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Practical Oncology

Practical Oncology. Wendy Blount, DVM. Housekeeping. Handouts other than PowerPoint slides are already in your notebook You will get copies of the PowerPoint slides after each section Natalie is our “concierge” C ourse materials are downloadable http://wendyblount.com

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Practical Oncology

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  1. Practical Oncology Wendy Blount, DVM

  2. Housekeeping • Handouts other than PowerPoint slides are already in your notebook • You will get copies of the PowerPoint slides after each section • Natalie is our “concierge” • Course materials are downloadable http://wendyblount.com • Table of Contents, Abbreviations • Blue subdividers

  3. Housekeeping • We’ll break the last 10 minutes of every hour • Lunch break is 11:50am-12:30pm today • Tomorrow, we will break from 11:30am to noon, and then start the lunch program at noon • PLEASE PARTICIPATE!! • But take private conversations out in the hall

  4. Practical Medicine Philosophy

  5. Definitions Cancer • The state in which normal growth controlling mechanisms are permanently impaired, permitting progressive growth of cells without reaching growth equilibrium Growth Equilibrium • Production of new cells = cell death • No net gain of tissue (liver) (heart)

  6. Definitions Hyperplasia • Normal tissue response to noxious stimuli • Reversible when regeneration is complete Neoplasia • Cell replication never “turns off” Anaplasia • Lack of cell differentiaion

  7. Definitions Malignant • propensity to spread by recurring locally and/or metastasizing Mitotic Index • Number of mitotic figures per high power field

  8. Definitions Carcinoma • Cancer arising from ectodermal or endodermal tissues Sarcoma • Cancer arising from mesodermal tissues

  9. Definitions Grade (based on histopathology) • Grade I behaves most benignly • Grade III behaves most malignantly Stage (based on tests to determine extent of tumor invasion) • Stage I is the least invasive • Stage 4-5+ are most invasive, and often carry poor prognosis for cure

  10. What Causes Cancer? Genetic derangement of the things that normally eventually turn cell replication off Faulty differentiation of pluripotent stem cells NOT anaplasia of differentiated cells • Except in rare circumstances Cancer most often arises from cells that continually replicate

  11. What Causes Cancer? Cancer is a disease of aging • odds of aberrant cell division increases • Immune surveillance weakens • Cell repair mechanisms fail • Genetic injury by exposure becomes more likely • Exposure to carcinogens • Infection by viruses carrying oncogenes • Physical damage by trauma or irritation

  12. What Causes Cancer? Oncogenes • Virus RNA that causes cancer when incorporated into host genes • Oncogenes make growth factors that are most often kinases • Basis of the new TKI anticancer drugs

  13. What Causes Cancer? Lost Tumor Suppressor genes • Normal people and animals have these • Lost in some individuals that will have genetic tendencies to particular pediatric cancers • Retinoblastoma • Osteosarcoma

  14. What Causes Cancer? Cancer Cell Immortalization • Normally a cell line eventually dies out because the telomeres required for cell division are used up • Telomerase allows extension of the telomeres for cell division ad infinitum • Telomerase products are sold as health food supplements to combat aging

  15. What Causes Cancer? Apoptosis defects • Apoptosis – programmed cell death • Important to growth equilibrium • Some genetic mutations eliminate apoptosis

  16. What Causes Cancer? It can take many years for a malignant cell to produce a detectable tumor • By the time you see the tumor, it has been there for a very long time

  17. What Causes Cancer? Biology of metastasis • Cancer cells shed into blood or lymphatics • Evade immune surveillance • Come to rest in capillary or lymphatic vessel beds • Disrupt the basement membrane (proteases, metalloproteinases) • New blood supply grows (angiogenesis)

  18. Treatment Modalities Surgery and Radiation • Local control • Exception – whole body radiation for lymphoma • After 11 week chemo induction • remission 16.5 months Chemotherapy • To manage widespread disease that is chemo responsive • To slow progression of metastatic disease

  19. Treatment Modalities Metronomic Chemotherapy • Low dose, long term chemo • Generally well tolerated • For less aggressive tumors • For palliation for advanced tumor stages

  20. Cytology Basics • Is cellularity adequate? • are there plenty of cells? • Are the cells those you intended to sample? • Are there cells other than RBC? • If there are few cells, is it possibly a cyst or hematoma? • Are the nucleated cells WBC or other cells? • If WBC, are they lymphoid cells?

  21. Cytology Basics • Are the lymphoid cells uniform or of various stages? • Various stages indicates inflammatory lymphoid response • All lymphoblasts – large cell lympoma • All plasma cells – plasmacytoma, myeloma • All lymphocytes can be normal in lymph node or spleen • Lymphocytic tumors can require histopathology for diagnosis

  22. Cytology Basics 6. If non-lymphoid WBC, what kind? • Neutrophils – suppurative • Degenerate toxic neutrophils – septic • Neutrophils + macrophages – pyogranulomatous • Macrophages – granulomatous • Eosinophils, basophils – allergic, parasitic • Mott cells, plasma cells – chronic antigenic stimulation • Fibroblasts can accompany chronic inflammation

  23. Cytology Basics Thillai Koothan – Friendswood TX

  24. Cytology Basics • Are cells round, epithelial or mesenchymal? • Nuclei • round - round cells and epithelial cells • Nuclei and cytoplasm oblong - mesenchymal cells • Clustering • With cell to cell adhesions - Epithelial cells • Separate cells - round cells or mesenchymal cells • Cytoplasmic borders • distinct - round cells and epithelial cells • Indistinct – mesenchymal cells

  25. Cytology Basics • Are cells round, epithelial or mesenchymal? Mixed populations • All three cell types present • anaplastic sarcoma • e.g., amelanoticmelanosarcoma • Multinucleated cells, mesenchymal cells, histiocytic round cells • Malignant fibrous histiocytoma • aka PUSS

  26. Cytology Basics Round Cells

  27. Cytology Basics Mesenchymal Cells

  28. Cytology Basics Epithelial Cells

  29. Cytology Basics Anaplastic melanoma

  30. Cytology Basics 8. Are there characteristics of malignancy? • Cells aren’t normally found there • Increased blast cells • Changes in nucleus • Increased, abnormal mitotic figures • Especially odd number of poles • Hyperchromatic nucleus • Prominent or abnormal nucleoli • Unexpected multinucleation • Especially different sizes

  31. Cytology Basics 8. Are there characteristics of malignancy? • Changes in cytoplasm • Loss of differentiation • Changes in Cell • Increased N:C ratio (nucleus takes over the cell) • Cell polymorphism – variation in size and shape

  32. Cytology Basics 9. Is sufficient inflammation present to explain dysplasia? • No – strong characteristic of malignancy • Mesothelial cells, macrophages and fibroblasts can look very dysplastic in response to severe inflammation

  33. Cytology Basics

  34. Cytology Basics

  35. Cytology Basics

  36. Cytology Basics

  37. Cytology Basics

  38. Cytology Basics Barton Cytologic Rubric • Is it inflammatory or non-inflammatory? • Is it round cell, epithelial cell, or mesenchymal cell? • Are there characteristics of malignancy? • Are they weak or strong?

  39. Cytology Basics Technique Tips • Try “coring” with needle only prior to attaching a syringe for aspiration • Start with a 22 or 25 gauge needle • If inadequate cellularity, try a bigger needle and/or aspiration • Use a 10-12cc syringe to spray the sample quickly onto a slide • Smear gently – vertical for lymph nodes, testicles and bone marrow

  40. Cytology Basics “Malignant” is a reasonable cytologic diagnosis “Benign” is almost never a cytologic diagnosis Cytology can not distinguish malignancy from wicked inflammation If the lump changes, aspirate it again

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