1 / 22

Chapter 101

Chapter 101. Anticancer Drugs I: Cytotoxic Agents. Cytotoxic Anticancer Drugs. Largest class of anticancer drugs Act directly on cancer cells and healthy cells to cause their death About 50% of cytotoxic anticancer drugs are phase-specific Subdivided into nine major groups.

aneko
Download Presentation

Chapter 101

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Chapter 101 Anticancer Drugs I: Cytotoxic Agents

  2. Cytotoxic Anticancer Drugs • Largest class of anticancer drugs • Act directly on cancer cells and healthy cells to cause their death • About 50% of cytotoxic anticancer drugs are phase-specific • Subdivided into nine major groups

  3. Anticancer Drugs • Cytotoxic drugs • Alkylating agents • Platinum compounds • Antimetabolites • Hypomethylating agents • Antitumor antibiotics • Mitotic inhibitors • Topoisomerase inhibitors • Miscellaneous cytotoxic drugs

  4. Cell-Phase Specificity • Sequence of events that a cell goes through from one mitotic division to the next • Cell-cycle phase–specific drugs • Toxic only to cells that are in a particular phase • Must be in the in the blood continuously over a long time • Cell-cycle phase–nonspecific drugs • Can act during any phase of the cell cycle

  5. Toxicity • Many anticancer drugs are toxic to normal tissues – especially tissue with high growth fraction • Bone marrow • Hair follicles • GI epithelium • Germinal epithelium

  6. Dosage, Handling, and Administration • Antineoplastic drugs are often mutagenic, teratogenic, and carcinogenic • Direct contact can result in local injury • Extravasation of vesicants • Carmustine, dacarbazine, dactinomycin, daunorubicin, doxorubicin, mechlorethamine, mitomycin, plicamycin, streptozocin, vinblastine, vincristine

  7. Alkylating Agents • Highly reactive compounds • Cells are killed by the alkalization of DNA • Cell-cycle phase–nonspecific agents • Drug resistance is common • Toxicities • Occur in tissues with high growth fraction • Bone marrow, hair follicles, GI mucosa, and germinal epithelium

  8. Fig. 101-1. Cross-linking of DNA by an alkylating agent. A, Reactions leading to cross-linkage between guanine moieties in DNA. B, Schematic representation of interstrand cross-linking within the DNA double helix. (A = adenine, C = cytosine, G = guanine, T = thymine.)

  9. Classes of Alkylating Agents • Nitrogen mustards • Cyclophosphamide (Cytoxan) • Nitrosoureas • Carmustine (BCNU) • Other • Temozolomide (Temodar) • Busulfan (Myleran)

  10. Platinum Compounds • Cell-cycle phase–nonspecific agents • Cisplatin (Platinol-AQ) • Carboplatin (Paraplatin) • Oxaliplatin (Eloxatin)

  11. Antimetabolites • Folic acid analog • Methotrexate (Rheumatrex) • Pemetrexed (ALIMTA) • Pyrimidine analogs • Cytarabine (Cytosar-U) • Fluorouracil (Adrucil) • Capecitabine (Xeloda) • Floxuridine (FUDR) • Gemcitabine (Gemzar)

  12. Antimetabolites • Purine analogs • Mercaptopurine (Purinethol) • Thioguanine (Tabloid) • Pentostatin (Nipent) • Fludarabine (Fludara) • Cladribine (Leustatin) • Nelarabine (Arranon)

  13. Fig. 101-2. Actions of methotrexate, leucovorin, and fluorouracil. (FdUMP = 5-fluoro-2'-deoxyuridine-5'-monophosphate, X = blockade of reaction.)

  14. Hypomethylating Agents • New class of anticancer drugs • Become incorporated into the DNA • Azacitidine (Vidaza) • Decitabine (Dacogen)

  15. Antitumor Antibiotics • Cytotoxic drugs originally isolated from cultures of Streptomyces • Used only to treat cancer – not infections • Injure cells through direct interaction with DNA • Poor GI absorption – IV administration • Two main groups • Anthracyclines and nonanthracyclines

  16. Anthracyclines • Doxorubicin (Adriamycin) • Doxorubicin liposomal (Doxil) • Daunorubicin (DaunoXome) • Epirubicin (Ellence) • Idarubicin (Idamycin) • Mitoxantrone (Novantrone)

  17. Nonanthracyclines • Dactinomycin (Actinomycin D) • Bleomycin (Blenoxane) • Mitomycin (Mutamycin)

  18. Mitotic Inhibitors • Vinca alkaloids • Vincristine (Oncovin) • Vinblastine (Velban) • Vinorelbine (Navelbine) • Taxanes • Paclitaxel (Taxol) • Docetaxel (Taxotere)

  19. Other Mitotic Inhibitors • Ixabepilone (Ixempra) • Estramustine (Emcyt)

  20. Topoisomerase Inhibitors • Nuclear enzymes that alter the shape of supercoiled DNA • Topotecan (Hycamtin) • Irinotecan (Camptosar) • Etoposide (VePesid) • Teniposide (Vumon)

  21. Miscellaneous Cytotoxic Drugs • Asparaginase (Elspar) • Pegaspargase (Oncaspar) • Hydroxyurea (Hydrea, Mylocel) • Mitotane (Lysodren) • Procarbazine (Matulane) • Dacarbazine (DTIC-Dome)

More Related