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BPH, PSA and Prostate Cancer

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Other symptoms are secondary symptoms or symptoms of other pathology ... Brachytherapy. No randomised controlled trials of treatment. All treatments have ... – PowerPoint PPT presentation

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Title: BPH, PSA and Prostate Cancer


1
BPH, PSA and Prostate Cancer
  • Mike Foster
  • Good Hope Hospital

2
Is it BPH ?
  • it could be
  • carcinoma prostate
  • stricture
  • primary unstable bladder
  • neuropathic bladder
  • overactive
  • underactive
  • UTI
  • prostatitis
  • bladder tumour
  • bladder stone
  • ureteric stone
  • diabetes

3
Symptoms of outflow obstruction
  • Hesitancy
  • Poor stream
  • Terminal dribbling
  • Difficulty starting
  • Difficulty going
  • Difficulty stopping
  • Sensation of incomplete emptying

4
  • Other symptoms are secondary symptoms or symptoms
    of other pathology
  • i.e. frequency, nocturia, urgency etc
  • secondary symptoms are more bothersome

5
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6
Chronic retention Dangerous because of -
renal failure bladder failure
7
Treatment options
  • No treatment
  • Drugs
  • 5 alpha reductase inhibitors
  • alpha blockers
  • Surgery
  • Heat treatment
  • Stents, catheters etc

8
5 alpha reductase inhibitors
  • Finasteride / Dutasteride
  • Genuine reduction in prostate size by up to 30
  • Work in c. 50 of patients
  • Better in bigger prostates
  • Dont work immediately
  • Small effect on symptom score and flow rates
  • Well tolerated can decrease libido

9
Alpha -blockers
  • Relax muscles around bladder neck
  • Work immediately
  • Doesnt effect natural history of disease
  • More side effects than 5 ? R I
  • Slightly better results than 5 ? R I
  • Work in all sizes of gland

10
Selective alpha blockers
  • Alpha - Phenoxybenzamine
  • Alpha 1 etc - Indoramin
  • Alpha 1a etc - Tamsulosin

11
Dutasteride Phase IIIa studies Pooled data for
first episode of acute urinary retention
6 5 4 3 2 1 0
Placebo Dutasteride 0.5 mg
Patients ()
0
6
12
18
24
Months
Placebo group No. of events, cumulative 28 49 70 9
0 No. at risk 2158 2039 1919 1793 Dutasteride
group No. of events, cumulative 19 27 31 39 No.
at risk 2167 2052 1928 1827
Roehrborn et al (2002)
12
Drug treatment
  • Improves symptoms
  • Decreases risk of retention / intervention by
    approx half
  • Combination therapy is more effective
  • 5 alpha reductase inhibitors work best in bigger
    prostates, but slowly
  • Alpha blockers work immediately

13
Managing BPH in the community
  • Is it BPH?
  • Are the symptoms right?
  • Flow rate?
  • Exclude cancer
  • Exclude chronic retention
  • U and E s
  • Scan ?
  • Trial of drugs
  • Refer if no response / symptoms worsen

14
TURP
  • Remains the gold standard for the treatment of
    BPH
  • 100 improvement in flow
  • Retrograde ejaculation but otherwise few side
    effects
  • Good results depend on good patient selection
  • 10 may need further surgery in 10 years

15
Heat treatment
  • Prostatic hyperthermia / thermatherapy / thermal
    ablation (TUMT, TUNA)
  • Laser prostatectomy
  • Short stay, safe, variable side effects, unproven
    in long term
  • Will almost certainly have a future
  • The best method of heat delivery is as yet
    uncertain

16
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17
PSA - specific for the prostate but not for
prostate cancer
  • PSA is raised in
  • cancer
  • prostatic infection
  • urinary retention
  • BPH

18
The normal PSA
  • PSA less than 4.0 Ca unlikely
  • PSA 4 10 Ca in 25
  • PSA 10 Ca in 33
  • PSA over 10 Ca in 66
  • PSA over 20 Ca highly likely
  • or age related reference range

19
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20
Improving the PSA test
  • PSA density
  • Age related PSA
  • 40 - 49 2.5
  • 50 - 60 3.5
  • 60 - 69 5.5
  • 70 - 79 6.5
  • PSA velocity
  • Free PSA

21
P.S.A.
  • To test or
  • not to test

22
  • Localised prostate
  • cancer is
  • not a fatal
  • disease

23
Survival at 5 years
24
  • Metastatic disease
  • rare if PSA is under 20
  • Very very rare if PSA under 10

25
  • No point searching for cancer aggressively if
    youre not going to treat it aggressively
  • Lots of old men die with prostate cancer without
    knowing they ever had it

26
Aggressive case finding and treatment, or not ?
  • Against
  • Lifetime risk of disease 9
  • Lifetime risk of mortality 3
  • Localised prostate cancer is not a fatal disease,
    and it may never progress in patients lifetime
  • Significant complication rate of treatment, so
    why overtreat ?
  • No proven overwhelming benefit to treatment

27
Aggressive case finding and treatment, or not ?
  • In favour
  • Some men do die of prostate cancer
  • Catch the disease early and remove it

28
Prostate cancer - treatment
  • Localised
  • No treatment
  • Radical prostatectomy
  • Radiotherapy
  • External beam
  • Brachytherapy
  • No randomised controlled trials of treatment

29
  • All treatments have
  • significant side effects

30
Is aggressive treatment effective?
  • Results are biased
  • by patient selection
  • by more accurate staging in surgical patients

31
191 patients with localised prostate cancer (all
grades) treated with radiotherapy
32
148 patients with localised prostate cancer
treated by radical prostatectomy
33
61 pts under 70 with mod / well diff T1 / T2
prostate cancer, no specific treatment
34
In the early years
  • Most patients with localised
  • prostate cancer do well,
  • however they are treated..

35
But after 10 years or more
  • Untreated patients do less well if they havent
    died of anything else in the meantime
  • 80 of men diagnosed age 60 or under who receive
    no treatment die of prostate cancer
  • cure rates after radical surgery of 70 - 90
    are often claimed

36
Common sense (and a little knowledge) suggests..
  • Some men will do well, treated or not, and die of
    other causes in due course
  • Some will progress and die of Ca
  • We cant predict who will do what
  • The younger you are, the more likely the disease
    will progress eventually
  • Radical treatment probably decreases the chance
    of progression

37
  • Consider radical treatment in patients with a
    life expectancy of 10 years (70 ish or less and
    fit)..

38
  • ...but accept that some patients may be having
    treatment (and complications of that treatment)
    which they may not need

39
P.S.A.
  • To test or
  • not to test

40
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41
Anti-screening
  • Not cost effective
  • Doesnt save enough (or even any) lives
  • No proven intervention which modifies the natural
    history of the disease
  • Poor take up rate

42
Pro-screening
  • It must save lives if you catch the tumours early
  • Its good enough for women
  • Trials in progress

43
If you have a PSA blood test
  • you have to seriously consider a biopsy if
    raised
  • what if the biopsy is equivocal ?
  • what if the biopsy is benign and PSA remains high
    ?

44
In an ideal world
  • Invite men under 70 for PSA screening after
    informed consent
  • .with serious consideration of radical treatment
    if cancer diagnosed

45
In the real world
  • Some men just want the test
  • Informed consent is difficult and time-consuming
  • Screening is not economically viable
  • Low take up rate
  • Questionable benefit in terms of population
    survival

46
Who should have a PSA ?
  • Patients with significant outflow symptoms
  • (? age cut off)
  • Patients over 40 with haemospermia, unexplained
    haematuria or abnormal DRE
  • Patients with suspected metastatic disease
  • Informed patients age 45 - 70 who ask for it

47
Who shouldnt have a PSA
  • Men under 40
  • Elderly asymptomatic men with normal feeling
    prostates
  • unless high suspicion of metastatic disease
  • Uninformed asymptomatic men of any age

48
Who should be referred?
  • Patients with significant outflow symptoms
  • Patients with likely cancer
  • Abnormal DRE
  • PSA over 20
  • Metastatic disease
  • Patients with life expectancy of 10 years or more
    with high age related PSA
  • ? Patients with PSA 10 -20 aged over 75

49
Do not be concerned about
  • Unfit elderly men with PSAs of under 15
  • Men unlikely to survive 10 years with PSA of less
    than 10
  • Raised PSA in men in retention or with infection
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