Prostate Cancer Flashcards

1
Q

Epidemiology

A

Most common cancer in men in the UK

26% of all male cancer diagnoses

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2
Q

Pathophysiology

A

Unclear

Widely agreed that growth of prostate cancer is influenced by androgens like testosterone and DHT

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3
Q

Type of prostate cancer

A

>95% are adenocarcinomas

Over 75% of prostate adenocarcinomas arise from the peripheral zone

20% from the transitional zone

5% in the central zone

Prostate cancers are often multifocal

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4
Q

Subtypes of prostate adenocarcinomas

A

Acinar adenocarcinoma originating in the glandular cells that line the prostate and is the most common form

Ductal adenocarcinoma that comes from cell lining of the duct. They tend to grow and metastasis faster.

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5
Q

Risk factors

A

Age

Ethnicity - Black african or Carribean ethnicity twice as likely.

FH of prostate cancer

BRCA2 or BRCA1 gene

Obesity, DM, smoking, degree of exercise

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6
Q

Clinical features

A

Usually presents with LUTS with a weak urinary stream, increased urinary frequency and urgency.

More advanced localised disease can also cause haemturia, dysuria, incontinence, haematospermia, suprapubic pain, loin pain and even rectal tenesmus.

Metastatic disease can also cause bone pain, lethargy, anorexia and unexplained wieght loss

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7
Q

Examinations

A

DRE is essential

Most arise from posterior peripheral zone so check for asymmetry, nodularity or fixed irregular mass.

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8
Q

Dx

A

BPH

Prostatitis

Bladder cancer, urinary stones, UTI and pyelonephritis

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9
Q

Lab test

A

PSA

A serum protein produced both by malignant and normal healthy cells in the prostate which can be elevated

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10
Q

When else might PSA be elevated?

A

BPH

Prostatitis

Vigorous exercise

Ejaculation

Recent DRE

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11
Q

Further calculations using PSA

A

Free:Total PSA ratio

A low ratio is associated with increased chance of diagnosig prostate cancer

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12
Q

Explain PSA density

A

Serum PSA level divided by the prostate volume which is determined on imaging.

High PSA densitiies = increased likelihood of prostate cancer

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13
Q

Further investigations

A

Current standard method for diagnosis is through biopsies of prostatic tissue

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14
Q

Potential methods of biopsy

A

Transperineal Template Biopsy

TransRectal Ultrasound guided (TRUS) biopsy

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15
Q

Explain Transperineal Template Biopsy

A

Sampling of biopsy transperineally.

This is done as a day case under general anaesthetics.

Transperineal approach allows for better access to the anterior part of the prostate and has a lower risk of infection.

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16
Q

Explain TransRectal UltraSound-guided TRUS biopsy

A

Sampling transrectally under local anaesthetics

12 cores are taken bilaterally in equal distribution from base to apex

1-2 % risk of sepsis.

Repeat prostate biopsy after previous negative biopse is recommended if there is a rise in PSA or peristently elevated.

17
Q

What grading system is used for prostate cancer?

A

Gleason Grading System

18
Q

Explain Gleason Grading System

A

Sample is assigned a score according to differentiation

Score is then calculated as the sum of the most common growth pattern + the second most common growth pattern seen.

Higher score = Less favourable prognosis

19
Q

Imaging in prostate cancer

A

Multiparametic magnetic resonance imaging mp-MRI is increasinly used to aid diagnosis.
It can identify abnormal areas which can then be targetted for biopsy by MRI-ultrasound fusion or cognitive-guidance techniques.

This means that mp-MRI is sometimes being used earlier in the diagnostic pathway prior to initial biopsy.

20
Q

When is staging of prostate cancer done?

A

Staging is typically done in intermediate and high-risk disease via CT-abdo-pelvic scan and bone scan.

21
Q

General management

A

Specialist prostate cancer MDT meeting

PSA levels, Gleason score and T staging decides further management.

22
Q

Low risk disease management

A

Active surveillance

Radical treatment only offered to those who show evidence of disease progression

23
Q

Intermediate and high risk management

A

Radical treatment options should be discussed.

Intermediate risk can also be offered active surveillane.

24
Q

Metastatic disease management

A

Chemotherapy agents and anti-hormonal agents

25
Q

Castrate-resistant disease management (Hormone-relapse prostate cancer)

A

Further chemotherapy like Docetaxel.

Corticosteroids can also be given as third line after androgen deprivation therapy and anti-androgen therapy.

26
Q

Explain the Watchful waiting and active surveillance management.

A

Symptom guided approach

Monitoring of patients with 3-monthly PSA

6 month to yearly DRE

Re-biopsy at 1-3 yearly intervals assessing for progression

mpMRI is also being used.

27
Q

Surgical management

A

Radical prostatectomy removing prostate gland, resection of the seminal vesicles + any surrounding tissue.

This can be done open approach, laparoscopically or robotically

28
Q

Complications of prostatectomy

A

ED

Stress incontinence

Bladder neck stenosis

29
Q

When is radiotherapy done?

A

External-beam radiotherapy and brachytherapy are both commonly used as alternatives to curative intervention of localised prostate cancer.

30
Q

Explain brachytherapy

A

Transperineal implantation of radioactive seeds of Iodine-125 directly into prostate gland

31
Q

Explain external-beam radiotherapy

A

External-beam radiotherapy uses focused radiotherapy to target the prostate gland and limits damage to surrounding tissue.

32
Q

Indications of chemotherapy

A

Metastatic prostate cancer.

33
Q

Give examples of chemotherapies in prostate cancer.

A

Docetaxel and cabazitaxel.

34
Q

What other chemical therapy can be done?

A

Androgen deprivation therapies since most prostate cancers are stimulated by circulating androgens.

GnRH receptor agonist like goserelin can be used
It becomes an LHRH agonist due to its action

Enzalutamide and abiraterone are new hormone therapies which act to lower levels of serum testosterone.

35
Q

Mainstay treatment for localised or locally advanced prostate cancer

A

Radical prostatectomy, external-beam radiotherapy and brachytherapy.

36
Q
A