Chemotherapy Drugs Flashcards
(42 cards)
Name the drug class that is a G-Phase DNA damage disruptors
DNA Intercalating Agents
Aside from hemorrhagic skin cystitis, What additional specific risk does cyclophosphamide pose?
CANCER (acute myelogenous leukemia)
Name the 2 drug classes that disrupt mitotic spindles
- Taxanes
2. Vinca Alkaloids
Name the 4 Drug classes that disrupt S phase
- Purine/Pyrimid Analogs
- Antimetabolites
- Antifolates
- Epipodophyllotoxins
When taking the deoxycytidine analog, Gemcitabine, watch out for ______ _____ Syndrome as a toxicity!
Hemolytic Uremic
Vinca alkaloids (vincristine) and Taxanes (paclitaxel) are both ______ _____
Microtubule disruptors
If a person has kidney disease, you would want to avoid the alkylating agent, _______ and instead use ______
Cisplatin, Carboplatin
What is they key highlighted Pyridine analog of Deoxyctidine that is used to treat cancer?
Gemcitabine
Gemcitabine is a ______ ____ drug
Deoxycytidine Analog
The epipodophyllotoxins (Etoposide), Capothecin (Irinotecan), and Anthracylcin (Doxonrubicin) all inhibit the enzyme ______
Topoisomerase
The MT disuptors Vin and Pac 3 key toxicities
- Neurotox
- ANS dysfxn
- SIADH
Considering the indication of Alkylating Agents, what are their 3 overall sideffects?
- GI problems
- Bone Marrow Depression (low immune cells)
- Reproductive system probs
Both of the Antifolate drugs, Pemetrexed and 5-FU target the enzyme _____(___) to reduce DHFR to lessen DNA & RNA biosynthesis
Thymidylate Synthase (TS)
The alkylating drug Cisplatin treats what types of cancer?
Basically all of them
Non-small and small, head, neck, lung, and GI
The deoxycytidine analog, Gemcitabine inhibits which two enzymes?
- Ribonucleatide Reductase
2. DNA polymerase
Aside from nephrotoxicity and ototoxicity, what major and speific toxicity occurs with Cisplatin?
Irreversible Nerve Dysfunction
Name the 3 Topoisomerase inhibitors
- Etoposide
- Irinotecan
- Doxorubicin
Etoposide, Irinotecan, and Doxorubicin are all _____ inhibitors
Topoisomerase
In order to become a Pur/Pyr, Folate become Dihydrofolate, then Tetrahydrofolate via the enzyme ______
DiHydrofolate Reductase (DHFR)
Considering that Irinotecan the Topo 1 inhibitor treats colorectal cancer, the most common toxicity is ______
Diarrhea
Vincristine and Paclitaxel are both MT disruptors disrupting mitosis, however Vin ____ polymerization, whereas Pac _____ polymerization
- Vin inhibits
- Pac promotes
Aside from myelosuppression and GI problems, the Anthracyclin, Doxorubicin’s MAJOR SEVERE toxicity is ______
CARDIOTOXICITY
2-3 days watch for arrhythmias
Purine/Pyrimidine analogs, antimetabolites, antifolates, and Epipodophyllo toxins all block the ____ phase of the cell cycle.
S
Pemetrexed and 5-Fluorouracil are both ______ Cancer Drugs
Anti-Folate