Prostate cancer Flashcards

1
Q

Localized treatment for early stage

A

observation
active surveillance

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2
Q

Localized treatment for advanced high risk early stage

A

radiation and LHRH (leuprolide or goserelin) - option for those who cannot handle surgery

Prostatectomy and lymph node dissection for those with greater than 10 year life expectancy will follow surgery with a Leuprolide or goserelin and possibly anti-androgen treatment if lymph positive or high rate or recurrence

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3
Q

SE with LHRH agonists

A

these will cause tumor flare because it needs to increase levels of hormones to desensitize the receptors
other side effects include ED, hot flashes, man boobs, edema - makes sense because its messing with the hormone levels in the body and stopping the production of man type hormones

Long term: osteoporosis, fracture, insulin resistance, increased risk in diabetes and cardiovascular events

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4
Q

Relugolix

A

oral option that is compated to the LHRH agonists and is a good option for those with cardiac history

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5
Q

Anti-androgens

A

given in combo with the LHRH agonists to prevent the flare up side effect

commonly used option is Bicalutamide
usually given 1 week before starting LHRH and stopped one month into therapy
can cause diarrhea and hematuria

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6
Q

M0HSPC

A

this is when patient has non-melaginancy but elevated PSA levels (greater than 4)
focus on the doubling time of PSA
If PSA doubles in less than 6 months patient can be treated with ADT
If PSA doubling time is longer than 6 months we will continue to observe the disease and testing levels every 6 months

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7
Q

M0HSPC and PSA doubled in less than 6 months - treatment

A

orchiectomy (removal of testes)
this causes an immediate drop in testosterone levels
toxicities include impotence (no boner) and hot flashes

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8
Q

intermittent ADT

A

FOR men with biochemical failure ONLY

Patients start a LHRH agonist with or without a ADT and PSA levels are monitored throughout the duration of therapy
If patients levels return to 4 ng/dl they can discontinue therapy but monitoring of PSA will continue and when patients PSA levels spikes again to 10-20 ng/dl we will restart therapy

this on and off therapy can be beneficial because it decreases the cost and decreases the side effects associated with the therapy regimen

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9
Q

M0CRPC tx

A

When patients PSA levels are continuing to increase although on proper ADT therapy and no distant metastasis found in scan

Continue on LHRH agonist
Add in ONE of the following: (darolutamide is safe option)
enzalutamide - DO NOT USE IN SEIZURE history, AVOID CYP2C8 inhibitors, decreases serum concentration of wafarin
Enzalutamide can cause seizures, diarrhea, confusion
apalutamide - Non-steroidal androgen receptor inhibitor, use with caution in seizure history, QT prolongation (watch out for heart problems)
apalutamide can cause hypertension, falls, rash, diarrhea, fatigue
darolutamide - NO seizure or falls - great for patients with seizure history or older patients that live alone
side effects in the two other drugs were less in darolutamide

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10
Q

M1HSPC

A

PSA level increased and metastasis found on scan
Therapy is determined based on volume which can either be low or high
before treating get patient MSI-H or dMMR testing as well as germline mutation testing - these will help us determine the treatment for the patient

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11
Q

Low volume M1HSPC treatment

A

start patient with leuprolide or any other GnRH agonist

continue ADT listed above and add any of the following
-Abiraterone + prednisone (prednisone must be given with because it is treating the adrenal insufficiency caused by abiraterone)
Causes hypertension, edema, increased triglycerides, liver toxicities, atrial fibrillation
- Enzalutamide - not great for seizure history and causes alot of confusion
- Apalutamide - not great for seizure and causes QT prolongation

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12
Q

High volume M1HSPC treatment

A

can give any of the following regimens
-Leuprolide and anti-androgen (ADT)
- ADT +/- abiraterone and prednisone
- ADT +/- enzalutamide
-ADT +/- apalutamide

Chemotherapy is now a possible treatment option

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13
Q

First line treatment for M1 disease high volume

A

Docetaxel + abiraterone + prednisone

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14
Q

M1CRPC

A

in addition to continuing ADT therapy
patient should add docetaxel + abiraterone + prednisone

if patient progresses on docetaxel regimen start them on cabazitaxel - this will work even with resistant tumors
cabazitaxel side effects include more severe neutropenia, more diarrhea, more febrile neutropenia

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15
Q

Treatment for bone mestastases

A

radium 223 dichloride
Used for CRPC symptomatic bone metastases
Cannot be given with chemotherapy
side effects include thrombocytopenia, anemia, and neutropenia

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16
Q

Prostate cancer with dMMR/MSI-H expression

A

Pembrolizumab

17
Q

Pluvicto (Lu-177)

A

For use in PSMA positive MCRPC
IV dosing - beta emitting therapeutic
side effects include myelosupression, renal toxicity, dry mouth, and GI toxicities

18
Q

Prostate screening

A

Screening should start around age 50
annual PSA if level is greater than or equal to 2.5
every 2 year screening if PSA is less than 2.5

digital rectal exam (DRE)
- normal prostate feels like the tip of your nose
- prostate cancer feels like your chin
- if there is presence of lumps and hardness we should test further
Prostate specific antigen (PSA) - normal range around 0-4 ng/dl
- greater than 4 means we should be evaluating
- greater than 10 means high probability of malignancy

Transrectal ultrasonography should be preformed if patient has abnormal findings in PSA and DRE

19
Q

High risk patients

A

include men age 45 and up African American who have a first degree relative with prostate cancer

those who have several first degree relatives with prostate cancer should be testing DRE and PSA at age 40

20
Q

Treatment options

A

go over slide 73