Prostate Flashcards

1
Q

How common is prostate cancer?

A

second most common cancer in the UK and the most common in men

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2
Q

What is the location of the prostate?

A

between the bladder & external urethral sphincter, and anterior to the rectum. It surrounds the prostatic urethra below the urinary bladder and is palpable on digital rectal exam (DRE)

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3
Q

What is the function of the prostate?

A

fluid is secreted during ejaculation, and consists of proteolytic enzymes, including the prostate-specific antigen (PSA), and prostatic acid phosphatase

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4
Q

What are the zones of the prostate?

A

transitional - BPH
central
peripheral - 75% cancer
anterior

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5
Q

Where is prostate cancer commonly found?

A

commonly found in peripheral zone (75%) and then transitional and lowest central

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6
Q

What type is common?

A
  • almost always adenocarcinoma
    • acinar adenocarcinoma (most common)
    • ductal adenocarcinoma (most aggressive)
    • growth of cancer usually influenced by androgens
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7
Q

What are some risk factors for developing prostate cancer?

A
  • family history - first degree relative increases risk by 2.5 times
  • ethnicity - men of black ethnicity
  • age
  • potential link with obesity
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8
Q

What are the clinical features?

A
  • can be asymptomatic if early
  • local disease
    • invasions of urethra: hesitancy, nocturia, frequency, haematuria
    • invasion of ejaculatory ducts: haematospermia
    • invasion of rectum: tenesmus
    • metastatic spread: weight loss, lethargy, anorexia, bone pain etc
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9
Q

What features might you feel on DRE?

A
  • asymmetry
  • hard, irregular surface
  • palpable mass
  • signs of mets
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10
Q

How would you investigate suspected PC?

A

Bloods
Prostate specific antigen measurement
Digital rectal examination
Trans rectal USS (+/- biopsy)
MRI/ CT and bone scan for staging
bone scan

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11
Q

What is PSA?

A

💁🏽‍♂️ protein produced within prostate epithelial cells and secreted into prostatic fluid, small quantities detected in blood normally

  • in cancer → abnormal architecture → higher levels in blood
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12
Q

Why might a PSA be indicated?

A

suspicious DRE, possible symptoms of prostate Ca, patient request over 50

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13
Q

Why might PSA be raised?

A

prostatitis, good DRE, BPH, UTI, catheterisation, prostate biopsy (upto 6w), vigorous exercise like cycling, ejaculation

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14
Q

Evaluate PSA as a screening tool.

A

Advantages as screening tool

  • minimally invasive, earlier detection, earlier treatment, low cost, simple and reproducible

Disadvantages as screening tool

  • false negatives, false positives, unnecessary investigations and treatment, over treatment
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15
Q

How is PC graded?

A

Graded using the Gleason grading system, two grades awarded 1 for most dominant grade (on scale of 1-5) and 2 for second most dominant grade (scale 1-5). The two added together give the Gleason score. Where 2 is best prognosis and 10 the worst

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16
Q

Where does PC spread to?

A

Lymphatic spread occurs first to the obturator nodes and local extra prostatic spread to the seminal vesicles is associated with distant disease

17
Q

How might PC be managed?

A

conservative
radical prostatectomy
radiotherapy
hormonal therapy - testosterone deprivation
chemo
palliative

18
Q

What is the difference between watch and wait and active surveillance?

A
  • watchful waiting: regular primary care follow up to monitor disease progression by assessing symptoms, PSA testing with avoidance of invasive Ix like DRE or biopsy
    • for older patient, multiple co-morbidities, more likely to die with rather than prostate Ca, in any risk group
  • active surveillance: regular monitoring of progression with MRI at diagnosis, regular DRE, PSA and biopsies
    • in low risk groups, only if patient is candidate for future radical treatment
19
Q

What is offered in active surveillance?

A

have had at least 10 biopsy cores taken
have at least one re-biopsy

*If men on active surveillance show evidence of disease progression, offer radical treatment. Treatment decisions should be made with the man, taking into account co-morbidities and life expectancy

20
Q

When might we opt for radical prostatectomy?

A

in intermediate or high risk localised cancer, failure of radical radiotherapy, locally advanced with adjunct, rarely in men over 70

21
Q

How is radiotherapy used in PC mx?

A
  • external beam radiotherapy: directed at tumour from outside body, for localised intermediate to high risk (with adjunctive for high), locally advanced (with brachy), relapse post surgery
  • brachytherapy: low or high dose commonly adjunct with ERBT for localised and locally advanced, can be used as monotherapy in low risk with implanted radioactive seeds
22
Q

What hormone therapies are utilised in PC?

A

testosterone dependent cancers, so reduce levels to reduce stimulation for cancer to grow
- testosterone antagonist cyproterone acetate
- GnRH agonist goserelin

23
Q

How might you manage bone pain?

A

nalgesics, hormone therapy, radiotherapy, radiopharmaceuticals and chemotherapy for pain relief

osteoclast inhibitor (e.g. denosumab, zoledronic acid) to reduce the risk of skeletal complications

24
Q

Why might there be problems with PC be managed as palliative?

A
  • prostate sx: retention due to tumour mass, clot retention
  • localised spread: lymphoedema
  • bone: pain, #, spinal cord compression, BM failure
  • psychosocial: altered body image, sexual dysfunction
25
Q

What are some complications for radical prostatectomy?

A
  • immediate - infection, bleeding, VTE, anastomotic leak, urinary retention
  • long term - incontinence, erectile dysfunction
26
Q

What are some complications in radiotherapy for PC?

A
  • damage to mucosa of urinary tract: LUTS, haematuria, radiation cystitis
  • damage to rectal mucosa: diarrhoea, rectal bleeding, rectal pain
  • urinary retention: prostatic swelling or urethral stricture