11-19 L1 Fundamentals of Chemotherapy Flashcards
define
Cell Kill hypothesis
States that a constant fraction of tumor cells will be killed with each chemotherapy cycle
Thus cell killing is a log-function and the tumor burden will (in theroy) never reach absolute zeroa
10^9 kill 99.999% only 10^5
Define
Phase I
Phase II
Phase III
-
Phase I: new drug don’t know much about it
- dose escalation to determine toxicity profile, dose-limiting toxicity (DLT) and max tolerated dose
-
Phase II: how it works
- Determine agent activity in specific diseases
-
Phase III: compare it to other drugs
- Compare efficacy of ABVD vs DEACOPP in HL
Whats the difference b/t
CCSA (cell cycle specific agents)
CCNSA (Cell cycle non-specific agents)
- CCSA:
- act at specific stages of the cell cycle espcially those stages representing active DNA/cell proliferation
- not effective in G0 phase
- CCNSA:
- Cytotoix to both cells that are actively cycling as well as to cells in the G0 phase
In the Cell-cycle specific agents
define the drugs for
- S (C-FFIrM)
- M (P-DoVV)
- S/G2
- G2 phase specific
- S phase
- Cytarabine
- Fludarabine
- Fluorouracil
- Irinotecan
- Methotrexate
- M phase
- Paclitaxel
- Docetaxel
- Vincristine
- Vinblastine
- S/G2 phase
- Bleomycin
- G2 phase
- Asparaginase
Name the 4 classical alkylating agents (CCIM)
- Carmustine
- Cyclophosphamide
- Ifosfamide
- Mechlorethamine
Carmustine
- primary brain tumors, HL, Cutaneous T-cell lymphoms
- hydrophobic (admin in alcohol)
- Toxicity: myelosuppression, delayed nadir (21-28 days) Adminstere every 6 weeks
Cyclophosphamide & Ifosfamide
- whats its byproduct
- what does it lead to
- how do we treat it
- Toxicity:
- Acroelin
- causes severe hemorrhagic cystitis
- MESNA: used as a cytoprotected
- Toxicity: Bone marrow suppresion (d 8-14), cystisi, cardiac (high doses), immunosuppression)
Name 2 non-classical alkylating agents
describe its toxicity
- Carboplatin: toxicity–> Myelosuppression
- Cisplatin: toxicity –> nephrotoxicity
Name the drugs associated with the following classes in antimetabolites
- Antifolates
- Fluoropyrimidines
- Deoxycitadine analods
- Purine antagonists
- Antifolates: Methotrexate
- Fluoropyrimidines: 5-FU (5 fluorouracil)
- Deoxycitabine analogs: Cytarabines
- Purine anatognists: Fludarabine
Methotrexates
- What is it used for?
- how do you treat it if given too much?
- solid & hematological tumors
- ALL, Breast, head nad neck cancer, lung, NHL
- Leucovorin rescue
What is an example of Topoisomerase I inhibitor?
- What is it used for?
- What is a major side effect
- how do you treat it
- acutely
- delayed
- Irinotecan
- Colorectal cancer
- diarrhea treat w/:
- acute: atropine
- delayed: loperamide
Provide 2 examples of microtubule inhibitors
What is a major side effect
- Vincristine
- Vinblastine
- SE: neuropathy, including constipation
Provide 2 drugs that stabilize the microtubules
- Paclitaxel
- Docetaxel
Bleomycin
- Composed of what
- Inidcation
- Toxicity
- Mixture of fungal glycopeptides (from streptomyces spps)
- Indicatoin: HL, NHL, head and neck, testicular
- Toxicity: Pulmonary toxicity, hypersensitivity rxn, chills, mucositis
Hydroxyurea
inhibits ribonucleotide reductase
AML: acute myelocytic leujemai