chemotherapy - pharm E4 Flashcards

(66 cards)

1
Q

cell cycle

A

G0: rest phase
G1: cell growth
S: DNA synthesis
G2: prepare to divide
M: mitosis (division)

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2
Q

growth fraction

A

the ration of proliferating cells to resting cells (G0)
higher amount in prolif = high GF, more in G0 = low G0

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3
Q

what growth fraction rate is harder to kill

A

the low growth rate

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4
Q

malignant tumors initially grow very

A

rapidly (high growth fraction)

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5
Q

as the size of the tumor increases, the growth fraction rate and what does it create

A

lowers -> a necrotic core, decreased nutrient supply at core, more cells in G0

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6
Q

barriers to success

A

-100% kill required for cure
-toxicity
-late detection
-tumor response
-drug resistance
-cell heterogeneity

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7
Q

same dose treatment

A

to kill the cancer cells, patient needs to have the same dose of chemo every time but the problem is that in the beginning the pt might be able to tolerate the dose for a few rounds but as they grow weaker they might not be able to tolerate it

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8
Q

what is the earliest we can detect cancer

A

when it is 1cm in diameter (& the cancer already has a billion cells)

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9
Q

intermittent chemo

A

Goal: 100% cancer cell death w/ limited normal cell injury
-needs a balance to let normal cells recover and aggressive treatment

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10
Q

combination therapy

A

-multiple drugs are better than one
-Adv: reduces drug resistance & normal cell injury
-increases cancer cell killed
don’t pair drugs that have the same toxicity

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11
Q

optimal dosing : dosing schedule

A

-maximize results
-cell cycle specific agents
-keep active drug present in body as long as possible so it can hit all parts of the cell cycle

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12
Q

optimal dosing: regional drug therapy

A

-access to tumors
-high drug concentrations
-decrease systemic toxicity
ex: intra arterial, intrathecal, intraperitoneal, intravesical
acting on the tumor, not the cell

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13
Q

usual toxicities from chemo

A

-N/v for several days after chemo
-1 to 2 wks after first round: decreased WBCs, RBCs, pallor, platelets, diarrhea, alopecia, fatigue
-neutropenia, erythrocytopenia, thrombocytopenia (bone marrow)
-stomatitis & GI tract injury & malnutrition
-hyperuricemia (kidney risk)

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14
Q

magic mouth wash

A

-prescription “cocktail” for stomatitis
-swish, gargle & spit 5-10ml q6 prn
-not curative

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15
Q

reproductive toxicities of chemo

A

do not take while pregnant / get pregnant while on
-can cause sterility in men

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16
Q

chemo is the treatment but aslo a

A

carcinogen so can cause organ damage

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17
Q

anti cancer agents

A

-cytotoxic agents
-hormonal agents
-biologicals
-targeted drugs

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18
Q

cytotoxic agent

A

cell death

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19
Q

hormonal agents

A

block effects of hormones on tumor
ex) tamoxifen

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20
Q

biologics

A

alter the body’s response to cancer
ex) interferon therapy

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21
Q

targeted drugs

A

new class, targets only cancer cells
ex) bevacizumab

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22
Q

cytotoxic agents: MOA

A

disrupt DNA synthesis & mitosis

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23
Q

what drugs are considered cytotoxic agents

A

alkylating agents
antimetabolites
antitumor antibiotics
mitotic inhibitors

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24
Q

immune check point inhibitors

A

allow for immune cells to respond more strongly to cancer

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25
T cell transfer therapy
boost natural ability of the T cells to fight cancer **taken out of body, grown in lab, put back in for this effect**
26
Monoclonal abx
used to mark the cancer cells so that they are better seen by body's immune system
27
Treatment vaccines
boosts immune systems response to cancer
28
Immune system modulators
enhance the body's immune response against cancer to prevent or slow tumor growth
29
what are the biological agents
Immune checkpoint inhibitors T cell transfer therapy Monoclonal abx Treatment vaccines Immune system modulators
30
biological agents MOA
Uses body’s immune system to kill cancer cells
31
biological agents indications
-Leukemias/ lymphomas -breast -bladder -brain -colon -lung -pancreatic
32
biological agents SE
Pain Swelling Soreness Flu like Wt gian Diarrhea Inc risk of infection
33
biological agents nursing considerations
Not as effective as surgery
34
cytotoxic agents MOA
Disrupt DNA synthesis & mitosis causing cell death
35
cytotoxic agents SE
N/v Hair loss Malnutrition
36
cytotoxic agents nursing considerations
Give through central line or port
37
what class is Cyclophosphamide
alkylating agents
38
alkylating agents MOA
Cell cycle phase nonspecific
39
Cyclophosphamide indication
Cancer
40
Cyclophosphamide SE
Vesicant Hemorrhagic cystitis Sterility Discoloration of skin & nails
41
Cyclophosphamide nursing considerations
**Includes G0** High likely hood of resistance Bladder injury
42
what class is Methotrexate
Antimetabolites
43
Antimetabolites MOA
Cell cycle specific
44
Methotrexate indications
Leukemia Lymphomas
45
Methotrexate SE
Nephrotoxicity Hepatotoxicity Fetal death or abnormalities
46
Methotrexate nursing considerations
**Interferes w/ S phase (DNA synthesis) of cell growth** Resistance likely
47
what class is Doxorubicin
Antitumor
48
Antitumor MOA
Cell cycle phase nonspecific
49
Doxorubicin indications
Cancer
50
Doxorubicin SE
Turns urine & sweat red Cardiotoxicity Acute & delayed rxn
51
Doxorubicin nursing considerations
Can be used in all phases
52
what class is Vincristine
Mitotic inhibitor
53
Mitotic inhibitor MOA
Cell cycle specific
54
Vincristine indications
cancer
55
Vincristine SE
Peripheral neuropathy Vesicant
56
Vincristine nursing considerations
Blocks mitosis Bone marrow sparing Good combo drug
57
what class is Ondansetron
Antiemetic: serotonin antagonist
58
Ondansetron MOA
Blocks serotonin receptors on vagal nerve & in the chemoreceptor trigger zone
59
Ondansetron indications
N/v
60
Ondansetron SE
Headache Diarrhea Dizziness
61
Ondansetron nursing considerations
Better w/ steroids
62
what class is Promethazine
Antiemetic: dopamine antagonist
63
Promethazine MOA
Blocks dopamine receptors in the CTZ
64
Promethazine indications
Chemo Post op General N/v
65
Promethazine SE
Respiratory depression Drowsiness, sedation
66
Promethazine nursing considerations
BBW: resp depression <2, gangrenous extravasation