Skip to main content
LGBT Health logoLink to LGBT Health
. 2016 Feb 1;3(1):49–56. doi: 10.1089/lgbt.2015.0090

The Health Effects of Masculine Self-Esteem Following Treatment for Localized Prostate Cancer Among Gay Men

Donald Allensworth-Davies 1,, James A Talcott 2, Timothy Heeren 3, Brian de Vries 4, Thomas O Blank 5, Jack A Clark 6,,7
PMCID: PMC4770849  PMID: 26698658

Abstract

Purpose: To identify factors associated with masculine self-esteem in gay men following treatment for localized prostate cancer (PCa) and to determine the association between masculine self-esteem, PCa-specific factors, and mental health factors in these patients.

Methods: A national cross-sectional survey of gay PCa survivors was conducted in 2010–2011. To be eligible for the study, men needed to be age 50 or older, reside in the United States, self-identify as gay, able to read, write, and speak English, and to have been treated for PCa at least 1 year ago. One hundred eleven men returned surveys.

Results: After simultaneously adjusting for the factors in our model, men aged 50–64 years and men aged 65–74 years reported lower masculine self-esteem scores than men aged 75 years or older. Lower scores were also reported by men who reported recent severe stigma. Men who reported feeling comfortable revealing their sexual orientation to their doctor reported higher masculine self-esteem scores than men who were not. The mental component score from the SF-12 was also positively correlated with masculine self-esteem.

Conclusion: PCa providers are in a position to reduce feelings of stigma and promote resiliency by being aware that they might have gay patients, creating a supportive environment where gay patients can discuss specific sexual concerns, and engaging patients in treatment decisions. These efforts could help not only in reducing stigma but also in increasing masculine self-esteem, thus greatly influencing gay patients' recovery, quality of life, and compliance with follow-up care.

Key words: : health disparities, health services, masculinity, prostatic neoplasms, quality of life (QoL), sexual minority men

Introduction

For many men, prostate cancer (PCa) treatment has profound effects on masculine identity and self-esteem.1 Self-esteem may be conceptualized as the totality of internal, external, and social factors that a person associates with their own personal attributes or identity.2 Masculine self-esteem is focused more narrowly on attributes associated with the gender role strain paradigm as described by Pleck and other clinical psychologists.3,4 Under this paradigm, masculine roles are defined by stereotypes and/or norms arising from societal gender ideologies. As a result, there has been a long-standing hypothesis that masculine gender role discrepancy strain (i.e., strain resulting from the extent that a man perceives his gender role as being different from societal stereotypes and/or norms) is negatively correlated with, and results in poorer, self-esteem.

A growing body of evidence describes masculinity in the context of PCa across the diagnosis and treatment spectrum, including studies about information seeking,5,6 screening and diagnosis,7,8 loss of sexual function following treatment,9–11 and the impact of treatment and its effects on spousal and intimate relationships.12–14 Regardless of the physiological outcome of treatment, which often involves a loss of urinary, bowel, and/or sexual function, men are expected to cope, adjust, and accept the impact of PCa on their lives and intimate relationships.15 Research has shown that sexual dysfunction and incontinence following treatment result in decreased self-esteem and that while these aftereffects of treatment and aspects of quality of life (QoL) may improve by 1 year postsurgery, decreases in masculine self-esteem are more enduring.1,16–19

The combination of poor sexual function following treatment with adherence to traditional norms of masculinity may result in poor social, role, and mental health functioning.20 Eton et al. reported a positive correlation between general self-esteem and general physical and mental functioning among men with localized PCa.11 One question that remains is whether these associations are also true for gay men. It has been estimated that at least 5000 gay or bisexual men are diagnosed each year with having PCa and that 50,000 or more are PCa survivors.21 Despite the growing number of gay PCa survivors, the extent to which PCa is associated with traditional masculine norms and QoL among gay men is still unknown.

The hypothesized association of enduring decrements in masculine self-esteem following PCa treatment with poor social, role, and mental health functioning is concerning among gay men who may already be experiencing social isolation before PCa treatment. One recent PCa study also reported worse mental health functioning and fear of cancer recurrence within a convenience sample of gay men following treatment for PCa when compared with published norms in the literature.22 For example, support, especially from partners, mitigates negative effects of PCa, but the first national study of lesbian, gay, bisexual, and transgender (LGBT) elders has reported that gay men are less likely to be partnered or married than their straight counterparts, which can result in decreased social support.23 In addition, older gay men have fewer children in the household and are more likely to live alone than straight older adult men.23 In a subsequent analysis, Fredriksen-Goldsen et al. also identified social support and social network size serving as protective factors among LGBT older adults—decreasing the odds of poor general health, disability, and depression.24

Studies have also shown that gay men, in general, may feel more dissatisfied with their bodies than heterosexual men due to the strong emphasis placed on appearance in the gay community.25–27 Historically, gay men have also demonstrated more stereotypically feminine interests, attitudes, speech patterns, and body movements when compared with their heterosexual peers.28–30Thus, we would expect that the experience of bodily changes following treatment for localized PCa would be different for gay men and that masculinity and sexual intimacy would be formulated differently. However, findings in the majority of PCa studies to date have been limited by the lack of diverse sexual orientation. Thus, similarities or differences cannot be determined until concepts such as masculine self-esteem are included among the growing, but still very limited, body of studies on PCa and gay men. To determine the association between masculine self-esteem, PCa-specific factors, and mental health factors in these patients, we examined these relationships using data from a cross-sectional national survey of gay PCa survivors in the United States conducted in 2010–2011.

Methods

Study population

To be eligible for the study, men needed to be age 50 or older, reside in the United States, self-identify as gay (i.e., bisexual men, transgender male-to-female and heterosexually identifying men who have sex with men were not included), and to have been treated for localized PCa (i.e., cancer stages I, II, or III) at least 1 year before the commencement of the study. Survey respondents were recruited almost exclusively through LGBT print publications across the United States, including a national gay magazine and LGBT community newspapers. Informed consent was obtained over the phone for all subjects before their participation in the survey, and all study procedures were reviewed and approved by the Boston University Medical Center Institutional Review Board.

Measures

Validated measures

The masculine self-esteem outcome was assessed using a validated scale developed as part of the PCa work of Clark et al. that asked questions such as feeling like a whole man, feeling weak and small, being too emotional, and comparing unfavorably to other men (eight items, Cronbach's α = 0.80).1,31 General physical and mental health were assessed using the physical and mental component scores (PCS and MCS, respectively) from the SF-12. The SF-12 is a validated short-form survey of 12 questions selected from the SF-36 Health Survey.32 Well-validated, expanded prostate cancer index composite (EPIC)33 subscales assessing urinary (11 items, Cronbach's α = 0.88), bowel (12 items, Cronbach's α = 0.85), and sexual functions (8 items, Cronbach's α = 0.79) were included to measure physical functional impacts of PCa treatments. Severe stigma was assessed using the MacDonald and Anderson social stigma scale with severe stigma defined post hoc as scoring in the top 15% of the scale (four items, with values ranging from 1 [Not at all] to 5 [Very much], Cronbach's α = 0.82).34 The stigma items comprised the following: “I avoid other people”, “I feel that other people are avoiding me”, “I feel odd and different from other people,” and “I feel self-conscious and embarrassed”. Among the social support measures, we included the partner or spouse support scale from the Medical Outcomes Study (five items ranging from 1 [Definitely true] to 5 [Definitely false], Cronbach's α = 0.79).35

Additional factors

The following factors were also assessed: time since PCa diagnosis, type of PCa treatment received, rising prostate-specific antigen (PSA) after the first treatment, an inventory of sexual activities developed by the authors (i.e., anal intercourse, oral sex, kissing, mutual masturbation, erotic massage, rimming, BDSM/S&M, sexual role play, sexual toys, fisting, and spanking), relationship with PCa doctor (adapted from the Patient–Doctor Relationship Questionnaire [PDRQ-9]36), a question about comfort in revealing one's sexual orientation to a doctor developed by the authors (“I am comfortable telling my PCa doctor that I am gay”, five-point Likert scale with values ranging from 1 [Strongly disagree] to 5 [Strongly agree]), anxiety, and depression. Anxiety and depression were each measured by two single-item questions, which asked whether a physician had ever provided a diagnosis of these conditions and whether daily activities were limited by these conditions. We also included a single five-point Likert scale item with values ranging from 1 (Not at all) to 5 (Very much), “I have replaced sex with other activities”. “Other activities” was left to the interpretation of the men responding to the question; no follow-up inventory was provided.

Data analyses

All variables to be included were specified before any analyses were conducted. For categorical variables, we calculated proportions, and for continuous variables, we calculated the mean, standard deviation, and quintiles. We then conducted bivariate analyses to assess for differences in masculine self-esteem scores by each factor. Since the masculine self-esteem scores were non-normally distributed (i.e., nonparametric) we used the Kruskal–Wallis test to calculate P-values to assess differences with categorical variables and Spearman's rho to assess for correlation with continuous variables.

A multivariate, generalized linear model was then developed to control for potential confounders and identify factors associated with masculine self-esteem. To ensure that no important variables were overlooked, we identified independent variables for inclusion in the model based on a combination of their importance in the PCa literature or their potentially confounding effect. The final model included all variables with a P < 0.15 on bivariate analysis, and we then eliminated variables in a stepwise manner, retaining those chosen a priori as relevant for clinical reasons. Confounders were identified based on either results reported in the PCa literature or when a statistically significant association was identified between both masculine self-esteem and our primary independent variable (age) on bivariate analysis.

Age was categorized into three age groups: 50–64, 65–74, and 75+ years. Since the time since PCa diagnosis was highly variable among the respondents, we also included this variable in the model to help preserve the validity of the results. All variables included in the final model were also assessed for colinearity (Spearman's rho >0.60), and if two variables were found to be colinear, then one was dropped from the model. For the anxiety and depression measures, we chose to use the MCS as a combined mental health measure rather than the two single-item questions since the MCS is better validated and has been found to be a useful screening tool for both depression and anxiety disorders.37,38 We then calculated the regression coefficients and accompanying 95% confidence intervals for all variables in the model. All analyses were conducted using SAS version 9.2 (Cary, NC).

Results

Sample characteristics

Most subjects (72%) learned about the study through our advertising in a national gay magazine or through a friend who had participated. Of the 138 surveys that were mailed, 133 were returned. Due to concerns of introducing selection and measurement bias, 22 men were excluded from the analysis because they did not meet our inclusion criteria (n = 16) or reported long-term hormone replacement therapy within the first 6 months postdiagnosis (n = 6). Our available sample for analysis was therefore 111 men.

Table 1 shows the characteristics of the gay men in our sample. Overall, men were predominantly white with proportionate representation of both younger (ages 50–64) and older men (ages 65–74 and age 75 or older); more than half were in partnered relationships. Men were well educated, all reported having health insurance, and half reported an annual income of $50,000 or more. The average number of years since PCa diagnosis was six; however, respondents reported a wide range of time since diagnosis (1–30 years). EPIC urinary and bowel function scores were high (82.0 ± 15.7 and 89.3 ± 12.4, respectively) with sexual function reported lower at 36.6 ± 20.6. Most men (60%) received a radical prostatectomy within the first 6 months after diagnosis and the majority (77%) reported feeling comfortable revealing their sexual orientation to their doctor. Approximately half reported having up to five close friends and relatives, while the remainder reported more than five close friends or relatives; a small percentage (4%) reported having no close friends or relatives. Sixty percent reported replacing sex with other activities following PCa treatment, 18% reported experiencing severe stigma over the past month, while the majority when asked about the helpfulness of their relationship with their PCa doctor reported scores of four or greater on a five-point Likert scale.

Table 1.

Characteristics of Gay Prostate Cancer Survivors

  Gay survivors (N = 111)
Age, n (%)
 50–64 46 (41.4)
 65–74 46 (41.4)
 ≥75 19 (17.2)
Partnership status, n (%)
 Partnered 69 (62.2)
 Unpartnered 42 (37.8)
Race, n (%)
 White 99 (89.2)
 Nonwhite 8 (7.2)
 Missing 4 (3.6)
Highest level of education, n (%)
 High school or less 12 (10.8)
 At least some college 99 (89.2)
Insurance, n (%)
 Private insurance 47 (42.4)
 Medicare 42 (37.8)
 Medicaid 7 (6.3)
 Other 15 (13.5)
Employment, n (%)
 Employed 47 (42.3)
 Unemployed 9 (8.1)
 Retired 55 (49.6)
Annual income, n (%)
 Less than $50,000 49 (44.1)
 $50,000 or more 54 (48.7)
 Missing 8 (7.2)
Years since prostate cancer diagnosis
 Mean ± SD 6.4 ± 5.4
 0/25th/50th/75th/100th 1/2/4/10/30
Prostate cancer treatments received first 6 months after diagnosis, n (%)
 Radical prostatectomy 67 (60.4)
 External beam radiation 16 (14.4)
 Brachytherapy 14 (12.6)
 Other 4 (3.6)
 Watch and wait 10 (9.0)
Rising PSA after first treatment, n (%)
 Yes 21 (18.9)
 No 83 (74.8)
 Do not know 7 (6.3)
EPIC scores
 Urinary function
  Mean ± SD 82.0 ± 15.7
  0/25th/50th/75th/100th 18/74/86/93/100
 Bowel function
  Mean ± SD 89.3 ± 12.4
  0/25th/50th/75th/100th 38/85/94/98/100
 Sexual function
  Mean ± SD 36.6 ± 20.6
  0/25th/50th/75th/100th 0/20/36/52/81
SF-12
 Physical component score
  Mean ± SD 48.6 ± 10.1
  0/25th/50th/75th/100th 21/42/52/56/63
 Mental component score
  Mean ± SD 48.6 ± 10.1
  0/25th/50th/75th/100th 22/42/52/57/61
Social support
 Social support (five items from MOS)
  Mean ± SD 3.9 ± 1.1
  0/25th/50th/75th/100th 1/3/4/5/5
 Number of close friends and relatives, n (%)
  0 4 (3.6)
  1–5 52 (46.9)
  6–10 22 (19.8)
  More than 10 33 (29.7)
Replaced sex with other activities, n (%)
 Yes 65 (58.6)
 No 46 (41.4)
Severe stigma, n (%)
 Yes 20 (18.0)
 No 91 (82.0)
Helpful relationship with prostate cancer doctor
  Mean ± SD 4.0 ± 1.2
  0/25th/50th/75th/100th 1/3/5/5/5
Patient comfortable revealing sexual orientation to doctor
 Yes 84 (77.1)
 No 25 (22.9)

Cell counts totaling less than 111 represent participant nonresponse.

EPIC, expanded prostate cancer index composite; MOS, medical outcomes study; PSA, prostate-specific antigen; SD, standard deviation.

Bivariate analyses

Table 2 shows the bivariate associations with the masculine self-esteem score. The strongest associations were found between replacing sex with other activities, severe stigma in the past month, and masculine self-esteem. On average, gay men who reported replacing sex with other activities also reported masculine self-esteem scores nearly 20 points lower than men who did not. A difference in scores of similar magnitude was also seen among men who reported experiencing severe stigma over the past month compared with men who did not. A moderate positive correlation was also identified between masculine self-esteem score and MCS (Spearman's rho = 0.36, P = 0.0002). Masculine self-esteem scores also differed significantly by age with men aged 50–64 years reporting the lowest scores and men aged 75 years or older reporting the highest scores (P = 0.002). Finally, men who were comfortable revealing their sexual orientation to their doctor reported masculine self-esteem scores that were 15 points higher on average than men who were not (P = 0.0001).

Table 2.

Associations with Masculine Self-Esteem Scores Among Gay Prostate Cancer Survivors

  Average masculine self-esteem score ± SD (N = 111) P
Age
 50–64 66.6 ± 19.8 0.002
 65–74 74.8 ± 19.0  
 ≥75 84.8 ± 13.6  
Partnership status   0.65
 Partnered 72.6 ± 19.2  
 Unpartnered 73.8 ± 20.3  
Race
 White 72.5 ± 19.0 0.50
 Nonwhite 76.8 ± 24.2  
 Missing 79.7 ± 26.6  
Highest level of education
 High school or less 70.6 ± 22.7 0.72
 At least some college 73.4 ± 19.2  
Insurance   0.19
 Private insurance 68.5 ± 20.0  
 Medicare 75.6 ± 19.0  
 Medicaid 78.6 ± 14.9  
 Other 77.7 ± 19.8  
Employment   0.26
 Employed 69.0 ± 22.0  
 Unemployed 78.9 ± 11.4  
 Retired 75.5 ± 17.8  
Annual income   0.31
 Less than $50,000 70.9 ± 19.2  
 $50,000 or more 73.8 ± 20.6  
 Missing 81.6 ± 11.7  
Years since prostate cancer diagnosis   0.34
 Spearman's rho 0.09  
Prostate cancer treatments received first 6 months after diagnosis   0.49
 Radical prostatectomy 70.4 ± 20.6  
 External beam radiation 75.1 ± 17.9  
 Brachytherapy 77.0 ± 18.6  
 Other 82.6 ± 22.3  
 Watch and wait 78.4 ± 13.2  
Rising PSA after first treatment   0.06
 Yes 64.7 ± 18.5  
 No 74.6 ± 19.7  
 Do not know 80.7 ± 13.3  
EPIC Scores
 Urinary Function
  Spearman's rho 0.19 0.06
 Bowel Function
  Spearman's rho 0.13 0.19
 Sexual Function
  Spearman's rho 0.22 0.02
SF-12
 Physical component score   0.04
  Spearman's rho 0.20  
 Mental component score   0.0002
  Spearman's rho 0.36  
Social support
 Social support  (five items from MOS)   0.01
  Spearman's rho 0.24  
Number of close friends and relatives   0.048
 0 80.5 ± 20.5  
 1–5 68.5 ± 19.5  
 6–10 73.1 ± 17.9  
 More than 10 79.0 ± 19.4  
Replaced sex with other activities   <0.0001
 Yes 66.3 ± 19.2  
 No 82.9 ± 15.4  
Severe stigma   <0.0001
 Yes 54.7 ± 15.8  
 No 77.2 ± 17.9  
Helpful relationship with prostate cancer doctor   0.01
 Spearman's rho 0.24  
Patient comfortable revealing sexual orientation to doctor   0.001
 Yes 76.7 ± 18.4  
 No 61.8 ± 19.6  

P-values were calculated based on the Kruskal–Wallis test or Spearman's correlation as appropriate.

Multivariate model

Our final adjusted model results (Table 3) closely reflected the associations we identified in our unadjusted bivariate results (Table 2). After simultaneously adjusting for the factors in our multivariate model, men aged 50–64 years and men aged 65–74 years reported lower masculine self-esteem scores than men aged 75 years or older (Table 3). A similar effect was also seen among men who reported recent severe stigma (i.e., past 4 weeks). Men who reported feeling comfortable revealing their sexual orientation to their doctor reported higher masculine self-esteem scores than men who were not. The mental component score from the SF-12 also remained positively correlated with masculine self-esteem after adjusting for other factors.

Table 3.

Multivariate Model of Masculine Self-Esteem Among Gay Prostate Cancer Survivors

  Masculine self-esteem score (N = 108)
Independent variables B (95% CI) P
Age
 50–64 −17.69 (−28.91, −6.46) 0.002
 65–74 −14.55 (−24.47, −4.64) 0.004
 ≥75 Referent  
Partnership status
 Unpartnered −1.86 (−8.67, 4.96) 0.59
 Partnered Referent  
Education
 Less than college −4.70 (−15.39, 5.99) 0.39
 At least some college Referent  
EPIC Scores
 Urinary function −0.09 (−0.32, 0.14) 0.44
 Bowel function 0.02 (−0.28, 0.31) 0.92
 Sexual function 0.09 (−0.07, 0.24) 0.26
Replaced sex with other activities
 Yes −6.36 (−13.59, 0.86) 0.08
 No Referent  
Severe stigma
 Yes −8.53 (−17.16, 0.09) 0.05
 No Referent  
Patient comfortable revealing sexual orientation to doctor
 Yes 17.47 (10.14, 24.79) <0.0001
 No Referent  
SF-12
 Physical component  score 0.23 (−0.10, 0.56) 0.17
 Mental component  score 0.38 (0.06, 0.71) 0.02

All P-values were calculated from generalized linear models using maximum likelihood estimation. Model simultaneously adjusts for all variables. Models also adjusted for years since prostate cancer diagnosis, prostate cancer treatment received first 6 months after diagnosis, and number of close friends and relatives.

Discussion

Similarities to straight PCa survivors

The negative impact of the loss of sexual functioning and other side effects of PCa treatment on the masculine self-esteem of our sample is similar to that reported by straight men. Reported decreases in masculine self-esteem following PCa treatment among straight men, especially when accompanied by loss of sexual function, may be found in the PCa literature.1,39,40 Correspondingly, while not found to be a differentiating factor within our sample, decrements in mental health status have also been reported following PCa treatment among straight men, most commonly manifesting as increased anxiety and/or depression.31,41–43

Gay men aging

Compared with older men, younger men reported lower masculine self-esteem. Studies of PCa survivors in presumptively straight populations are consistent with these findings, indicating that life experience such as dealing with cancer in their friends and family or their own experiences with other chronic conditions may increase the confidence and coping ability of older men when faced with a PCa diagnosis. Younger men are also more likely to be employed (rather than retired) with greater access to resources and may have different health expectations than their older counterparts, especially concerning cancer diagnoses. In addition, younger men may feel the loss of sexual function more acutely than older men,44 especially as sexuality plays a central role in both gay and straight masculine identity.45

Older gay men reporting higher masculine self-esteem is also consistent with emerging research on resiliency in LGBT aging populations. Fredriksen-Goldsen et al. found that a high proportion of LGBT elders feel good about belonging to their communities and many (similar to the gay men in our study) have at least moderate levels of social support.23 In addition, a large number of LGBT older adults in this study were found to engage regularly in wellness activities and moderate physical activity.23 These may represent uniquely protective factors for LGBT communities in terms of physical and mental health and ones which help to promote resiliency over time, especially during a health crisis such as intensive cancer treatment and recovery.

Stigma and disclosure of sexual orientation

While there have been studies that have documented feelings of stigma, guilt, shame, and self-blame among cancer survivors and the negative effect of these feelings on psychological adjustment following treatment,46,47 for LGBT patients, these feelings are also compounded by stigma experienced as part of their sexual orientation, magnifying the risk associated with poor mental health among gay elders. Men who reported feeling comfortable revealing their sexual orientation to their doctor also reported higher masculine self-esteem scores. This finding suggests that open communication with one's PCa physician may be an important factor in a gay man's recovery from PCa. Given that few PCa support groups exist specifically for gay men, increased opportunities for speaking openly and in a safe environment about treatment concerns and changes in sexual function could benefit post-treatment QoL for gay and bisexual men.

Methodological recommendations and limitations

This study has some important limitations. Its cross-sectional design precludes examination of causal or temporal relationships. In addition, varying time intervals between diagnosis and the survey may influence reported outcomes through recall bias and adaptation to post-treatment changes, resulting in improved QoL in the time since diagnosis and treatment, despite our attempt to control for this in our multivariate analyses. Our single-item questions on anxiety and depression were included as measures of relevant comorbidity, modeled after the format of the self-report version of the Charlson Comorbidity Index,48 and were included as part of this inventory. We chose this approach to ascertain significant diagnosed depression and anxiety as relevant comorbidity. There was also some concern that using additional validated scales might overlap with the measurement of depression and anxiety symptoms by the MCS in the SF-12. Future studies should compare the performance of single-item anxiety and depression questions to the MCS in larger LGBT samples using a clinical mental health diagnosis as the gold standard. Our social support items also only measured positive social support relationships without considering important detrimental social interactions.49

Our subjects were self-selected, limiting our study's generalizability. Due to a lack of national health data sources in the United States that collect information on sexual orientation and gender identity, many researchers of LGBT health cannot recruit survey respondents or analyze data from the general population and instead use LGBT-oriented sources such as LGBT websites and community publications.50–53 However, men who contacted us were highly motivated to participate in the hope that their participation might help other gay PCa survivors, as our high response rate indicates. In addition, despite our best outreach and recruitment efforts, few racial or ethnic minority men contacted us. However, our population is one of the largest samples of gay PCa survivors ever studied. The large sample size, high response rate, and comprehensive survey instrument, which allowed us to adjust for important known confounders of PCa QoL, provide important previously unavailable information about the QoL of gay PCa survivors.

Conclusion

This study draws attention to gay men as an invisible minority among PCa survivors who share many of the same effects as their heterosexual peers, although they are distinguished by experiences of resiliency and stigma. PCa providers are in a unique position to help reduce stigma and promote resiliency by being aware that they might have gay patients, creating a supportive environment where gay patients can discuss specific sexual concerns, and engaging patients in treatment decisions. These efforts by providers could help not only in reducing stigma but also in increasing masculine self-esteem, which may in turn positively influence gay patients' recovery, QoL, and compliance with follow-up care.

Acknowledgments

This research was supported by a grant from the National Cancer Institute (Co-PIs: D.A.-D./J.C., 1R03CA136114-01A1). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Cancer Institute or the National Institutes of Health. The authors would like to thank the gay PCa survivors who agreed to participate in this study.

Author Disclosure Statement

No competing financial interests exist.

References

  • 1.Clark JA, Inui TS, Silliman RA, et al. : Patients' perceptions of quality of life after treatment for early prostate cancer. J Clin Oncol 2003;21:3777–3784 [DOI] [PubMed] [Google Scholar]
  • 2.Baumeister RF. The self. In: The Handbook of Social Psychology. Edited by Gilbert DT, Fiske ST, Lindzey G. New York: Random House, 1998, p. 680 [Google Scholar]
  • 3.Pleck JH: The Myth of Masculinity. Cambridge: MIT Press, 1981 [Google Scholar]
  • 4.Pleck JH: The Gender Role Strain Paradigm: An Update. In: A New Psychology of Men. Edited by Levant RF, Pollack WS. New York: Basic Books, 1995. [Google Scholar]
  • 5.Broom A: Virtually he@lthy: The impact of internet use on disease experience and the doctor-patient relationship. Qual Health Res 2005;15:325–345 [DOI] [PubMed] [Google Scholar]
  • 6.Broom A: The eMale: Prostate cancer, masculinity and online support as a challenge to medical expertise. J Sociol 2005;41:87–104 [Google Scholar]
  • 7.Oliffe J, Thorne S: Men, masculinities, and prostate cancer: Australian and Canadian patient perspectives of communication with male physicians. Qual Health Res 2007;17:149–161 [DOI] [PubMed] [Google Scholar]
  • 8.Paiva EP, Motta MC, Griep RH: Barriers related to screening examinations for prostate cancer. Rev Lat Am Enfermagem 2011;19:73–80 [DOI] [PubMed] [Google Scholar]
  • 9.Chen RC, Clark JA, Manola J, Talcott JA: Treatment “mismatch” in early prostate cancer: Do treatment choices take patient quality of life into account? Cancer 2008;112:61–68 [DOI] [PubMed] [Google Scholar]
  • 10.Davison BJ, Goldenberg SL: Decisional regret and quality of life after participating in medical decision-making for early-stage prostate cancer. BJU Int 2003;91:14–17 [DOI] [PubMed] [Google Scholar]
  • 11.Eton DT, Lepore SJ, Helgeson VS: Early quality of life in patients with localized prostate carcinoma: An examination of treatment-related, demographic, and psychosocial factors. Cancer 2001;92:1451–1459 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Badr H, Taylor CL: Sexual dysfunction and spousal communication in couples coping with prostate cancer. Psychooncology 2009;18:735–746 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Couper J, Bloch S, Love A, et al. : Psychosocial adjustment of female partners of men with prostate cancer: A review of the literature. Psychooncology 2006;15:937–953 [DOI] [PubMed] [Google Scholar]
  • 14.Garos S, Kluck A, Aronoff D: Prostate cancer patients and their partners: Differences in satisfaction indices and psychological variables. J Sex Med 2007;4:1394–1403 [DOI] [PubMed] [Google Scholar]
  • 15.Wall D, Kristjanson L: Men, culture and hegemonic masculinity: Understanding the experience of prostate cancer. Nurs Inq 2005;12:87–97 [DOI] [PubMed] [Google Scholar]
  • 16.Helgeson VS, Lepore SJ, Eton DT: Moderators of the benefits of psychoeducational interventions for men with prostate cancer. Health Psychol 2006;25:348–354 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Messaoudi R, Menard J, Ripert T, et al. : Erectile dysfunction and sexual health after radical prostatectomy: Impact of sexual motivation. Int J Impot Res 2011;23:81–86 [DOI] [PubMed] [Google Scholar]
  • 18.Powel LL: Quality of life in men with urinary incontinence after prostate cancer surgery. J Wound Ostomy Continence Nurs 2000;27:174–178 [DOI] [PubMed] [Google Scholar]
  • 19.Thornton AA, Perez MA, Oh S, Crocitto L: A prospective report of changes in prostate cancer related quality of life after robotic prostatectomy. J Psychosoc Oncol 2011;29:157–167 [DOI] [PubMed] [Google Scholar]
  • 20.Burns SM, Mahalik JR: Understanding how masculine gender scripts may contribute to men's adjustment following treatment for prostate cancer. Am J Mens Health 2007;1:250–261 [DOI] [PubMed] [Google Scholar]
  • 21.Blank TO: Gay men and prostate cancer: Invisible diversity. J Clin Oncol 2005;23:2593–2596 [DOI] [PubMed] [Google Scholar]
  • 22.Hart TL, Coon DW, Kowalkowski MA, et al. : Changes in sexual roles and quality of life for gay men after prostate cancer: Challenges for sexual health providers. J Sex Med 2014;11:2308–2317 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Fredriksen-Goldsen KI, Hyun-Jun K, Emlet CA, et al. : The Aging And Health Report: Disparities and Resilience Among Lesbian, Gay, Bisexual, and Transgender Older Adults. Seattle: University of Washington, 2011 [Google Scholar]
  • 24.Fredriksen-Goldsen KI, Emlet CA, Kim HJ, et al. : The physical and mental health of lesbian, gay male, and bisexual (LGB) older adults: The role of key health indicators and risk and protective factors. Gerontologist 2013;53:664–675 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Beren SE, Hayden HA, Wilfley DE, Grilo CM: The influence of sexual orientation on body dissatisfaction in adult men and women. Int J Eat Disord 1996;20:135–141 [DOI] [PubMed] [Google Scholar]
  • 26.Siever MD: Sexual orientation and gender as factors in socioculturally acquired vulnerability to body dissatisfaction and eating disorders. J Consult Clin Psychol 1994;62:252–260 [DOI] [PubMed] [Google Scholar]
  • 27.Herzog DB, Newman KL, Warshaw M: Body image dissatisfaction in homosexual and heterosexual males. J Nerv Ment Dis 1991;179:356–359 [DOI] [PubMed] [Google Scholar]
  • 28.Johnson K, Gill S, Reichman V, Tassinary LG: Swagger, sway, and sexuality: Sexual orientation from body motion and morphology. J Pers Soc Psychol 2007;93:321–334 [DOI] [PubMed] [Google Scholar]
  • 29.Lippa RA: Sexual orientation and personality. Ann Rev Sex Res 2005;16:119–153 [PubMed] [Google Scholar]
  • 30.Pierrehumbert JB, Bent T, Munson B, et al. : The influence of sexual orientation on vowel production (L). JASA 2004;116:1905–1908 [DOI] [PubMed] [Google Scholar]
  • 31.Clark JA, Bokhour BG, Inui TS, et al. : Measuring patients' perceptions of the outcomes of treatment for early prostate cancer. Med Care 2003;41:923–936 [DOI] [PubMed] [Google Scholar]
  • 32.Ware J, Kosinski M, Keller SD: A 12-item short-form health survey: Construction of scales and preliminary tests of reliability and validity. Med Care 1996;34:220–233 [DOI] [PubMed] [Google Scholar]
  • 33.Wei JT, Dunn RL, Litwin MS, et al. : Development and validation of the expanded prostate cancer index composite (EPIC) for comprehensive assessment of health-related quality of life in men with prostate cancer. Urology 2000;56:899–905 [DOI] [PubMed] [Google Scholar]
  • 34.MacDonald LD, Anderson HR: Stigma in patients with rectal cancer: A community study. J Epidemiol Community Health 1984;38:284–290 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Stewart AL, Ware JE, eds.: Measuring Functioning and Well-Being: The Medical Outcomes Study Approach. Durham, Duke University Press, 1992 [Google Scholar]
  • 36.Van der Feltz-Cornelis CM, Van Oppen P, Van Marwijk HW, et al. : A patient-doctor relationship questionnaire (PDRQ-9) in primary care: Development and psychometric evaluation. Gen Hosp Psychiatry 2004;26:115–120 [DOI] [PubMed] [Google Scholar]
  • 37.Gill SC, Butterworth P, Rodgers B, Mackinnon A: Validity of the mental health component scale of the 12-item short-form health survey (MCS-12) as measure of common mental disorders in the general population. Psychiatry Res 2007;152:63–71 [DOI] [PubMed] [Google Scholar]
  • 38.Vilagut G, Forero CG, Pinto-Meza A, et al. : The mental component of the short-form 12 health survey (SF-12) as a measure of depressive disorders in the general population: Results with three alternative scoring methods. Value Health 2013;16:564–573 [DOI] [PubMed] [Google Scholar]
  • 39.Chambers SK, Schover L, Nielsen L, et al. : Couple distress after localised prostate cancer. Support Care Cancer 2013;21:2967–2976 [DOI] [PubMed] [Google Scholar]
  • 40.Zaider T, Manne S, Nelson C, et al. : Loss of masculine identity, marital affection, and sexual bother in men with localized prostate cancer. J Sex Med 2012;9:2724–2732 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Kohler N, Friedrich M, Gansera L, et al. : Psychological distress and adjustment to disease in patients before and after radical prostatectomy. Results of a prospective multi-centre study. Eur J Cancer Care (Engl) 2014;23:795–802 [DOI] [PubMed] [Google Scholar]
  • 42.Ravi P, Karakiewicz PI, Roghmann F, et al. : Mental health outcomes in elderly men with prostate cancer. Urol Oncol 2014;32:1333–1340 [DOI] [PubMed] [Google Scholar]
  • 43.Taoka R, Matsunaga H, Kubo T, et al. : Impact of trait anxiety on psychological well-being in men with prostate cancer. Int Braz J Urol 2014;40:620–626 [DOI] [PubMed] [Google Scholar]
  • 44.Diefenbach M, Mohamed NE, Horwitz EM, Pollack A: Longitudinal associations among quality of life and its predictors in patients treated for prostate cancer: The moderating role of age. Psychol Health Med 2008;13:146–161 [DOI] [PubMed] [Google Scholar]
  • 45.Lodge AC, Umberson D: Age and embodied masculinities: Midlife gay and heterosexual men talk about their bodies. J Aging Stud 2013;27:225–232 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Else-Quest NM, LoConte NK, Schiller JH, Hyde JS: Perceived stigma, self-blame, and adjustment among lung, breast and prostate cancer patients. Psychol Health 2009;24:949–964 [DOI] [PubMed] [Google Scholar]
  • 47.LoConte NK, Else-Quest NM, Eickhoff J, et al. : Assessment of guilt and shame in patients with non-small-cell lung cancer compared with patients with breast and prostate cancer. Clin Lung Cancer 2008;9:171–178 [DOI] [PubMed] [Google Scholar]
  • 48.Chaudhry S, Jin L, Meltzer D: Use of a self-report-generated Charlson Comorbidity Index for predicting mortality. Med Care 2005;43:607–615 [DOI] [PubMed] [Google Scholar]
  • 49.Mehnert A, Lehmann C, Graefen M, et al. : Depression, anxiety, post-traumatic stress disorder and health-related quality of life and its association with social support in ambulatory prostate cancer patients. Eur J Cancer Care (Engl) 2010;19:736–745 [DOI] [PubMed] [Google Scholar]
  • 50.Fernandez MI, Warren JC, Varga LM, et al. : Cruising in cyber space: Comparing internet chat room versus community venues for recruiting hispanic men who have sex with men to participate in prevention studies. J Ethn Subst Abuse 2007;6:143–162 [DOI] [PubMed] [Google Scholar]
  • 51.Fisher HH, Purcell DW, Hoff CC, et al. : Recruitment source and behavioral risk patterns of HIV-positive men who have sex with men. AIDS Behav 2006;10:553–561 [DOI] [PubMed] [Google Scholar]
  • 52.Grov C, Bux D, Jr., Parsons JT, Morgenstern J: Recruiting hard-to-reach drug-using men who have sex with men into an intervention study: Lessons learned and implications for applied research. Subst Use Misuse 2009;44:1855–1871 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Harro CD, Judson FN, Gorse GJ, et al. : Recruitment and baseline epidemiologic profile of participants in the first phase 3 HIV vaccine efficacy trial. J Acquir Immune Defic Syndr 2004;37:1385–1392 [DOI] [PubMed] [Google Scholar]

Articles from LGBT Health are provided here courtesy of Mary Ann Liebert, Inc.

RESOURCES