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The New Zealand Medical Journal

 Journal of the New Zealand Medical Association, 20-June-2003, Vol 116 No 1176

Prostate cancer screening: knowledge, experiences and attitudes of men aged 40–79 years
Bruce Arroll, Salil Pandit and Stephen Buetow
Abstract
Aim The purpose of this study was to explore the knowledge, experiences and attitudes of men aged 40–79 years regarding screening for prostate cancer.
Methods This study was a cross-sectional telephone survey of men aged 40–79 years whose names were randomly selected from the Auckland telephone directory. The study was undertaken in the summers of 2000/2001 and 2001/2002.
Results The response rate was 77% (120/156). Of the men surveyed, 81% (91/113) stated that it was necessary to test for prostate cancer in men without concerns or symptoms. The majority were not aware of complications of treatment.
Conclusions Misconceptions surround prostate cancer screening. We recommend that doctors inform their patients that prostate cancer screening is controversial, and that the effectiveness of treatment for screen-detected prostate cancer is unknown. Individual patients would then be an improved position to decide about participation in screening.

Prostate cancer is the most common cause of cancer-related death in men (3.8%) behind lung cancer (6.1%) and bowel cancer (4%).1 In terms of new cancers it is the most commonly diagnosed, with 2439 cases reported in 1998. In the same year 1247 new cases of large-bowel cancer and 967 cases of lung cancer were reported. The number of deaths from prostate cancer was 502. This was in the absence of agreement about treatment for clinically localised prostate cancer. A USA study of urologists and radiation oncologists found that urologists would choose radical prostatectomy as their treatment option. Meanwhile, 72% of the oncologists considered surgery and external beam radiotherapy to be equivalent treatments.2
Some observational studies show benefit from diagnosing prostate cancer early. However, this does not, in itself, justify screening.3 Randomized controlled trials are required to assess screening because diagnostic tests in low prevalence settings yield large numbers of false-positive results, each of which requires invasive investigation.4 The harms from surgical treatment are well documented. In one study 8.4% of men experienced incontinence and 41.9% erectile dysfunction after radical prostatectomy for clinically localised prostate cancer.5 Moreover, although one published trial claims benefit from screening for prostate cancer,6 no published randomized controlled trials have yet found a mortality benefit for screening. In the absence of sufficient evidence to screen, the Cancer Society of New Zealand’s recommendation of not screening for prostate cancer should stand.7 A New Zealand editorial noted that different USA institutions had different recommendations for screening for prostate cancer.8 It further commented that two thirds of the men undergoing an ultrasound and biopsy of the prostate will not have the disease and many will die with their prostate cancer, not of it. The purpose of this study was to explore the knowledge, experiences and attitudes of men aged 40–79 years regarding screening for prostate cancer.

Methods

Participants were randomly selected from the Auckland 2000 telephone directory and phoned in the summer of 2000/2001 or 2001/2002. The caller asked if any men present were aged between 40 and 79. If more than one were present, the person whose birthday was first in the calendar year was chosen for the interview. He had the study explained to him and, on giving verbal consent, was administered a structured interview. It comprised 38 questions on knowledge, experiences and attitudes concerning issues around prostate cancer. The questions were taken from other studies and generated by the authors to answer relevant research questions. This study had received ethical approval from the Auckland Ethics Committee. Results were analysed using descriptive statistics and chi-square tests, performed on SPSS v11.

Results

The response rate was 77% (120/156). Where the denominator does not add up to 120 in the following results, this is due to missing responses.
Table 1 shows the demographic characteristics of the group.

Table 1. Demographics of study participants (n = 120)

Age mean (SD)
57 (12) years
Ethnicity
NZ European
Maori
Pacific
Other

104 (89%)
6 (5%)
3 (3%)
4 (3%)
Hold community services card
34 (29%)
Educational history
Left school before School Certificate
Secondary school qualification
Tertiary qualification

27 (23%)
38 (32%)
52 (44%)
Annual gross income
<$28 000
$28 000 to $49 999
$50 000+

30 (27%)
38 (34%)
45 (40%)
Perceived health status
Excellent
Very good
Good
Fair
Poor

29 (24%)
46 (38%)
32 (27%)
11 (9%)
2 (2%)
Ever had or been told have prostate cancer
8 (7%)
Health care
Median number of visits to a GP in previous 12 months
Number of prostate cancer screening tests undergone

2 visits, range 0–12
57 men had tests from 1 to 12 times over the past 5 years
Have health insurance
52 (43%)

Table 2 shows their knowledge of prostate cancer. Table 3 shows experiences and Table 4 documents attitudes.

Table 2. Knowledge of prostate cancer and screening among study participants

Areas of knowledge
n (%)
Knowledge of prostate cancer
No knowledge
Little knowledge
Moderate or high knowledge

29 (24)
66 (55)
25 (21)
Symptoms producing prostate problems*
Dribbling or thin stream
Having to go again
Frequent urination
Blood in urine
Getting up at night
Stopping and starting

21 (32)
8 (12)
24 (37)
7 (11)
4 (6)
1 (2)
Possible cause of these problems*
Prostate cancer
Benign prostatic hypertrophy
Kidney disease
Ageing
Other
Identified no cause

27 (19)
33 (24)
2 (1)
11 (8)
24 (17)
43 (31)
Treatments known about*
Surgery
Radiation
Drugs
Don’t know

49 (30)
46 (28)
20 (12)
47 (29)
Complications of treatment*
Incontinence
Impotence
Other complications
Don’t know

1 (0)
23 (16)
20 (16)
81 (65)
Cancer Society advice about prostate cancer screening
Recommends screening
Does not recommend screening
Don’t know

60 (52)
2 (2)
54 (47)
*percentage of responses

Table 3. Experiences regarding prostate cancer and screening among study participants

All participants:
n (%)
Have you ever been offered a test for prostate cancer?
No
Yes

50 (45)
60 (55)
Of those offered test:
Has the doctor encouraged or discouraged you from having the test?
Encouraged
Neither encouraged nor discouraged me


45 (75)
15 (25)
Has your doctor ever given you anything to read about the test?
No
Yes

51(85)
9 (15)
Duration of time doctor talked about the pros and cons of the test
Not at all
<5 minutes
5–15 minutes
>15 minutes

26 (44)
26 (44)
6 (10)
1 (2)
Has the doctor told you enough about the pros and cons of the test?
No
Yes

8 (14)
51 (86)
Which tests do you usually have?
PSA alone
DRE alone
PSA and DRE

16 (29)
16 (29)
24 (43)
Who usually tests you for prostate cancer?
GP
Specialist

53 (98)
1 (2)
Why did you agree to be tested for prostate cancer?
Had symptoms of prostate cancer
Wife or friend recommended it
Media publicity
Male friend or colleague recommended it
Doctor suggested it as had cancer symptoms
Doctor suggested it as part of a regular health check

16 (30)
2 (4)
11 (21)
8 (16)
1 (2)
15 (28)
Where did you learn about treatment?*
GP
Specialist
Other medical provider
Friends and relatives
Media sources

37 (25)
10 (7)
1 (0)
40 (27)
56 (38)
DRE = digital rectal examination; PSA = prostate specific antigen test; *responses rather than respondents

Table 4. Attitudes to prostate cancer and screening among study participants


n (%)
Do you think routine health examinations in well people are important?
Unimportant
Important

7 (6)
103 (94)
How concerned are you about getting prostate cancer?
Unconcerned
Concerned
Don’t know

40 (33)
72 (60)
8 (7)
How necessary is it to test for prostate cancer in people without concerns or symptoms?
Unnecessary
Necessary
Don’t know


9 (8)
91 (81)
13 (12)
How concerned are you about getting prostate cancer?
Unconcerned
Concerned
Missing and other

40 (33)
72 (60)
8 (7)

Ownership of health insurance was associated with having both a prostate specific antigen (PSA) test and a digital rectal examination (DRE), p = 0.020. Ownership of health insurance was more likely to be associated with concern about getting prostate cancer (p <0.0001) and with having ever been offered a test for prostate cancer (p <0.0001). A history of tertiary education was associated with having ever been offered a test for prostate cancer (p <0.001). Marginally non-significant was an association between an annual gross income of $50 000 or more and concern about getting prostate cancer (p = 0.059 one-sided).

Discussion

Of the men interviewed, 94% (103/110) said that having routine health examinations was important and 81% (91/113) stated that screening asymptomatic men for prostate cancer was necessary. Fifty two per cent (60/116) of respondents indicated that the Cancer Society recommends routine screening; only 2% knew that it does not recommend screening for prostate cancer. Fifty five per cent (60/110) had been offered a test for prostate cancer. Seventy five per cent of those offered the test (45/60) reported that their doctor encouraged them to have a prostate-cancer screening test despite the fact that the Cancer Society does not recommend this. This suggests a need to inform doctors regarding screening practice. All but one of the men who reported an offer of prostate cancer screening accepted it. Forty four per cent of them (26/59) recalled no discussion with their doctor about the advantages and disadvantages of having the test. This is a matter of concern given the high proportion of men who believe that screening for prostate cancer is worthwhile, and the high morbidity from surgery. However, most were satisfied with the information they received about the benefits and harms of screening. Ownership of health insurance increased the likelihood of having a DRE and PSA test. Having a digital examination probably represents more thorough practice (although not recommended for screening, it is recommended when looking for clinically presenting prostate cancer) suggesting that the inverse care law applies to those with health insurance; they were more concerned about getting prostate cancer and more likely to be offered a screening test for this disease.9
The strength of this study was that it involved a random selection of men in the Auckland telephone directory. However, this source favours the 97% of households with telephones in the Auckland urban area10 and may therefore have missed some men with the lowest incomes. Our sample comprised mainly New Zealand European men (89% compared with 67% in the Auckland urban area and 80% in all of New Zealand).10 Forty four per cent (52/117) of the participants had a tertiary qualification; the expected percentage in the Auckland urban area for men aged at least 15 is 36%. The response rate of 77% may not be a true reflection of the actual response rate. The interviewer had a concern that, in order to terminate the call, the person answering the telephone might have used the excuse that no one in the defined age group was at home. Reports of past screening behaviour and, in particular, what the doctor did indicate only what participants could recall rather than necessarily what took place.
In telephone interviews with men in Western Australia11 and New Mexico,12 56% and 48% respectively said that they had been tested for prostate cancer. These statistics are similar to the 55% (60/110) offered a test in this study. Another study, conducted in New South Wales, Australia, found that 44% had ever been screened for prostate cancer.13 Ninety per cent of the New Mexico men stated that prostate cancer screening was important compared with 81% (91/113) in our study.
In the Western Australian study, almost two in every five of the men who reported testing for prostate cancer said they received minimal pre-test counselling or written information.11 In a USA study of men aged 45 to 70 years with no history of prostate cancer and presenting to a university-based family medicine clinic most could not identify the principal advantages and disadvantages of PSA screening.14
An Australian survey found that 68% of general practitioners considered a combination of DRE and PSA effective for prostate cancer screening.15 A New Zealand survey found that 40% of general practitioners believed that all men aged 50 years or over should be screened using DRE, PSA or both.16 However, regardless of their beliefs in these tests, over 80% of these doctors screened at least some of these patients with these tests. A study in the USA likewise found that most family physicians screened for prostate cancer using a PSA test in men older than 50 years.2 Another study of primary care physicians in Missouri found that the majority believed that PSA testing for prostate cancer was a useful procedure.17 These findings suggest that misconceptions about prostate cancer screening exist, and that they are an issue in a number of countries. There are implications for both doctors and patients.
Three in every five men (72/120) in our study reported concern about getting prostate cancer. When diagnosed with prostate cancer a high proportion of men are asymptomatic.18 Other men might not be sure whether they have symptoms because some are not well defined. It is understandable, therefore, that patients and doctors should feel a need to screen for the disease. However, our findings indicate that many men and their doctors are unaware of the current evidence on screening for prostate cancer. Men with positive tests are likely to be exposed to potentially harmful and costly diagnostic and therapeutic interventions without knowing whether or not treatment for screen-detected prostate cancer is effective. It is difficult for groups such as the Cancer Society to get their message across to the public unless scientific evidence informs the media publicity surrounding prostate cancer in high-profile men. In our study, media sources accounted for 38% (56/148) of the responses describing where participants learnt about treatment. We would suggest a campaign to alert the public to the fact that it is unknown whether treatment for screen-detected prostate cancer is effective and that individuals should discuss this issue with their doctor. Our findings suggest that doctors need appropriate information to deal with such questions. It should include the complications of diagnostic procedures and treatment.
Author information: Bruce Arroll, Associate Professor; Salil Pandit, Medical Student; Stephen Buetow, Senior Research Fellow, Department of General Practice and Primary Health Care, University of Auckland, Auckland
Acknowledgements: We thank the Health Research Council for funding the summer studentship for Salil Pandit.
Correspondence: Associate Professor Bruce Arroll, Department of General Practice and Primary Health Care, University of Auckland, Private Bag 92019, Auckland. Fax: (09) 373 7006; email: b.arroll@auckland.ac.nz
References:
  1. New Zealand Health Information Service. Mortality statistics: totals for 1998 and 1999. Available online. URL: http://www.nzhis.govt.nz/stats/mortstats.html#01 Accessed June 2003.
  2. Fowler FJ Jr, McNaughton Collins M, Albertsen PC, et al. Comparison of recommendations by urologists and radiation oncologists for treatment of clinically localized prostate cancer. JAMA 2000;283:3217–22.
  3. Bolla M, Collette L, Blank L, et al. Long-term results with immediate androgen suppression and external irradiation in patients with locally advanced prostate cancer (an EORTC study): a phase III randomised trial. Lancet 2002;360:103–6.
  4. Barratt A, Irwig L, Glasziou P, et al. Users’ guide to the medical literature: XVII. How to use guidelines and recommendations about screening. Evidence-Based Medicine Working Group. JAMA 1999;281:2029–34.
  5. Stanford JL, Feng Z, Hamilton AS, et al. Urinary and sexual function after radical prostatectomy for clinically localized prostate cancer: the Prostate Cancer Outcomes Study. JAMA 2000;283:354–60.
  6. Labrie F, Candas B, Dupont A, et al. Screening decreases prostate cancer deaths: first analysis of the 1988 Quebec prospective randomized controlled trial. Prostate 1999;38:83–91.
  7. Cancer Society of New Zealand. Prostate screening not recommended. Cancer Update 1996;1:1–4.
  8. Davidson P. Prostate specific antigen and screening for early prostate cancer. NZ Med J 2001;114:150.
  9. Tudor Hart J. Three decades of the inverse care law. BMJ 2000;320:18–9.
  10. Statistics NZ. Census 2001. URL: http://www.stats.govt.nz/domino/external/web/aboutsnz.nsf/htmldocs/ Accessed June 2003.
  11. Slevin TJ, Donnelly N, Clarkson JP, et al. Prostate cancer testing: behaviour, motivation and attitudes among Western Australian men. Med J Aust 1999;171:185–8.
  12. Hoffman RM, Gilliland FD. A population-based survey of prostate cancer testing in New Mexico. J Community Health 1999;24:409–19.
  13. Perkins JJ, Sanson-Fisher RW, Clarke SJ, Youman P. An exploration of screening practices for prostate cancer and the associated community expenditure. Br J Urol 1998;82:524–9.
  14. O’Dell KJ, Volk RJ, Cass AR, Spann SJ. Screening for prostate cancer with the prostate-specific antigen test: are patients making informed decisions? J Fam Pract 1999;48:682–8.
  15. Ward J, Young J, Sladden M. Australian general practitioners’ views and use of tests to detect early prostate cancer. Aust NZ J Pub Health 1998;22:374–80.
  16. Morris J, McNoe B. Screening for prostate cancer: what do general practitioners think? NZ Med J 1997;110:178–82.
  17. Lawson DA, Simoes EJ, Sharp D, et al. Prostate cancer screening – a physician survey in Missouri. J Community Health. 1998;23:347–58.
  18. Holleb AI, Fink DJ, Murphy GP. American Cancer Society textbook of clinical oncology. Atlanta Georgia: American Cancer Society; 1991.


     
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