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163 Cards in this Set

  • Front
  • Back
cytotoxic chemotherapy agents
antimetabolites
antitumor antibiotics
antimiotics
alkylating agent
topoisomerase inhibitor
antimetabolites
kill cancer cells by interrupting a specific phase of cell reproduction
antitumor antibiotics
kill cancer cells by stopping the synthesis of RNA, DNA, or proteins
antimitotics
kill cancer cells by inhibiting mitosis and preventing cell division
anklyating agents
kill fast-growing cancer cells by altering DNA structure and preventing cell reproduction
topisomerase inhibitors
kill cancer cells by interrupting DNA synthesis
other
kill cells by various mechanisms including interrupting DNA and RN synthesis in leukemia cells
cytotoxic chemotherapy agents adverse
nausea, vomiting, myelosuppression, alopecia
antimetabolites
folic acid analog
pyrimidine analog
purine analogs
antimetabolite agents adverse
bone marrow suppression, GI discomfort
intervention: monitor WBC, absolute neutrophil count, platelet count, Hgb, and Hct
assess clients for bruising and bleeding gums
avoid crowds and contact with infectious individual
administer antiemetic before beginning chemo
methotrexate adverse (Folic acid analog)
mucositis, gastric ulcers, perforation
reproductive toxicity
renal damage due to hyperuricemia or elevated levels of uric acid

intervention: monitor for GI bleeding, provide frequent oral hygeine, advise client not to become pregnant while taking these meds and 6 months after
monitor kidney function and BUN, administer allopurinol if uric acid is elevated.
cytarabine adverse (pyrimidine analog)
liver disease, pulmonary edema, arachnoiditis- manifestations may be treated with dethmethasone (Decadron)
mercaptopurine (purine)
liver toxicity, mucositis, gastric ulcers, perforation, reproductive toxicity
methotrexate interactions
salicylates, NSAIDs, sulfanomides, penicillin, and tetracyclines- methotrexate toxicity

folic acid changes the body's response to methotrexate- avoid folic acid supplements
cytarabine interactions
may reduce digoxin (Lanoxin) level
may reduce gentamicin response to Klebsiella pneumonae
Mercaptopurine interactions
allopurinol (Zyloprim) may reduce breakdown of mercaptopurine
mercaptopurine may either increase or decrease anticoagulant effect of warfarin- monitor PT and INR
folic acid analog
proto: methotrexate (Rheumatrex, Trexall)
pyrimidine analog
proto: cytarabine
fluorouracil (Adrucil, Carac)
Capecitabine (Xeloda)
floxuridine (FUDR)
purine analog
prot: mercaptopurine (Purinethol)
thioguanine (Tabloid)
pentostatin (Nipent)
fludarabine (Fludara)
folic acid analog MOA
stops cell reproduction by inhibiting folic acid conversion
S-phase specific
pyrimidine analog MOA
inhibits RNA and DNA synthesis of cancer cells
S- phase specific
purine analogs MOA
interrupts RNA and DNA synthesis of cancer cells
S-phase specific
folic acid analog use
choriocarcinoma, solid tumors, (breast, lung, head and neck sarcomas, acute lymphocytic leukemia, non-Hodgkins lymphoma)
pyrimidine use
acute myelogenous leukemia
solid tumors- such as breast and colon
superficial skin cancers (flourouracil)
purine use
acute lymphocytic leukemia
acute nonlymphocytic leukemia
methotrexate contraindications
contraindicated in renal or hepatic failure, blood dyscrasias, or lactation
cytarabine contraindications
liver disease
mercaptopurine
contraindicated in clients who are resistant to medication
antimetabolites admin
give with sodium bicarbonate capsules to alkalinize urine
do not use birth control during treatment
avoid alcohol during treatment
monitor for bleeding and bruising
jaundice
methotrexate admin
administer leucovorin rescue to reduce toxicity to healthy cells.
take med on empty stomach
protect skin from sunlight
use birth control during and 6 months after
cytarabine admin
monitor for indications of neurotoxicity, such as nystagmus
antitumor antibiotics
anthracyclines
nonanthracyclines
anthracyclines (antitumor)
proto: doxorubicin (Adriamycin)

other: liposomal doxorubicin (Doxil)
daunorubicin (Cerubidine)
nonanthracyclines (antitumor)
proto: dacintomycin (Cosmegen)

other: bleomycin (Belnoxane)
mitomycin (Mutamycin)
dacintomycin, liposomal (Doxil)
anthracyclines MOA
binds to DNA, altering it's structure
cell phase nonspecific
anthracycline use
includes solid tumors, such as lung, bone, stomach, and breast cancer, Hodgkin's and non-Hodgkin's lymphoma
nonanthracyclines MOA
binds to DNA, altering structure
nonanthracycline use
Wilms tumor
rhabdomyosacroma
choriocarcinoma
Ewings sarcoma
Kaposi's sarcoma
all antitumor drugs adverse
bone marrow suppression
GI manifestations
severe tissue damage due to extravasations of vesicants
alopecia
doxorubicin (antitumor) adverse
acute cardiac toxicity, dysrhythmias- can be treated with dexraoxane (Zinecard)
cardiomyopathy- may be treated with ACE inhibitor
red coloration to urine and sweat- not a harmful effect
doxorubicin contraindications
contraindicated in clients who have severe myelodepression and those who have had a lifetime cumulative dose of 550 mg/m2
dacintomycin contraindications
acute infections
doxorubicin interactions
calcium channel blockers- increase cardiotoxicity
phenobarbital- may increase metabolism of doxorubicin
paclitaxel (Taxol) may decrease metabolism of doxorubicin
doxorubicin may reduce phenytoin (Dilantin) levels
dacintomycin contraindications
none noted
antitumor admin
reduce dose in liver disease
monitor for bleeding
monitor CBC and liver enzymes

doxorubicin- monitor for delayed cardiac toxicity
antimitotics
Vinca alkaloids
Taxanes
vinca alkaloids (antimitotics)
proto: vincristine (Oncovin, Vincasar PFS)
other: vinblastine (Velban)
vinorelbine (Navelbine)
taxanes (antimitotics)
proto: paclitaxel (Abraxane)
docetaxel (Taxotere)
vinca alkaloids MOA
useful in combination with other chemotherapy med
stops cell division during mitosis
not bone marrow toxic
M-phase specific
vinca alkaloids use
acute lymphocytic leukemia, Wilms tumor, rhabdomyosarcoma, solid tumors
taxanes use
ovarian , non-small cell lung tumors and Kaposi's sarcoma
taxanes MOA
stop cell division during mitosis
vincristine (Vinca alkaloids) adverse
peripheral neuropathy effects
alpopecia
paclitaxel (Taxane) adverse
bone marrow suppression
bleeding caused by thrombocytopenia or low platelet count, anemia, or low RBCs
bradycardia
heart block
MI
Alopecia
vincristine contraindications
contraindicated in CHarcot-Marie-Tooth syndrome
liver disease of neuromuscular disease
paclitaxel contraindications
neutrophil count less than 1500 mm
use with caution who have myelosuppression
vincristine interactions
vincristine may reduce effects of digoxin
mitomycin may increase risk for brochospasm
vincristine may decrease level of phenytoin
paclitaxel interactions
cisplatin or doxorubin may increase myelosuppression
cardiac meds that decrease heart rate such as beta blockers, calcium channel blockers and digoxin, can increase bradycardia
paclitaxel interactions
meds that increase risk for bleeding such as NSAIDs and anticoagulants may increase bleeding risk
antimitotic admin
reduce dose for clients who have liver disease
assess for bronchospasm
monitor for bleeding and infection
monitor CBC and liver enzymes
stop chemotherapy if extravasation occurs
use birth control during treatment
ankylating agents
nitrogen mustards
nitrosoureas
platinum compounds
nitrogen mustards (ankylating agent)
proto: cyclophosphamide (Cytoxan, Neosar)

other: mechlorethamine (Mustargen)
bendamustine (Treanda)
chlorambucil (Leukeran)
nitrogen mustards MOA
kills rapid growing cells by interrupting DNA and RNA synthesis
nitrogen mustards use
acute lymphomas, solid tumors: head, neck, breast cancers, Hodgkins and non-Hodgkins lymphoma
nitrogen mustards adverse
acute hemmorrhagic cystitis- increase fluids (3L)
monitor for blood in urine, Mesna (Mesnex) may be given if needed
alopecia
nitrosoureas (ankylating agent) MOA

carmustine (BiCNU, Gliadel)
kills rapid growth cells by interrupting DNA and RNA synthesis
crosses blood brain barrier
nitrosoureas (ankylating agent) use
brain tumors, Hodgkins, non-Hodgkins, and multiple myeloma
nitrosoureas adverse
pulmonary fibrosis
liver and kidney toxicity
platinum compounds (ankylating agent) MOA

cisplatin (Platinol)
kills rapid growing cells by interrupting DNA and RNA synthesis
platinum compounds use
bladder, testicular, and ovarian cancers
platinum compounds adverse
renal toxicity
hearing loss
monitor for tinnitus and hearing loss
nitrogen mustard (Cyclophosphamide) contraindications
severe myelosuppression or severe infection
kidney or liver disorder or leukocytopenia or thrombocytopenia
nitrosoureas (Carmustine) contraindications
severe myelosuppression or impaired liver function
platinum compounds (Cisplatin)
severe myelosuppression, kidney disorders, hearing loss
cyclophasphamide interactions
concurrent use of succinylcholine may cause increased neuromuscular blockage
carmustine interactions
concurrent use with cimetidine (Tagament) may increase bone marrow suppression
cisplatin
concurrent use with aminoglycosides may increase risk for renal toxicity
concurrent use with furosemide may increase hearing loss
ankylating agents admin
monitor for blood in urine- Mesna (Mesnex) may be indicated
monitor CBC
monitor hearing prior to treatment with cisplatin
topoisomerase inhibitors
proto: topotecan (Hycamtin)
topoisomerase inhibitor MOA
kills cancer cells by interrupting DNA synthesis
topoisomerase inhibitor use
treats metastatic ovarian cancer, cervical cancer, and small cell lung cancer
topoisomerase inhibitor adverse
bone marrow suppression
bleeding caused by thrombocytopenia
low platelet count
anemia
GI discomfort
alopecia
topoisomerase inhibitor contraindications
severe myelosuppression with a neutrophil count less than 1500 mm
topoisomerase inhibitor interactions
cisplatin may increase myelosuppression
topoisomerase inhibitor admin
monitor for bleeding, bruising, infection
CBC
good oral hygiene
use birth control during treatment
asparaginase (Elspar) (antineoplastic agent)
kills cancer cells by interrupting DNA synthesis in leukemia cells
G1 specific
asparaginase (Elspar) use
acute lymphocytic leukemia
hydroxurea (Hydrea, Mylocel) (antineoplastic)
kill cancer cells by interrupting DNA synthesis
s specific
may cross blood brain barrier
hydroxurea use
chronic myelogenous leukemia, ovarian, squamous cell cancers
procarazine (Matulane) (antineoplastic agent)
kills cancer cells by interrupting DNA and RNA synthesis
cell phase nonspecific
may cross blood brain barrier
procarzine (Matulane) use
brain tumors, Hodgekin, non-Hodgkin lymphoma
asparaginase, hyroxurea, procarbazine adverse
GI discomfort
aspariginase adverse
hypersensitivity
CNS effects ranging from confusion to coma, temporary tremor may occur
liver and pancreas toxicity
renal toxicity
hydroxurea and procarbazine adverse
bone marrow suppression
may occur 4-6 weeks after infusion
procarbazine adverse
peripheral neuropathy may include weakness and paresthesia
asparaginase contraindications
history of pancreatitis, exposure to chickenpox, herpes simplex infection
liver disease
hydroxyurea contraindications
severe myelosuppression or anemia
use with caution in clients who have kidney disease
procarbazine contraindications
severe myelosuppression
liver or kidney disease
asparaginase interactions
may decrease effects of methotrexate
prednisone and vincristine may increase asparaginase toxicity
decreased effect of antidiabetic meds
hydroxyurea interactions
cytotoxic meds may increase hydroxyurea
procarbazine interactions
increase depressant effects of CNS depressants
MAOI or TCA, foods containing tyramine, and many OTC preparations such as cough medicines may cause hypertensive crisis
alcohol may cause a disulfiram reaction
asparaginase admin
allergic reaction
use birth control during treatment
use good mouth care
hydroxyurea admin
monitor for bleeding, bruising, or infection
withhold med and notify the provider for a WBC less than 2500 mm or a platelet count less than 100,000 mm3
procarbazine admin
monitor for neurologic effects such as confusion or paresthesia
withold meds and notify provider for a WBC less than 4,000 mm3 and a platelet count less than 100,000 mm3
noncytotoxic chemotherapy agents
gonadotropin-releasing hormone agents
androgen receptor blockers
gonadotropin-releasing hormone agents
testes stop producing testosterone

use: palliative treatment for advanced prostate cancer
androgen receptor blockers
blocks testosterone at receptor site
used in conjunction with gonadotropin-releasing hormone agonists to block androgen receptors and suppress the growth of prostate cancer

use: treatment of prostate cancer
gonadotropin-releasing hormone agonist proto
leuprolide (Eligard, Lupron)
other: triptorelin (Trestar Depot)
androgen receptor blockers proto
flutamide (Eulexin)
other: bicalutamide (Casodex)
leuprolide adverse (GRH)
hot flushes, decreased libido, gynecomastia
decreased bone density
arrythmias, pulmonary edema
flutamide adverse
hot flushes, decreased libido, gynecomastia
nausea, vomiting, diarrhea
hepatitis
leuprolide contraindications
hypersensitive to gonadotropin-releasing agents
flutamide contraindications
severe liver disease
leuprolide interactions
none noted
flutamide interactions
concurrent use with warfarin may increase anticoagulation
leuprolide admin
increase calcium and vit D intake
minimize bone loss with weight-bearing exercises
monitor PSA and testosterone levels, which should both decrease with treatment
flutamide admin
administered with gonadotropin-releasing hormone agonist or alone following a surgical castration
hormonal agents- breast cancer meds
estrogen receptor blockers
aromatase inhibitors
monoclonal antibody
estrogen receptor blockers
prototype: tamoxifen (Nolvadex)
other: raloxifene (Evista)
fulvestrant (Faslodex)
aromatase inhibitors
proto: anastrozole (Arimidex)
letrozole (Femara)
exemestane (Aromasin)
monoclonal antibody
trastuzumab (Herceptin)
estrogen receptor blocker MOA
stops growth of breast cancer cells, which are estrogen dependent cancers
estrogen receptor blocker use (tamoxifen)
used to treat or prevent breast cancer
aromatase inhibitors use (anastrozole)
treats breast cancer in postmenopausal women
monoclonal antibody use (trastuzumab)
treat metastatic breast cancer
alone or in conjunction with paclitaxel
tamoxifen adverse
endometrial cancer
hypercalcemia
nausea and vomiting
pulmonary embolus
hot flushes
vaginal discharge or bleeding
anastrozole adverse
muscle and joint pain
nausea
vaginal bleeding
increased risk for osteoporosis
hot flushes
trastuzumab adverse
cardiac toxicity, tachycardia, heart failure
hypersensitivity
nausea and vomiting
tamoxifen contraindications
taking warfarin or history of blood clots or pulmonary embolism
anastrozole contraindications
women before menopause and in severe liver disease
mild to moderate liver disease
trastuzumab contraindications
hypersensitive
heart disease
tamoxifen interactions
anticoagulation action of warfarin
some SSRI antidepressants decrease effectiveness of tamoxifen
anastrozole interactions
tamoxifen and estrogenlike meds may reduce anstrozole effects
anastrozole and anthracyclines may increase the risk for cardiac effects
breast cancer meds admin
increase calcium and vit d
perform monthly breast exam
monitor CBC
use birth control
biologic response modifiers
proto: interferon alfa-2b (Intron A)
other: aldesleukin (Inteleukin 2) BCG vaccine (TheraCys)
biologic response modifiers MOA
increases immune response and decreases production of cancer cells
biologic response modifiers use
treat or prevent hairy cell leukemia, chronic myelogenos leukemia, malignant melanoma, and AIDS-related Kaposi's sarcoma
biologic response modifier adverse
flulike symptoms
bone marrow suppression, alopecia, cardiotoxicity, neurotoxicity
depression, anxiety, insomnia, altered mental states.
biologic response modifier contraindications
hypersensitivity to the medication, suicidal thoughts, colitis, pancreatitis
severe liver, kidney, heart, or pulmonary disease and in DM or history of depression
biologic response modifier interactions
concurrent use of theophylline (Theo-Dur) can lead to theophylline toxicity
Zidophine (Retrovir) may increase the risk of neutropenia or thrombocytopenia
concurrent use with meds that are cardiotoxic or netrotoxic may increase cardiotoxicity or neurotoxicity
concurrent use with vaccines using a live virus may reduce antibody response
biologic response modifier admin
monitor for flu symptoms
monitor CBC, platelets, electrolytes
monitor fluid status
Targeted antineoplastic meds
EGFR-tyrosine Kinase inhibitors
BCR_ABL tyrosine kinase inhibitors
CD2- Directed antibodies
angiogenesis inhibitors
EGFR-tyrosine kinase inhibitor
proto: cetuximab (Erbitux)

other: panitumumab (Vectibix)
BCR-ABL tyrosine kinase inhibitor
prototype med: imatinib (Gleevec)
CD20-Directed antibodies
proto: rituximab (Rituxan)
angiogenesis inhibitors
proto: bevacizumab (Avastin)
cetuximab MOA and use
antibody that stops cancer cell growth and increases cell death

USE: treat cancers that are EGRF positive, such as colorectal nd solid tumors of the head and neck
imatinib MOA and use
stops cancer growth by inhibiting intracellular enzymes

use: treat chronic myeloid leukemia
rituximab MOA and use
antibody that stops cancer cell growth and increases cell death

use: treats non-Hodgkins lymphoma
bevacizumab MOA and use
antibody that stops cancer cell growth and increases cell death

use: treat colorectal and lung cancer
cetuximab adverse
infusion reaction, rash, hypotension, wheezing
pulmonary emboli
skin toxicity, rash
imatinib adverse
GI discomfort
flulike symptoms
edema
hypokalemia
neutropenia, anemia
rituximaba adverse
infusion reaction, rash, hypotension, wheezing
flulike symptoms
tumor lysis syndrome due to rapid cell death, may lead to kidney failure, hypocalcemia and hyperuricemia
bevacizumab adverse
thromboembolism, including CVA, MI, TIA
alopecia
hemorrhage, GI, vaginal, nasal, intracranial, or pulmonary
hypertension
gastric perforation
cetuximab contraindications
hypersensitivity
imatinib adverse
liver disease
rituximab adverse
liver or kidney failure
bevacizumab adverse
low WBC, nephrotic syndrome, recent surgery or dental work, hypertensive crisis
cardiac, renal disease history or hypersensitivity
cetuximab interactions
sun exposure may increase skin toxicity
imatinib interactions
may increase chance of liver failure
concurrent use with warfarin may increase anticoagulant effect
clarithromycin, erythromycin, and ketoconazole may slow imatinib metabolism and cause toxicity
carbamazepine and phenytoin may increase imatinib metabolism
rituximab interactions
calcium channel blockers and other antihypertensive meds increase chance of hypotension
bevacizumab interactions
may increase irinotecan level
targeted antineoplastic meds admin
monitor for infusion reaction
protect skin from sun
notify provider for shortness of breath
good oral hygiene
CBC, platelets, and electrolytes
fluid status
edema
abdominal pain, skin lesions, headache, episodes of bleeding