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TO SCREEN OR NOT TO SCREEN: THE PROSTATE CANCER

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(1)

TO SCREEN OR NOT TO SCREEN:

THE PROSTATE CANCER

DILEMMA

DILEMMA

Thomas J Stormont MD

January 2012

y

(2)

http://www.youtube.com/watch?v=8jD

7bAHVp0A&feature=related

7bAHVp0A&feature related

(3)

INTRODUCTION

 A government health panel

(the USPSTF) recently

recommended against PSA screening for prostate cancer screening for prostate cancer because it does “more harm than good”.

 This contradicts most other  This contradicts most other

society guidelines.

 This summary is to help the

patient/doctor understand the role of PSA screening and screening guidelines.

(4)

Background

Prostate cancer is

common~ 240,890

new cases and

33,720 deaths in US

2011

2011.

Initial surge in new

cases but lately 3%

cases but lately 3%

yearly decline in

incidence.

incidence.

(5)

Decreasing numbers

Since PSA screening

there has been a

profound decrease

in

d  Age at diagnosis  Stage at diagnosis Death rate  Death rate

(6)

70 80 50 60 40 50 Pre PSA P t PSA 20 30 Post PSA 0 10 0

(7)

Most Prostate Cancer Indolent

 Autopsy studies show 70%

of men over 70 have occult prostate cancer

prostate cancer.

 PSA screening alone does

not ‘risk stratify’ those y innocuous from the life threatening tumors.

Th t j it f

 The vast majority of men

with prostate cancer die of other causes.

(8)

PSA Considerations

 PSA levels can vary

 May increase from BPH,

UTI or instrumentation

 PSA accuracy-only ~1 in

4 men with abnormal PSA have prostate UTI or instrumentation  Decreases by 50% with finasteride or d t t id p cancer.  PSA cutoff of 4.0ng/dl

not a valid threshold dutasteride

 Ejaculation or DRE has

negligible effect.

 Age adjusted PSA, free

PSA, PSA velocity and density

g g

 Lab variation can yield

results up to 25% difference

 New biomarkers (the

PCA3 urine test)-all have shown promise, but none proven PSA difference but none proven-PSA

(9)

Screening Cost and Morbidity

Abnormal PSA leads to a prostate

biopsy-5min office procedure which can

biopsy 5min office procedure which can

cause stress, pain, bleeding and rarely

infection.

infection.

The main problem with PSA screening is

that diagnosis is almost uniformly

that diagnosis is almost uniformly

associated with aggressive

treatment and thus overtreatment

treatment and thus overtreatment.

(10)

Screening Cost and Morbidity

FDA approved treatments include-alone or in

combination-active surveillance, radiation,

cryoablation radical prostatectomy and

cryoablation, radical prostatectomy and

androgen ablation.

The main long term side effects may include

i

l k

l d f

ti

t l

urinary leakage, sexual dysfunction, rectal

injury and depression.

The yearly cost of just screening is over

e yea y cost o just sc ee

g s o e

$2billion. This does not include the accruing

cost of primary therapy and subsequent

treatments of side effects and or salvage

treatments of side effects and or salvage

therapy for failures.

(11)

3 major PSA Screening Studies

 PLCO study (NEJM 2009)76,963 US men. Authors

concluded no improvement in mortality at 7 years between control and screened men Recent

between control and screened men. Recent

subgroup analysis found significant survival benefit in screened men <65 (JCO Feb 2011).

ERSPC (NEJM 2009) 181 160 European men

 ERSPC (NEJM 2009) 181,160 European men.

Authors found no difference at 7 years, but at 9

years 20% reduction in death from prostate cancer. G b S d (LO 2010)10 000 i A 10

 Goteborg, Sweden (LO 2010)10,000 patients. At 10

years findings similar to the ERSPC study, at 14 years increasing survival benefit.

(12)

PSA Screening Studies

Conclusions

Differences in methodology between these 3

studies.

With longer follow up there appears to be a

With longer follow-up there appears to be a

significant and increasing survival benefit.

There is overdiagnosis/overtreatment of

g

/

prostate cancer.

At best it is estimated that 293 men need to

be screened and 12 treated to prevent one

be screened and 12 treated to prevent one

death. At worst, there is no statistical

(13)

Screening Guidelines

 Screening often includes

both PSA and DRE.

 High risk usually means

blacks and 1st degree

blacks and 1st degree

relatives.

 Shared decision making

means informed discussion b t ti t

between patient an physician.

 Testing interval is usually

annual.

 Most recommend no

screening if no symptoms and <10 yr life expectancy.

(14)

Sceening Guidelines

 ACS (American Cancer Society)

 Age 50, 40-45 if high risk.

 ACPM (American College of Preventive Medicine)

 Age 50. High risk at younger age.

 AUA(American Urological Association)

 Age 40

 EAU(European Association of Urology)  EAU(European Association of Urology)

 Age 40

 NCCN (National Comprehensive Cancer Network)

 Age 40g

 USPSTF (United States Preventive Services Task Force)

(15)

Discussion

 It is important for patients and

physicians to remain open minded about PSA screening and not dismiss it uniformly as y nonbeneficial.

 It is only one group (USPTF)

that is averse to any screening.

 PSA screening does detect g

prostate cancer at earlier stages when there are more options and success with treatment.

 Studies show varied results but

th t b

there appears to be some survival benefit that accrues over time.

 Overdiagnosis and

overtreatment clearly occurs overtreatment clearly occurs.

(16)

Discussion

 Virtually all guidelines

recommend a “Shared

Decision” between physcian and patient But is this

and patient. But is this realistic and really possible given all the complexities and the constraints of an office visit?

office visit?

 It can help to have a PSA

screening decision aid available to the patient.

li i /h lt

www.mayoclinic.com/healt

h/psa-test/MY00180/METHOD=pri

(17)

KEY POINTS

 An informed decision by the

patient is best-overdiagnosis needs to be discussed.

 Screening should include history

 Interpretation of the PSA by the

primary physician to assess risk is critical-the PSA threshold of 4 is no longer valid. The decision

 Screening should include history

of urinary troubles, bone pain and DRE and PSA.

 Informed men should be offered

the test at age 40 or 50 if they

g

for urology referral and possible biopsy should include DRE, age, family history, ethnicity,

symptoms, PSA velocity, etc)

N bi k b i

g y

have 10 yrs life expectancy. If symptoms, these age limits are not as valid.

 New biomarkers are being

developed, but unproven. PSA is still the best test.

 There needs to be an

“unlinking” by urologistsunlinking by urologists between diagnosis and immediate aggressive treatment.

(18)

References

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