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Anti-Cancer Drug
(Bevacizumab)
Department of
Pharmacy
Daffodil International
University
Development of biopharmaceuticals based
on cloning technology
Anticancer drug, also
called antineoplastic
drug, any drug that is
effective in the treatment
of malignant, or
cancerous, disease.
ANTI-CANCER
DRUG
1) Polyfunctional alkylating agents- Nitrosoureas, Mustards
2) Other alkylating agents- Cisplatin, Procarbazine
3) Antimetabolites- Amino acid antagonist
4) Purine antagonist- Mercaptopurine
5) Pyrimidine antagonist- Flurouracil
6) Plant alkaloids- Vinblastine
7) Antibiotics- Doxorubicin
8) Monoclonal Antibodies
9) Hormonal agents- Anastrozole
10) Miscellaneous anticancer agents- Amifostine
Classification of Anti-Cancer Drugs
Mechanism action of Anticancer drugs
Brand name: Trinstin
Generic name: Bevacizumab
Dosage form: Injection
Dose: 100mg/4ml or 400mg/16ml
Therapeutic class: Drugs for Age-related
Macular Degeneration, Targeted Cancer
Martin Luther King, Jr. – Civil Rights Activist and Pastor
Formulation
5 mg/kg every 2 weeks intravenously in combination with bolus-IFL.
10 mg/kg every 2 weeks intravenously in combination with FOLFOX4.
1)Avastin is provided as a concentrate for solution for infusion in a
single-use vial, which contains a nominal amount of either 100 mg of
bevacizumab in 4 ml or 400 mg of bevacizumab in 16 ml (concentration
of 25 mg/ml).
2) Bevacizumab is formulated with 51 mM sodium phosphate pH 6.2,
60 mg/ml α,α-trehalose dihydrate and 0.04% polysorbate 20.
3) The drug product is a clear to slightly opalescent, colourless to pale
brown sterile liquid solution that has to be diluted in 0.9 % sodium
chloride solution prior to administration.
Pharmacology & Pharmacodynamics:
Bevacizumab is derived from the murine VEGF monoclonal antibody A4.6.
It is ∼93% human and 7% murine protein sequence, producing an agent with the same
biochemical and pharmacologic properties as the parental antibody, but with reduced
immunogenicity, and a longer biological half-life.
Experimental studies show that bevacizumab and A4.6.1 neutralize all isoforms of
human VEGF with a dissociation constant (Kd) of 1.1 and 0.8 nmol/L, respectively.
They also inhibit VEGF-induced proliferation of endothelial cells in vitro with ED50 of 50 ±
5 and 48 ± 8 ng/mL, respectively.
Both also block tumor angiogenesis and growth with almost identical potency and
efficacy.
Pharmacokinetics
Administration: Bevacizumab is not administered as a single agent: it is always
administered with chemotherapy. If the Bevacizumab is held, however the chemotherapy
may continue under standard parameters. Bevacizumab must be diluted in normal saline
(not a dextrose-containing solution). Please refer to the Parenteral Drug Manual
(PDM)Sheet for further administration instructions. Administer Bevacizumab at a rate of
0.5 mg/kg/minute.
Storage & Handling: Avastin vials [100 mg (NDC 50242-060-01) and 400 mg
(NDC 50242-061-01)] are stable at 2−8°C (36−46°F). Avastin vials should be protected
from light. Do not freeze or shake. Diluted Avastin solutions may be stored at 2−8°C
(36−46°F) for up to 8 hours. Store in the original carton until time of use. No
incompatibilities between Avastin and polyvinylchloride or polyolefin bags have been
observed.
Side effects: •trouble breathing,
•swelling of ankles or feet,
•sudden weight gain,
•fast heartbeat,
•signs of infection (e.g., fever, persistent sore
throat),
•muscle cramps,
•muscle loss,
•yellowing eyes or skin,
•frothy or dark urine,
•difficulty urinating, or
•decreased amount of urine.
Contraindication: 1) Defective Internal Secretion of Ovaries
2) Decrease of Neutrophils in the Blood from Cancer
Chemotherapy
3) Decreased Neutrophils a Type of White Blood Cell
4) high blood pressure
5) heart attack
6) Angina
7) chronic heart failure
8) Transient Ischemic Attack
9) Obstruction of a Blood Vessel by a Blood Clot
10) bleeding
11) Inflammation of the Esophagus with Erosion
12) Abnormal Connection Between Esophagus and Windpipe

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Anti cancer-drug (Bevacizumab)

  • 1. Anti-Cancer Drug (Bevacizumab) Department of Pharmacy Daffodil International University Development of biopharmaceuticals based on cloning technology
  • 2. Anticancer drug, also called antineoplastic drug, any drug that is effective in the treatment of malignant, or cancerous, disease. ANTI-CANCER DRUG
  • 3. 1) Polyfunctional alkylating agents- Nitrosoureas, Mustards 2) Other alkylating agents- Cisplatin, Procarbazine 3) Antimetabolites- Amino acid antagonist 4) Purine antagonist- Mercaptopurine 5) Pyrimidine antagonist- Flurouracil 6) Plant alkaloids- Vinblastine 7) Antibiotics- Doxorubicin 8) Monoclonal Antibodies 9) Hormonal agents- Anastrozole 10) Miscellaneous anticancer agents- Amifostine Classification of Anti-Cancer Drugs
  • 4. Mechanism action of Anticancer drugs
  • 5. Brand name: Trinstin Generic name: Bevacizumab Dosage form: Injection Dose: 100mg/4ml or 400mg/16ml Therapeutic class: Drugs for Age-related Macular Degeneration, Targeted Cancer
  • 6.
  • 7. Martin Luther King, Jr. – Civil Rights Activist and Pastor
  • 8.
  • 9. Formulation 5 mg/kg every 2 weeks intravenously in combination with bolus-IFL. 10 mg/kg every 2 weeks intravenously in combination with FOLFOX4. 1)Avastin is provided as a concentrate for solution for infusion in a single-use vial, which contains a nominal amount of either 100 mg of bevacizumab in 4 ml or 400 mg of bevacizumab in 16 ml (concentration of 25 mg/ml). 2) Bevacizumab is formulated with 51 mM sodium phosphate pH 6.2, 60 mg/ml α,α-trehalose dihydrate and 0.04% polysorbate 20. 3) The drug product is a clear to slightly opalescent, colourless to pale brown sterile liquid solution that has to be diluted in 0.9 % sodium chloride solution prior to administration.
  • 10. Pharmacology & Pharmacodynamics: Bevacizumab is derived from the murine VEGF monoclonal antibody A4.6. It is ∼93% human and 7% murine protein sequence, producing an agent with the same biochemical and pharmacologic properties as the parental antibody, but with reduced immunogenicity, and a longer biological half-life. Experimental studies show that bevacizumab and A4.6.1 neutralize all isoforms of human VEGF with a dissociation constant (Kd) of 1.1 and 0.8 nmol/L, respectively. They also inhibit VEGF-induced proliferation of endothelial cells in vitro with ED50 of 50 ± 5 and 48 ± 8 ng/mL, respectively. Both also block tumor angiogenesis and growth with almost identical potency and efficacy.
  • 12. Administration: Bevacizumab is not administered as a single agent: it is always administered with chemotherapy. If the Bevacizumab is held, however the chemotherapy may continue under standard parameters. Bevacizumab must be diluted in normal saline (not a dextrose-containing solution). Please refer to the Parenteral Drug Manual (PDM)Sheet for further administration instructions. Administer Bevacizumab at a rate of 0.5 mg/kg/minute. Storage & Handling: Avastin vials [100 mg (NDC 50242-060-01) and 400 mg (NDC 50242-061-01)] are stable at 2−8°C (36−46°F). Avastin vials should be protected from light. Do not freeze or shake. Diluted Avastin solutions may be stored at 2−8°C (36−46°F) for up to 8 hours. Store in the original carton until time of use. No incompatibilities between Avastin and polyvinylchloride or polyolefin bags have been observed.
  • 13. Side effects: •trouble breathing, •swelling of ankles or feet, •sudden weight gain, •fast heartbeat, •signs of infection (e.g., fever, persistent sore throat), •muscle cramps, •muscle loss, •yellowing eyes or skin, •frothy or dark urine, •difficulty urinating, or •decreased amount of urine.
  • 14. Contraindication: 1) Defective Internal Secretion of Ovaries 2) Decrease of Neutrophils in the Blood from Cancer Chemotherapy 3) Decreased Neutrophils a Type of White Blood Cell 4) high blood pressure 5) heart attack 6) Angina 7) chronic heart failure 8) Transient Ischemic Attack 9) Obstruction of a Blood Vessel by a Blood Clot 10) bleeding 11) Inflammation of the Esophagus with Erosion 12) Abnormal Connection Between Esophagus and Windpipe

Editor's Notes

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