The impact of prostate cancer diagnosis and treatment decision-making on health-related quality of life before treatment onset.

OBJECTIVE: The objective of this study is to test if patients' health-related quality of life (HRQoL) declines after prostate biopsy to detect Pca, and after subsequent treatment decision-making in case Pca is confirmed, and to test whether personality state and traits are associated with these potential changes in HRQoL.
METHODS: Patients who were scheduled for prostate biopsy to detect Pca (N = 377) filled out a baseline questionnaire about HRQoL (EORTC QLQ-C30 and PR25), "big five" personality traits (BFI-10), optimism (LOT-r), and self-efficacy (Decision Self-efficacy Scale) (t0). Patients with confirmed Pca (N = 126) filled out a follow-up questionnaire on HRQoL within 2 weeks after treatment was chosen but had not yet started (t1).
RESULTS: HRQoL declined between t0 and t1, reflected in impaired role and cognitive functioning, and elevated fatigue, constipation, and prostate-specific symptoms. Sexual activity and functioning improved. Baseline HRQoL scores were unrelated to the selection of a particular treatment, but for patients who chose a curative treatment, post-decision HRQoL showed a greater decline compared to patients who chose active surveillance. Optimism was associated with HRQoL at baseline; decisional self-efficacy was positively associated with HRQoL at follow-up. No associations between HRQoL and the "big five" personality traits were found.
CONCLUSION: Patients who have undergone prostate biopsy and treatment decision-making for Pca experience a decline in HRQoL. Choosing treatment with a curative intent was associated with greater decline in HRQoL. Interventions aimed at optimism and decision self-efficacy could be helpful to reduce HRQoL impairment around the time of prostate biopsy and treatment decision-making.

Background

An aging population and increased use of prostate cancer (Pca) screening contribute to a growth in Pca detection in The Netherlands and other Western countries [1-3]. When Pca is suspected, patients undergo prostate biopsy [4]. In The Netherlands only, at least 25,000 Dutch men undergo this procedure every year, resulting in approximately 10,000 Pca diagnoses (Netherlands Cancer Registry, 2015) [5]. The largest proportion of Pca diagnoses consist of localized cancer (stage I or II), for which surgery, radiotherapy (either brachy or external beam), and active surveillance (AS) are seen as equally acceptable treatments [4, 6]. However, adverse effects from treatment can impair patients’ health-related quality of life (HRQoL) [7-10]. Common side effects from treatments with curative intent (surgery, radiotherapy) include sexual, urinary, and bowel-related complaints [9, 11], while AS can increase anxiety symptoms due to postponing treatment [12, 13]. Therefore, impact on HRQoL is an important factor when considering treatment options [14-16].

Changes in HRQoL after Pca treatment are well described and generally consist of a major decline in HRQoL in the first 1–2 years after treatment [9, 17–19]. Besides the consequences of treatment, changes in HRQoL are related to psychological factors. Optimism and self-efficacy are associated with better HRQoL outcomes, while anxiety, depression, and personality traits (e.g., neuroticism, distress) are associated with worse HRQoL outcomes [20-23]. However, most of these studies measured HRQoL from diagnosis onwards, lacking a pre-diagnosis baseline to also capture the psychological burden from prostate biopsy, receiving a Pca diagnosis, and treatment selection. Studies that did take a pre-diagnosis baseline focused on aspecific (older) patient population and did not measure immediately before and after diagnosis [24, 25].

To increase our understanding about the impact of Pca on HRQoL, including receiving a Pca diagnosis and choosing treatment, this study measured HRQoL pre-biopsy and post-treatment decision-making. Our hypothesis was that a significant decline in HRQoL would already appear prior to treatment onset from the psychological burden of diagnosis and treatment decision-making. Moreover, we expected changes in HRQoL would be associated with psychological factors (personality traits, optimism, and self-efficacy).

Methods

Participants and recruitment

Between January 2013 and May 2014, ten Dutch hospitals participated in this study and recruited 388 patients who were scheduled for a first prostate biopsy due to suspected Pca (M age = 66.5, SD = 6.6; Fig. 1). A host hoc power analysis revealed that this sample size was sufficient to achieve a power of 0.80 for detecting differences with an effect size from Cohen’s d = 0.2 (with alpha 0.05). During consultation, patients were informed that the goal of the study was to investigate quality of care in prostate examination and quality of life of patients undergoing this procedure. Together with an information letter, patients received the first questionnaire (t0) on paper and a pre-stamped envelope to return the questionnaire. Follow-up questionnaires were sent to patients whose biopsy result confirmed Pca. These patients received this second questionnaire and a pre-stamped envelope at their home address within 2 weeks after treatment decision-making (t1). Diagnosis and the moment of treatment decision-making were monitored for all included patients from their (electronic) medical record. After review of the study protocol, the medical ethics review board of the initiating hospital waived the need for formal ethical approval (reference 2012.103) and all participating hospitals approved conducting the study. All patients signed an informed consent.

Fig. 1

Patient flow

Questionnaires

Demographics and clinical data

Participants were asked to indicate their age, education, marital status, last known prostate-specific antigen (PSA) level, and choice of treatment. PSA levels were asked at both t0 and t1 to control for the possibility that treatment had already taken place before completing the t1 questionnaire.

Health-related quality of life

HRQoL was measured with the Dutch version of the EORTC QLQ-C30 questionnaire, which assesses functional HRQoL aspects (physical, role, cognitive, emotional, and social functioning and global health) and symptoms common for cancer patients (fatigue, nausea, pain, dyspnea, sleep disturbance, appetite loss, constipation, diarrhea, and financial impact) [26]. The prostate cancer-specific EORTC QLQ-PR25 module was added to assess prostate cancer-specific (urinary, bowel, and hormonal) symptoms and (sexual) functioning [27]. Scale reliability was low for the bowel and hormonal symptoms, and sexual activity subscale (alpha’s 0.50–0.60), and adequate (alpha ≥ 0.70) for all other subscales. Similar scale reliability scores have been found earlier [27].

Psychological factors

As possible moderating variables, three measures for individual differences measures were included. First, the Big Five Inventory-10 (BFI-10) was included to measure extraversion, agreeableness, conscientiousness, neuroticism, and openness, also known as the “big five” personality traits [28]. The BFI-10 was included in t0. With only two items per trait, low reliability scores were found (α < 0.50), which is common for this scale [29]. A subsequent confirmatory factor analysis confirmed five underlying factors, with each set of two items per trait yielding highest factor loadings.

Secondly, dispositional optimism, a generalized expectation that good things will happen, was assessed with the Life Orientation Test-Revised (LOT-R) [30]. Some minor textual adjustments were made to an existing and previously validated Dutch version of the LOT-R [31]. Scale reliability was sufficient (α = 0.67).

Thirdly, the Decision Self-Efficacy Scale was used as a subjective measure of the perceived ability to make a healthcare decision [32]. Rather than focusing on one specific decision, the goal of this scale was to measure feelings of self-confidence in a healthcare setting. The scale was included at t0 to measure a person’s baseline decisional self-efficacy before the distress from diagnosis. In the absence of an existing and validated Dutch version of this scale, a forward-backward translation was made by two researchers and the result was evaluated and consented on by two other researchers who were not involved to the translation. Scale reliability was good (α = 0.85).

Statistical analysis

Descriptive statistics are presented as means and standard deviations (SD) for continuous variables and as frequencies and percentages for categorical variables. Mean HRQoL scores at t0 were compared to the scores obtained at t1 using paired-samples t tests. The association between personality traits and HRQoL scores was assessed using bivariate correlation analyses (Pearson’s). Linear regression modeling was carried out with global health as dependent variable and personality characteristics as independent variables, controlling for age, education, PSA levels, and diagnosis (dummy variable; for t0 only). All analyses were performed using SPSS version 22.0 (Statistical Package for Social Sciences, Chicago, IL, USA). p values < 0.05 were considered statistically significant.

Results

Three hundred and 88 patients gave informed consent of which 377 patients completed the first questionnaire (t0, response rate 97.2%). All patients whose biopsy confirmed Pca (n = 126 patients, 32%) received the follow-up questionnaire (t1, response rate 63%) (Fig. 1). There were no statistically significant differences in demographics between patients with cancer and patients without cancer at t0, between responders at t0 and t1, or between responders and non-responders at t1. Patient demographics are presented in Table 1.

Table 1

Demographics

	t0—no cancer (N = 254)	t0—Pca (N = 123)	t1—Pca (N = 80)
Age at inclusion
≤ 65 years	106 (44%)	40 (33%)	24 (30%)
66–75 years	115 (48%)	73 (60%)	50 (63%)
≥ 76 years	20 (8%)	9 (7%)	5 (6%)
Education
Low	109 (43%)	48 (39%)	31 (39%)
Medium	60 (24%)	37 (30%)	25 (31%)
High	78 (31%)	36 (29%)	23 (29%)
Other/not specified	4 (2%)	2 (2%)	1 (1%)
Current occupation
Employed	70 (28%)	28 (23%)	15 (19%)
Not employed	183 (72%)	93 (77%)	64 (81%)
Partnership
Partner	224 (89%)	115 (94%)	74 (95%)
No partner	28 (11%)	7 (6%)	5 (6%)
Children
Yes	228 (91%)	118 (96%)	77 (96%)
No	24 (9%)	5 (4%)	3 (4%)
Prostate-specific antigen (PSA)
≤ 5 ng/ml	42 (17%)	19 (16%)	19 (25%)
5.01–10 ng/ml	125 (49%)	59 (48%)	37 (49%)
≥ 10.01 ng/ml	85 (34%)	44 (36%)	20 (26%)
Selected treatment
Active surveillance			26 (34%)
Radical prostatectomy			22 (29%)
Radiotherapy			28 (37%)

Numbers do not always add up to the same total due to item non-response. Differences between groups did not reach statistical significance

Health-related quality of life

At the pre-biopsy baseline (t0), HRQoL did not differ between patients whose biopsy result confirmed Pca and patients with a negative biopsy result (Table 2). After receiving diagnosis and treatment decision-making (t1), patients reported worse role and cognitive functioning and more symptoms (fatigue, constipation, urinary, bowel, and hormonal). Sexual activity and functioning improved after treatment were chosen (all with p < 0.05; Table 2).

Table 2

HRQoL scores

	No Pca	Pca
	t0 (N = 254)	t0 (N = 123)	t1 (N = 80)
HRQoL core	Mean (SD)	Mean (SD)	Mean (SD)	Mean difference (t1−t0)1
Global health	83.5 (14.8)	83.7 (15.4)	80.7 (16.1)	− 3.0
Physical functioning	94.2 (10.4)	94.3 (10.1)	92.8 (12.7)	−1.5
Role functioning	94.7 (14.9)	96.0 (12.9)	86.1 (24.2)	− 9.9***
Emotional functioning	85.3 (16.0)	85.0 (16.8)	83.4 (19.9)	− 1.6
Cognitive functioning	91.2 (15.0)	92.3 (12.5)	88.9 (16.9)	− 3.4*
Social functioning	95.0 (13.9)	96.2 (10.1)	93.9 (14.3)	− 2.3
Fatigue	11.4 (17.3)	10.7 (15.5)	17.0 (22.3)	6.3**
Nausea/vomiting	1.0 (4.7)	1.1 (5.2)	2.4 (11.9)	1.3
Pain	6.8 (15.8)	5.8 (12.6)	9.4 (19.8)	3.6
Dyspnoea	7.7 (16.9)	6.5 (15.3)	6.8 (17.3)	0.3
Insomnia	14.4 (23.8)	13.8 (21.5)	15.0 (25.6)	1.2
Appetite loss	1.9 (8.2)	2.0 (7.9)	4.7 (16.8)	2.7
Constipation	1.7 (8.0)	4.2 (12.7)	7.7 (20.0)	3.5*
Diarrhea	4.0 (13.4)	3.4 (11.0)	6.8 (18.9)	3.4
Financial difficulties	2.6 (12.3)	0.8 (5.3)	2.6 (12.9)	1.8
Prostate specific
Urinary symptoms	15.9 (13.4)	13.3 (11.8)	17.6 (15.6)	4.3*
Bowel symptoms	3.0 (6.3)	2.7 (5.8)	5.6 (10.5)	2.9**
Hormonal symptoms	3.5 (5.8)	3.8 (5.8)	7.0 (9.4)	3.2***
Sexual activity	63.1 (21.6)	61.5 (22.2)	65.4 (21.3)	3.9**
Sexual functioning	22.9 (20.3)	23.4 (19.6)	34.5 (24.0)	11.1*

All scales are 0–100; for functioning subscales, full functioning is represented by a score of 100; for symptoms, absence of symptoms is represented by a score of 0. All comparisons at t0 between patients with and without cancer were non-significant

1Paired comparison t1 vs t0 (N = 70)

*p < 0.05

**p < 0.01

***p < 0.001

Treatment choice

In case Pca was detected, symptoms and functioning reported prior to biopsy (t0) were not associated with selection of a particular treatment. At the time point after treatment decision-making (t1), men who chose a curative treatment reported reduced functioning and more symptoms compared to men who selected AS (Table 3). No associations were found between treatment choice and personality characteristics (data not shown).

Table 3

HRQoL changes grouped per treatment decision

	AS N = 23		Curative treatment (RP or RT) N = 38
	t0Mean (SD)	t1Mean (SD)	t0Mean (SD)	t1Mean (SD)
HRQoL core
Global health	86.4 (15.8)	87.9 (10.5)	81.4 (14.4)	75.0 (18.8)
Physical functioning	93.9 (10.1)	94.2 (10.7)	93.3 (13.2)	92.3 (15.3)
Role functioning	97.0 (9.8)	97.0 (9.8)	95.5 (16.0)	79.7 (29.3)**
Emotional functioning	89.8 (14.5)	92.0 (13.0)	85.1 (17.7)	77.6 (23.7)*
Cognitive functioning	90.5 (13.5)	92.1 (10.2)	91.2 (12.1)	85.5 (20.9)*
Social functioning	93.1 (11.0)	99.2 (3.6)*	96.8 (8.6)	90.5 (18.7)*
Fatigue	10.1 (12.8)	8.6 (12.8)	10.5 (16.1)	21.6 (26.8)**
Nausea/vomiting	3.0 (8.4)	2.3 (5.9)	0 (0.0)	16.5 (2.7)
Pain	5.3 (14.9)	3.0 (8.4)	7.0 (14.3)	15.4 (25.8)
Dyspnoea	7.6 (14.9)	6.1 (16.7)	7.9 (19.7)	8.8 (20.0)
Insomnia	9.1 (15.2)	6.1 (16.7)	16.7 (24.2)	22.8 (31.1)
Appetite loss	4.5 (11.7)	1.5 (7.1)	2.6 (9.1)	8.8 (22.8)
Constipation	1.5 (7.1)	1.5 (7.1)	4.4 (13.8)	13.2 (26.3)*
Diarrhea	3.0 (9.8)	3.0 (9.8)	4.4 (11.4)	11.4 (24.8)
Financial difficulties	0.0 (0.0)	1.5 (7.1)	0.9 (5.4)	3.5 (17.0)
Prostate specific
Urinary symptoms	19.3 (12.9)	14.1 (10.4)	10.3 (8.7)	19.0 (18.4)**
Bowel symptoms	2.2 (6.3)	2.2 (4.5)	3.1 (5.2)	8.6 (13.4)*
Hormonal symptoms	3.9 (4.9)	5.6 (6.7)	3.0 (4.9)	6.4 (10.0)*
Sexual activity	60.9 (27.3)	63.0 (18.1)	58.6 (20.3)	68.0 (20.9)*
Sexual functioning	25.0 (17.9)	23.8 (19.6)	22.2 (16.4)	29.6 (18.4)

All scales are 0–100; for functioning subscales, full functioning is represented by a score of 100; for symptoms, absence of symptoms is represented by a score of 0

AS active surveillance, RP radical prostatectomy, RT radiotherapy

*p < 0.05

**p < 0.01

Psychological variables

Prior to biopsy (t0), optimism was a significant predictor for global health (B = .31, p < .001). After receiving diagnosis and treatment decision-making (t1), a positive association was found between global health and decisional self-efficacy (B = 0.29, p = .04). Of the big five traits, extraversion (B = 0.14, p = .03) and neuroticism (B = − 0.17, p = .01) were significant predictors for global health at t0; no relations were found at t1.

Discussion

This study investigated the HRQoL impacts of undergoing prostate biopsy, receiving Pca diagnosis, and choosing treatment. Prior to prostate biopsy, when Pca is suspected but not yet confirmed, HRQoL was similar between patients who were later confirmed to have Pca and patients without Pca. When a Pca diagnosis was received, and treatment was chosen but had not yet started, patients reported more symptoms and reduced functioning compared to the pre-biopsy baseline. HRQoL at baseline did not predict treatment choice, but patients who chose a curative treatment instead of AS reported more symptoms and reduced functioning compared to patients who chose AS. Overall global health at baseline was related to optimism; after diagnosis and treatment selection, an association with decisional self-efficacy was found.

HRQoL outcomes

Differences in HRQoL between patients who selected curative treatment over AS are not surprising. Men eligible for AS could be expected to be in a more favorable condition compared to men who need (immediate) curative treatment [33]. However, it is remarkable that most HRQoL differences were not present in our sample at baseline but were only reported after diagnosis and treatment selection. Moreover, the highest level of urinary symptoms at t0 was reported by men who later selected AS, while after the treatment decision was made, most symptoms were reported by men who selected a curative treatment. Therefore, changes in HRQoL appear to be influenced by the impact of diagnosis and treatment decision-making, rather than by changes in the patient’s physical condition. Possibly, the Pca diagnosis made men more aware of their symptoms and led them to attribute their overall condition more to their disease. Increased symptom burden and impaired functioning at t1 could also be explained by cognitive dissonance reduction [34]; consequently of a finalized treatment decision, men could be motivated to justify this decision as being the right one. This could have resulted in a revised HRQoL evaluation at t1 to make it consonant with the characteristics that would fit to the selected treatment [35, 36]. If biopsy itself caused a decline in HRQoL, all patients should have reported lower HRQoL at t1, while this was only the case for patients who chose a curative treatment, patients from the AS group even reported (non-significant) improvements [37].

Earlier studies on physical and psychological outcomes in Pca patients highlighted the perceived masculinity threat men could experience [38, 39]. This threat affects how men cope with their condition and the perceived threat could cause a further decline of HRQoL after treatment. Although most of the work on masculinity threats in Pca patients focused on post-treatment outcomes, it is likely that this perceived threat is already present from diagnosis onwards. In our results, reduced role functioning and increased sexual functioning (compensatory behavior) could be indicative for the presence of a masculinity threat [40, 41].

Personality factors

Optimism and decisional self-efficacy were associated with better global health; this is in line with previous research that found optimism and decisional self-efficacy to be associated with less distress and better coping [21, 42]. In the current study, patients scoring higher on optimism report better HRQoL prior to biopsy, when Pca was suspected but not yet confirmed. After diagnosis, and a treatment decision was required, optimism seemed to play less of a role and decisional self-efficacy, the subjective feeling of being able to take the right action, making good decisions, and to ask questions, was positively associated with HRQoL. This adds to previous findings about knowledgeable (and therefore possibly more self-efficated) patients reporting better HRQoL [43].

Instead of focusing on a single trait (e.g., neuroticism), this study investigated a broader spectrum of the big five personality traits. At t0, extraversion and neuroticism were related to global health, while at t1, no relations were present anymore. Hence, we found no evidence of a moderating role of specific traits affecting changes in HRQoL. Another explanation could be that the brief measure we used was not sensitive enough to also detect statistically significant differences in the smaller t1 sample. Future studies should use more extensive measures to investigate this relation in more detail.

Study limitations

Some limitations need to be discussed. First, no detailed clinical data about tumor stage was available, and PSA was self-reported by participants. However, patients were only eligible for inclusion if Pca was suspected, following pre-biopsy screening (rectal examination and PSA testing). Therefore, we were still able to sample a homogeneous patient population. And although we had no registration of the number of patients refusing participation, the average Pca detection rate in our sample was similar to what was expected based on literature [5]. Secondly, dropout of men without Pca diagnosis and non-response at t1 led to a limited number of patients per treatment group available for further analyses. Moreover, the comparison between t1 and t0 on group level had sufficient power; however, the subgroup comparisons were lacking power. As we found no statistically significant differences in patient characteristics between responders and non-responders, we estimate the risk for selection bias was low. Our results should therefore be seen as exploratory findings on the development of HRQoL in Pca patients with a pre-diagnosis baseline. Follow-up studies preferably use larger samples.

Future studies

Based on the changes in HRQoL we found in this study, future studies should focus on determining the impact of the individual aspects of undergoing biopsy, receiving Pca diagnosis, and selecting treatment. Compared to the current design, this would require an additional measurement in between receiving diagnosis and making a treatment decision.

Furthermore, the current study did not follow up on patients with a negative biopsy result. To have a complete comparison of HRQoL after prostate biopsy, post-biopsy HRQoL should also be compared between patients with a positive and patients with a negative biopsy result. Recently, a prospective study found similar HRQoL before and after diagnosis between Pca patients on AS and a non-cancer control group, indicating HRQoL of patients on AS is similar to that of patients without cancer [44]. However, it would be interesting to investigate if decisional self-efficacy is still associated with HRQoL outcomes when no treatment decision has to be made.

Clinical implications

This study emphasizes the impact of undergoing prostate biopsy, receiving a Pca diagnosis, and selecting treatment. Clinicians should be aware that optimism and decisional self-efficacy are associated with HRQoL prior to treatment onset. To ensure that optimism does not backfire post-treatment, it is important to ensure accurate risk perceptions in patients about the chances of treatment success and the occurrence of treatment side effects. Interventions to stimulate shared decision-making, like decision aids, could be helpful for achieving this, as well as to contribute to patients’ decisional self-efficacy levels [45].

Conclusion

So far, most studies investigating HRQoL in Pca patients have focused on the impact of treatment, while neglecting the psychological burden caused by diagnosis and the treatment selection process. This study showed that prior to treatment onset, patients reported reduced functioning, more symptoms, and lower overall global health, in particular if a curative treatment was selected. During clinical counseling, managing optimism when Pca is suspected (before and after biopsy) and (decisional) self-efficacy when Pca is confirmed could help to reduce the pre-treatment impact on HRQoL.