Volume 20, Issue 1 (January 2022)                   IJRM 2022, 20(1): 1-12 | Back to browse issues page


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Hosseini S E, Ilkhani M, Rohani C, Nikbakht Nasrabadi A, Ghanei Gheshlagh R, Moini A. Prevalence of sexual dysfunction in women with cancer: A systematic review and meta-analysis. IJRM 2022; 20 (1) :1-12
URL: http://ijrm.ir/article-1-2074-en.html
1- Department of Medical Surgical Nursing, School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
2- Department of Medical Surgical Nursing, School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Cancer Research Center, Shahid Beheshati University of Medical Sciences, Tehran, Iran. , m_ilkhani@yahoo.com
3- Department of Health Care Sciences, Palliative Care Center, Ersta Sköndal Bräcke University College, Campus Ersta, Stockholm, Sweden. Department of Community Health Nursing, School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4- School of Nursing and Midwifery, Tehran University of Medical Sciences, Tehran, Iran.
5- Spiritual Health Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
6- Breast Disease Research Center (BDRC), Tehran University of Medical Sciences, Tehran, Iran. Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran. Department of Obstetrics and Gynecology, Arash Women's Hospital, Tehran University of Medical Sciences, Tehran, Iran.
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1. Introduction
Cancer is one of the most widespread concerns of human beings, affecting both their emotional and physical wellbeing (1). It is projected that in 2028, over 1.7 million people will be living with cancer and over 600,000 of these people will lose their lives (2). Fortunately, nowadays many cancer patients survive due to timely diagnosis, accessibility of new treatments, and improvement in support systems (3). According to the National Cancer Institute, the rate of five-year survival increased from 58% in 1975 to 83% in 2013 (4). It is expected that by 2024, there will be over 9.5 million survivors of cancer (5). Therefore, more attention should be paid to the problems of people with cancer, including quality of life considerations and complications resulting from late diagnosis. Among these concerns, sexual desirability has been an important point requiring sober and meticulous attention (1).
Sexual dysfunction (SD) has been categorized into four classifications encompassing problems related to arousal, interest, orgasm and pain (6). Female SD (FSD) in cancer patients is multidimensional, and includes factors related to psychology, physiology and sociology (7). The type of cancer and its treatment approaches (including chemotherapy, radiotherapy, surgery etc.) play an essential role in SD. Hence, SD in women with cancer is distinctively different from other women’s impairments (8). One study revealed that females who underwent post-treatment chemotherapy had a higher risk of SD in comparison with those patients receiving no chemotherapy (9).
The insufficient attention given to sexual problems leads to negative impacts on couples’ bilateral and mutual relationships (10). In addition to the time limitations of medical examinations, the reluctance of physicians and nurses to research this aspect of life, as well as the embarrassment of asking about sexual issues, create further obstacles to addressing SD (7). The effort to expand the focus on FSD is limited due to lack of sufficient screening tools and valid instruments (11).
The female sexual function index (FSFI) is one of few valid and reliable measurements to assess sexual-related problems among women with and without cancer (12). FSFI is a six-dimensional tool by which female performance indices over the past four weeks, such as desire, arousal, lubrication, orgasm, satisfaction and pain, are assessed through 19 questions. A score of 26 is considered the cut-off, and scores above this indicate satisfactory sexual performance (13). Data from studies about FSD among cancer survivors are highly heterogeneous.
The aim of this research was to examine the prevalence of SD in females with cancer through a systematic review and meta-analysis.
 
2. Materials and Methods
The present research utilized the meta-analysis of observational studies in epidemiology (MOOSE) checklist for reporting systematic reviews and meta-analyses (14). All scientific articles concerning SD in women with cancer were collected in January 2019. To do so, the following databases were systematically searched: PubMed, Web of Science, Google Scholar, Embase, and Scopus. The following keywords were used: “Neoplasia”, “Tumor”, “Cancer”, “Malignancy”, “Female Sexual Function Index”, “FSFI”, and “female sexual dysfunction”, using coordinating conjunctions “AND” and “OR”. The reference lists of articles were also searched to find additional articles not found through the initial searching process. Two researchers independently performed the search, extraction, and quality analysis of the studies. To be selected, the articles had to meet the following criteria: females with a cancer diagnosis were studied, FSD was a primary or secondary outcome, FSFI was used to evaluate the scope of SD; published in the English language in a peer-reviewed journal. Unpublished full articles, posters, conference abstracts, letters to the editor, case reports and commentaries were excluded. Studies that did not report a total score, studies with inadequate data, studies that used only one dimension of the FSFI, studies with a sample size of less than 50 people, articles without full text, and studies published in non-English languages were excluded.
The name of the first author, year of article publication, cancer type, design of the study, FSFI scores, country where the study was performed, and total number of patients were extracted from the articles. The methodological quality was evaluated by two independent reviewers in compliance with the Newcastle–Ottawa Scale. In case of disagreement, a third party’s assessment prevailed. The articles were graded with stars from 0 (the poorest quality) to 9 (the highest quality).
 
2.1. Statistical analysis
We calculated the variance of the prevalence of SD in each of the selected articles based on the binomial distribution formula. Heterogeneity was assessed using Cochran’s Q test and I2 statistics and due to the high heterogeneity, a random-effects model was used to combine studies and estimate the pooled prevalence. According to the I2 index, heterogeneities were divided into three categories: low (> 25%), medium (25 to 75%) and high (< 75%) (13). To ensure the stability of the results, a sensitivity analysis was performed so that the pooled prevalence was assessed by omitting each study to identify a study whose omission had a significant effect on the pooled prevalence. To investigate the relationship between the prevalence of SD with the mean age of women, the year of publication, the sample size of the selected studies, and quality score, meta-regression was used. Also, with subgroup analysis, the prevalence of SD was estimated by geographical area. A funnel plot based on Egger's regression test was used to evaluate the publication bias. Data analysis was performed using the Stata software (version 11).
 
3. Results
A PRISMA flow diagram of the search strategy is illustrated in figure 1. The first attempt to search identified 1205 articles. 582 duplicate articles were removed. In the next stage, the individual papers were investigated based on title and abstract and 542 articles were excluded due to not conforming to the inclusion criteria. Then, 81 full-text papers were studied. 24 studies were included in the final analysis, of which 17 were cross-sectional, four were prospective studies, two were retrospective studies, and one was a case-control study. 11 studies (15-25) addressed breast cancer, one study colorectal cancer (26), four studies cervical cancer (27-29), three studies endometrial cancer (30-32), one study ovary and uterus cancer (33), and one study rectum cancer (34). Two studies (35, 36) dealt with patients categorized based on different cancer sites. The sample size ranged from 59 patients (26) to 1071 patients (27). Three studies were conducted in developing countries (15, 18, 22) and others were performed in developed countries (Table I and Figure 1).
To decide whether to include all of the articles examining SD or not, a publication bi:as char:t was created. The results showed that publication bias was not significant (p = 0.20) (Figure 2).
The results of the sensitivity analyses showed that the elimination of each article bore no effect upon the prevalence of the disorder. Pooled prevalence of FSD in patients was 66% (95% CI: 59-74%). Most of the studies were conducted in the United States of America. The findings of the subgroup analyses demonstrated that the prevalence of SD in the continents of Africa, America, Asia, and Europe was 75% (95% CI: 66-83%), 68% (95% CI: 61-75%), 62% (95% CI: 48-75%) and 43% (95% CI: 26-60%), respectively (Figure 3).
Regarding the type of cancer, the subgroup analysis showed that the highest and lowest prevalence of FSD was in women with genital and colorectal cancers, respectively. Meta-regression revealed that the prevalence of FSD bore no relationship with publication year (p = 0.40), mean age of the women (p = 0.31), sample size (p = 0.97), or article methodological quality score (0.38) (Figure 4).







 
4. Discussion
This study presented a meta-analysis of the literature on cancer and FSD. The purpose was to study and address the problems of SD in women. We only included observational studies that evaluated sexual function with a validated test. Sensitivity analyses showed that the results were strong, and there was no significant diffusion bias. The results of meta-regression showed that neither FSD prevalence nor sexual function scores in women with cancer were affected by the mean age of the women, year of publication, sample size, or quality of score.
The findings of this study showed that two-thirds of these patients (66%) suffered from SD, which was similar to the findings previously reported (> 60%) by Maiorino et al. (37).
Other studies have shown that upon starting treatment, 40% of women with cancer suffer from SD and 50% of breast cancer patients experience SD long term (38, 39). Another study revealed that cancer and its treatment can have a direct and conclusive impact on desire, arousal, orgasm, and dyspareunia, and that the severity of SD and how long it lasts depend on radiotherapy and its duration (40).
Lawman et al. reported that 43% of American female patients in their study experienced FSD, while approximately 63% developed FSD in a study conducted in mainland China (39, 41). A study conducted in Iran on 100 women with cancer showed that 60% of patients had moderate SD (42). Anderson adds that surgery on patients with cancer, such as hysterectomy, mastectomy and ovarian resection, can significantly impair sexual function, which can threaten the quality of life in women with cancer (43).
The findings show that the prevalence of gynecological cancer in women has the highest rate, so that in a meta-analysis, female dysfunction was reported as the highest rank (78%) (37). Survivors of gynecological cancers have been found to experience SD at higher rates than survivors of other cancers (44). In addition, gynecological cancer treatments usually involve surgery, which can be combined with radiation therapy, chemotherapy, and hormone therapy that often have direct effects on sexual organs (45).
Gynecological issues and sexual function for women with cancer are considered great challenges, originating from patient social status and disease impacts, as well as side effect complications (46). Cancer type and treatment modalities have an impact on FSD. These distinctions partially affect FSFI scores (47). One study indicated that the most prevalent dysfunctions among women with cancer are loss of desire for sex (39%), vaginal dryness (24%), dyspareunia (9%), difficulty feeling excitement and pleasure (21%), and issues in orgasm (15%) (48). Vaginal spasm and dryness can be due to the effects of chemotherapy drugs and a lack of sexual arousal in these women. Also, lack of stimulation prevents the secretion of viscous vaginal fluid and so leads to painful intercourse (49). In these women, constant mental preoccupation with the defect may cause low stimulation or even lack of stimulation (50, 51). Frederickson and Robert point out that when people are distracted by their appearance, they cannot focus on their sexual pleasure, and this negatively affects their sexual function (49). Estrogen levels drop naturally during chemotherapy. It is well known that a lack of estrogen results in atrophy of the urogenital system and dyspareunia, lowering sexual desire and arousal (48, 52). Given these findings, it is important to pay more attention to changes in the sexual function of women with cancer. Thus, these results can help to increase the availability of assistance to women.
The subgroup analyses showed that most articles on FSD have been published in the United States. Most valid tools for measuring FSD are designed by Americans, are in English and are tailored to the American culture (53). Sexuality is a concept based on cultural norms and influences. In other words, cultural factors determine the importance and meaning of sexual behaviors. Therefore, sexual issues should be discussed within the framework of the prevailing culture of that society (54). For this reason, the World Health Organization recommends explaining the concept of sexual health in a cultural context (55). Sex has always been a taboo subject especially in Asian society. This has led researchers in Eastern countries to focus less on sexuality, especially in women. These countries often use translated tools that are not based on their own culture and historical background, which creates problems in collecting data and interpreting results. In his review, Lewis showed that because there are fundamental methodological problems in data collection, there are no articles comparing sexual performance in Asia with other parts of the world. In addition, there are few studies on the incidence of SD in Asian populations (53).
Our finding showed that FSD is more prevalent in American and African women with cancer than in Asia and Europe. Ethnic, social or cultural differences seem to be the reason for this finding. Therefore, more studies are needed to confirm the reliability of these regional differences.
The present research focused on the FSFI because it is one of the only valid instruments for cancer survivors, and it was created by the National Comprehensive Cancer Network (56) and the Patient‐Reported Outcomes Measurement Information System (PROMIS) committee (11). A widespread epidemiology study on 7243 healthy females with ages ranging from 40 to 59 was conducted to evaluate FSFI scores which resulted in a FSFI score 25.2 (57). However, the average score of FSFI in middle-aged women can be lower than the cut-off on account of sexual performance dysfunction, menopause, and hormone and metabolism-related changes (58).
At present, there are some tools for evaluation of SD in cancer patients such as the Sexual Function-Vaginal Changes Questionnaire (59) and the sexual function after treatment for gynecologic cancer (60). Some tools are sex-specific (i.e., Derogatis Sexual Functioning Inventory (61) and Changes in Sexual Functioning Questionnaire (62). Furthermore, numerous site-specific measurements have been developed to assess cancer patients’ quality of life, with function or symptom subscales for sexual function assessment (e.g., the European Organization for Research and Treatment of Cancer quality-of-life questionnaires (63). Most of these tools encompass a few items in a general scale to assess SD. Accordingly, they deal with the general quality of life of cancer survivors (63).
It is noted that the sample sizes of most surveys are small. We excluded research with fewer than 50 subjects as well as those studies with questionnaires other than the FSFI. A limitation of our study is that studies which were written in languages other than English were omitted. We also did not perform subgroup analyses for the clinical stage, treatment regimen, or other possible factors that may have affected the results.
 
5. Conclusion
Overall, our results confirm that the prevalence of FSD in women with cancer is high. Women with cancer in Africa and the United States have a higher prevalence of FSD than those in Asia and Europe. Since the sexual needs of women with cancer are different from those of healthy women, the development of a dedicated, specialized tool to evaluate the FSD of women with cancer is necessary.
 
Acknowledgments
The study had no financial support. The authors appreciate all the researchers whose articles were used in the present research.
 
Conflict of Interest
The authors declare that there is no conflict of interest.
 
Type of Study: Review Article | Subject: Reproductive Oncology

References
1. Agboola SO, Ju W, Elfiky A, Kvedar JC, Jethwani K. The effect of technology-based interventions on pain, depression, and quality of life in patients with cancer: A systematic review of randomized controlled trials. J Med Internet Res 2015; 17: e65. [DOI:10.2196/jmir.4009] [PMID] [PMCID]
2. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018; 68: 394-424. [DOI:10.3322/caac.21492] [PMID]
3. Maiorino M, Bellastella G, Giugliano D, Esposito K. From inflammation to sexual dysfunctions: A journey through diabetes, obesity, and metabolic syndrome. J Endocrinol Invest 2018; 41: 1249-1258. [DOI:10.1007/s40618-018-0872-6] [PMID]
4. Jemal A, Ward EM, Johnson ChJ, Cronin KA, Ma J, Ryerson B, et al. Annual report to the nation on the status of cancer, 1975-2014, featuring survival. J Natl Cancer Inst 2017; 109: djx030. [DOI:10.1093/jnci/djx030]
5. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin 2016; 66: 7-30. [DOI:10.3322/caac.21332] [PMID]
6. American Psychiatric Association. Association, AP Diagnostic and statistical manual of mental disorders. Arlington, USA: American Psychiatric Pub; 2013. [DOI:10.1176/appi.books.9780890425596]
7. Alicikus ZA, Gorken IB, Sen RC, Kentli S, Kinay M, Alanyali H, et al. Psychosexual and body image aspects of quality of life in Turkish breast cancer patients: A comparison of breast conserving treatment and mastectomy. Tumori 2009; 95: 212-218. [DOI:10.1177/030089160909500213] [PMID]
8. Frieben RW, Lin HCh, Hinh PP, Berardinelli F, Canfield SE, Wang R. The impact of minimally invasive surgeries for the treatment of symptomatic benign prostatic hyperplasia on male sexual function: A systematic review. Asian J Androl 2010; 12: 500-508. [DOI:10.1038/aja.2010.33] [PMID] [PMCID]
9. Avis NE, Crawford S, Manuel J. Psychosocial problems among younger women with breast cancer. Psychooncology 2004; 13: 295-308. [DOI:10.1002/pon.744] [PMID]
10. Frimer M, Turker LB, Shankar V, Cardaci R, Van Arsdale AR, Rosenthal E, et al. The association of sexual dysfunction with race in women with gynecologic malignancies. Gynecol Oncol Rep 2019; 30: 100495. [DOI:10.1016/j.gore.2019.100495] [PMID] [PMCID]
11. Jeffery DD, Tzeng JP, Keefe FJ, Porter LS, Hahn EA, Flynn KE, et al. Initial report of the cancer patient‐reported outcomes measurement information system (PROMIS) sexual function committee: Review of sexual function measures and domains used in oncology. Cancer 2009; 115: 1142-1153. [DOI:10.1002/cncr.24134] [PMID] [PMCID]
12. Rosen RC, Bachmann GA. Sexual well-being, happiness, and satisfaction, in women: The case for a new conceptual paradigm. J Sex Marital Ther 2008; 34: 291-297. [DOI:10.1080/00926230802096234] [PMID]
13. Stabile C, Gunn A, Sonoda Y, Carter J. Emotional and sexual concerns in women undergoing pelvic surgery and associated treatment for gynecologic cancer. Transl Androl Urol 2015; 4: 169-185.
14. Stroup DF, Berlin JA, Morton SC, Olkin I, Williamson GD, Rennie D, et al. Meta-analysis of observational studies in epidemiology: A proposal for reporting; meta-analysis of observational studies in epidemiology (MOOSE) group. JAMA 2000; 283: 2008-2012. [DOI:10.1001/jama.283.15.2008] [PMID]
15. Faten E, Nader M, Raies H, Sana M, Amel M, Fadhel M. [Body image disorder in 100 Tunisian female breast cancer patients]. Bull Cancer 2018; 105: 350-356. (in French) [DOI:10.1016/j.bulcan.2018.01.008] [PMID]
16. Robinson PJ, Bell RJ, Christakis MK, Ivezic SR, Davis SR. Aromatase inhibitors are associated with low sexual desire causing distress and fecal incontinence in women: An observational study. J Sex Med 2017; 14: 1566-1574. [DOI:10.1016/j.jsxm.2017.09.018] [PMID]
17. Gass JS, Onstad M, Pesek S, Rojas K, Fogarty S, Stuckey A, et al. Breast-specific sensuality and sexual function in cancer survivorship: Does surgical modality matter? Ann Surg Oncol 2017; 24: 3133-3140. [DOI:10.1245/s10434-017-5905-4] [PMID]
18. Paiva CE, Rezende FF, Paiva BSR, Mauad EC, Zucca-Matthes G, Carneseca EC, et al. Associations of body mass index and physical activity with sexual dysfunction in breast cancer survivors. Arch Sex Behav 2016; 45: 2057-2068. [DOI:10.1007/s10508-016-0758-7] [PMID]
19. Boquiren VM, Esplen MJ, Wong J, Toner B, Warner E, Malik N. Sexual functioning in breast cancer survivors experiencing body image disturbance. Psychooncology 2016; 25: 66-76. [DOI:10.1002/pon.3819] [PMID]
20. Raggio GA, Butryn ML, Arigo D, Mikorski R, Palmer SC. Prevalence and correlates of sexual morbidity in long-term breast cancer survivors. Psychol Health 2014; 29: 632-650. [DOI:10.1080/08870446.2013.879136] [PMID] [PMCID]
21. Schover LR, Baum GP, Fuson LA, Brewster A, Melhem‐Bertrandt A. Sexual problems during the first 2 years of adjuvant treatment with aromatase inhibitors. J Sex Med 2014; 11: 3102-3111. [DOI:10.1111/jsm.12684] [PMID] [PMCID]
22. Safarinejad MR, Shafiei N, Safarinejad S. Quality of life and sexual functioning in young women with early‐stage breast cancer 1 year after lumpectomy. Psychooncology 2013; 22: 1242-1248. [DOI:10.1002/pon.3130] [PMID]
23. Pumo V, Milone G, Iacono M, Giuliano SR, Di Mari A, Lopiano C, et al. Psychological and sexual disorders in long-term breast cancer survivors. Cancer Manag Res 2012; 4: 61-65. [DOI:10.2147/CMAR.S28547] [PMID] [PMCID]
24. Harirchi I, Montazeri A, Bidokhti FZ, Mamishi N, Zendehdel K. Sexual function in breast cancer patients: A prospective study from Iran. J Exp Clin Cancer Res 2012; 31: 20. [DOI:10.1186/1756-9966-31-20] [PMID] [PMCID]
25. Boehmer U, Ozonoff A, Timm A, Winter M, Potter J. After breast cancer: Sexual functioning of sexual minority survivors. J Sex Res 2014; 51: 681-689. [DOI:10.1080/00224499.2013.772087] [PMID]
26. Reese JB, Handorf E, Haythornthwaite JA. Sexual quality of life, body image distress, and psychosocial outcomes in colorectal cancer: A longitudinal study. Support Care Cancer 2018; 26: 3431-3440. [DOI:10.1007/s00520-018-4204-3] [PMID] [PMCID]
27. He H, Yang Z, Zeng D, Yao D, Fan J, Zhao R, et al. [Comparison of the short-term and long-term outcomes of laparoscopic surgery and open surgery for early-stage cervical cancer]. Zhonghua Zhong Liu Za Zhi 2017; 39: 458-466. (in Chinese)
28. Tsai TY, Chen SY, Tsai MH, Su YL, Ho CM, Su HF. Prevalence and associated factors of sexual dysfunction in cervical cancer patients. J Sex Med 2011; 8: 1789-1796. [DOI:10.1111/j.1743-6109.2010.01745.x] [PMID]
29. Carter J, Sonoda Y, Baser RE, Raviv L, Chi DS, Barakat RR, et al. A 2-year prospective study assessing the emotional, sexual, and quality of life concerns of women undergoing radical trachelectomy versus radical hysterectomy for treatment of early-stage cervical cancer. Gynecol Oncol 2010; 119: 358-365. [DOI:10.1016/j.ygyno.2010.07.016] [PMID] [PMCID]
30. Damast Sh, Alektiar K, Eaton A, Gerber NK, Goldfarb S, Patil S, et al. Comparative patient-centered outcomes (health state and adverse sexual symptoms) between adjuvant brachytherapy versus no adjuvant brachytherapy in early stage endometrial cancer. Ann Surg Oncol 2014; 21: 2740-2754. [DOI:10.1245/s10434-014-3562-4] [PMID]
31. Damast Sh, Alektiar KM, Goldfarb S, Eaton A, Patil S, Mosenkis J, et al. Sexual functioning among endometrial cancer patients treated with adjuvant high-dose-rate intra-vaginal radiation therapy. Int J Radiat Oncol Biol Phys 2012; 84: e187-e193. [DOI:10.1016/j.ijrobp.2012.03.030] [PMID] [PMCID]
32. Onujiogu N, Johnson T, Seo S, Mijal K, Rash J, Seaborne L, et al. Survivors of endometrial cancer: Who is at risk for sexual dysfunction? Gynecol Oncol 2011; 123: 356-359. [DOI:10.1016/j.ygyno.2011.07.035] [PMID]
33. Chan JL, Senapati S, Johnson LNC, DiGiovanni L, Voong Ch, Butts SF, et al. Risk factors for sexual dysfunction in BRCA mutation carriers following risk-reducing salpingo-oophorectomy. Menopause 2019; 26: 132-139. [DOI:10.1097/GME.0000000000001176] [PMID] [PMCID]
34. Segelman J, Martling A, Machado M, Holm T, Bergmark K, Rådestad AF. Preoperative sexual function in women with rectal cancer. Eur J Surg Oncol 2013; 39: 1079-1086. [DOI:10.1016/j.ejso.2013.07.091] [PMID]
35. Moroney MR, Flink D, Sheeder J, Blake EA, Carrubba AR, Fisher CM, et al. Radiation therapy is not an independent risk factor for decreased sexual function in women with gynecologic cancers. Rep Pract Oncol Radiother 2018; 23: 331-336. [DOI:10.1016/j.rpor.2018.07.007] [PMID] [PMCID]
36. Carter J, Stabile C, Seidel B, Baser RE, Gunn AR, Chi S, et al. Baseline characteristics and concerns of female cancer patients/survivors seeking treatment at a female sexual medicine program. Support Care Cancer 2015; 23: 2255-2265. [DOI:10.1007/s00520-014-2573-9] [PMID] [PMCID]
37. Maiorino MI, Chiodini P, Bellastella G, Giugliano D, Esposito K. Sexual dysfunction in women with cancer: A systematic review with meta-analysis of studies using the female sexual function index. Endocrine 2016; 54: 329-341. [DOI:10.1007/s12020-015-0812-6] [PMID]
38. Schofield Ch, Newton RU, Cohen PA, Galvão DA, McVeigh JA, Mohan GR, et al. Health-related quality of life and pelvic floor dysfunction in advanced-stage ovarian cancer survivors: associations with objective activity behaviors and physiological characteristics. Support Care Cancer 2018; 26: 2239-2246. [DOI:10.1007/s00520-018-4069-5] [PMID]
39. Jing L, Zhang Ch, Li W, Jin F, Wang A. Incidence and severity of sexual dysfunction among women with breast cancer: A meta-analysis based on female sexual function index. Support Care Cancer 2019; 27: 1171-1180. [DOI:10.1007/s00520-019-04667-7] [PMID]
40. Falk SJ, Dizon DS. Sexual dysfunction in women with cancer. Fertil Steril 2013; 100: 916-921. [DOI:10.1016/j.fertnstert.2013.08.018] [PMID]
41. Laumann Eo, Paik A, Rosen RC. Sexual dysfunction in the United States: Prevalence and predictors. JAMA 1999; 281: 537-544. [DOI:10.1001/jama.281.6.537] [PMID]
42. Irandoost S, Nasiri A, Izadpanahi P. [Evaluation of sexual function and its related factors in females with breast cancer undergoing chemotherapy in Iran-Mehr medical center, Birjand, Iran, 2018]. J Birjand Univ Med Sci 2020; 27: 366-375. (in Persian)
43. Andersen BL. Yes, there are sexual problems. Now, what can we do about them? Gynecol Oncol 1994; 52: 10-13. [DOI:10.1006/gyno.1994.1003] [PMID]
44. Lindau ST, Gavrilova N, Anderson D. Sexual morbidity in very long term survivors of vaginal and cervical cancer: A comparison to national norms. Gynecol Oncol 2007; 106: 413-418. [DOI:10.1016/j.ygyno.2007.05.017] [PMID] [PMCID]
45. Carter J, Stabile C, Gunn A, Sonoda Y. The physical consequences of gynecologic cancer surgery and their impact on sexual, emotional, and quality of life issues. J Sex Med 2013; 10 (Suppl.): 21-34. [DOI:10.1111/jsm.12002] [PMID]
46. Hopkins TG, Stavraka C, Gabra H, Fallowfield L, Hood C, Blagden S. Sexual activity and functioning in ovarian cancer survivors: an internet-based evaluation. Climacteric 2015; 18: 94-98. [DOI:10.3109/13697137.2014.929104] [PMID]
47. Harding Y, Ooyama T, Nakamoto T, Wakayama A, Kudaka W, Inamine M, et al. Radiotherapy-or radical surgery-induced female sexual morbidity in stages IB and II cervical cancer. Int J Gynecol Cancer 2014; 24: 800-805. [DOI:10.1097/IGC.0000000000000112] [PMID]
48. Sertoz OO, Mete HE, Noyan A, Alper M, Kapkaç M. [Effects of surgery type on body image, sexuality, self-esteem, and marital adjustment in breast cancer: A controlled study]. Turk Psikiyatri Derg 2004; 15: 264-275. (in Turkish)
49. Fredrickson BL, Roberts TA. Objectification theory: Toward understanding women's lived experiences and mental health risks. Psychol Women Quarter 1997; 21: 173-206. [DOI:10.1111/j.1471-6402.1997.tb00108.x]
50. Holzner B, Kemmler G, Kopp M, Moschen R, Schweigkofler HR, Du Nser M, et al. Quality of life in breast cancer patients-not enough attention for long-term survivors? Psychosomatics 2001; 42: 117-123. [DOI:10.1176/appi.psy.42.2.117] [PMID]
51. Hannoun-Levi J. [Treatment of breast and uterus cancer: Physiological and psychological impact on sexual function]. Cancer Radiother 2005; 9: 175-182. (in French) [DOI:10.1016/j.canrad.2004.11.005] [PMID]
52. Angelopoulos N, Barbounis V, Livadas S, Kaltsas D, Tolis G. Effects of estrogen deprivation due to breast cancer treatment. Endocr Relat Cancer 2004; 11: 523-535. [DOI:10.1677/erc.1.00783] [PMID]
53. Lewis RW. A critical look at descriptive epidemiology of sexual dysfunction in Asia compared to the rest of the world-a call for evidence-based data. Transl Androl Urol 2013; 2: 54-60.
54. Hosseini SE, Ilkhani M, Rohani C, Nikbakht Nasrabadi A. Sexual experience of Iranian women with cancer: A qualitative content analysis. Middle East J Cancer 2021; in Press.
55. WHO. World health statistics 2015. Geneva (Switzerland): World Health Organization; 2015. in Press.
56. Denlinger CS, Carlson RW, Are M, Baker KS, Davis E, Edge SB, et al. Survivorship: Aexual dysfunction (female), version 1.2013. J Natl Compr Canc Netw 2014; 12: 184-192. [DOI:10.6004/jnccn.2014.0019] [PMID] [PMCID]
57. Blümel JE, Chedraui P, Baron G, Belzares E, Bencosme A, Calle A, et al. Sexual dysfunction in middle-aged women: A multicenter Latin American study using the female sexual function index. Menopause 2009; 16: 1139-1148. [DOI:10.1097/gme.0b013e3181a4e317] [PMID]
58. Maiorino MI, Bellastella G, Esposito K. Sexual activity in midlife women and beyond. JAMA Intern Med 2014; 174: 1203-1204. [DOI:10.1001/jamainternmed.2014.1621] [PMID]
59. Jensen PT, Klee MC, Thranov I, Groenvold M. Validation of a questionnaire for self‐assessment of sexual function and vaginal changes after gynaecological cancer. Psychooncology 2004; 13: 577-592. [DOI:10.1002/pon.757] [PMID]
60. Bransfield DD, Horiot JC, Nabid A. Development of a scale for assessing sexual function after treatment for gynecologic cancer. J Psychosoc Oncol 1984; 2: 3-19. [DOI:10.1300/J077v02n01_02]
61. Derogatis LR. The Derogatis interview for sexual functioning (DISF/DISF-SR): An introductory report. J Sex Marital Ther 1997; 23: 291-304. [DOI:10.1080/00926239708403933] [PMID]
62. Clayton AH, McGarvey EL, Clavet G. The changes in sexual functioning guestlonnaire (CSFO): Development, reliability, and validity. Psychopharmacol Bull 1997; 33: 731-745.
63. Press P. European organization for research on treatment of cancer (eortc) eortc symposium on treatment of neoplastic lesions of the nervous system. Available at: https://www.eortc.org.

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