Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Pharmacology – IV PHL-425 Chapter 2: CANCER CHEMOTHERAPY: The basic Concepts By: Dr. Abdulaziz Bin Saeedan Ph.D. Department of Pharmacology E mail: [email protected] Pathogenesis of Neoplasia DNA is altered via mutagens including chemical carcinogens, viruses, and radiation. This mutations is inherted by at least one cell division (initiation). This mutation mainly lead to activation of proto-oncogene into oncogenes (leading to uncontrolled cell proliferation) and/or inactivation of tumor suppressor genes (leading to resistance to apoptosis.) Once the cell reproduction process is altered, other factors (epigenetic factors ) indirectly allow and promote these cells to proliferate unchecked (promotion) These promoters can be (hormones, co- carcinogens, immunosuppressant…which themselves are non carcinogenic). • Initiation - point at which an irreversible alteration, usually genetic, is introduced into a target cell. Initiation: (1) is essentially irreversible (2) caused only by carcinogenic compounds (3) occurs rapidly after carcinogen exposure (4) alone does not result in tumor formation • Promotion is the process whereby an initiated tissue or organ develop focal proliferations and it requires the presence of continuous stimulation. Promotion: (1) reversible (2) acts only after exposure to an initiating agent (3) requires repeated administration of a promoter (4) is not carcinogenic in itself Etiolopathology 50.2 Rang Apoptosis Programmed cell death Cascade of proteases initiate process Characteristics of Cancer Cells The problem: Cancer cells divide rapidly (cell cycle is accelerated) They are “immortal” Cell-cell communication is altered uncontrolled proliferation invasiveness Ability to metastasise The Goal of Cancer Treatments Curative Total irradication of cancer cells Curable cancers include testicular tumors Palliative Alleviation of symptoms Avoidance of life-threatening toxicity Increased survival and improved quality of life Adjuvant therapy Attempt to eradicate microscopic cancer after surgery e.g. breast cancer & colorectal cancer Rx Modalities (Cancer Treatments) 1. 2. 3. 4. 5. 6. Surgery Radiotherapy Chemotherapy Endocrine therapy (hormonal therapy) Immunotherapy Targeted therapy or molecularly targeted therapy: blocks the growth of cancer cells by interfering with specific targeted molecules needed for carcinogenesis and tumor growth, rather than interfering with all rapidly dividing cells - Small molecule inhibitors: Tyrosine kinase inhibitors (e.g imatinib) - Genetic material (RNA or DNA) Major approaches to therapy of cancers Cell Cycle = Growth, Division 18_01_cell_cycle.jpg Cancer Chemotherapy After completion of mitosis, the resulting daughter cells have two options: (1) they can either enter G1 & repeat the cycle or (2) they can go into G0 and not participate in the cell cycle. Growth fraction - at any particular time some cells are going through the cell cycle whereas other cells are resting. The ratio of proliferating cells to cells in G0, is called the growth fraction. A tissue with a large percentage of proliferating cells & few cells in G0 has a high growth fraction. Conversely, a tissue composed of mostly of cells in G0 has a low growth fraction. Cell Cycle Specific (CCS) & Cell Cycle NonSpecific Agents (CCNS) Log kill hypothesis According to the log-kill hypothesis, chemotherapeutic agents kill a constant fraction of cells (first order kinetics), rather than a specific number of cells, after each dose. In other words, at a given dose, in a given tumor the drug will kill a constant % of cells, regardless the tumor size 1. Solid cancer tumors - generally have a low growth fraction thus respond poorly to chemotherapy & in most cases need to be removed by surgery 2. Disseminated cancers- generally have a high growth fraction & generally respond well to chemotherapy Log kill hypothesis: LOG kill hypothesis The example shows the effects of tumor burden, scheduling, initiation/duration of treatment on patient survival. The tumor burden in an untreated patient would progress along the path described by the RED LINE – The tumor is detected (using conventional techniques) when the tumor burden reaches 109 cells The patient is symptomatic at 1010-1011 cells Dies at 1012 cells. Cancer Chemotherapy Combinations of agents with differing toxicities & mechanisms of action are often employed to overcome the limited cell kill of individual anti cancer agents. Each drug selected should be effective alone 3 advantages of combination therapy: 1. Suppression of drug resistance - less chance of a cell developing resistance to 2 drugs than to 1 drug. 2. Increased cancer cell kill - administration of drugs with different mechanisms of action. 3. Reduced injury to normal cells - by using a combination of drugs that do not have overlapping toxicities, we can achieve a greater anticancer effect than we could by using any one agent alone. Resistance to Cytotoxic Drugs Increased expression of MDR-1 gene for a cell surface P-glycoprotein MDR-1 gene is involved with drug efflux Drugs that reverse MDR : verapamil, quinidine, cyclosporine MDR increases resistance to natural drug products including the anthracyclines, vinca alkaloids, and epipodophyllotoxins Modes of Resistance to Anticancer Drugs Mechanism Drugs or Drug Groups Change in sensitivity or ↓ binding Etoposide, methotrexate, vinca affinity of target enzymes or alkaloids, estrogen & androgen receptors receptors Decreased drug accumulation via ↑ expression of glycoprotein transporters, or ↓ permeability Methotrexate, alkylating agents, dactinomycin Formation of drug-inactivating enzymes Purine & pyrimidine antimetabolites Production of reactive chemicals that “trap” the anticancer drug Alkylators, bleomycin, cisplatin. doxorubicin Increased nucleic acid repair mechanisms Alkylating agents, cisplatin Reduced activation of pro-drugs Purine & pyrimidine antimetabolites General problems with anticancer drugs Most of them are antiproliferative, i.e. they damage DNA and so initiate apoptosis. They also affect rapidly dividing normal cells. This leads to toxicity which are usually severe. To greater or lesser extent the following toxicities are exhibits by all anticancer drugs. ADR of Antineoplastic Drugs in Humans Tissue Undesirable Effects Bone marrow Leukopenia and resulting infections Immunosuppression Thrombocytopenia Anemia GI tract Oral or intestinal ulceration Diarrhea Hair follicles Alopecia Gonads Menstrual irregularities, including premature menarche; impaired spermatogenesis Wounds Impaired healing Fetus Teratogenesis (especially during first trimester) Distinctive Toxicities of Some Anticancer Drugs Toxicity Drug(s) Renal Cisplatin,* methotrexate Hepatic 6-MP, busulfan, cyclophosphamide Pulmonary Bleomycin,* busulfan, procarbazine Cardiac Doxorubicin, daunorubicin Neurologic Vincristine,* cisplatin, paclitaxel Immunosuppressive Cyclophosphamide, cytarabine, dactinomycin, methotrexate Other Cyclophosphamide (hemorrhagic cystitis); procarbazine (leukemia); asparaginase* (pancreatitis) Chemotherapeutic agents are much more toxic to tissues that have a high growth fraction than to tissues that have a low growth fraction. Proliferating cells are especially sensitive to chemotherapy because cytotoxic drugs usually act by disrupting DNA synthesis or mitosis, cellular activities that only proliferating cells carry out. Unfortunately, toxicity to the anticancer agents is to any rapidly dividing cells. (e.g. bone marrow, hair follicles, sperm forming cells). Prevention or Management of Drug Induced toxicities The toxicities of some anticancer drugs can be well anticipated and hence be prevented by giving proper medications E.g. mesna is given to prevent hemorrhagic cystitis by cyclophosphamide (How? it reacts with the drug metabolite) Dexrazoxane, is used to reduce the risk of anthracycline-induced cardiomyopathy Anti-cancer drugs Classification Cell Cycle–Specific (CCS) Agents Cell Cycle–Nonspecific (CCNS) Agents Antimetabolites (S phase) Alkylating agents Capecitabine Altretamine Cladribine Bendamustine Clofarabine Busulfan Cytarabine (ara-C) Carmustine Fludarabine Chlorambucil 5-Fluorouracil (5-FU) Cyclophosphamide Gemcitabine Dacarbazine 6-Mercaptopurine (6-MP) Lomustine Methotrexate (MTX) Mechlorethamine 6-Thioguanine (6-TG) Melphalan Epipodophyllotoxin (topoisomerase II inhibitor) (G1–S phase) Etoposide Taxanes (M phase) Temozolomide Thiotepa Anthracyclines Daunorubicin Albumin-bound paclitaxel Doxorubicin Docetaxel Epirubicin Paclitaxel Idarubicin Vinca alkaloids (M phase) Vinblastine Mitoxantrone Antitumor antibiotics Vincristine Dactinomycin Vinorelbine Mitomycin Antimicrotubule inhibitor (M phase) Ixabepilone Antitumor antibiotics (G2–M phase) Camptothecins (topoisomerase I inhibitors) Irinotecan Topotecan Platinum analogs Bleomycin Carboplatin Cisplatin Targeted agents Monoclonal antibodies bevacizumab humanized monoclonal antibody with a circulatory system target (VEGF-A) cetuximab monoclonal antibody with a tumor target (EGFR) ipilimumab fully human antibody with an immune system target (CTLA-4) Small molecules bortezomib small molecule proteasome inhibitor imatinib small molecule tyrosine kinase inhibitor seliciclib small molecule cyclin-dependent kinase inhibitor THANK YOU