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55 Cards in this Set

  • Front
  • Back
what are some characteristics of uncontrolled growth in tumors?
invasiveness
metastases - via MMP
capacity for dedifferentiation
ability to accumulate mutations
uncontrolled growth
what is a kill ratio
given dose of a cytotoxic drug that destorys a constant fraction of the malignant cells
what is the difference between cell cycle specific and non specific?
CCS only acts in active cells/cells traversing the cell cycle
CCNS acts on Go/resting phase, has worse toxicity
what are some alkylating agents that can be used in tx of brain tumors because they can cross the BBB
lomustine, carmustine
what is the MOA of alkylating agents?
alkylation @ n7 position of guanine. they allows cross linking within a DNA strand to occur --> miscoding, depurination, and strand breakage
what are some SE of nitrosoureas?
neurotoxicity --> nausea and vomiting in acute phase

chronic phase :
leukopenia sterility carcinogenic alopecia thrombocytopenia
which alkylating drug will give you pulmonary fibrosis and hepatic toxicity?
busulfan
which will be activated in the liver and could lead to hemorrhagic cystitis if acrolein is made
cychlophosphamide
what is the rescue agent to form an inactive compound with acrolein so hemorrhagic cystitis doesn't occur with cyclophosphamide use?
mesna
what is a SE of cyclophosphamide?
hepatotoxicity
what are some Rx uses of cyclphosphamide?
BON NHL

breast ovarian neuroblastoma NHL
what is the MOA of procarbazine?
forms h202 --> free radicals and dna strand scission
what are some SE of procarbazine?
bone marrow suppression, *leukomogenic, teratogenic, *pulmonary toxicity
what are some platinum analogs and how do they work?
they complex and react with DNA, forming intra interstrand cross links --> cytotoxic effects

cisplatin
carboplatin
what are some SE of cisplatin/carboplatin?
cisplatin : nephrotoxicity, ototoxicity

carboplatin: myelosuppression
what is an inhibitor of dihydrofolate reductase --> inhibition of formation of thymidine and therfore no DNA synthesis
mtx
mtx does NOT cross the BBB. how does it get into the brain?
if injected intrathecally
what are some SE of mtx?
nephrotoxicity
bone marrow depression
mucositis
what is a rescue drug for mtx?
leucovorin
leukemias, lymphomas, breast cancer all use what drug that they all have in common?
mtx
this drug needs HGPRT to convert it to its active form. inhibits several enzymes needed for purine synthesis and with formation of NDA/RNA
6 thiopurines
what are some SE of 6 mercaptoppurine, 6-thioguanine
HIM
hepatotoxicity
immunosuppression
myelosuppresion
what is the main tx for ALL (acute loymphocytic leukemia)
purine antagonists
this inhibits DNA pol alpha and beta
fludarabine
pyrimidine antagonist
SE: nausea, diarrhea, mucositis, bone marrow depression, alopecia
5 FU
what are the therapeutic uses for 5FU
think of follicles and upper
ovarian, breast, head and neck cancers
this drug is S phase specific and activity is limited to hematologic malignancies

- blocks DNA pol a and b
cytabarine
what does cytabarine treat?
ALL
Acute myelogenous leukemia
what is the MOA of gemcitabine?
inhibits ribonucleotide reductase --> decreases pool of nucleotides for DNA synthesis
what is the only durg that is first line treatment of pancreatic ca?
gemcitabine
what drug blocks the formation of mitotic spindles and thus prevents assembly of MT
vinca alkaloids
what SE include myelosuppresion, painful ulcerations if extravasation occurs, and GI problems
vinblastine
i am used to treat hodgkin, NHL, breast cancer, testicular and i am a plant alkaloid that works on the M phase
vinblastine
i am used to treat ALL, hodgkin, leukemia, wilms and i also have tingling in my extremities and constipation as a SE and i am a plant alkaloid
vincrinstine
this drug's MOA is to build MT and then interfere with the mitotic spindle, preventing the MT disassembly into tubulin monomers
taxanes (paclitaxel and docetaxel)
what drugs work in the M phase?
paclitaxel, vincristine, vinblastine
what drugs have neurotoxicity?
paclitaxel, vinblastine, cisplatin
which drug works in the late s phase to the g2 phase?
etoposides
what is the MOA of etoposides
inhibit dna pol II by forming a tertiary compelx --> strand breakage
which one is used for solid tumors, lung cancer, hodkins, and NHL
etoposide
what is the MOA of camptothecins
inhibits topoisomerase I and prevents tsrand ligation --> DNA damage
which camptothecin must be converted to its active form
irinotecan
this anthracycline has major cardiotoxicity as a SE and may exacerbate CHF and cardiomyopathies
doxorubicin
which drug is cell cycle specific and chelates Fe2+ on one end and binds DNA on the other end and stops the cell cycle at g2?
bleomycin
what are the se of bleomycin
pulmonary fibrosis ** main one
mucocutaneous rxn
alopecia
what inhibits topoisomerase Ii but is an anthracycline and is used for pediatric tumors
dactiniomycin
what is used for hypoxic tumor cells
mitomycin
this is used to suppress the immune system before you get an organ transplant
prednisone
name the 2 treatments for breast cancer
tamoxifen and trastuzumab
which drug has a specific affinity for breast CA via binding to HER-2
trastuzumab
what is a tx for prostate cancer
flutamide leuprolide goserelin
what is a treatment for advanced breast cancer via inhibiting estrogen from being made by blocking aromatase
anastrozole letrozol exemestane
this inhibits PDGF and should NOT be used if you have torsades
nilotinib
what are the bone marrow sparing agents
cisplatin, bleomycin, vincristine
combining what 2 drugs can decrease the likelihood of gaining resistance?
mtx + vincristine

if resistance does develop it is dt p glycoprotein which transports foreign molecules out of the cell