have been reported to be approximately 95%, 75% and 57% for 2, 5, and 7 years, respectively, 80% after 5 years, and 60% after 10 years (5). During the course of the disease, >40% of ACC patients are diagnosed with distant metastases, and a diagnosis of the solid form of ACC is associated with a high risk of mortality (6,7).
At present, the preferred therapeutic method for patients with ACC is complete surgical resection with or without post-operative radiotherapy regardless of the location of the primary tumor (8). Radiotherapy is often administered post-operatively to improve locoregional control or as a primary therapy for unresectable diseases (9). A growing numbers of studies have indicated that treatment methods are associated with the prognosis of ACC patients (10,11). Post-operative radiotherapy has been reported to increase the local control rate by 89–95% within 5 years (12); however, the disease-free survival rates have been reported to decline dramatically at 10 and 15 years (13). It is not yet known whether radiotherapy is needed for ACC patients.
ACC is a kind of rare disease, and due to its scarcity and heterogeneity, it is difficult to explore and gain an understanding of all the histologic subtypes. According to the classification of tumors of the salivary glands of the World Health Organization (WHO), ACC has 22 subtypes with a distinct incidence rates and diverse biological heterogeneity (3,14). Previously, Cavalieri et al. revealed that gender, disease-free interval, lung metastases, liver metastases and bone metastases were factors associated with the prognosis of ACC patients (15). A study indicated that age, primary site, lymph node metastasis, distant metastasis, radiotherapy and surgery were prognostic factors for disease-specific survival of ACC patients (16). The effects of surgery or surgery combined with radiotherapy in the treatment of ACC varies in different subtypes of ACC. Previous studies have evaluated the outcomes of patients receiving surgery or surgery combined with radiotherapy in the treatment of ACC of the head and neck (12,17,18). There was evidence showing that surgery or surgery combined with radiotherapy might improve the survival of ACC patients (12). Other studies also reported that the role of postoperative radiotherapy might be unfavorable prognostic factor for ACC patients in locally advanced lesions or in case of high risk of local relapse (18,19). These findings were controversies and the patients were mainly ACC patients. There is very little evidence of the prognostic effects of surgery and radiotherapy on ACC of the head and neck.
In the present study, the prognostic effects of surgery and radiotherapy on ACC of the head and neck, including the tumor sites of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear, were examined based on the data from the Surveillance, Epidemiology and End Results (SEER) database. The findings of this study might provide insights into the prognosis effects of surgery or radiotherapy on ACC of the head and neck at different tumor sites, which might help the clinicians select better treatment for ACC of head and neck at different primary tumor sites. We present the following article in accordance with the STROBE reporting checklist (available at https://gs.amegroups.com/article/view/10.21037/gs-22-526/rc).
Methods
Study design and participants
In this retrospective cohort study, the data of 2,392 participants with ACC of the head and neck were extracted from the SEER database (www.seer.cancer.gov). The SEER database is the most representative tumor databases in the United States (US), was established by the National Cancer Institute in 1973, and covers about 28% of the US population (20). The SEER database comprises 18 population-based registries that collect the demographic, clinicopathological, and follow-up survival data of different kinds of tumors, especially rare tumors (21). SEER*Stat (version 8.3.6) software was applied to extract the data from the SEER database. The sub-database used had the following designation: “Incidence—SEER 18 Regs Custom Data (with additional treatment fields), Nov 2018 Sub (1975–2016 varying)”.
The approval of the Institutional Review Board was not required for this study, as the SEER data are publicly available. The participants were divided into the salivary gland group (n=1,351), the mouth and oropharynx group (n=563), and the nose, nasal cavity, and middle ear group (n=478). The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013).
Potential confounders
In our study, the following were considered potential confounders: sex, age (years), marriage status (married, alone or other), race (non-Hispanic White, Hispanic, non-Hispanic Black, non-Hispanic Asian or Pacific Islander, non-Hispanic unknown race, or non-Hispanic American Indian/Alaska native), primary location (salivary gland, mouth and oropharynx, or nose, nasal cavity, and middle ear), T stage (T0/T1, T2, T3, T4 or unknown), N stage (N0, N1/N2/N3 or unknown), M stage (M0, M1 or unknown), the American Joint Commission on Cancer (AJCC) grade (I, II, III, IV or unknown), and tumor size (<40, ≥40 mm, or unknown).
Outcome variables and follow-up
The outcome variables for this study were the all-cause death and cancer-specific death of patients. The baseline data were collected in 2004, and the patients were followed-up to 2016. The survival times of all the patients were also recorded. Among the patients, 766 died and 1,626 survived. The patients had a median survival time of 9.92 years.
Statistical analysis
The normally distributed measurement data are described as the mean ± standard deviation (mean ± SD), and the independent sample t-test was used to compare differences between the groups. The non-normally distributed data are expressed as the median and quaternary spacing [M (Q1, Q3)], and the Mann-Whitney U rank-sum test was used to compare differences between the groups. The enumeration data are presented as the number (percentage) [n (%)], and the Chi-square test or Fisher’s exact probability method was used to compare differences between the groups. Bayesian multiple regression was used to fill in the missing data, and a sensitivity analysis was performed to compare the difference between the data before and after filling. Univariate and multivariate Cox regression analyses were conducted to explore the effects of surgery and radiotherapy on the all-cause mortality of ACC of different sites. And Fine-Gray test was applied for assessing the effects of surgery and radiotherapy on the cancer-specific mortality of the ACC patients. In the multivariable Cox regression model exploring the effects of surgery and radiotherapy on the all-cause mortality of ACC of the salivary gland, confounders including sex, marriage status, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy were adjusted. In the multivariable Fine-Gray test model exploring the effects of surgery and radiotherapy on the cancer-specific mortality of ACC of the salivary gland, confounders including race, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy were adjusted. In the multivariable Cox regression model exploring the effects of surgery and radiotherapy on the all-cause mortality of ACC of the mouth and oropharynx, confounders including marriage status, race, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy were adjusted. In the multivariable Fine-Gray test model exploring the effects of surgery and radiotherapy on the cancer-specific mortality of ACC of the mouth and oropharynx, confounders including race, T stage, N stage, M stage, AJCC, tumor size, and chemotherapy were adjusted. In the multivariable Cox regression model exploring the effects of surgery and radiotherapy on the all-cause mortality of ACC of the nose, nasal cavity, and middle ear, confounders including marriage status, N stage, M stage, AJCC, age, tumor size, and chemotherapy were adjusted. In the multivariable Fine-Gray test model exploring the effects of surgery and radiotherapy on the cancer-specific mortality of ACC of the nose, nasal cavity, and middle ear, confounders including T stage, N stage, and M stage were adjusted. The survival of the ACC patients was analyzed via the log-rank test, and the results were displayed by plotting Kaplan-Meier survival curves. R 4.1.1 was used for the data analyses, and a two-sided P value <0.05 was considered statistically significant.
Results
Comparisons of the characteristics of patients with ACC of the salivary gland, mouth and oropharynx, and nose, nasal cavity, and middle ear
In this study, the data of 2,726 patients were extracted from the SEER database. Among them, those who were lost to follow-up or lacked data about the treatment methods were excluded (n=334). Ultimately, the data of 2,392 patients were analyzed. The average age of all patients was 58.91 years. The average age of patients in the ACC of the salivary gland group, the ACC of the mouth and oropharynx group, and the ACC of the nose, nasal cavity, and middle ear group differed significantly (58.04 vs. 60.70 vs. 59.28 years, respectively). The percentages of patients with ACC of the salivary gland, mouth and oropharynx, and nose, nasal cavity, and middle ear at different T stage (χ2=235.643, P<0.001), N stage (χ2=112.668, P<0.001), M stage (χ2=78.656, P<0.001), and AJCC grade (χ2=183.145, P<0.001) differed. Among the patients, 1,280 patients (53.51%) were aged <60 years. The percentages of patients with ACC of the salivary gland, mouth and oropharynx, and nose, nasal cavity and middle ear in different age groups differed (χ2=6.660, P=0.036). The proportions of patients who died for all-cause (χ2=37.584, P<0.001) and cancer-specific (χ2=40.243, P<0.001) reasons differed among patients in the ACC of the salivary gland group, the ACC of the mouth and oropharynx group, and the ACC of the nose, nasal cavity, and middle ear group (see Table 1).
Table 1
Variables | Total (n=2,392) | Salivary gland (n=1,351) | Mouth and oropharynx (n=563) | Nose, nasal cavity, and middle ear (n=478) | Statistics | P |
---|---|---|---|---|---|---|
Gender, n (%) | χ2=4.706 | 0.095 | ||||
Male | 986 (41.22) | 531 (39.30) | 246 (43.69) | 209 (43.72) | ||
Female | 1,406 (58.78) | 820 (60.70) | 317 (56.31) | 269 (56.28) | ||
Age, years, mean ± SD | 58.91±16.09 | 58.04±16.57 | 60.70±15.61 | 59.28±15.06 | F=5.602 | 0.004 |
Marriage, n (%) | χ2=4.575 | 0.334 | ||||
Married | 1,418 (59.28) | 786 (58.18) | 343 (60.92) | 289 (60.46) | ||
Alone | 440 (18.39) | 268 (19.84) | 95 (16.87) | 77 (16.11) | ||
Other | 534 (22.32) | 297 (21.98) | 125 (22.20) | 112 (23.43) | ||
Race, n (%) | χ2=10.820 | 0.372 | ||||
Non-Hispanic White | 1,521 (63.59) | 879 (65.06) | 352 (62.52) | 290 (60.67) | ||
Hispanic (all races) | 307 (12.83) | 164 (12.14) | 73 (12.97) | 70 (14.64) | ||
Non-Hispanic Black | 258 (10.79) | 131 (9.70) | 69 (12.26) | 58 (12.13) | ||
Non-Hispanic Asian or Pacific Islander | 269 (11.25) | 159 (11.77) | 56 (9.95) | 54 (11.30) | ||
Non-Hispanic unknown race | 22 (0.92) | 12 (0.89) | 7 (1.24) | 3 (0.63) | ||
Non-Hispanic American Indian/Alaska Native | 15 (0.63) | 6 (0.44) | 6 (1.07) | 3 (0.63) | ||
T stage, n (%) | χ2=235.643 | <0.001 | ||||
T0 or T1 | 611 (25.54) | 372 (27.54) | 177 (31.44) | 62 (12.97) | ||
T2 | 492 (20.57) | 335 (24.80) | 110 (19.54) | 47 (9.83) | ||
T3 | 394 (16.47) | 274 (20.28) | 29 (5.15) | 91 (19.04) | ||
T4 | 632 (26.42) | 251 (18.58) | 180 (31.97) | 201 (42.05) | ||
Unknown | 263 (10.99) | 119 (8.81) | 67 (11.90) | 77 (16.11) | ||
N stage, n (%) | χ2=112.668 | <0.001 | ||||
N0 | 1,915 (80.06) | 1,073 (79.42) | 478 (84.90) | 364 (76.15) | ||
N1/N2/N3 | 277 (11.58) | 203 (15.03) | 49 (8.70) | 25 (5.23) | ||
Unknown | 200 (8.36) | 75 (5.55) | 36 (6.39) | 89 (18.62) | ||
M stage, n (%) | χ2=78.656 | <0.001 | ||||
M0 | 2,078 (86.87) | 1,190 (88.08) | 504 (89.52) | 384 (80.33) | ||
M1 | 190 (7.94) | 122 (9.03) | 36 (6.39) | 32 (6.69) | ||
Unknown | 124 (5.18) | 39 (2.89) | 23 (4.09) | 62 (12.97) | ||
AJCC, n (%) | χ2=183.145 | <0.001 | ||||
I | 557 (23.29) | 343 (25.39) | 163 (28.95) | 51 (10.67) | ||
II | 426 (17.81) | 279 (20.65) | 101 (17.94) | 46 (9.62) | ||
III | 350 (14.63) | 246 (18.21) | 28 (4.97) | 76 (15.90) | ||
IV | 795 (33.24) | 369 (27.31) | 206 (36.59) | 220 (46.03) | ||
Unknown | 264 (11.04) | 114 (8.44) | 65 (11.55) | 85 (17.78) | ||
Age, n (%) | χ2=6.660 | 0.036 | ||||
<60 | 1,280 (53.51) | 752 (55.66) | 278 (49.38) | 250 (52.30) | ||
≥60 | 1,112 (46.49) | 599 (44.34) | 285 (50.62) | 228 (47.70) | ||
Tumor size, mm, n (%) | χ2=240.028 | <0.001 | ||||
<40 | 1,584 (66.22) | 991 (73.35) | 412 (73.18) | 181 (37.87) | ||
≥40 | 406 (16.97) | 211 (15.62) | 72 (12.79) | 123 (25.73) | ||
Unknown | 402 (16.81) | 149 (11.03) | 79 (14.03) | 174 (36.40) | ||
All-cause, n (%) | χ2=37.584 | <0.001 | ||||
Alive | 1,626 (67.98) | 959 (70.98) | 398 (70.69) | 269 (56.28) | ||
Dead | 766 (32.02) | 392 (29.02) | 165 (29.31) | 209 (43.72) | ||
Cancer-specific, n (%) | χ2=40.243 | <0.001 | ||||
Alive | 1,626 (67.98) | 959 (70.98) | 398 (70.69) | 269 (56.28) | ||
Dead of this cancer | 441 (18.44) | 227 (16.80) | 87 (15.45) | 127 (26.57) | ||
Dead of other cause | 325 (13.59) | 165 (12.21) | 78 (13.85) | 82 (17.15) |
ACC, adenoid cystic carcinoma; SD, standard deviation; AJCC, the American Joint Commission on Cancer.
The effects of surgery and radiotherapy on the survival of patients with ACC of the salivary gland
As Table 2 shows, the univariate analysis revealed that surgery [hazard ratio (HR) =0.25; 95% confidence interval (CI): 0.20–0.31] and radiotherapy [HR =0.55; 95% CI: 0.45–0.67] might be associated with the all-cause mortality of patients with ACC of the salivary gland. After adjusting for a number of covariables, including gender, marital status, T stage, N stage, M stage, AJCC grade, age, tumor size, and chemotherapy, the results showed that surgery was associated with a decreased risk of all-cause mortality (HR =0.51; 95% CI: 0.36–0.71). However, no significant association was found between radiotherapy and the risk of all-cause mortality (P>0.05). The results of the univariate analysis are set out in Table S1. Additionally, the univariate analysis results showed that both surgery and radiotherapy might be correlated with the cancer-specific mortality of patients with ACC of the salivary gland. Notably, patients with ACC of the salivary gland who received surgery had a decreased risk of cancer-specific mortality (HR =0.57; 95% CI: 0.34–0.97), but after adjusting for variables with a P value <0.1 in the univariate analysis, the effects of radiotherapy on the cancer-specific mortality of patients was not statistically significant (see Table S2). As Figure 1 shows, the overall survival probability of the patients with ACC of the salivary gland who received surgery was higher than that of those who did not receive surgery. Patients with ACC of the salivary gland who received radiotherapy had a lower survival probability than those who did not receive radiotherapy (see Figure 2).
Table 2
Variables | Groups | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | P | HR (95% CI) | P | |||
All-cause mortality | ||||||
Surgery | Yes (vs. no) | 0.25 (0.20, 0.31) | <0.001 | 0.51 (0.36, 0.71) | <0.001 | |
Radiotherapy | Yes (vs. no) | 0.55 (0.45, 0.67) | <0.001 | 0.81 (0.63, 1.04) | 0.103 | |
Cancer-specific mortality* | ||||||
Surgery | Yes (vs. no) | 0.29 (0.21, 0.40) | <0.001 | 0.57 (0.34, 0.97) | 0.037 | |
Radiotherapy | Yes (vs. no) | 0.75 (0.58, 0.98) | 0.036 | 1.14 (0.78, 1.67) | 0.490 |
Multivariate analysis adjusting for sex, marriage status, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy. *, multivariate analysis adjusting for race, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy. ACC, adenoid cystic carcinoma; HR, hazard ratio; CI, confidence interval; AJCC, the American Joint Commission on Cancer.
The effects of surgery and radiotherapy on patients with ACC of the mouth and oropharynx
According to the univariate analysis results, surgery (HR =0.32; 95% CI: 0.24–0.42) and radiotherapy (HR =0.61; 95% CI: 0.45–0.84) might be associated with the all-cause mortality of patients with ACC of the mouth and oropharynx. The multivariate analysis revealed a 0.53-fold decrease in the risk of all-cause mortality in patients with ACC of the mouth and oropharynx who underwent surgery (HR =0.47; 95% CI: 0.28–0.78). Radiotherapy did not have a statistically significant effect on the risk of all-cause mortality of patients with ACC of the mouth and oropharynx (P>0.05) (see Table 3). However, surgery was correlated with the cancer-specific mortality of patients with ACC of the mouth and oropharynx (HR =0.42; 95% CI: 0.26–0.66). The results of the multivariate analysis (see Table 3) showed that after adjusting for confounding variables, surgery was a protective factor for the risk of cancer-specific mortality of patients with ACC of the mouth and oropharynx (HR =0.70; 95% CI: 0.33–1.50). No statistically significant association was found between radiotherapy and the risk of cancer-specific mortality of patients with ACC of the mouth and oropharynx (P>0.05). The detailed information on adjusted confounders of all-cause mortality and cancer-specific mortality in patients with ACC of the mouth and oropharynx are shown in Table S3 and Table S4, respectively. The overall survival probability of patients with ACC of the mouth and oropharynx who received surgery was higher than that of those who did not receive surgery (see Figure 3). Patients with ACC of the mouth and oropharynx who received radiotherapy had a lower survival probability than those who did not receive radiotherapy (see Figure 4).
Table 3
Variables | Groups | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | P | HR (95% CI) | P | |||
All-cause mortality | ||||||
Surgery | Yes (vs. no) | 0.32 (0.24, 0.42) | <0.001 | 0.47 (0.28, 0.78) | 0.003 | |
Radiotherapy | Yes (vs. no) | 0.61 (0.45, 0.84) | 0.002 | 1.00 (0.65, 1.54) | 0.998 | |
Cancer-specific mortality* | ||||||
Surgery | Yes (vs. no) | 0.42 (0.26, 0.66) | <0.001 | 0.70 (0.33, 1.50) | 0.360 | |
Radiotherapy | Yes (vs. no) | 0.94 (0.62, 1.42) | 0.75 | 1.35 (0.74, 2.44) | 0.370 |
Multivariate analysis adjusting for marriage status, race, T stage, N stage, M stage, AJCC, age, tumor size, and chemotherapy. *, multivariate analysis adjusting for race, T stage, N stage, M stage, AJCC, tumor size, and chemotherapy. ACC, adenoid cystic carcinoma; HR, hazard ratio; CI, confidence interval; AJCC, the American Joint Commission on Cancer.
The effects of surgery and radiotherapy on patients with ACC of the nose, nasal cavity, and middle ear
In relation to patients with ACC of the nose, nasal cavity, and middle ear, the univariate analysis showed that surgery (HR =0.32; 95% CI: 0.24–0.42) and radiotherapy (HR =0.39; 95% CI: 0.30–0.52) might be associated with the risk of all-cause mortality of patients with ACC of the nose, nasal cavity, and middle ear. After adjusting for confounding variables with a P value <0.1 in the univariate analysis, a decreased risk of all-cause mortality was observed in patients with ACC of the nose, nasal cavity, and middle ear who underwent surgery (HR =0.46; 95% CI: 0.30–0.70). After adjusting for confounding variables, the risk of cancer-specific mortality in patients with ACC of the nose, nasal cavity, and middle ear was also reduced in patients who underwent surgery (HR =0.35; 95% CI: 0.20–0.61) (Table 4). The detailed information of adjusted confounders of all-cause mortality and cancer-specific mortality in patients with ACC of the nose, nasal cavity, and middle ear are shown in Tables S5,S6, respectively. The overall survival probability of patients with ACC of the nose, nasal cavity, and middle ear who underwent surgery was higher than those who did not undergo surgery (see Figure 5). Patients with ACC of the nose, nasal cavity, and middle ear who received radiotherapy had a lower survival probability than who did not receive radiotherapy (see Figure 6).
Table 4
Variables | Groups | Univariate | Multivariate | |||
---|---|---|---|---|---|---|
HR (95% CI) | P | HR (95% CI) | P | |||
All-cause mortality | ||||||
Surgery | Yes (vs. no) | 0.32 (0.24, 0.42) | <0.001 | 0.46 (0.30, 0.70) | <0.001 | |
Radiotherapy | Yes (vs. no) | 0.39 (0.30, 0.52) | <0.001 | 0.75 (0.50, 1.12) | 0.165 | |
Cancer-specific mortality* | ||||||
Surgery | Yes (vs. no) | 0.34 (0.24, 0.49) | <0.001 | 0.35 (0.20, 0.61) | <0.001 | |
Radiotherapy | Yes (vs. no) | 0.53 (0.37, 0.74) | <0.001 | 1.07 (0.62, 1.84) | 0.810 |
Multivariate analysis adjusting for marriage status, N stage, M stage, AJCC, age, tumor size, and chemotherapy, *, multivariate analysis adjusting for T stage, N stage, and M stage. ACC, adenoid cystic carcinoma; HR, hazard ratio; CI, confidence interval; AJCC, the American Joint Commission on Cancer.
Discussion
In this study, the prognostic effects of surgery and radiotherapy on ACC of the head and neck, including the tumor sites of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear, were evaluated. The results indicated that surgery was associated with a decreased risk of all-cause mortality and cancer-specific mortality in ACC patients with the tumor sites of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear. Radiotherapy was not statistically associated with the all-cause mortality and cancer-specific mortality of patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear. The findings of this study might provide a reference for the treatment of ACC of the head and neck.
Previously, Ciccolallo et al. conducted a study based on a European population and found that the survival of ACC patients might differ depending on the different primary sites of the tumor, and that ACC of the nasal cavity was associated with an increased risk of death (14). In our study, the all-cause mortality rate of patients with ACC of the nose, nasal cavity, and middle ear was 26.57% and the cancer-specific mortality was 17.15%, which were higher than the rates of patients with ACC of the salivary gland, and mouth and oropharynx. Further research needs to be conducted to determine whether surgery or radiotherapy affect the prognosis of patients with ACC of different primary sites.
Currently, there is no consensus about the appropriate treatment for ACC of the head and neck. The preferred treatment modalities for patients with ACC of the head and neck is surgical excision (22). Surgery has been widely accepted as a prognostic factor for ACC patients, and the overall survival of ACC patients who receive surgery has been shown to be improved (2,16). Meyers et al. showed that surgery is the preferred treatment for ACC to achieve complete resection regardless of the primary location (23). Similarly, our study showed that surgery was associated with a decreased risk of mortality in patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear.
Post-operative radiotherapy is often recommended for patients with ACC of the head and neck to reduce local relapse (24). Some previous studies have shown that post-operative radiotherapy improves the survival of ACC patients (25,26). However, another study has shown post-operative radiotherapy has no significant effect on the prognosis of ACC patients. A review by Mur et al. identified that the 5-year disease-specific survival of patients with ACC of the larynx was 92.9% in those receiving surgery alone and 74.3% in those receiving surgery and radiotherapy, but no significant difference in survival was found among those receiving both surgery and radiotherapy (27). Lloyd et al. found that post-operation radiotherapy does not significantly affect the survival outcomes of patients (28). Similarly, another study evaluated the incidence rates and survival outcomes of patients diagnosed with ACC of the head and neck and found that adjuvant radiotherapy confers little survival advantage for those patients (29). In the present study, we found that radiotherapy had no statistically significant effect on the survival of patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear.
In the present study, the prognostic effect of surgery and radiotherapy on ACC of the head and neck, including the tumor sites of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear, was evaluated. Due to the rarity of ACC, sample size may be an issue in the evaluation of the prognostic roles of surgery and radiotherapy. Our study extracted data from the SEER database for 2,392 participants with ACC of the head and neck. Thus, our results were based on a relatively large population, and might be more reliable than the results of other studies. Additionally, prognostic effects of different primary tumor sites of ACC of the head and neck were measured, which might provide a reference for clinicians in selecting the optimal treatments for ACC patients with different primary tumor sites. In the current study, surgery was found to be associated with a decreased risk of mortality in patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear. Radiotherapy was not statistically associated with the mortality of patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear. In recent years, research has shown that cancers are overtreated (30,31). The findings of our study should serve to remind clinicians that radiotherapy should be used with caution in ACC patients.
The current study had several limitations. First, all the data of the patients were extracted from the SEER database, and some variables that may affect the outcomes of ACC patients, including pathological factors, and cancer biomarkers, were not analyzed. Second, the sample size in some subgroups was small; thus, the results still required validation by prospective studies.
Conclusions
The present study assessed the prognostic effects of surgery and radiotherapy on ACC of the head and neck. The results indicated that surgery was associated with a decreased risk of mortality, while radiotherapy was not statistically associated with the risk of mortality in patients with ACC of the salivary gland, oropharynx, and nose, nasal cavity, and middle ear. The findings of this study might provide a reference for the treatment of ACC of the head and neck.
Acknowledgments
Funding: None.
Footnote
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at https://gs.amegroups.com/article/view/10.21037/gs-22-526/rc
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://gs.amegroups.com/article/view/10.21037/gs-22-526/coif). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013).
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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