Skip to main content
Springer logoLink to Springer
. 2016 Jun 17;25(12):3027–3035. doi: 10.1007/s11136-016-1341-3

The role of mindfulness in distress and quality of life for men with advanced prostate cancer

Suzanne K Chambers 1,2,3,4,5,6,, Elizabeth Foley 7, Samantha Clutton 2,6, Robert McDowall 2,6, Stefano Occhipinti 6,8, Martin Berry 6,9, Martin R Stockler 6,10,11, Stephen J Lepore 12, Mark Frydenberg 6,13,14, Robert A Gardiner 4,5,6,15, Ian D Davis 6,16,17, David P Smith 1,6,18
PMCID: PMC5102949  PMID: 27315118

Abstract

Objective

To examine the extent to which mindfulness skills influence psychological distress and health-related quality of life (HRQOL) in men with metastatic or castration-resistant biochemical progression of prostate cancer.

Patients and methods

A cross-sectional survey of 190 men (46 % response; mean age 71 years, SD = 8.7, range 40–91 years) with advanced prostate cancer, assessed psychological and cancer-specific distress, HRQOL. Mindfulness skills were assessed as potential predictors of adjustment outcomes.

Results

Overall, 39 % of men reported high psychological distress. One third had accessed psychological support previously although only 10 % were under current psychological care. One quarter had accessed a prostate cancer support group in the past six months.

Higher HRQOL and lower cancer-specific and global psychological distress were related to non-judging of inner experience (p < 0.001).

Higher HRQOL and lower psychological distress were related to acting with awareness (p < 0.001). Lower distress was also related to higher non-reactivity to inner experience and a lower level of observing (p < 0.05).

Conclusions

Men with advanced prostate cancer are at risk of poor psychological outcomes. Psychological flexibility may be a promising target for interventions to improve adjustment outcomes in this patient group.

Clinical Trial Registry

Trial Registration: ACTRN12612000306819

Keywords: Quality of life, Advanced prostate cancer, Psychological distress

Introduction

Prostate cancer is the second most frequently diagnosed cancer in men worldwide, with an estimated 1.1 million new cases diagnosed in 2012 [1]. It is the fifth most common cause of cancer death internationally. Incidence rates vary 25-fold worldwide, with highest rates in Australia and New Zealand. An estimated 1 in 5 Australian men will develop prostate cancer in their lifetime, and 1 in 28 will die of prostate cancer [2]. Approximately, 5–10 % of newly diagnosed Australian men have locally advanced or metastatic disease [3, 4]. Although prostate cancer is generally a slow-growing cancer, recurrence or progression can develop over the long term, even among patients considered to have low risk at diagnosis [5]. Further, an estimated 1 in 5 Australian men diagnosed with localised disease progress to metastatic disease [6].

Most prostate cancer deaths arise as a result of disease progression, and historically the median survival for men with metastatic castrate-resistant prostate cancer has been less than 2 years. The relatively recent availability of new agents for advanced disease has provided greater hope of cancer control for these men as trials indicate improved survival time [7]. However, the reality is that advanced prostate cancer is an incurable disease, and for many men, their disease progression is associated with more frequent healthcare interventions due to increasing morbidities from disease and treatments [8], diminished quality of life [9], increased psychological burden [10] and an increased risk of suicide [11, 12].

To date no randomised controlled trials have reported interventions to improve psychological outcomes for men with advanced prostate cancer, with clinicians relying on studies in men with localised disease for practice recommendations [13]. Given that the psychological challenges of advanced versus localised disease will differ (i.e. hope for cure vs. knowledge of progression), this extrapolation is likely inappropriate. In developing psychological interventions for such men, a first step is to consider what modifiable variables might be relevant therapeutic targets in a context where disease is progressive and the future highly threatened. We propose that psychological flexibility may be important for men confronting the novel, complex and uncertain challenges of advanced prostate cancer. Psychological flexibility can be broadly defined as the ability to shift mindsets in the face of changing and challenging situational demands. This includes being more aware of and able to accommodate, rather than deny or distract from, unpleasant emotions and physical morbidities and from this guide ones thoughts and actions in a constructive direction [14]. Psychological flexibility is a high level and overarching construct that includes both acceptance and mindfulness, with these processes proposed as relevant to both clinical and general populations [15]. At its centre is an interaction between psychological content, the present moment and chosen values. Mindfulness is a key and core component that speaks to the cognitive fusion and experiential avoidance that is proposed to contribute to psychological inflexibility [16]. In both laboratory and clinical settings, greater psychological flexibility has been found to be linked to more positive psychological outcomes. Finally, psychological flexibility is proposed to be stable over time, but importantly appears to be amenable to psychological intervention and as such a potential intervention target [17].

Interventions to encourage psychological flexibility, and in particular mindfulness facets or skills, are increasingly being applied in cancer populations as a psychotherapeutic approach to improving adjustment after cancer. Mindfulness approaches aim to lead the person to be less reactive to difficult experiences and to approach equanimity regarding the illness experience [18]. These approaches assume therefore a connection between these psychological facets and a person’s psychological outcomes and quality of life. However, to our knowledge no research to date has tested this assumption in men with prostate cancer, and hence it is unknown empirically whether the facets of mindfulness are related to these patients’ adjustment outcomes. Accordingly, the present study aimed to describe psychological distress and quality of life in men with advanced prostate cancer and examine the influence of mindfulness on these outcomes.

Patients and methods

The present study utilised baseline data from an Australian randomised controlled trial of a mindfulness intervention for men with advanced prostate cancer [19]. Eligible participants were men with metastatic prostate cancer or castration-resistant biochemical progression who were referred to the trial by their treating medical specialist. Other eligibility criteria included: ability to read and speak English; no history of head injury, dementia or current psychiatric illness; and no concurrent cancer. All participants provided written informed consent. The trial received approval from the Griffith University Human Research Ethics Committee and the human research ethics committees of participating hospitals across Australia. Further detail about this trial is provided in Chambers et al. [19].

Sociodemographic information was collected in a telephone interview. Trained researchers used a data collection protocol to obtain clinical, disease and treatment information through medical records review. Psychosocial measures were completed by participants via mailed self-administered questionnaires. These measures are outlined below.

Mindfulness facets

The 39-item Five Facet Mindfulness Questionnaire (FFMQ) measures engagement with the principles of mindfulness and contains five subscales: observing or noticing ones reaction; being able to describe this reaction; acting with awareness; non-judging of inner experience; and non-reactivity to inner experience [20]. Items were scored 1 (never or very rarely true) to 5 (very often or always true) and summed to create subscale scores with higher scores indicating greater engagement with each principle or facet (score range for observing, describing, acting with awareness, non-judging of inner experience 8–40; non-reactivity to inner experience 7–35). Internal reliability was acceptable for subscales (α = 0.78–0.90) and the total scale (α = 0.86).

Health-related quality of life

The 39-item Functional Assessment of Cancer Therapy-Prostate (FACT-P) assesses men’s perceived global quality of life across five domains: physical, social/family, emotional, functional well-being and prostate cancer-specific concerns [21]. For this study, items were scored 0 (not at all) to 5 (very much) and averaged to create subscale scores, with these subscale scores then summed to create a global quality of life score (score range 0–156). Higher scores indicated greater perceived quality of life (α = 0.91). The average FACT-P total score for men with advanced disease was reported by Esper et al. as 109.8 [21].

Psychological distress

The Brief Symptom Inventory-18 (BSI-18) provides a global measure of current psychological distress with subscale scores for anxiety, depression and somatisation [22]. In the current study, the 18 items were scored 0 (not at all) to 4 (extremely) and summed to create a Global Severity Index (GSI) with higher scores indicating greater distress (score range 0–72; α = 0.91). Raw scores were transformed into standardised t scores to determine the proportion of men who met the criteria for caseness. Caseness has been reported as a standardised t score of 57 or above on the GSI or any two subscales in men with cancer [23]. This cut-off score was used to indicate the percentage of men with clinical psychological distress in this sample.

Cancer-specific distress

The 15-item Impact of Events Scale (IES) measures men’s cancer-specific distress and contains two subscales: intrusive symptoms and avoidance symptoms [24]. Items were scored 0 (not at all) to 5 (extremely) and summed to create an overall score with higher scores indicating greater distress (score range 0–75; α = 0.93). A score of 20 or above on either the intrusive or avoidance symptoms subscale was used to calculate the proportion of men with clinical cancer-specific distress, and this is in line with the cut-off score used for the IES in advanced cancer patients [25].

Statistical analyses

Three hierarchical regressions examined the factors associated with quality of life, cancer-specific distress and psychological distress. Variables were entered into the regression in the following order: Step 1: sociodemographic and clinical characteristics (age, marital status, education level, the presence of a limiting comorbidity, time since diagnosis) and Step 2: the five facets of the FFMQ (observing, describing, acting with awareness, non-judging of inner experience, non-reactivity to inner experience). Categorical variables of marital status (1 married/de facto; 0 single), education level (1 tertiary; 0 high school or less) and the presence of a limiting comorbidity (1 yes; 0 no) were coded dichotomously for the analysis. Pairwise deletion was used for missing data.

Results

Patients

Between September 2012 and January 2015, 472 patients were referred to participate in the study; of these 190 completed the assessment (61 were ineligible and 221 declined to participate). Thirteen of the 190 men self-referred to the project team in response to media about the project and were assessed for eligibility prior to recruitment. The sociodemographic characteristics, self-reported health status and prostate cancer history are reported in Table 1. For prostate cancer history, medical record data were not obtainable for all patients and are reported accordingly.

Table 1.

Sample sociodemographic characteristics, self-reported health status and prostate cancer history (n = 190)

Variable
Age 70.8 years (8.7 years)
Married or de facto relationship 75 %
Retired 68 %
Born in Australia 66 %
University or college degree 66 %
BMI
Overweight range 47 %
Obese range 28 %
Smoking history
Ex-smoker 45 %
Current smoker 7 %
Comorbid health conditions
Any condition 92 %
Back pain 59 %
Osteoarthritis or degenerative arthritis 54 %
High blood pressure 48 %
Depression or anxiety 27 %
Heart disease 22 %
Diabetes 18 %
Lung disease 11 %
At least one condition limited current activities 58 %
Time since prostate cancer diagnosis 6 years (4.9 years)
Gleason score ≥ 8a 71 %
Prostate cancer stage b
T2 20 %
T3 55 %
T4 24 %
PSA levelc 50.6 ng/mL* (106.3 ng/mL)
Prostate cancer treatment d
Androgen deprivation therapy 97 %
Radiation therapy 69 %
Prostatectomy 44 %
Chemotherapy 31 %
Active surveillance 4 %
Watchful waiting 4 %
Orchidectomy 2 %

Values in parentheses are standard deviations for continuous variables

* PSA range = 0.01–588.9 ng/mL; PSA median = 7.94 ng/mL

a n = 114; b n = 83; c n = 160; d n = 171

Psychological care and support

Thirty-nine per cent of men met the criteria for clinical psychological distress as indicated by the BSI-18 [23]. Eighteen per cent of men met the criteria for clinical cancer-specific distress as indicated by the IES [25]. However, only 6 % of participants were currently receiving psychological care (psychiatrist, 2 %; psychologist, 4 %), and 11 % were taking medication for depression or anxiety. Thirty-four per cent had accessed some psychological care in the past (psychiatrist 10 %; psychologist 12 %; counsellor 14 %).

In the 6 months prior to the study, 56 % of men had received support for prostate cancer and this was predominantly from prostate cancer support groups (26 %), their doctor (26 %), books or brochures provided by their doctor (26 %), or the Internet (26 %). Men also received support from family or friends (17 %), a nurse or other health professional (16 %) and prostate cancer related newsletters (13 %). Although 58 % of participants reported previous use of the Internet for information about their prostate cancer, only 7 % used this to access online support groups or other social services.

Quality of life

Table 2 provides the descriptive statistics and inter-correlations for all variables in the main analyses. Sociodemographic and clinical characteristics entered at Step 1 of the hierarchical regression explained 13.3 % of the variance in quality of life, F(5, 149) = 4.58, p < 0.001. Limitation by comorbidity was the only significant predictor of quality of life at this step (B = −13.44, SE = 3.09, β = −.33, p < 0.001). The addition of the five facets of mindfulness in Step 2 significantly increased the explained variance by 30.4 %, F(5, 144) = 15.52, p < 0.001. Limitation by comorbidity remained a significant predictor of quality of life at this step contributing 2.8 % unique variance. Of the five facets acting with awareness and non-judging of inner experience were the only significant predictors of quality of life, contributing 3.1 and 9.3 % unique variance, respectively. Both of these facets had a positive relationship with quality of life (Table 3).

Table 2.

Descriptive statistics and inter-correlations among analysis variables

Variable M (SD) 1 2 3 4 5 6 7 8 9 10 11 12 13
1. QOL 111.74 (20.12)
2. Cancer-specific distress 15.72 (15.58) −.59**
3. Psychological Distress 52.40 (10.32) −.73** .64**
4. Age 70.79 (8.68) .11 −.15* −.14
5. Marital statusa .04 .01 −.05 −.05
6. Educationa .05 .09 −.04 −.15 −.04
7. Limited by comorbiditya −.35** .27** .30** −.06 .12 −.09
8. Time since diagnosis 5.95 (4.89) .14 −.15 −.07 .24* .05 −.06 .03
9. Observing 22.33 (6.73) −.05 .15* .18* −.01 .19* .11 .25* −.07
10. Describing 28.54 (6.63) .30** −.27** −.31** .06 .06 .15 −.03 .02 .28**
11. Acting with awareness 31.39 (6.10) .51** −.51** −.56** .12 .05 .04 −.30** .05 −.14 .42**
12. Non-judging of inner experience 31.93 (7.00) .53** −.60** −.57** .00 .04 .07 −.24* .04 −.27** .25** .55**
13. Non-reactivity to inner experience 20.78 (5.82) .06 .05 −.03 −.03 .04 .12 .08 −.01 .53** .37** −.04 −.11

Range of obtained scores for QOL 39–151; cancer-specific distress 0–61; psychological distress 0–45; age 40.38–91.80 years; time since diagnosis 0–25.90 years; observing 8–38; describing 11–40; acting with awareness 15–40; non-judging of inner experience 12–40; non-reactivity to inner experience 7–34

p < 0.05; ** p < 0.001

aCategorical variable; correlations calculated using Spearman’s Rho

Table 3.

Final step of hierarchical regression predicting quality of life (n = 155)

Predictors B SE β
Sociodemographic and clinical characteristics
Age −.03 .15 −.01
Marital status .37 3.00 .01
Education −.83 2.73 −.02
Limited by a comorbidity −7.27 2.74 −.18*
Time since diagnosis .37 .26 .09
Mindfulness facets
Observing .09 .26 .03
Describing .16 .24 .05
Acting with awareness .77 .27 .23*
Non-judging of inner experience 1.10 .23 .39**
Non-reactivity to inner experience .36 .27 .11

At the final step, the overall model was significant and explained 43.7 % of the variance in quality of life, F(10, 144) = 11.17, p < 0.001

p < 0.05; ** p < 0.001

Cancer-specific distress

In Step 1, sociodemographic and clinical characteristics explained 8.2 % of the variance in cancer-specific distress, F(5, 148) = 2.66, p = 0.02. Limitation by comorbidity was the only significant predictor of cancer-specific distress at this step (B = 7.14, SE = 2.59, β = .22, p < 0.01). The addition of the five facets of mindfulness in Step 2 significantly increased the explained variance by 42.8 %, F(4, 143) = 24.98, p < 0.001. At this final step, non-judging of inner experience was the only significant predictor of cancer-specific distress and contributed 18.3 % of unique variance. Greater non-judging was related to lower cancer-specific distress. Limitation by comorbidity was no longer significant at the second step with the addition of the mindfulness facets to the model (Table 4).

Table 4.

Final step of hierarchical regression predicting cancer-specific distress (n = 154)

Predictors B SE β
Sociodemographic and clinical characteristics
Age −.12 .12 −.06
Marital status .73 2.30 .02
Education 3.57 2.07 .11
Limited by a comorbidity .81 2.08 .02
Time since diagnosis −.20 .20 −.06
Mindfulness facets
Observing .05 .19 .02
Describing −.21 .18 −.09
Acting with awareness −.39 .21 −.15a
Non-judging of inner experience −1.25 .17 −.55**
Non-reactivity to inner experience −.03 .21 −.01

At the final step, the overall model was significant and explained 51.0 % of the variance in cancer-specific distress, F(10, 143) = 14.89, p < 0.001

p < 0.05; ** p < 0.001; a p = 0.057

Psychological distress

Sociodemographic and clinical characteristics in Step 1 explained 10.2 % of the variance in psychological distress, F(5, 148) = 3.36, p < 0.01. Limitation by comorbidity was the only significant predictor of psychological distress at this step (B = 6.11, SE = 1.65, β = .29, p < 0.001). In Step 2, the addition of the five facets of mindfulness significantly increased the explained variance by 41.3 %, F(5, 143) = 24.33, p < 0.001. Four out of the five facets were significant predictors of psychological distress at this final step. Non-judging of inner experience contributed the most unique variance (10 %) followed by acting with awareness (4.5 %), non-reactivity to inner experience (3.2 %) and observing (1.6 %). Each facet had a negative relationship with psychological distress with the exception of observing which had a positive relationship with distress. Limitation by comorbidity was no longer significant at the second step with the addition of the mindfulness facets to the model (Table 5).

Table 5.

Final step of hierarchical regression predicting psychological distress (n = 154)

Predictors B SE β
Sociodemographic and clinical characteristics
Age −.06 .08 −.05
Marital status −1.08 1.46 −.04
Education .23 1.33 .01
Limited by a comorbidity 1.88 1.33 .09
Time since diagnosis −.01 .13 −.00
Mindfulness facets
Observing .27 .12 .17*
Describing −.12 .11 −.08
Acting with awareness −.48 .13 −.28**
Non-judging of inner experience −.60 .11 −.40**
Non-reactivity to inner experience −.41 .13 −.23*

At the final step, the overall model was significant and explained 51.5 % of the variance in psychological distress, F(10, 143) = 15.16, p < 0.001

p < 0.05; ** p < 0.001

Discussion

Many of the men in this study reported high levels of psychological distress, with health-related quality of life similar to previous research with men with advanced prostate cancer [21]. Importantly, three key psychological mechanisms or mindfulness facets were associated with better outcomes: awareness, non-judgement and non-reactivity. Evidence suggests that people who judge their (especially negative) experiences can end up in a ruminative loop of “why am I feeling this way” which ironically has the effect of worsening distress [26]. Our results support this contention and suggest that interventions that promote awareness paired with non-judgement and non-reactivity may be useful in the setting of advanced prostate cancer. With regard to intervention research, to date a few preliminary studies have reported applying mindfulness approaches with men with prostate cancer. One single-arm trial of mindfulness-based stress reduction groups with 49 breast cancer patients and 10 men with localised prostate cancer found post-intervention improvements in quality of life and stress symptoms [27], with benefits maintained over time [28]. In a more recent study, men with advanced prostate cancer who participated in a mindfulness-based cognitive intervention targeting self-awareness, non-judgement and acceptance, reported moderate to large improvements in anxiety and fear of cancer recurrence [29]. In the present study, non-judging of inner experience demonstrated the strongest effect across both quality of life and psychological distress and this may be of particular relevance given masculine values around stoicism in the face of adversity that may exacerbate distress and isolation in a chronic illness [30]. Specifically, as cancer progresses and fears and concerns about the future naturally arise, a stoic approach may become difficult to maintain. Hence the development of a less judgemental and more flexible approach to coping may be crucial for men facing advanced prostate cancer. These are important and novel findings.

Despite high distress, most men were currently not receiving psychological care. This is consistent with previous research showing that men with prostate cancer often report unmet psychological needs [31] and again reinforces the need for action to detect men with high distress and provide targeted intervention [32]. Taking into account the apparent strong role of mindfulness facets across both QOL and distress, acceptance focussed approaches such as mindfulness-based cognitive therapies may be indicated [33]. Uptake of support groups was high in this cohort and was more accessed than professional psychological care. This may relate at least in part to the social isolation that can be experienced when cancer has advanced leading a person to seek support by connecting with others in a similar situation [34, 35]. These approaches appear worthy of future research.

It is noteworthy that being limited by comorbid conditions was an independent predictor of HRQOL, but not cancer-specific or global distress. This may be due to the fact that the HRQOL measure captures limitations in social and physical functioning which might be directly due to comorbid conditions, particularly arthritis and back pain that were highly prevalent in this population. The finding that physical limitations imposed by comorbid conditions were not strong predictors of distress after psychological flexibility was entered into the models suggests that this flexibility may mediate the distressing effects of other physical health problems, not just prostate cancer.

Limitations of the present study include the cross-sectional design such that causality cannot be inferred. However, the inclusion of modifiable psychological variables using well-validated assessment measures is novel, and the use of a relatively large national sample is a strength. Future longitudinal research is needed to test if these relationships persist over time. As well, the participation rate was only 46 % with men in the study reporting high levels of education. It may be that men who did not participate differed in other background or clinical characteristics as well as their levels of distress and as a result our study may well underrepresent levels of distress in this vulnerable patient group. Finally, we note that the observed facet was associated with greater distress, a direction of effect consistent with earlier research suggesting this subscale may not capture the quality of noticing one’s experience that is central to mindfulness-based approaches [20]. Future research in the cancer context is needed to expand assessments of psychological flexibility beyond mindfulness to include other processes, such as values exploration and committed action and from this fine-tune potential therapy targets [16].

In conclusion, several facets of mindfulness may hold promise as therapeutic targets to reduce psychological distress and improve QOL in men with advanced prostate cancer. Future longitudinal descriptive research is needed to examine the influence of not only psychological flexibility in its broader definition, but also other relevant constructs such as masculinity [36]. This would assist both practitioners and researchers to better understand the dynamic of how men adjust and learn to live with serious and chronic illness. Finally, larger randomised controlled trials controlled trials are needed to move knowledge forward in the effectiveness of psychological interventions for men with cancer.

Acknowledgments

This project was a collaboration between Cancer Council Queensland, Griffith University and the Australian and New Zealand Uro-genital and Prostate (ANZUP) Cancer Trials Group that was funded by an Australian National Health and Medical Research Council Project Grant (ID: APP1024989). SKC had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. The sponsors did not participate in the design or conduct of the study; collection, management, analysis, and interpretation of the data; or in the preparation, review, or approval of the manuscript. SKC is an Australian Research Council Future Fellow. IDD is supported by an NHMRC Practitioner Fellowship. We gratefully acknowledge the support of the Prostate Cancer Foundation of Australia and the Urological Society of Australia and New Zealand; of Bill McHugh and Peter Dornan as consumer advisors; of the medical centres that recruited for this trial (Austin Health, Australian Urology Associates, Bankstown Private Practice, Brisbane Urology Clinic, Concord General Repatriation Hospital, Eastern Health, Flinders Medical Centre, Fremantle Hospital, Genisis CancerCare QLD, Greenslopes Hospital, Cancer Council Queensland 13 11 20 Information and Support Service, Highfields Specialist Centre Port Macquarie, John Flynn Hospital, Liverpool Hospital, Lyell-McEwin Hospital, Nepean Hospital, Northern Cancer Institute, Prince of Wales Hospital, Princess Alexandra Hospital, Radiation Oncology Mater Centre, Redcliffe Hospital, Repatriation General Hospital, Royal Brisbane and Women’s Hospital, Royal Prince Alfred Hospital, Sir Charles Gairdner Hospital, St John of God Hospital, Sydney Adventist Hospital, Townsville Urology, Westmead Hospital, Westmead Private, Whyalla Hospital, and Yaxley Urology); of Tahlee Marian, Sonali Munot, Jan Howell, Cailyn Rogers and Brigid Hanley who facilitated the recruitment of participants in this trial; and of the men who participated in this project. ANZUP is supported by funding through Cancer Australia and Cancer Institute New South Wales.

Compliance with ethical standards

Conflict of interest

All authors had no conflict of interest, including relevant financial interests, activities, relationships, and affiliations to declare relating to this manuscript.

References

  • 1.Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A. Global cancer statistics, 2012. CA: A Cancer Journal for Clinicians. 2015;65(2):87–108. doi: 10.3322/caac.21262. [DOI] [PubMed] [Google Scholar]
  • 2.AIHW. (2015). Australian Cancer Incidence and Mortality. In A. I. o. H. a. Welfare (Ed.), ACIM books. Canberra: AIHW.
  • 3.Evans SM, Millar JL, Davis ID, Murphy DG, Bolton DM, Giles GG, et al. Patterns of care for men diagnosed with prostate cancer in Victoria from 2008 to 2011. Medical Journal of Australia. 2013;198(10):540–545. doi: 10.5694/mja12.11241. [DOI] [PubMed] [Google Scholar]
  • 4.Luo Q, Yu XQ, Cooke-Yarborough C, Smith DP, O’Connell DL. Characteristics of cases with unknown stage prostate cancer in a population-based cancer registry. Cancer Epidemiology. 2013;37(6):813–819. doi: 10.1016/j.canep.2013.09.008. [DOI] [PubMed] [Google Scholar]
  • 5.Popiolek M, Rider JR, Andrén O, Andersson S-O, Holmberg L, Adami H-O, et al. Natural history of early, localized prostate cancer: A final report from three decades of follow-up. European Urology. 2013;63(3):428–435. doi: 10.1016/j.eururo.2012.10.002. [DOI] [PubMed] [Google Scholar]
  • 6.Luo Q, Yu XQ, Smith DP, O’Connell DL. A population-based study of progression to metastatic prostate cancer in Australia. Cancer Epidemiology. 2015;39(4):617–622. doi: 10.1016/j.canep.2015.04.013. [DOI] [PubMed] [Google Scholar]
  • 7.Agarwal N, Di Lorenzo G, Sonpavde G, Bellmunt J. New agents for prostate cancer. Annals of Oncology. 2014 doi: 10.1093/annonc/mdu038. [DOI] [PubMed] [Google Scholar]
  • 8.Nguyen PL, Alibhai SMH, Basaria S, D’Amico AV, Kantoff PW, Keating NL, et al. Adverse effects of androgen deprivation therapy and strategies to mitigate them. European Urology. 2015;67(5):825–836. doi: 10.1016/j.eururo.2014.07.010. [DOI] [PubMed] [Google Scholar]
  • 9.White WM, Sadetsky N, Waters WB, Carroll PR, Litwin MS. Quality of life in men with locally advanced adenocarcinoma of the prostate: An exploratory analysis using data from the CaPSURE database. The Journal of urology. 2008;180(6):2409–2414. doi: 10.1016/j.juro.2008.08.079. [DOI] [PubMed] [Google Scholar]
  • 10.Eton DT, Lepore SJ. Prostate cancer and health-related quality of life: A review of the literature. Psycho-Oncology. 2002;11(4):307–326. doi: 10.1002/pon.572. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Bill-Axelson A, Garmo H, Lambe M, Bratt O, Adolfsson J, Nyberg U, et al. Suicide risk in men with prostate-specific antigen-detected early prostate cancer: A nationwide population-based cohort study from PCBaSe Sweden. European Urology. 2010;57(3):390–395. doi: 10.1016/j.eururo.2009.10.035. [DOI] [PubMed] [Google Scholar]
  • 12.Fang F, Keating NL, Mucci LA, Adami H, Stampfer MJ, Valdimarsdottir U, et al. Immediate risk of suicide and cardiovascular death after a prostate cancer diagnosis: Cohort study in the United States. Journal of the National Cancer Institute. 2010;102(5):307–314. doi: 10.1093/jnci/djp537. [DOI] [PubMed] [Google Scholar]
  • 13.Chambers SK, Pinnock C, Lepore SJ, Hughes S, O’Connell DL. A systematic review of psychosocial interventions for men with prostate cancer and their partners. [Research Support, Non-U.S. Gov’t Review] Patient Education and Counseling. 2011;85(2):e75–e88. doi: 10.1016/j.pec.2011.01.027. [DOI] [PubMed] [Google Scholar]
  • 14.Kashdan TB, Rottenberg J. Psychological flexibility as a fundamental aspect of health. Clinical Psychology Review. 2010;30(7):865–878. doi: 10.1016/j.cpr.2010.03.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Levin ME, Hildebrandt MJ, Lillis J, Hayes SC. The impact of treatment components suggested by the psychological flexibility model: A meta-analysis of laboratory-based component studies. Behavior Therapy. 2012;43(4):741–756. doi: 10.1016/j.beth.2012.05.003. [DOI] [PubMed] [Google Scholar]
  • 16.White RG, Gumley AI, McTaggart J, Rattrie L, McConville D, Cleare S, et al. Depression and anxiety following psychosis: Associations with mindfulness and psychological flexibility. Behavioural and Cognitive Psychotherapy. 2013;41(01):34–51. doi: 10.1017/S1352465812000239. [DOI] [PubMed] [Google Scholar]
  • 17.Gloster AT, Klotsche J, Chaker S, Hummel KV, Hoyer J. Assessing psychological flexibility: What does it add above and beyond existing constructs? Psychological Assessment. 2011;23(4):970–982. doi: 10.1037/a0024135. [DOI] [PubMed] [Google Scholar]
  • 18.Foley E, Baillie A, Huxter M, Price M, Sinclair E. Mindfulness-based cognitive therapy for individuals whose lives have been affected by cancer: A randomized controlled trial. Journal of Consulting and Clinical Psychology. 2010;78(1):72–79. doi: 10.1037/a0017566. [DOI] [PubMed] [Google Scholar]
  • 19.Chambers, S. K., Smith, D. P., Berry, M., Lepore, S. J., Foley, E., Clutton, S., et al. (2013). A randomised controlled trial of a mindfulness intervention for men with advanced prostate cancer. BMC Cancer, 13(89). doi:10.1186/1471-2407-13-89. [DOI] [PMC free article] [PubMed]
  • 20.Baer RA, Smith GT, Hopkins J, Krietemeyer J, Toney L. Using self-report assessment methods to explore facets of mindfulness. Assessment. 2006;13(1):27–45. doi: 10.1177/1073191105283504. [DOI] [PubMed] [Google Scholar]
  • 21.Esper P, Mo F, Chodak G, Sinner M, Cella D, Pienta KJ. Measuring quality of life in men with prostate cancer using the Functional Assessment Of Cancer Therapy-Prostate instrument. Urology. 1997;50(6):920–928. doi: 10.1016/S0090-4295(97)00459-7. [DOI] [PubMed] [Google Scholar]
  • 22.Derogatis L, Lopez M. Brief symptom inventory 18: Administration, scoring and procedures manual. Minneapolis: National Computer Systems Inc; 2000. [Google Scholar]
  • 23.Zabora J, BrintzenhofeSzoc K, Jacobsen P, Curbow B, Piantadosi S, Hooker C, et al. A new psychosocial screening instrument for use with cancer patients. Psychosomatics. 2001;42(3):241–246. doi: 10.1176/appi.psy.42.3.241. [DOI] [PubMed] [Google Scholar]
  • 24.Horowitz M, Wilner N, Alvarez W. Impact of event scale: A measure of subjective stress. Psychosomatic Medicine. 1979;41(3):209–218. doi: 10.1097/00006842-197905000-00004. [DOI] [PubMed] [Google Scholar]
  • 25.Kaasa S, Malt U, Hagen S, Wist E, Moum T, Kvikstad A. Psychological distress in cancer patients with advanced disease. Radiotherapy and Oncology. 1993;27(3):193–197. doi: 10.1016/0167-8140(93)90073-H. [DOI] [PubMed] [Google Scholar]
  • 26.Williams JMG, Kuyken W. Mindfulness-based cognitive therapy: A promising new approach to preventing depressive relapse. The British Journal of Psychiatry. 2012;200(5):359–360. doi: 10.1192/bjp.bp.111.104745. [DOI] [PubMed] [Google Scholar]
  • 27.Carlson LE, Speca M, Patel KD, Goodey E. Mindfulness-based stress reduction in relation to quality of life, mood, symptoms of stress, and immune parameters in breast and prostate cancer outpatients. Psychosomatic Medicine. 2003;65(4):571–581. doi: 10.1097/01.PSY.0000074003.35911.41. [DOI] [PubMed] [Google Scholar]
  • 28.Carlson LE, Speca M, Faris P, Patel KD. One year pre–post intervention follow-up of psychological, immune, endocrine and blood pressure outcomes of mindfulness-based stress reduction (MBSR) in breast and prostate cancer outpatients. Brain, Behavior, and Immunity. 2007;21(8):1038–1049. doi: 10.1016/j.bbi.2007.04.002. [DOI] [PubMed] [Google Scholar]
  • 29.Chambers SK, Foley E, Galt E, Ferguson M, Clutton S. Mindfulness groups for men with advanced prostate cancer: A pilot study to assess feasibility and effectiveness and the role of peer support. Supportive Care in Cancer. 2011;20(6):1183–1192. doi: 10.1007/s00520-011-1195-8. [DOI] [PubMed] [Google Scholar]
  • 30.Hyde, M., Zajdlewicz, L., Lowe, A., Wootten, A., Oliffe, J., & Dunn, J. (2015). Measuring masculinity in the context of chronic disease. Psychology of Men & Masculinity. Accepted September 2015.
  • 31.Watson E, Shinkins B, Frith E, Neal D, Hamdy F, Walter F, et al. Symptoms, unmet needs, psychological well-being and health status in survivors of prostate cancer: Implications for redesigning follow-up. BJU International. 2015 doi: 10.1111/bju.13122. [DOI] [PubMed] [Google Scholar]
  • 32.Chambers SK, Zajdlewicz L, Youlden DR, Holland JC, Dunn J. The validity of the distress thermometer in prostate cancer populations. Psycho-Oncology. 2014;23(2):195–203. doi: 10.1002/pon.3391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Segal Z, Williams J, Teasdale J. Mindfulness-based cognitive therapy for depression: A new approach to preventing relapse. New York: Guilford Press; 2002. [Google Scholar]
  • 34.Dunn J, Steginga SK, Rosoman N, Millichap D. A review of peer support in the context of cancer. Journal of Psychosocial Oncology. 2003;21(2):55–67. doi: 10.1300/J077v21n02_04. [DOI] [Google Scholar]
  • 35.Steginga SK, Pinnock C, Gardner M, Gardiner R, Dunn J. Evaluating peer support for prostate cancer: The Prostate Cancer Peer Support Inventory. BJU International. 2005;95(1):46–50. doi: 10.1111/j.1464-410X.2005.05247.x. [DOI] [PubMed] [Google Scholar]
  • 36.Chambers S, Hyde M, Zajdlewicz L, Lowe A, Wootten A, Oliffe J, et al. Measuring masculinity in the context of chronic disease. Psychology of Men & Masculinity. 2015 [Google Scholar]

Articles from Quality of Life Research are provided here courtesy of Springer

RESOURCES