Chemotherapy and Biologic Therapy Flashcards
Components of Drug Effect with Chemotherapy
Drug Concentration x Duration of Exposure
How is Dosage Calculated for chemotherapy?
Milligrams per meter squared of body surface area
Definition of Area Under the Curve
attenuate doses based on functional or induced impairment of body systems
Definition of Complete response to Chemotherapy treatment
Disappearance of all evidence of tumor
Definition of Partial response to chemotherapy treatment
a 50% reduction in the cross product of measurable lesions and absence of any new disease
Definition of Cell Cycle Specific Chemo agents
Depend on proliferative capacity of cells and phase of cells.
Chemotherapy agents that work in DNA synthesis (S) phase
Antimetabolites: Methotrexate, Gemcitabine
Chemotherapy agents that work in the mitotic phase (M) phase
Alkaloids: Taxanes, Topotecan, Etoposide, Vincristine
Definition of Cell Cycle non specific Chemo agents
acts in all phases of the cell cycle, not dependent on proliferative capacity
Classes of cycle non specific chemo agents
Platinum agents, Antibiotics, Alkylating agents
Common Platinum agents
Cisplatin, carboplatin
Antibiotics used in Chemotherapy regimens
Doxorubicin, Bleomycin
Common Alkylating agents
Cyclophosphamide, Ifosfamide
Methotrexate: Mechanism of action
Active during S phase, Combines with dihydrofolate reductase. Inhibits conversion of di-hydrofolate to tetrahydrofolate
Methotrexate: Toxicities
Mucositis, Myelosupression, Liver and renal impairment
Methotrexate: Uses
GTN, Breast cancer`
Gemcitabine: Mechanism of action
Active during S phase
Gemcitabine: Toxicities
Myelosupression
Gemcitabine: Uses
Ovarian Cancer
Paclitaxel: Mechanism of action
Active in M phase. Stabilization of micro tubular aparatus, cells die in metaphase arrest
Paclitaxel: Toxicities
Hypersensitivity reaction, Dysrhythmias, alopecia, neuropathy, myelosupression
Paclitaxel: Dose limiting toxicity
Myelosupression
Vincristine: Mechanism of action
Active in M phase: Inhibits polymerization of tubulin
Vincristine: Toxicities
Neuropathy, Alopecia
Vinblastine: Mechanism of action
Active in M phase: Inhibits polymerization of tubulin
Vinblastine: Toxicities
Myelosupression
Cyclophosphamide and Ifosfamide: Mechanism of Action
Alkylating agent, reactive species bind to DNA, Cross link DNA, produce breaks in DNA chains and Interfere with base pairing
Cyclophosphamide and Ifosfamide: Toxicities
Increased risk of second malignancy, premature gonadal failure, hemorrhagic cystitis, CNS confusion (Ifosphamide)
Cisplatin: Mechanism of action
Platinum Drug, mechanism similar to alkylating agent. reactive species bind to DNA, Cross link DNA, produce breaks in DNA chains and Interfere with base pairing
Cisplatin: Toxicities
Emetogenic, Neuropathy, Nephropathy
Carboplatin: Mechanism of action
Platinum drug, Forms adducts/complexes with DNA, causes single and double strand breaks
Carboplatin: Toxicities
More marrow Supressive, less emetogenic, neurotoxic and nephrotoxic
Doxorubicin: mechanism of action
Antibiotic. Direct DNA intercalation, Free radical formation
Doxorubicin: Toxicities
Mucositis, Myelosupression, Cardiomyopathy
Doxil: Mechanism of action
liposomal pegylated Doxirubicin. Direct DNA intercalation, Free radical formation
Doxil: Toxicities
Mucositis, Myelosupression, Cardiomyopathy, Palmar plantar erythrodysesthesia (peeling from sking on palmar and platar surfaces)
Bleomycin: Mechanism of action
Antibiotic. Forms complexes with DNA, breaking DNA helix
Bleomycin: Toxicities
Pneumonitis, pulmonary fibrosis
Bevacizumab (Avastin): Mechanism of action
Antivascular. Inhibit new blood vessel formation, regression of tumor microvessels, normalization of tumor vascularity.
Bevacizumab (Avastin): Toxicities
Hypertension, Proteinuria, Bowel perforation
Olaparib: Mechanism of action
PARP Inhibitor. used for treatment and maintenance. Binds PARP enzyme to prevent single stranded DNA repair
Olaparib: Toxicities
Nausea, vomiting, dyspepsia, diarrhea
Rucaparib: Mechanism of action
PARP inhibitor. used for treatement and maintenance. same mechanism as olaparib. BRCA mutation enhanced effect
Rucaparib: Toxicities
Fatigue, anemia
Niraparib: Mechanism of action
PARP inhibitor. used only for maintenance. Same mechanism as olaparib.
Niraparib: Toxicities
rarely causes AML/MDS
Pembrolizumab: Mechanism of action
Anti-PDL1 monoclonal antibody. Inhibits programmed cell death activity by binding to PD1 receptor on T cells, induces antitumor response and reverses T cell supression
Pembrolizumab: Toxicities
Fatigue, rash, endocrine/metabolic disorders
Pebrolizumab: Uses in Uterine cancer
MSI +/high tumor, dMMR positive tumor
Pembolizumab: Uses in Cervical cancer
PDL1 positive tumor, CPS > 1 tumor
Chemotherapy treatment: Epithelial Ovarian Cancer
Primary - Taxanes, platinums (Carboplatin, Paclitaxol)
Secondary - Doxorubicin, Topetecan, Gemcitabine, Olaparib, Pembro
Chemotherapy Treatment: Germ Cell Ovarian Cancer
BEP - Bleomycin, Etoposide, Cisplatin
VAC - Vinblastine, Actinomycin-D, Cyclophosphamide
Chemotherapy Treatment: Uterine Cancer
Primary - Taxanes, Platinums (Carboplatin, Paclitaxol
Secondary - Doxorubicin, Ifosphamide, megace, Pembro
Chemotherapy Treatment: Cervico-Vaginal
Primary - Cisplatin + Radiation
Secondary- Carbotaxol, carboplatin/cisplatin, Bevacizumab, Pembro
Chemotherapy Treatment: GTN
MAC - Methotrexate, Actinomycin-D, Cyclophosphamide
EMACO - Methotrexate, Actinomycin-D, Cyclophosphamide, Etoposide, Vincristine