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Characteristics of men responding to an invitation to undergo testing for prostate cancer as part of a randomised trial

Abstract

Background

Sociodemographic characteristics are associated with participating in cancer screening and trials. We compared the characteristics of those responding with those not responding to a single invitation for prostate-specific antigen (PSA) testing for prostate cancer as part of the Cluster randomised triAl of PSA testing for Prostate cancer (CAP).

Methods

Age, rurality and deprivation among 197,763 men from 271 cluster-randomised primary care centres in the UK were compared between those responding (nā€‰=ā€‰90,300) and those not responding (nā€‰=ā€‰100,953) to a prostate cancer testing invitation.

Results

There was little difference in age between responders and nonresponders. Responders were slightly more likely to come from urban rather than rural areas and were slightly less deprived than those who did not respond.

Conclusion

These data indicate similarities in age and only minor differences in deprivation and urban location between responders and nonresponders. These differences were smaller, but in the same direction as those observed in other screening trials.

Trial registration

ISRCTN92187251. Registered on 29 November 2004.

Peer Review reports

Background

Screening for prostate cancer (PCa) has been shown to reduce disease-specific morbidity and mortality through early detection, but at the expense of overdiagnosis and overtreatment of indolent cancer [1ā€“3]. The UK National Screening Committee (UKNSC) does not currently recommend population screening for PCa, although testing can be performed on request [4]. The UKNSC awaits the results of ongoing nationwide trials to further inform UK PCa screening policy. The Cluster randomised triAl of PSA testing for Prostate cancer (CAP) is an effectiveness trial comparing PCa-specific mortality in men invited (intervention arm) and men not invited (control arm) to prostate-specific antigen (PSA) testing in primary care [5] and the Prostate testing for cancer and treatment (ProtecT) randomised controlled trial (RCT), which evaluates the effectiveness and cost-effectiveness of treatment for localised, PSA-detected PCa [6].

Material and social deprivation is associated with lower rates of attending cancer screening programmes for both men [7ā€“9] and women [10ā€“14], as well as RCT participation [15]. Failure to enroll participants who are representative of the target population can compromise the generalisability of trial findings [16], for example, due to a healthy volunteer effect (HVE) [17] with younger, healthier, more-educated individuals taking part compared with nonattendees [18]. Here we compare the characteristics of those who responded to the invitation to take part in the intervention arm of the CAP trial with those who did not, using routine data available from primary care centres.

Methods

Men aged 50ā€“69 years from 271 primary care (GP) practices in England and Wales were cluster-randomised to receive the intervention in the CAP trial (Fig.Ā 1) of a postal invitation to attend a one-off appointment for a PSA test screening for PCa. Those who returned a reply slip by post accepting this invitation (i.e. ā€˜respondersā€™) were given an appointment and invited to participate in the screening and diagnostic stage of the ProtecT trial [6]. Responders who were ineligible or decided not to participate in the ProtecT study were followed up as part of the CAP trial (discussed in full elsewhere; [5]). Those who declined the initial invitation (i.e ā€˜nonrespondersā€™) were also followed up as part of the CAP trial [5].

Fig. 1
figure 1

Trial and follow-up organisation

Data

Date of birth and postcode were provided by the primary care practices for all men who were invited to screening for recruitment purposes. These are the only demographic data items available for both responders and nonresponders due to governance and ethical permissions. Postcode was used to calculate the Index Multiple Deprivation (IMD) score and the Rural and Urban Area Classification (RUAC).

Index Multiple Deprivation (IMD)

The IMD is a widely used measure of area deprivation in England and Wales and has been shown to represent deprivation appropriately for both urban and rural areas [19]. The IMD is an overall composite score of weighted domains with higher scores indicating more deprivation encompassing aspects of socioeconomic status including unemployment, claiming financial support from the state, poor health, low educational attainment, criminal victimisation, household condition and overcrowding. English 2004 and Welsh 2005 IMD scores are not directly comparable and are, therefore, analysed separately [20].

Rural and Urban Area Classification (RUAC)

The RUAC (2004) is a measure of population density and sparseness in the UK. For RUAC, areas of more than 10,000 people are considered to be urban, otherwise they are classified as rural (i.e. less than 10,000 people).

Statistical analysis

A t test was used to compare mean age and deprivation in responders and nonresponders. Odds ratios (ORs) were used to compare the proportion of responders and nonresponders living in an urban location. Gartner et al. [19] found that deprivation accounted for the differences they found in outcomes by urban-rural location, and we therefore adjusted this analysis by IMD score. Analyses were conducted in STATA version 13.

Results

Of 197,763 men registered at primary care practices who were randomised to receive invitations to the PSA testing clinic, 46Ā % (nā€‰=ā€‰90,300) accepted the invitation (responders) and 51Ā % did not respond (nā€‰=ā€‰100,953; i.e. nonresponders). The remaining men either explicitly refused the invitation (1.5Ā %; nā€‰=ā€‰3,010) or, having attended, refused to take part in the trial (1.8Ā %; nā€‰=ā€‰3,499). Eighty-four percent (nā€‰=ā€‰75,753) of responders ultimately attended the clinic, of which 98Ā % (nā€‰=ā€‰65,836) reported themselves as being of White ethnic origin.

The mean age of both responders and nonresponders was 59Ā years (5.47 and 5.66 standard deviations (SDs), respectively; see TableĀ 1). Responders in England and Wales were less deprived on average compared to nonresponders (IMD 20.66 (SD 15.49) versus 25.04 (SD 17.74); pā€‰<ā€‰0.001 and 19.04 (SD 14.08) versus 22.27 (SD 15.28); pā€‰<ā€‰0.001, respectively). The distribution of IMD scores between responders and nonresponders are comparable (see Fig.Ā 2a and b), as demonstrated by the interquartile range (IQR) of both IMD scores in England (respondersā€™ IQR 9.3ā€“28.5 versus nonrespondersā€™ IQR 10.9ā€“37.2) and Wales (respondersā€™ IQR 8.2ā€“26.9 versus nonrespondersā€™ IQR 10.3ā€“31.8).

Table 1 Demographics of responders and nonresponders to screening invitation
Fig. 2
figure 2

a Frequency distribution of Welsh Index Multiple Deprivation (IMD) scores for those responding (solid line) to a one-off invite to a PSA test compared to those who did not respond (dash) to this invitation. b Frequency distribution of English IMD scores for those responding (solid line) to a one-off invite to a PSA test compared to those who did not respond (dash) to this invitation

Responders were also slightly less likely to live in urban areas with a population of more than 10,000 than nonresponders (85Ā % [95Ā % confidence interval (CI) 0.85 to 0.86] versus 87Ā % [95Ā % CI 0.87 to 0.87]; pā€‰<ā€‰0.001), and slightly more likely to be from urban locations when controlling for deprivation, in both England (crude OR 0.85, 95Ā % CI 0.83 to 0.87 compared with adjusted OR 1.04, 95Ā % CI 0.99 to 1.09) and Wales (crude OR 1.01, 95Ā % CI 0.91 to 1.13 compared with adjusted OR 1.11, 95Ā % CI 0.95 to 1.30).

There was no difference in the results when classifying those who accepted the invitation, but did not ultimately attend the clinic or undergo a PSA test (nā€‰=ā€‰22,964), as nonresponders rather than responders.

Discussion

There were very small differences between those who responded and those who did not respond to a single invitation to receive a PSA test as the intervention in the CAP trial. Responders and nonresponders were similar in age. Responders were only slightly less deprived than the nonresponders, and there were negligible differences in urban-rural location. Although we report small p values, these reflect the large numbers in the study as the absolute differences are very small in magnitude.

The CAP trial gained consent after randomisation to receive or not receive an invitation to screening and, by analysing on this intention-to-screen basis, reduces the risk of self-selection bias influencing the representativeness to the target population. This is compared to other trials where consent was gained prior to randomisation [21]. However, differences between men who did and did not actually undergo a PSA test is a key issue for policy-makers and cannot be ruled out as having an impact on the effectiveness of screening.

It was only possible to derive age, urban/rural location and an ecological measure of deprivation from the available data because of ethical and governance regulations. The large randomly allocated cohort and intention-to-screen analysis in the CAP trial helps to mitigate the effect of unmeasured factors on generalisability of the trial. While the responders and nonresponders were similar according to the characteristics measured, it cannot be ruled out that there were other differences between the groups. Important differences in comorbidities, education, income and decision-making between attendees and nonattendees have been shown elsewhere [32, 33] and remain key factors for policy-makers.

We are unable to comment on the impact of any post-randomisation differences between the groups on mortality and PCa incidence. Previous trials have suggested that nonparticipation in the screening arm is associated with higher mortality [22] and that controlling for ā€˜healthierā€™ attenders in the screening arm is important to avoid overestimating the effect of screening on mortality [18]. This is something that could be investigated in the future once the median 10-year intention-to-screen analyses have been reported.

This RCT invited over 190,000 patients to attend a one-off blood test from different geographical regions across the UK. According to these characteristics, those who responded to the invitation were representative of the population who were invited as a whole and comparable with those enrolled in other screening trials [23, 24]. Compared to other PCa screening trials, considerably more men were invited in this trial and overall response rates were studied [6]. Other trials have not consistently reported the numbers initially invited (cf. [25ā€“31]) or have reported on a sample of participant uptake of invitations to testing prior to publication of the primary analysis [21].

Group-level data (i.e. postcode) limits the sensitivity of deprivation data at an individual level, and area measures of deprivation are an average of the overall deprivation of the population, which arguably cannot represent the level of deprivation in the age- and gender-specific group included in this trial [34]. Further, without ethnicity information for all those invited we cannot investigate the lack of ethnic diversity among attenders (more than 90Ā % of whom are of White ethnicity). Although, this figure does reflect the 2001 UK Census, which reported that 89Ā % and 97Ā % of English and Welsh residents, respectively, from urban areas were classified as of ā€˜Whiteā€™ ethnicity [35].

Despite changes in the most recent Consolidated Standards of Reporting Trials (CONSORT) guidelines, there are very few trials that report the figures required to assess the impact of trial participation on health outcomes and survival [36]. It is difficult to assess who is likely to attend screening if trials do not publish prerecruitment figures and the details of those who are being enrolled remain under-reported [37, 38]. Without adequate reporting of the groups who do and do not participate potential external validity and barriers to screening and treatment cannot be properly assessed. Describing the characteristics of those enrolled and those not enrolled in trials, to ascertain the generalisability of the trial results and to assess the validity of the recruited sample, has been recommended [39].

Conclusions

We have reported key characteristics that describe those who did and those who did not respond to a single invitation to undergo a PSA test in the ProtecT and CAP RCTs. Overall, there were only minor differences in area-deprivation measures and urban-rural location between those who responded and did not respond to the invitation. Therefore, this is unlikely to affect the generalisability of the ProtecT and CAP trials. Despite restricted access to routine data limiting the comparisons that could be made between responders and nonresponders, this analysis suggests that those who are likely to engage with screening do not differ from those who would not in a meaningful way. Moreover, the characteristics of those who responded are comparable to those observed in other screening trials and add to knowledge about who might accept an invitation to PCa screening, if a programme were to be initiated in England and Wales.

Abbreviations

CAG:

Confidentiality Advisory Group

CAP:

Cluster randomised triAl of PSA testing for Prostate cancer

CI:

Confidence interval

GP:

General practitioner

HVE:

Healthy Volunteer Effect

IMD:

Index Multiple Deprivation

IQR:

Interquartile range

MREC:

Multicentre Research Ethics Committee

OR:

Odds ratio

PCa:

Prostate cancer

PIAG:

Patient Information Advisory Group

ProtecT:

Prostate testing for cancer and treatment

PSA:

Prostate-specific antigen

RCTs:

Randomised controlled trials

RUAC:

Rural and Urban Area Classification

SD:

Standard deviation

UKNSC:

UK National Screening Committee

References

  1. Andriole GL, et al. Prostate cancer screening in the randomized Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial: mortality results after 13Ā years of follow-up. J Natl Cancer Inst. 2012;104(2):125ā€“32.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  2. Buzzoni C, et al. Metastatic prostate cancer incidence and prostate-specific antigen testing: new insights from the European Randomized Study of Screening for Prostate Cancer. Eur Urol. 2015;68(5):885ā€“90.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  3. Schrƶder FH, et al. Screening for prostate cancer decreases the risk of developing metastatic disease: findings from the European Randomized Study of Screening for Prostate Cancer (ERSPC). Eur Urol. 2012;62(5):745ā€“52.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  4. UKNSC. Screening for Prostate Cancer Review 2014 Update: review against programme appraisal criteria for the UK National Screening Committee (UKNSC). 2015. Available from: http://legacy.screening.nhs.uk/prostatecancer. Accessed 12 Oct 2016.

  5. Turner EL, et al. Design and preliminary recruitment results of the Cluster randomised triAl of PSA testing for Prostate cancer (CAP). Br J Cancer. 2014;110(12):2829ā€“36.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  6. Lane JA, et al. Active monitoring, radical prostatectomy, or radiotherapy for localised prostate cancer: study design and diagnostic and baseline results of the ProtecT randomised phase 3 trial. Lancet Oncol. 2014;15(10):1109ā€“18.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  7. Morgan RM, et al. Socioeconomic variation and prostate specific antigen testing in the community: a United Kingdom based population study. J Urol. 2013;190(4):1207ā€“12.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  8. Moss SM, et al. Performance measures in three rounds of the English bowel cancer screening pilot. Gut. 2012;61(1):101ā€“7.

    ArticleĀ  CASĀ  PubMedĀ  Google ScholarĀ 

  9. Williams N, et al. Prostate-specific antigen testing rates remain low in UK general practice: a cross-sectional study in six English cities. BJU Int. 2011;108(9):1402ā€“8.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  10. Banks E, et al. Comparison of various characteristics of women who do and do not attend for breast cancer screening. Breast Cancer Res. 2002;4(1):R1.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  11. Hansen BT, et al. Factors associated with non-attendance, opportunistic attendance and reminded attendance to cervical screening in an organized screening program: a cross-sectional study of 12,058 Norwegian women. BMC Public Health. 2011;11:264.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  12. Johns LE, Moss SM, Trial Management Group. Randomized controlled trial of mammographic screening from age 40 (ā€˜Ageā€™ trial): patterns of screening attendance. J Med Screen. 2010;17(1):37ā€“43.

    ArticleĀ  CASĀ  PubMedĀ  Google ScholarĀ 

  13. Moser K, Patnick J, Beral V. Inequalities in reported use of breast and cervical screening in Great Britain: analysis of cross sectional survey data. BMJ. 2009;338:b2025.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  14. Ouedraogo S, et al. European transnational ecological deprivation index and participation in population-based breast cancer screening programmes in France. Prev Med. 2014;63:103ā€“8.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  15. Ford JG, et al. Barriers to recruiting underrepresented populations to cancer clinical trials: a systematic review. Cancer. 2008;112(2):228ā€“42.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  16. Sheikh A. Why are ethnic minorities under-represented in US research studies? PLoS Med. 2005;3(2):e49.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  17. Burnell M, et al. Impact on mortality and cancer incidence rates of using random invitation from population registers for recruitment to trials. Trials. 2011;12(1):1ā€“10.

    ArticleĀ  Google ScholarĀ 

  18. Kranse R, et al. Excess all-cause mortality in the evaluation of a screening trial to account for selective participation. J Med Screen. 2013;20(1):39ā€“45.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  19. Gartner A, et al. Rural/urban mortality differences in England and Wales and the effect of deprivation adjustment. Soc Sci Med. 2011;72(10):1685ā€“94.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  20. ONS. Similarities and differences between the Indices of Deprivation across the UK. 2016. Available from: http://www.neighbourhood.statistics.gov.uk/dissemination/Info.do?m=0&s=1472057104682&enc=1&page=analysisandguidance/analysisarticles/indices-of-deprivation.htm&nsjs=true&nsck=false&nssvg=false&nswid=1920. Accessed 12 Oct 2016.

  21. Otto SJ, Schrƶder FH, de Koning HJ. Low all-cause mortality in the volunteer-based Rotterdam section of the European randomised study of screening for prostate cancer: self-selection bias? J Med Screen. 2004;11(2):89ā€“92.

    ArticleĀ  CASĀ  PubMedĀ  Google ScholarĀ 

  22. Kilpelainen TP, et al. The Finnish prostate cancer screening trial: analyses on the screening failures. Int J Cancer. 2015;136(10):2437ā€“43.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  23. Andriole GL, et al. Mortality results from a randomized prostate-cancer screening trial. N Engl J Med. 2009;360(13):1310ā€“9.

    ArticleĀ  CASĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  24. Green BB, et al. Nonparticipation in a population-based trial to increase colorectal cancer screening. Am J Prev Med. 2012;42(4):390ā€“7.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  25. Berenguer A, et al. The Spanish contribution to the European Randomized Study of Screening for Prostate Cancer. BJU Int. 2003;92:33ā€“8.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  26. Ciatto S, et al. Specific features of the Italian section of the ERSPC. BJU Int. 2003;92:30ā€“2.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  27. Finne P, et al. The Finnish trial of prostate cancer screening: where are we now? BJU Int. 2003;92:22ā€“6.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  28. Hugosson J, et al. Population-based screening for prostate cancer by measuring free and total serum prostate-specific antigen in Sweden. BJU Int. 2003;92:39ā€“43.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  29. Kwiatkowski M, et al. Features and preliminary results of prostate cancer screening in Canton Aargau, Switzerland. BJU Int. 2003;92:44ā€“7.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  30. Nelen V, et al. ERSPC: features and preliminary results from the Antwerp study centre. BJU Int. 2003;92:17ā€“21.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  31. Roobol MJ, Kirkels WJ, Schrƶder FH. Features and preliminary results of the Dutch centre of the ERSPC (Rotterdam, the Netherlands). BJU Int. 2003;92:48ā€“54.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  32. Nijs HG, et al. Randomised trial of prostate cancer screening in The Netherlands: assessment of acceptance and motives for attendance. J Med Screen. 1997;4(2):102ā€“6.

    ArticleĀ  CASĀ  PubMedĀ  Google ScholarĀ 

  33. Nijs HG, et al. Why do men refuse or attend population-based screening for prostate cancer? J Public Health Med. 2000;22(3):312ā€“6.

    ArticleĀ  CASĀ  PubMedĀ  Google ScholarĀ 

  34. Zarrouk M, et al. The importance of socioeconomic factors for compliance and outcome at screening for abdominal aortic aneurysm in 65-year-old men. J Vasc Surg. 2013;58(1):50ā€“5.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  35. ONS. Census 2001. 2014. Available from: http://www.ons.gov.uk/ons/guide-method/census/census-2001/index.html. Accessed 12 Oct 2016.

  36. Vist GE, et al. Systematic review To determine whether participation in a trial influences outcome. BMJ: Br Med J. 2005;330(7501):1175ā€“9.

    ArticleĀ  Google ScholarĀ 

  37. Kane RL, Wang J, Garrard J. Reporting in randomized clinical trials improved after adoption of the CONSORT statement. J Clin Epidemiol. 2007;60(3):241ā€“9.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  38. Mills EJ, et al. The quality of randomized trial reporting in leading medical journals since the revised CONSORT statement. Contemp Clin Trials. 2005;26(4):480ā€“7.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

  39. Wright JR, et al. The importance of reporting patient recruitment details in phase III trials. J Clin Oncol. 2006;24(6):843ā€“5.

    ArticleĀ  PubMedĀ  Google ScholarĀ 

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Acknowledgements

The authors acknowledge the contribution of the CAP trial group. Investigators: Richard Martin (lead PI), Jenny Donovan (PI), David Neal (PI), Freddie Hamdy (PI), Emma Turner (trial co-ordinator), Chris Metcalfe (statistician), Jonathan Sterne (statistician) and Sian Noble (health economist). Research staff: Liz Hill, Siaw Yein Ng, Naomi Williams, Liz Down (data manager), Eleanor Walsh (data manager), Joanna Thorn (health economist), Charlotte Davies, Laura Hughes, Mari-Anne Rowlands and Lindsey Bell. Management Committee: Emma Turner (chair), Richard Martin, Jenny Donovan, Chris Metcalfe, Jonathan Sterne, Sian Noble, Yoav Ben- Shlomo, Athene Lane, Steven Oliver, Peter Brindle and Simon Evans. CAP & ProtecT Trial Steering Committee: Michael Baum (chair), Peter Albertsen, Tracy Roberts, Mary Robinson, Jan Adolfsson, David Dearnaley, Anthony Zeitman, Fritz Schrƶder, Tim Peters, Peter Holding, Teresa Lennon, Sue Bonnington, Malcolm Mason, Jon Oxley, Richard Martin, Jenny Donovan, David Neal, Freddie Hamdy, Emma Turner and Athene Lane. Data Monitoring Committee: Lars Holmberg (chair), Robert Pickard, Simon Thompson and Usha Menon. Cause of Death Committee: Peter Albertsen (chair), Colette Reid, Jon McFarlane, Jon Oxley, Mary Robinson, Jan Adolfsson, Michael Baum, Anthony Zeitman, Amit Bahl and Anthony Koupparis. Administrative staff: Marta Tazewell and Genevieve Hatton-Brown.

We acknowledge the tremendous contribution of all the ProtecT study participants, investigators, researchers and the Steering and Data Monitoring Committees. The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the Department of Health.

Funding

The CAP trial is funded by Cancer Research UK and the UK Department of Health (C11043/A4286, C18281/A8145, C18281/A11326 and C18281/A15064).

The ProtecT study is funded by the UK National Institute for Health Research (NIHR) Health Technology Assessment Programme (96/20/06, 96/20/99).

Availability of supporting data

The dataset supporting the conclusions of this article cannot be shared with third parties due to conditions within the Section 251 approval that governs this research.

Authorsā€™ contributions

JAL, JD, FCH, DN and RMM were involved in the trial design and concept. EW and ET were involved in the date collection, preparation and statistical analysis. EW, ET and RMM were responsible for interpreting the data and drafting the manuscript. All authors critically revised the manuscript and approved the final version.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethical approval and consent to participate

Ethical approval to access information about all those in the CAP study was obtained from UK Trent Multicentre Research Ethics Committee (MREC/03/4/093). The CAP study was exempt from gaining individual consent to participant having obtained Section 251 approval from the UK Patient Information Advisory Group (PIAG) (now the Confidentiality Advisory Group, CAG), under Section 251 of the NHS Act 2006 (PIAG 4-09 (k)/2003). The CAP study is sponsored by the University of Bristol and is registered at Current Controlled Trials (ISRCTN92187251).

Individual consent to participate was gained from those enrolled in the ProtecT trial. Trent MREC in the UK also provided ethical approval for the ProtecT trial (01/4/025) with the University of Oxford as trial sponsor. The ProtecT trial is registered at Current Controlled Trials (ISRCTN20141297) and at ClinicalTrials.gov (NCT00632983).

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Walsh, E.I., Turner, E.L., Lane, J.A. et al. Characteristics of men responding to an invitation to undergo testing for prostate cancer as part of a randomised trial. Trials 17, 497 (2016). https://0-doi-org.brum.beds.ac.uk/10.1186/s13063-016-1624-6

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