Less gastrointestinal and renal toxicity:
- cisplatin (Platinol)
- carboplatin (Paraplatin)
Side effect(s)-cisplatin (Platinol):
- nausea, vomiting
- significant bone marrow effects
- significant renal dysfunction
- A & C
- A, B & C
major acute side effect of cisplatin (Platinol)
- bone marrow depression
- renal dysfunction
- nausea and vomiting
- acoustic nerve dysfunction
Most important toxic effect associated with alkylating agents:
- renal dysfunction
- hepatic failure
- neurotoxicity
- bone marrow suppression
- alopecia
Secondary to bone marrow suppression associate with alkylating agent chemotherapy:
- septicemia
- severe infection
- hemorrhage
- A & C
- A, B & C
More likely to cause nausea and vomiting:
- IV cyclophosphamide (Cytoxan)
- oral cyclophosphamide (Cytoxan)
- equally likely
Most antimetabolite anticancer drugs interfere with nucleic acid synthesis or nucleotide synthesis:
- true
- false
Methotrexate:
- tumor resistance associated with decreased polyglutamate formation
- may be used in treating rheumatoid arthritis
- induces abortion when combined with a prostaglandin
- B & C
- A, B & C
Methotrexate-mechanism action: Folic acid antagonist, acting at dihydrofolate reductase catalytic site:
- true
- false
Synergistic with cytarabine (ARA-C) in treating acute adult leukemia:
- thioguanine
- mercaptopurine (Purinethol)
Drug resistance-thioguanine
- decreased HGPRT activity
- increased alkaline phosphatase which dephosphorylates thiopurine nucleotides
- both
- neither
More likely to be associated with drug toxicity when given concurrently with allopurinol (Zyloprim, Purinol)
- mercaptopurine (Purinethol)
- thioguanine
In hematologic cancer chemotherapy with purine antagonists, allopurinol (Zyloprim, Purinol) coadministration is used to prevent:
- cardiotoxicity
- retroperitoneal fibrosis
- nephrotoxicity and gout
- hepatotoxicity
- depletion of bone calcium
Purine antagonist(s)
- fludarabine (Fludara)
- cladribine (Leustatin)
- pentostatin (Nipent)
- A & B
- A, B & C
Pyrimidine antagonists:
- cytarabine (ARA-C)
- azatadine (Optimine)
- fluorouracil (5-FU)
- B & C
- A, B & C
Primary mechanism of action: inhibition of topoisomerase II
- vincristine (Oncovin)
- teniposide (Vumon)
- vinblastine (Velban)
- A & C
- A, B & C
Clinical use teniposide (Vumon)
- monocytic leukemia
- lymphoma
- testicular cancer
- oat cell carcinoma
In combination with prednisone (Deltasone): induction of remission in children with acute leukemia
- vinblastine (Velban)
- vincristine (Oncovin)
- both
- neither
Significant frequency-adverse effect associated with vincristine (Oncovin)
- bone marrow depression
- neurotoxicity
- equal frequency
Used in management of colon: & rectal cancer, including tumors not responding to fluorouracil (5-FU)
- irinotecan (Camptosar)
- topotecan (Hycamtin)
Primary adverse effect(s): topotecan (Hycamtin)
- neutropenia
- thrombocytopenia
- anemia
- A & C
- A, B & C
Dose-limiting adverse effect for irinotecan (Camptosar):
- diarrhea
- nausea
- vomiting
- myelosuppression
Clinical uses:taxanes: (paclitaxel (Taxol) & docetaxel (Taxotere))
- ovarian cancer
- advanced breast cancer
- both
- neither
Taxanes: dose limiting adverse effect(s):
- peripheral neuropathy
- thrombocytopenia
- neutropenia
- B & C
- A, B & C
Anticancer antibiotics act by DNA intercalation-blocking DNA & RNA synthesis
- true
- false