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Inclusion of these cohort studies would also make clear

that the 13-yr horizon to which the

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USPSTF guideline refers

is far too short. For a 55-yr-old man, the question is

outcomes at 30 yr andmore. While the guideline reflects the

latest follow-up reported to date for the ERSPC trial, the

evidence is abundantly clear that mortality risk increases

sharply with longer follow-up, and that, by extension, the

number of lives saved rises and the numbers needed to

screen and treat fall accordingly

[14–17]

. Randomized trials

yield valuable insights, but a new trial randomizing men

younger than 50 yr is extremely unlikely at this stage, and

avoiding contamination in a control arm in any developed

country would be pragmatically impossible. Ignoring all

nonrandomized evidence on principle yields an incomplete

picture of the knowledge base on PSA screening, and does a

large disservice to at-risk men.

This problem is particularly salient for African-Amer-

icans, men with a positive family history, and other groups

with a higher risk of lethal prostate cancer. While

acknowledging higher rates of cancer and lethal disease

in these populations, the guideline cites no screening

research outside the PLCO or ERSPC trials, both of which

involved overwhelmingly Caucasian cohorts. The call for

more research in these groups is of course appropriate, but

randomized trials will not provide the answers in any

foreseeable future, and better consideration must be paid to

cohort studies, modeling

[18]

, and other complementary

sources of information, most of which would support earlier

screening in high-risk groups.

Despite explicitly excluding nonrandomized evidence in

defining benefits, the USPSTF opted to include both trials

and cohorts in measuring harms. Their choice of cohorts to

include, moreover, was far from inclusive and overempha-

sized outdated studies, thus leading to overestimation of

the harms. The inadequacy of the literature review on this

question is evident, for example, in the selection of

references for the PCOS and CaPSURE cohorts which were

over a decade out of date relative to more recent papers

[19,20]

. Cohorts such as PROST-QA

[21]

were excluded

entirely, as were large meta-analyses

[22–25]

and other

data sources. While there is no argument that surgery and

radiation can adversely affect urinary, bowel, and sexual

functions, the statements that one in five men need diapers

in the long term after surgery, two in three suffer long-term

sexual dysfunction, and one in six men suffer long-term

bowel complications after radiation are simply not defen-

sible in light of more contemporary data.

The new guideline reiterates a ‘‘D’’ recommendation

against any screening for men aged 70 yr. While the ratio

of benefits and harms may be different for older men—and

certainly a somewhat elevated PSA can be more difficult to

interpret in this age group—life expectancy for healthy men

at age 70 is now quite protracted, and there is a big

difference between a man who has had prior reassuring PSA

results in his 50s and 60s and one who has never been

screened before. Older men who are not treated effectively

for high-grade prostate cancer face an approximately 25%

risk of prostate cancer mortality

[26]

, and conversations

with healthy men in their 70s should be more individual-

ized and nuanced than the new guideline suggests.

Finally, the USPSTF has againmissed a major opportunity

to advocate that screening efforts should focus on

identification of higher-risk cancers. The statement that

we cannot distinguish aggressive, potentially lethal cancer

frommore indolent disease ignores decades of research and

progress. In fact, prostate cancer can be risk-stratified with

approximately 80% accuracy using clinical parameters

alone

[27]

, accuracy that can be further improved with

emerging imaging, genomic, and other tests.

The evidence review stated that a single investigator

abstracted all the study data

[9]

. Given the massive volume

of prostate cancer research published in the past 5 yr, this

may have been an insurmountable challenge for any

individual, especially one without prior experience in

prostate cancer research.

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In fact, the evidence review and

guideline miss many critical studies directly addressing the

priority questions identified in the

Research Needs and Gaps

section. In contrast to the 2012 guideline, this time the

USPSTF actively sought informal input from four urologic

oncology experts, although none of these contributed

directly to the evidence review or final guideline.

The draft recommendation

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closed for

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formal comment

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on May 8, 2017,

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but readers

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can

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certainly continue to

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voice

their

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opinions

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to the

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USPSTF

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leadership, and

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should

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continue

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to

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engage with their local primary care communi-

ties. Following the draft and final ‘‘D’’ recommendations in

2011 and 2012, Twitter proved to be an active forum for

debate on the subject

[28]

, one monitored by many patients

and policymakers. Those with opinions on this subject are

encouraged to make their thoughts heard on Twitter and

other social media platforms using the hashtags #pcsm and

#uspstf.

The new ‘‘C’’ recommendation represents substantial

progress in the right direction towards offering men a fair

opportunity to discuss the risks and benefits of screening

with their primary care providers.

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Hope

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springs

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eternal the

finalized recommendation will reflect a fairer and more

comprehensive consideration of the available evidence

base. The USPSTF should, like other guidelines panels,

formally engage stakeholders and experts with both

breadth and depth of knowledge and experience in order

to give men and their physicians the best possible guidance

on the perennially complex questions surrounding early

detection of prostate cancer.

Conflicts of interest:

The author has nothing to disclose.

References

[1] Tasian GE, Cooperberg MR, Cowan JE, et al. Prostate specific antigen

screening for prostate cancer: knowledge of, attitudes towards, and

utilization among primary care physicians.

Urol Oncol

2012;30:155–60

http://dx.doi.org/10.1016/j.urolonc.2009.12.019

[2] Moyer VA. U.S. Preventive Services Task Force. Screening for pros-

tate cancer: U.S. Preventive Services Task Force recommendation

statement. Ann Intern Med 2012;157:120–34

http://dx.doi.org/10. 7326/0003-4819-157-2-201207170-00459

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