growth factor, major determinant of chemotherapy effectiveness
3 properties unique to cancer cells
growth factor
enzyme production
vascularization
3 tumor cell properties that could present problems
uncontrolled proliferation
ectopic growht sites
cell life cycle
4 mechanisms for drug resistance
cellular adaptation
reduced drug transport into cells
reduced molecular target affinity
stimulation of alternative biosynthetic pathways
4 bad results of tumor lysis syndrome
hyperuricemia
hyperkalemia
hyperphosphatemia
hypocalcemia
tumor lysis causing metabolic and electrolyte disturbances can progress to 4
renal insufficiency
cardiac arrhythmia
seizures
death due to multiorgan failure
causes chemotherapy-induced hyperpigmentation of the tongue
doxorubicin & cyclophasphamide
preventative vaccine against strains of HPV attributed to cause 70% of cervical cancers
gardasil
cervarix
therapeutic vaccine which utilizes personalized medicine to treat prostate cancer
sipuleucel-T
disrupt DNA synthesis
block mitosis
disrupt protein synthesis
target cell replication
cycle specific and non
cytotoxic drugs
act during any phase
synergistic w/cell cycle specific drugs
more toxic to proliferatind cells
cell cycle nonspecific drugs
3 criteria for cancer drug therapy
each drug effective alone
different mechanism of action
minimal overlapping toxicities
which drug class causes a formation of a covalent bond between drug and DNA to form crosslinks
methylation at N7
alkylating agents
Administer with caution in hepatic failure, DO NOT take this drug with calcium containing foods (dairy products) or antacids, thrombosis and hypertension possible side effects
USE contraception due to mutagenic, carcinogen and tetratogenic potential
alkylating agents
DNA virus agent
acyclovir - zovirax
RNA virus agent
didanosine - videx
MOA: Spindle poison – unique mechanism such that these drugs promote assembly of microtubules and stabilize them such that
depolymerization can not occur
taxoids
cytotoxic intercalation
not cell cycle specific
streptomyces or streptococcus origin
most have I.V administration
antitumor antibiotics
DNA cleavage agents
significant antitumor activity
minimal myelosupression
pulmonary fibrosis
bleomycin
aquation or hydration necessary to produce active species
explains difference in pharmacokinetics and potency
platinum coordination complexes
Side-effects include:
Hepatotoxicity & renal damage
severe vomiting
ototoxicity (more severe in children)
Analyphylaxis (immediate-treat with epinephrine, antihistamines,corticosteroids)
platinum coordination complexes
Bone marrow suppression is dose related producing infection and
anemia---may be cumulative and require transfusions
Dosage adjustment a function of renal creatinine clearance
Carefully monitor platelet and neutrophil counts
DO NOT use aluminum containing administration sets
platinum coordination complexes
target post menopausal women
blocks estrone and estradiol production
does not block ovarian production in pre-menopausal women
aromatase inhibitors
Nonreceptor TK’s
Maintained in the inactive state by
cellular inhibitor proteins
lipids
intramolecular autoinhibition
These inhibitors also induce growth arrest, cell differentiation, and apoptosis of tumor cells.