GI cancer drugs Flashcards
(19 cards)
bevacizumab moa
anti-VEGF
bevacizumab adverse effects
bleeding, GI perforation, wound dehiscence, HTN
cetuximab moa
anti-EGFR
cetuximab adverse effects
cardiac arrest, respiratory arrest, and sudden death; acne form rash in 80%
erlotinib moa
EGFR tyrosine kinase inhibitor
erlotinib adverse effects
Bleeding, elevated LFTs, ocular toxicity, interstitial lung disease
glutamic acid moa
nutritional supplement; used to counterbalance deficiencies of HCl in the gastric juice
imatinib moa
KIT tyrosine kinase inhibitor
imatinib adverse effects
CHF in some patients, neurologic toxicity, GI toxicity
leucovorin moa
reduced folate; synergies with 5-FU
methysergide moa
serotonin inhibitor in the GI tract, causing vasoconstriction; used for migraines
octreotide moa
somatostatin analog; reduces duodenal bicarb and amylase, gastric acidity, inhibition of GB contractility and bile secretion, meal induced increases in SMA and portal flow.
octreotide adverse effects
inhibition of insulin and glucagon. dose related diarrhea
sorafenib moa
oral multikinase inhibitor targeting serine/threonine and receptor tyrosine kinases in both tumor and vasculature:
Raf, VEGFR 2&3, PDGFR-beta, KIT, FLT-3, and RET
sorafenib adverse effects
hand-food skin reaction characterized by redness, pain, swelling, or blisters on the palms of the hands or soles of the feet, generally in first 6 weeks of treatment
sunitinib moa
inhibitor of >80 RTKs including PDGFR alpha and beta, VEGFR1,2,3, KIT, FLT-3, CSF-1R, and RET
sunitinib adverse effects
thrombocytopenia and bleeding, QT prolongation, sometimes fatal GI complications including perforation
trastuzumab moa
HER-2/neu antibody, causing HER2 downregulation, leading to accumulation of CDK inhibitor p27, causing cell cycle arrest; also inhibits HER2 cleavage mediated by metalloproteases, which may correlate with the clinical activity
trastuzumab adverse effects
LVEF dysfunction and cardiomyopathy, severe infusion-related reactions including anaphylaxis, angioedema, and pulmonary toxicity; pulmonary toxicity is worse in patients with interstitial lung disease