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uncertainty. As a result, Schroek and colleagues

[1]

may still

be overestimating the cost-effectiveness of newer technolo-

gy. Evaluation against the ‘‘wrong’’ comparator in treatment

trials and cost analyses is one factor leading to the authors’

proclaimed ‘‘revolution in prostate cancer treatment’’

[1] .

In

the US, direct-to-consumer marketing of new technologies

[5]

, opportunities for self-referral

[6] ,

and a quantity versus

quality based reimbursement model further feed into

overdiagnosis and overtreatment that contribute to spiraling

health care costs.

SR, including those of treatment costs, provide a critical

role in helping us reflect on the appropriateness of medical

care and guide future evidence-based decision-making

[7]

. This is particularly true in prostate cancer; a prevalent

and potentially fatal disease with a highly variable natural

history. Schroeck et al

[1]

note: ‘‘Understanding the value of

treatment with new technologies will become increasingly

important as society and policy makers are moving towards

accountable care organizations, bundled payments, and

value based reimbursement.’’ They also highlight that cost

utility may depend on the time horizon (early high

acquisition costs, treatment harms, and lack of benefit

versus later lower operational costs, harms reduction, and

mortality/morbidity benefits) and the payer perspective

(patient, insurer, society, costs, versus charges). Unfortu-

nately, consideration of resource use remains an under-

utilized component for optimizing health care value

delivery. In theory, expensive interventions, including those

studied by Schroeck et al

[1] ,

should only be implemented

based on reliable evidence demonstrating greater benefits

or fewer harms than less expensive options (higher value).

However, historically, more expensive technologies have

rarely proven to be higher value. Early adoption of more

expensive technologies prior to demonstration of better

value has much to do with the pathway by which new

technologies are approved including lower evidentiary

standards by the US Food and Drug Administration than

used for pharmaceutical therapies

[8,9]

.

Where do we go for here? Decision makers need higher

quality evidence summarized in well performed SR of

comparative benefits, harms, and resource utilization to

make well informed decisions. Aside from its approach for

making clinical practice guidelines, the Grades of Recom-

mendation, Assessment, Development, and Evaluation

Working Group has recently developed an approach for

moving from evidence to decisions including those about

coverage

[7]

. Ideally, evidence should be available prior to

widespread approval and adoption, a situation that is rare in

prostate cancer. Experience shows that the uptake of

‘‘negative’’ trial evidence that stands in contrast to

prevailing opinion and subsequent attempts to deimple-

ment low value practices, are frequently hampered by an

uncritical passion for the new and advanced—referred to as

‘‘gizmo idolatry’’

[10]

. Rather than a continued escalation in

prostate cancer diagnostic and treatment complexity and

resulting costs we suggest a simple, safe, scientifically

sound solution as proposed by the IDEAL Collaboration in

which rigorous evaluation precede, not follow, wide-spread

new device implementation

[9]

. When it comes to prostate

cancer detection, less intensive screening limited to well-

informed men aged 55–69 yr who inquire about the test are

in excellent health, performed no more frequently than

every 2 yr, and using higher PSA thresholds to define

abnormality is higher value; places the focus on individuals

most likely to benefit and least likely to be harmed while

reducing costs

[11]

. For most men with PSA detected

tumors, especially those with low-risk disease, observation

or PSA-based monitoring is preferred. Aggressive

[2_TD$DIFF]

, resource-

intense

[3_TD$DIFF]

, and potentially harmful approaches should be

targeted towards younger, healthier men with higher risk

prostate cancer who are at greatest risk for succumbing to

their disease. The findings by Schroeck and colleagues

[1]

add valuable new information on our approach to prostate

cancer: radical interventions, especially newer more

expensive therapies, are unlikely to be higher value and

less treatment is likely to mean more health and lower cost.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Schroeck FR, Jacobs BL, Bhayani SB, Nguyen PL, Penson D, Hu J. Cost of new technologies in prostate cancer treatment: systematic re- view of costs and cost effectiveness of robotic-assisted laparoscopic prostatectomy, intensity-modulated radiotherapy, and proton beam therapy. Eur Urol 2017;72:712–35

.

[2]

Wilt TJ, Brawer MK, Jones KM, et al. Radical prostatectomy versus observation for localized prostate cancer. N Engl J Med 2012;367:203–13.

[3]

Hamdy FC, Donovan JL, Lane JA, et al. 10-Year outcomes after monitoring, surgery, or radiotherapy for localized prostate cancer. N Engl J Med 2016;375:1415–24.

[4]

Hayes JH, Ollendorf DA, Pearson SD, et al. Observation versus initial treatment for men with localized, low-risk prostate cancer: a cost- effectiveness analysis. Ann Intern Med 2013;158:853–60

.

[5]

Mirkin JN, Lowrance WT, Feifer AH, Mulhall JP, Eastham JE, Elkin EB. Direct-to-consumer Internet promotion of robotic prostatectomy exhibits varying quality of information. Health Aff (Millwood) 2012;31:760–9

.

[6]

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.

[7]

Dahm P, Oxman AD, Djulbegovic B, et al. Applying GRADE to coverage decisions: results of a Stakeholder Survey and Workshop. J Clin Epidemiol 2017;86:129–39

.

[8]

Dahm P. Envisioning an IDEAL future for urological innovation. BJU Int 2016;117:387–8

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[9]

Sedrakyan A, Campbell B, Merino JG, Kuntz R, Hirst A, McCulloch P. IDEAL-D: a rational framework for evaluating and regulating the use of medical devices. BMJ 2016;353:i2372.

[10]

Leff B, Finucane TE. Gizmo idolatry. JAMA 2008;299:1830–2.

[11]

Wilt TJ, Dahm P. PSA screening for prostate cancer: why saying no is a high-value health care choice. J Natl Comp Cancer Network 2015;13:1566–74.

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