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Yeganegi M, Behnampour A, Mirzaei F, Tabrizi A, Zokaee H. Psychological status in Head and Neck Cancer Patients with Xerostomia due to Radiotherapy. Jorjani Biomed J 2020; 8 (4) :26-33
URL: http://goums.ac.ir/jorjanijournal/article-1-765-en.html
1- General Dentist, Gorgan, Iran
2- Golestan University of Medical Sciences, Gorgan, Iran
3- Student Research Committee, Golestan University of Medical Sciences, Gorgan, Iran
4- Dental Research Center, Golestan University of Medical Sciences, Gorgan , halehzokaee2020@gmail.com
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Introduction
Head and Neck Cancer (HNC) is the seventh most common cancer in the world with an estimation of more than 550,000 occurrences and 380,000 deaths annually. It consists of malignancies originating from the skin, nasal cavity, paranasal sinuses, oral cavity, salivary glands, throat and larynx which includes squamous cell carcinoma, malignant salivary gland tumors, malignant lesions of the jaw, nasopharyngeal carcinoma, basal cell carcinoma, malignant melanoma, Non-Hodgkin's lymphoma, and soft tissue sarcomas (1, 2).
Treatment methods for HNC patients include surgery, chemotherapy and radiotherapy. Radiotherapy is a reliable way to treat HNC patients. Salivary glands would be more protected in advanced types of radiotherapy; however, it can lead to complications such as mucositis, difficulty in swallowing, trismus, tooth decay, and hyposalivation. When salivary flow below than 0.1-1.2 ml/min, it is defined as hyposalivation in such these cases (radiotherapy induced hyposalivation) which is the most suffering complication for patients (3-5).
The prevalence of hyposalivation has been estimated about 20%, mostly induced by medication and it tends to be more common among women (5). Preventing the occurrence of hyposalivation is an important subject since there is no effective treatment for it and as a result patient's quality of life is affected negatively by impairment of their physical function, social life and cognitive abilities. Based on previous studies, patients' QOL scores have decreased at least 25% after radiotherapy (6-8).
Psychological status as one of the QOL indices can be reduced by hyposalivation. (9). Poor prognosis makes HNC patients suffer from psychological imbalance more than any other cancer patients and hyposalivation exacerbates their psychological disorders including depression, anxiety, and behavioural disorders. Therefore, diagnosis and treatment of these complications improve QOL and life expectancy in HNC patients (10, 11).
Few articles have studied the subject of HNC-related psychological status and also most of the studies are conducted on physical side effects of cancer treatment and their impact on the quality of life while mental side effects were disregarded (12-15) accordingly, this study aimed to assess the psychological status of the HNC patients after at least one week of receiving radiotherapy.
Materials and Methods
This cross-sectional study with the aim of assessing the psychological status of patients with hyposalivation due to radiotherapy was performed in 5 Azar hospital from 1397 to 1398. Inclusion criteria were as follows: patients with no history of mental illness, at least one week after radiotherapy and no medical record of using medication including analgesics, anticholinergics, antidepressants, antihistamines, antihypertensive, anti-Parkinson, antipsychotics, anticonvulsants, cytotoxic, diuretics, muscle relaxants, sedatives and antidepressants (2).
This study was conducted on 44 patients and oral informed consent was obtained (ethical code: IR.GOUMS.1397.205).
Patients were asked to fill out the GHQ-28 questionnaire. General Health Questionnaire-28 (GHQ-28) is a 28-item measure for psychological status. The first part of the questionnaire includes demographic and clinical information, and the second part includes several questions about psychological status. It was developed by Goldberg, and its validity and reliability was confirmed in 1978. The GHQ-28 is divided into 4 subscales and each subscale has 7 questions. These subscales are Somatic symptoms (question 1-7), anxiety/insomnia (question 8-14), social dysfunction (question 15-21), and severe depression (question 22-28). All the questions of GHQ-28 have 4 options. In this study the Likert scoring
method was used. According to this method, the scoring of each question is (0.1.2.3); therefore the total score of an individual varies from 0 to 84. Lower score indicates a better psychological status (16, 17). Questions number 1, 15, 17, 21 are scored inversely in the final scoring since they are reverse questions.
Descriptive statistics including frequency, percentage, mean, standard deviation and plotting of frequency distribution tables were used to describe the data. Parametric and non-parametric inferential tests and Spss18 software were used to analyse the data. Shapiro-Wilk test was used to evaluate the normality of data distribution. The significance level was considered 0.05 in all tests.
Result
A total of 44 patients participated in this study, of whom 26 (59.9%) were men and 18 (40.91) were women. A comparison between the mean components of psychological status revealed that depression was in the best and anxiety/insomnia in the worst condition (Table 1).
Table 1: Interaction between hyposalivation and psychological status on GHQ-28 scores
Mean ± SD score Subscales
7.39 ± 3.75 Physical health
6.16 ± 3.25 Social functioning
12.64 ± 2.99 Anxiety/insomnia
1.33 ± 1.54 depression
27.50 ± 8.21 Total







Aging caused an increase in the overall score of both general psychological status and it's components except for depression; but there was no significant relationship between patients' age and psychological status, physical health, social functioning, anxiety/insomnia and depression. The mean psychological status was 26.38±8.71 in men and 29.11±7.36 in women and the difference between genders was not statistically significant (Table 2).
There was no statistical significant difference between the 4 components of psychological status and gender (Table 3).
 
Table 2: Spearman’s correlation coefficient between subscales of GHQ-28 and age
Age Depression Anxiety/ insomnia Social functioning Physical health  
0.224 0.464 0.551 0.874 0.866 Total
0.225 0.382 0.261 0.727   Physical health
0.212 0.320 0.335     Social functioning
0.233 0.018       Anxiety/insomnia
-0.018         Depression










Table 3: Relation between GHQ-28 subscales and female and male patients

 
P-Value Mean (SD) Gender  
0.869 7.30 (3.82) Male Physical health
7.50 (3.74) Female
0.128 5.53 (3.64) Male Social functioning
7.05 (2.73) Female
0.798 12.53 (3.00) Male Anxiety/insomnia
12.77 (3.05) Female
0.136 1.00 (1.13) Male Depression
1.77 (1.92) Female
0.28 26.38 (8.71) Male Total
29.11 (7.36) Female
 

According to the Spearman test, a significant direct correlation was observed between physical health status and social functioning (P <0.001), physical health status and depression (P = 0.011), anxiety/insomnia status and social functioning (P = 0.026) and also depression and social functioning (P = 0.034) (Table 2).
Among participants, there were 4 illiterate people, 9 primary educated, 11 middle school educated, 12 diploma graduated and 7 higher level educated. The highest scores of psychological status, physical condition, anxiety/insomnia and social functioning status were related to illiterate people, while depression had a higher score among people with diploma.
Discussion
This study aimed to evaluate the psychological status of HNC patients with hyposalivation due to radiotherapy. In this study, the average psychological status was reported to be 27.50. According to Ebrahimi et al.'s study, the clinical cut-off point for the GHQ-28 questionnaire in Iran was 24, so cancer and its complications overshadowed the psychological status of the subjects in this study(16).
In different studies, different questionnaires such as mental component summary (MCS), Hospital anxiety and depression scale, PSQI, ESS, hospital anxiety and depression scale (HADS), Taiwanese depression questionnaire (THQ) and also clinical interview has been used for assessing the psychological status of HNC patients (5, 18-22).
In a study conducted by Nielson et al., the prevalence of depression was initially 15%, increased to 29% by 3 weeks after treatment, and decreased to 8% at the end of 18 months. The prevalence of anxiety was 20% at the beginning and reached 17% 3 weeks after treatment and 22% at the end of 18 months (19). In the Lopez-Jornet study, hyposalivation was significantly associated with depression (5). In the study of Pelland et al., 345 patients (25.6%) had moderate to severe anxiety and 120 patients (8.9%) had moderate to severe depression (20). In the study conducted by Lee et al., 13 patients (14%) had depression after 6 months, which had increased compared to the beginning of treatment (8.5%) (21). In the study of Wu et al., Pre-treatment anxiety rate was high which decreased over time (from 27.3% to 6.4% and then 3.3%) and the rate of pre-treatment depression was 8.5% and then decreased to 24.5% and 14%, respectively, and hyposalivation was significantly associated with depression (22). In the study of Astrup GL et al., mental health status in HNC patients decreased and after 6 months, returned to the previous state (18). In the study of Nikoloudi et al., Depression and anxiety in HNC patients significantly increased after radiotherapy (23).
This significant increase between radiation-induced hyposalivation and depression was also observed in the present study. Comparison between that study and ours showed that cancer individually makes no significant effect on psychological, but the side effects of cancer and radiotherapy such as hyposalivation can result in depression and mental illness. In most studies, the rate of hyposalivation was closely related to the psychological status, however after a long period and partial return for saliva production ability, psychological status and its components have been improved after 1 year of radiotherapy and approached to primary state (5, 19, 21, 22).
In the present study, as age increased, psychological status and its components such as anxiety, insomnia, physical health problems and social functioning issues increased. These results were in contrast to Nielson et al.'s study, in which younger patients were more anxious (19).
In Malekian et al.'s study, depression rate was higher in 50-65 years old patients in comparison with other age groups (24). In the study of Rajabizadeh et al., the prevalence of depression was significantly associated with ages over 45 years (25).
It is very difficult to diagnose depressive mood indicators in the elderly; since the symptoms of depression in the elderly vary from those in adolescence. These differences can be originated from depressing experiences such as heartburn, painful illness, or cognitive impairment such as memory loss. Depression in the elderly is the second disability after physical causes. People who have had a history of depression during their lifetime show more depression in older ages (26).
In this study, the psychological status average among men and women was not statistically significant. Other components (depression, social functioning, anxiety/insomnia, and physical health) were not statistically significant despite being lower in men. In the study of Malekian et al., despite the higher prevalence of anxiety and depression in women, no statistically significant differences were observed between the two groups (24). In the study of Rajabizadeh et al., No significant relationship was observed between gender, severity and prevalence of depression (25).
Also in the study of Astrup GL et al., There was no significant difference between mental health and gender (P = 0.348) (18). In the study conducted by Linden et al., the prevalence of anxiety in women was significantly higher (P <0.001) that can be explained by women's higher tendency to express emotions (27). The study by Pelland et al. did not agree with the results of our study in this regard (20).
Social anxiety is the clinically significant anxiety due to social or functional situations that often leads to avoidant behavior. Epidemiological reports have estimated that women more likely develop social anxiety disorders, like other anxiety disorders; but few studies equate this ratio. The reason for this discrepancy may be the difference in diagnostic characteristics and examination indexes. In other words, this heterogeneity in the relationship between social anxiety and gender is always seen in the articles. Researchers have found that masculinity is negatively related to anxiety. Masculinity is negatively related to general levels of fear and panic such as fear of failure and criticism and fear of the unknown and medical fear; while there is a direct relationship between femininity and anxiety as well as sensitivity to anxiety symptoms. As a result, gender role is a mediator between femininity and sensitivity to anxiety symptoms (28).
Among the patients of this study, the highest scores of psychological status, physical condition, anxiety/insomnia and social functioning were in illiterate individuals, while the highest scores of depression were in those with diploma degree. In the study of Naseri et al, patients with higher education had higher rates of depression (29).
In the study of Rajabizadeh et al., a significant relationship was observed between the level of education and depression of oncology patients, so with increasing education, the severity of depression decreased (P <0.001) (25). There was a significant relationship between the rate of depression in women with breast cancer and the level of education (P = 0.001) (28). In the study of WU et al., no significant relationship between anxiety and depression and education level and other demographic characteristics was found (22).
Conclusion
To justify the results of this study, it can be stated that an increase in a person's level of education increases access to information resources and raises the level of knowledge and awareness about cancer and ways to treat it, and despite positive results, this can also make an individual sad and depressed.
The limitation of the present study was difficulty in assessing patients due to their poor physical condition. In this study, only the mental status of HNC patients was evaluated. It is recommended to consider the psychological status of patients with various head and neck cancers treatment.

References
1. Fitzmaurice C, Allen C, Barber RM, Barregard L, Bhutta ZA, Brenner H, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 32 cancer groups, 1990 to 2015: a systematic analysis for the global burden of disease study. JAMA Oncol. 2017;3(4):524-48.
2. Glick M. Burket's oral medicine: PMPH USA; 2015.
3. Kırca K, Kutlutürkan S. Symptoms of patients with head and neck cancers undergoing radiotherapy. Eur J Cancer Care (Engl). 2017;26(6):e12584.
4. Braam PM, Terhaard CH, Roesink JM, Raaijmakers CP. Intensity-modulated radiotherapy significantly reduces xerostomia compared with conventional radiotherapy. Int J RadiatOncolBiol Phys. 2006;66(4):975-80.
5. Lopez-Jornet P, Lucero Berdugo M, Fernandez-Pujante A, Lavella C Z, Silvestre FJ. Sleep quality in patients with xerostomia: a prospective and randomized case-control study. ActaOdontol Scand.2016;74(3):224-8.
6. Wijers OB, Levendag PC, Braaksma MM, Boonzaaijer M, Visch LL, Schmitz PI. Patients with head and neck cancer cured by radiation therapy: A survey of the dry mouth syndrome in long‐term survivors. Head Neck. 2002;24(8):737-47.
7. Almståhl A, Alstad T, Fagerberg‐Mohlin B, Carlén A, Finizia C. Explorative study on quality of life in relation to salivary secretion rate in patients with head and neck cancer treated with radiotherapy. Head Neck. 2016;38(5):782-91.
8. Allal AS, Dulguerov P, Bieri S, Lehmann W, Kurtz JM. Assessment of quality of life in patients treated with accelerated radiotherapy for laryngeal and hypopharyngeal carcinomas. Head Neck. 2000;22(3):288-93.
9. Organization WH. WHOQOL-BREF: introduction, administration, scoring and generic version of the assessment: field trial version, December 1996. WHO, 1996.
10. Robinson D, Renshaw C, Okello C, Møller H, Davies E. Suicide in cancer patients in South East England from 1996 to 2005: a population-based study. Br J Cancer. 2009;101(1):198-201.
11. Kallay E, Dégi CL, Vincze AE. Dysfunctional attitudes, depression and quality of life in a sample of Romanian. J CognBehavPsychother. 2007;7(1):95-106.
12. Rabiei M, Rahimi A, KazemnezhadLeyli E, Jalalian B, Massoudi Rad S. Complication of post radiation in patients with head and neck cancer. J GorganUniv Med Sci. 2014;16(2):114-20.
13. Chambers MS, Garden AS, Kies MS, Martin JW. Radiation‐induced xerostomia in patients with head and neck cancer: pathogenesis, impact on quality of life, and management. Head Neck. 2004;26(9):796-807.
14. Duncan GG, Epstein JB, Tu D, Sayed SE, Bezjak A, Ottaway J, et al. Quality of life, mucositis, and xerostomia from radiotherapy for head and neck cancers: a report from the NCIC CTG HN2 randomized trial of an antimicrobial lozenge to prevent mucositis. Head Neck. 2005;27(5):421-8.
15. Pow EH, Kwong DL, McMillan AS, Wong MC, Sham JS, Leung LH, et al. Xerostomia and quality of life after intensity-modulated radiotherapy vs. conventional radiotherapy for early-stage nasopharyngeal carcinoma: initial report on a randomized controlled clinical trial. Int J RadiatOncolBiol Phys. 2006;66(4):981-91.
16. Ebrahimi A, Molavi H, Moosavi G, Bornamanesh A, Yaghobi M. Psychometric Properties and Factor Structure of General Health Questionnaire 28 (GHQ-28) in Iranian Psychiatric Patients. J Res Behav Sci. 2007;5(1):5–11.
17. Nazifi M, Mokarami H, Akbaritabar A, FarajiKujerdi M, Tabrizi R, Rahi A. Reliability, validity and factor structure of the persian translation of general health questionnire (ghq-28) in hospitals of kerman university of medical sciences. J FasaUniv Med Sci. 2014;3:336–42.
18. Astrup GL, Rustøen T, Hofsø K, Gran JM, Bjordal K. Symptom burden and patient characteristics: Association with quality of life in patients with head and neck cancer undergoing radiotherapy. Head Neck. 2017;39(10):2114-26.
19. Neilson K, Pollard A, Boonzaier A, Corry J, Castle D, Smith D, et al. A longitudinal study of distress (depression and anxiety) up to 18 months after radiotherapy for head and neck cancer. Psychooncology. 2013;22(8):1843-8.
20. Pelland M, Lambert L, Filion E, Bahig H, Beaudry M, Ouellette A, et al., editors. Depression, anxiety and claustrophobia in patients undergoing radiotherapy for head and neck cancer. RadiotherOncol. 2017 May 1;123(2):318-9.
21. Lee Y, Wu Y-S, Chien C-Y, Fang F-M, Hung C-F. Use of the Hospital Anxiety and Depression Scale and the Taiwanese Depression Questionnaire for screening depression in head and neck cancer patients in Taiwan. Neuropsychiatr Dis Treat. 2016;12:2649.
22. Wu Y-s, Lin P-Y, Chien C-Y, Fang F-M, Chiu N-M, Hung C-F, et al. Anxiety and depression in patients with head and neck cancer: 6-month follow-up study. Neuropsychiatr Dis Treat. 2016;12:1029.
23. Nikoloudi M, Lymvaios I, Zygogianni A, Parpa E, Strikou D-A, Tsilika E, et al. Quality of life, anxiety, and depression in the head-and-neck cancer patients, undergoing intensity-modulated radiotherapy treatment. Indian J Palliat Care. 2020;26(1):54.
24. Malekian A, Alizadeh A, Ahmadzadeh GH. Anxiety and Depression in Cancer Patients. J Res Behavior Sci. 2007;5:115–118.
25. Rajabizadeh G, Mansoori SM, Shakibi MR, Ramazani MR. Determination of Factors Related to Depression in Cancer Patients of the Oncology Ward in Kerman. J Kerman Univ Med Sci. 2005;12(2):142-7.
26. Norton MC, Singh A, Skoog I, Corcoran C, Tschanz JT, Zandi PP, et al. Church attendance and new episodes of major depression in a community study of older adults: the Cache County Study. J Gerontol B PsycholSciSoc Sci. 2008;63(3):P129-P37.
27. Linden W, Vodermaier A, MacKenzie R, Greig D. Anxiety and depression after cancer diagnosis: prevalence rates by cancer type, gender, and age. J Affect Disord. 2012;141(2-3):343-51.
28. AliakbariDehkordi M, Zare H, AsgharnejadFarid A, Hashemian R. Investigations of the Relation Between Social Anxiety, Cognitive and Behavioral Aspect of It and Sex and Gender-Role in Adolescence. Iran J PsychiatrClin Psychol. 2017;22(4):340-7.
29. Naseri N, Taleghani F. Depression in cancer patients: the role of demographic variables. IJCA. 2019;1(1):55-61.
How to cite:
Yeganegi M, Behnampour A, Mirzaei F, Tabrizi A, Zokaee,H. Psychological status in Head and Neck Cancer Patients with Xerostomia due to Radiotherapy. Jorjani Biomedicine Journal. 2020; 8(4): 26-33.
 
 
Type of Article: Brief Report | Subject: General medicine
Received: 2020/10/1 | Accepted: 2020/10/15 | Published: 2020/11/30

References
1. Fitzmaurice C, Allen C, Barber RM, Barregard L, Bhutta ZA, Brenner H, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 32 cancer groups, 1990 to 2015: a systematic analysis for the global burden of disease study. JAMA Oncol. 2017;3(4):524-48. [view at publisher] [DOI] [Google Scholar]
2. Glick M. Burket's oral medicine: PMPH USA; 2015. [view at publisher] [Google Scholar]
3. Kırca K, Kutlutürkan S. Symptoms of patients with head and neck cancers undergoing radiotherapy. Eur J Cancer Care (Engl). 2017;26(6):e12584. [view at publisher] [DOI] [Google Scholar]
4. Braam PM, Terhaard CH, Roesink JM, Raaijmakers CP. Intensity-modulated radiotherapy significantly reduces xerostomia compared with conventional radiotherapy. Int J RadiatOncolBiol Phys. 2006;66(4):975-80. [view at publisher] [DOI] [Google Scholar]
5. Lopez-Jornet P, Lucero Berdugo M, Fernandez-Pujante A, Lavella C Z, Silvestre FJ. Sleep quality in patients with xerostomia: a prospective and randomized case-control study. ActaOdontol Scand.2016;74(3):224-8. [DOI] [Google Scholar]
6. Wijers OB, Levendag PC, Braaksma MM, Boonzaaijer M, Visch LL, Schmitz PI. Patients with head and neck cancer cured by radiation therapy: A survey of the dry mouth syndrome in long‐term survivors. Head Neck. 2002;24(8):737-47. [view at publisher] [DOI] [Google Scholar]
7. Almståhl A, Alstad T, Fagerberg‐Mohlin B, Carlén A, Finizia C. Explorative study on quality of life in relation to salivary secretion rate in patients with head and neck cancer treated with radiotherapy. Head Neck. 2016;38(5):782-91. [view at publisher] [DOI] [Google Scholar]
8. Allal AS, Dulguerov P, Bieri S, Lehmann W, Kurtz JM. Assessment of quality of life in patients treated with accelerated radiotherapy for laryngeal and hypopharyngeal carcinomas. Head Neck. 2000;22(3):288-93. https://doi.org/10.1002/(SICI)1097-0347(200005)22:3<288::AID-HED12>3.0.CO;2-B [view at publisher] [DOI] [Google Scholar]
9. Organization WH. WHOQOL-BREF: introduction, administration, scoring and generic version of the assessment: field trial version, December 1996. WHO, 1996. [Google Scholar]
10. Robinson D, Renshaw C, Okello C, Møller H, Davies E. Suicide in cancer patients in South East England from 1996 to 2005: a population-based study. Br J Cancer. 2009;101(1):198-201. [view at publisher] [DOI] [Google Scholar]
11. Kallay E, Dégi CL, Vincze AE. Dysfunctional attitudes, depression and quality of life in a sample of Romanian. J CognBehavPsychother. 2007;7(1):95-106. [Google Scholar]
12. Rabiei M, Rahimi A, KazemnezhadLeyli E, Jalalian B, Massoudi Rad S. Complication of post radiation in patients with head and neck cancer. J GorganUniv Med Sci. 2014;16(2):114-20. [view at publisher] [Google Scholar]
13. Chambers MS, Garden AS, Kies MS, Martin JW. Radiation‐induced xerostomia in patients with head and neck cancer: pathogenesis, impact on quality of life, and management. Head Neck. 2004;26(9):796-807. [view at publisher] [DOI] [Google Scholar]
14. Duncan GG, Epstein JB, Tu D, Sayed SE, Bezjak A, Ottaway J, et al. Quality of life, mucositis, and xerostomia from radiotherapy for head and neck cancers: a report from the NCIC CTG HN2 randomized trial of an antimicrobial lozenge to prevent mucositis. Head Neck. 2005;27(5):421-8. [view at publisher] [DOI] [Google Scholar]
15. Pow EH, Kwong DL, McMillan AS, Wong MC, Sham JS, Leung LH, et al. Xerostomia and quality of life after intensity-modulated radiotherapy vs. conventional radiotherapy for early-stage nasopharyngeal carcinoma: initial report on a randomized controlled clinical trial. Int J RadiatOncolBiol Phys. 2006;66(4):981-91. [view at publisher] [DOI] [Google Scholar]
16. Ebrahimi A, Molavi H, Moosavi G, Bornamanesh A, Yaghobi M. Psychometric Properties and Factor Structure of General Health Questionnaire 28 (GHQ-28) in Iranian Psychiatric Patients. J Res Behav Sci. 2007;5(1):5-11. [view at publisher] [Google Scholar]
17. Nazifi M, Mokarami H, Akbaritabar A, FarajiKujerdi M, Tabrizi R, Rahi A. Reliability, validity and factor structure of the persian translation of general health questionnire (ghq-28) in hospitals of kerman university of medical sciences. J FasaUniv Med Sci. 2014;3:336-42. [view at publisher] [DOI] [Google Scholar]
18. Astrup GL, Rustøen T, Hofsø K, Gran JM, Bjordal K. Symptom burden and patient characteristics: Association with quality of life in patients with head and neck cancer undergoing radiotherapy. Head Neck. 2017;39(10):2114-26. [view at publisher] [DOI] [Google Scholar]
19. Neilson K, Pollard A, Boonzaier A, Corry J, Castle D, Smith D, et al. A longitudinal study of distress (depression and anxiety) up to 18 months after radiotherapy for head and neck cancer. Psychooncology. 2013;22(8):1843-8. [view at publisher] [DOI] [Google Scholar]
20. Pelland M, Lambert L, Filion E, Bahig H, Beaudry M, Ouellette A, et al., editors. Depression, anxiety and claustrophobia in patients undergoing radiotherapy for head and neck cancer. RadiotherOncol. 2017 May 1;123(2):318-9. [view at publisher] [DOI] [Google Scholar]
21. Lee Y, Wu Y-S, Chien C-Y, Fang F-M, Hung C-F. Use of the Hospital Anxiety and Depression Scale and the Taiwanese Depression Questionnaire for screening depression in head and neck cancer patients in Taiwan. Neuropsychiatr Dis Treat. 2016;12:2649. [view at publisher] [DOI] [Google Scholar]
22. Wu Y-s, Lin P-Y, Chien C-Y, Fang F-M, Chiu N-M, Hung C-F, et al. Anxiety and depression in patients with head and neck cancer: 6-month follow-up study. Neuropsychiatr Dis Treat. 2016;12:1029. [view at publisher] [DOI] [Google Scholar]
23. Nikoloudi M, Lymvaios I, Zygogianni A, Parpa E, Strikou D-A, Tsilika E, et al. Quality of life, anxiety, and depression in the head-and-neck cancer patients, undergoing intensity-modulated radiotherapy treatment. Indian J Palliat Care. 2020;26(1):54. [view at publisher] [DOI] [Google Scholar]
24. Malekian A, Alizadeh A, Ahmadzadeh GH. Anxiety and Depression in Cancer Patients. J Res Behavior Sci. 2007;5:115-118. [Google Scholar]
25. Rajabizadeh G, Mansoori SM, Shakibi MR, Ramazani MR. Determination of Factors Related to Depression in Cancer Patients of the Oncology Ward in Kerman. J Kerman Univ Med Sci. 2005;12(2):142-7. [view at publisher] [Google Scholar]
26. Norton MC, Singh A, Skoog I, Corcoran C, Tschanz JT, Zandi PP, et al. Church attendance and new episodes of major depression in a community study of older adults: the Cache County Study. J Gerontol B PsycholSciSoc Sci. 2008;63(3):P129-P37. [view at publisher] [DOI] [Google Scholar]
27. Linden W, Vodermaier A, MacKenzie R, Greig D. Anxiety and depression after cancer diagnosis: prevalence rates by cancer type, gender, and age. J Affect Disord. 2012;141(2-3):343-51. [view at publisher] [DOI] [Google Scholar]
28. AliakbariDehkordi M, Zare H, AsgharnejadFarid A, Hashemian R. Investigations of the Relation Between Social Anxiety, Cognitive and Behavioral Aspect of It and Sex and Gender-Role in Adolescence. Iran J PsychiatrClin Psychol. 2017;22(4):340-7. [DOI] [Google Scholar]
29. Naseri N, Taleghani F. Depression in cancer patients: the role of demographic variables. IJCA. 2019;1(1):55-61. [view at publisher] [DOI] [Google Scholar]

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