Prostate cancer Flashcards

1
Q

Risk factors for prostate cancer

A

Age
Black african ethnicity, then caucasian and hispanic/ Asian and natice american men lower rates
FH and genetics
Hormonal factors
Environemantla factors - chemical exposure, high fat diet, sediantary, obsesity

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2
Q

Initial genetic mutations genes

A

oncogenes (e.g., MYC, ERG) and tumour suppressor genes (e.g., TP53, PTEN).

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3
Q

what causing clonal expansion of caner cells

A

hormones (e.g., androgens), growth factors (e.g., IGF-1), and inflammatory mediators (e.g., IL-6).

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4
Q

What genetic mutations in final stage selective advantage for invading tissues and resisting apoptosis

A

PI3K/AKT/mTOR, MAPK, and Wnt signalling pathways.

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5
Q

Clinical features of prostate cancer

A

Often asymptomatic as cancers tend to develop peripherally - dont cause obstruction
-bladder outlet obstruction - hesitancy, urinary retention
Haematuria, haemaatospermia
Pain - back, perineal or testicular
PR exam - asymetrical hard nodular enlargement with loss of median sulcus

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6
Q

When refer for suspected prostate cancer

A

Prostate feels malignant on PR exam
PSA above normal levels

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7
Q

When consider a PSA test and PR exam for prostate cance r

A

Any lower urinary symptoms eg nocturia, urinary frequency, hesitancy, urgency or retnetion or
Erectile dysfunciton
Visible haematuria

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8
Q

Investigaiton for prostate cancer

A

NICE first line= multiparametric MRI as first line
(was US TRUS biopsy)

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9
Q

TRUS biopsy complications

A

sepsis: 1% of cases
pain: lasting >= 2 weeks in 15% and severe in 7%
fever: 5%
haematuria and rectal bleeding

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10
Q

What determines whether do a biospy for prostate cancer

A

Likhert scale 1-5 from multiparametric MRI

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11
Q

What likhert scale means offer biopsy vs discuss pros and cons

A

> 3 -> biopsy
1-2 = discuss

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12
Q

Localised prostate cancer T1/2 management

A

Watch and wait - active monitoring
Radical prostatectomy
Radiotherapy - external beam and brachytherapy

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13
Q

Localised advanced prostate cancer (T3/T4)) managmenet

A

Hormonal therap
Radical prostatectomy
Radiotherapy

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14
Q

What chemo is used in prostate cancer

A

Docetaxel

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15
Q

antiandrogen therapy options in prostate cancer

A

Synthetic GnRH agonist or antagonist eg goserelin, zoladex
Bicalutamide - non steroid anti androgen
Cyproterone acetate - steroidal above
Abiraterone - androgen synthesis inhibitor
Bilateral orchidectomy to reduce testosterone levels rapidly

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16
Q

Risks with radical prostatectomy

A

Erectile dysfunction common complication

17
Q

Radiotherapy side effects in prostate cancer

A

Proctitis
Increased risk of bladder, colon and rectal cacner

18
Q

How do GnRH agonist/antagonsits MOA prostate cancer

A

Reduce testosterone levels
paradoxically result in lower LH levels longer term by causing overstimulation, resulting in disruption of endogenous hormonal feedback systems. The testosterone level will therefore rise initially for around 2-3 weeks before falling to castration levels

19
Q

Why need to prescribe an anti androgen with GnRH agonsits

A

prevent a rise in testosterone - ‘tumour flare’. The resultant stimulation of prostate cancer growth may result in bone pain, bladder obstruction and other symptoms

20
Q

prognosis prostate cancer 5 year survivalrates

A

99% and 96% localised and regional (III)
IV /distant mets = 30%

21
Q

Factors affecting prognosis prostate cancer

A

Stage
Fleason score - how aggresisive cancer is 1-10
PSA level
Age and health

22
Q

PSA age related limits recommended

A

NICE - >3 aged 50-69 or abnormal DRE
>4 for 60-60
>5 for 70

23
Q

What can raise PSA levels

A

BPH
Prostatits and UTI
Ejaculation - ideally not in last 48 hrs
Vigorous exercise - as above
Urinary retention
iNSTRUMENTATation of unrinary tract eg catheter

24
Q

Sensitivity and specificity of PSA

A

Poor
around 33% of men with a PSA of 4-10 ng/ml will be found to have prostate cancer. With a PSA of 10-20 ng/ml this rises to 60% of men
around 20% with prostate cancer have a normal PSA
various methods are used to try and add greater meaning to a PSA level including age-adjusted upper limits and monitoring change in PSA level with time (PSA velocity or PSA doubling time)