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Point

of

Focus Debate:

Against

Smoking

Status

Is

Not

Sufficient

to

Accurately

Target

Patients

Who Would

Benefit

from

Screening

for

Bladder

and Kidney

Cancer

Morgan

Roupreˆt

*

Academic Urology Department,

Pitie´-Salpe´trie`re Hospital,

Assistance

Publique

- Hopitaux

de

Paris, Universiy

Pierre

and Marie

Curie,

Paris,

France

Screening

is

a

strategy

used

to

detect

disease within

an

asymptomatic population. The underlying hypothesis

is

that

asymptomatic

disease

detection

leads

to

earlier

staged

disease

(stage migration)

and

better

outcomes

from

treat-

ment. However,

the

disease

needs

to

be

common

or

severe

enough

to warrant

detection, must

have

a

known

natural

history

for which earlier

treatment

improves outcomes, and

the detection method

(test) must be

accurate,

safe,

reliable,

and

cost

effective.

Screening

programmes

have

yet

to

be

implemented

for

two major diseases

in

the

field of urologic

oncology

and

should

be

considered:

bladder

cancer

(BCa)

and

renal

cell

carcinoma

(RCC).

Both

cancers

have

a

poor

outcome

when

advanced,

are

extremely

expensive

to

manage, and many patients present with metastatic disease

[1] .

However,

the

background

prevalence

rates

for

both

cancers

is

low; BCa

is

the sixth most common cancer overall,

with

an

estimated

72

570

new

cases

and

15

210

deaths

in

2013

in

the United

States

[1,2]

.

RCC

represents

2–3%

of

all

cancers, with

an

age-standardised

rate

incidence

of 5.8

and

mortality

of 1.4 per 100 000

in Western nations

[1,3] .

BCa

screening

in

the

general

population

has

been

evaluated

(reviewed

by

Chou

and Dana

[4]

and

Larre

et

al.

[5] )

. However, partly because of

the

low overall

incidence of

BCa,

screening

is

currently

not

recommended

in

routine

practice.

For

RCC,

>

50%

of

tumours

are

detected

inciden-

tally

when

noninvasive

imaging

is

used

to

investigate

nonspecific

symptoms

or

other

diseases.

Because

advanced

disease at diagnosis

is now

rare

[1,3] ,

there are no published

data

or

screening

recommendations

for

RCC

in

the

general

population.

Although

general

population-based

screening

for

BCa

and

RCC

seems

illogical,

targeted

screening

of

high-risk

populations makes

clinical

and

economic

sense. However,

as

often

the

case,

the

devil

is

in

the

details.

How

do

we

define

these

high-risk

populations

(beyond

familial

syn-

dromes

[3] )

,

and what

test do we

screen with? The

answer

may

be

smokers.

Cigarette

smoking

is

the

best

established

risk

factor

for

BCa,

with

a

relative

risk

of

1.5–3

in

past

smokers

and

a

relative

risk

(RR)

of

4–5

in

active

smokers

[6] .

Cigarette

smoking

is also

the best established

risk

factor

for RCC

(RR:

1.25–1.55)

[7]

.

In

a

previous

report,

the

most

efficient

screening

tool

for

BCa was

the

combination

of

UroVysion

(Abbott

Molecular,

Des

Plaines,

IL,

USA),

cytology,

and

urinary

dipstick

testing

[8]

.

Screening

a

high-risk

group

with

a

history

of

smoking

of

40

pack-years

revealed

a

significant proportion

(3.3%)

of

individuals with malignan-

cy.

Lotan

et

al.

used

the

NMP22

BladderChek

(Alere,

Waltham, MA,

USA)

to

screen

an

asymptomatic

high-risk

population.

BladderChek

can

detect

noninvasive

cancers,

but

the

low

prevalence

of

BCa

in

this

population

did

not

permit

the

assessment

of

intervention

efficacy

(ie,

the

incidence

of BCa was

0.13%)

[9] .

In

a

recent

screening

trial,

the optimal high-risk population most

likely

to benefit

from

screening was men

aged

>

60

yr with

a

smoking

history

of

>

30

pack-years;

this

group

had

incidence

rates

>

2

in

1000 person-years

[10]

. Consequently, a

screening

strategy

for

BCa,

particularly

in

smokers,

has

been

previously

used

without

any

convincing

data.

No

such

data

are

available

for

RCC.

E U R O P E A N U R O L O G Y F O C U S 1 ( 2 0 1 5 ) 5 2 – 5 3

available

at

www.sciencedirect.com

journal

homepage:

www.europeanurology.com

* Corresponding

author.

Academic Urology Department, Hoˆpital

Pitie´,

47-83

blvd

de

l’Hoˆpital,

75013

Paris,

France.

E-mail

address:

morgan.roupret@psl.aphp.fr

.

http://dx.doi.org/10.1016/j.euf.2014.12.006

2405-4569/

#

2015

European

Association

of Urology.

Published

by

Elsevier

B.V.

All

rights

reserved.