| Question |
Answer |
| The ability of a test to rule out a disease |
Sensitivity |
| The percentage of people with cancer who will have an abnormal test |
Sensitiviy |
| The percentage of people without cancer whose test is negative |
Specificity |
| The ability of a test to rule in disease |
Specificity |
| Probability that people with an abnormal test actually have cancer |
Positive predictive value |
| Probability that a negative test will predict that a person does not have cancer |
Negative predictive value |
| Proteins normally found in larger amounts during fetal development |
Antigens |
| These are examples of which type of tumor marker; AFP, CEA, PSA, CA-125, Bence Jones Proteins |
Antigens |
| These are examples of which type of tumor marker; Prostatic Acid Phosphatase, Galactosyl transferase II |
Enzymes |
| This marker is often associated with tumors of endocrine glands |
Hormones |
| These are examples of which type of tumor marker; Beta-HCG, Human Calcitonin |
Hormones |
| Genes that are useful in fetal development but when activate in mature cells trigger tumor growth |
Oncogenes |
| These are examples of which type of tumor marker; BRCA 1, BRCA 2, Philadelphia chromosome |
Oncogenes |
| Philadelphia Chromosome is associated with which type of cancer |
Chronic Myelogenous Leukemia-CML |
| Cell surface proteins that affect the rate of tumor development by binding to hormones and growth factors |
Tissue receptors |
| These are examples of which type of tumor marker; ER assay, PR assay, EGFR |
Tissue receptors |
| What goes down as prevalence of disease goes down |
Positive predictive value |
| Increased in 80-90% of patients with hepatocellular carcinoma |
Alpha-Fetoprotein (AFP) |
| Patients with cirrhosis and active hepatitis should be screened with which tumor marker every 3-4 months |
Alpha-Fetoprotein (AFP) |
| Used primarily to detect and monitor clinical course of Multiple Myeloma. It is not found in the blood b/c it is effeciently filtered by the kidneys. Considered to be the first tumor marker. |
Bence Jones Proteins |
| This hormone tumor marker is normally negative except in pregnancy, and is never found in cancer free males. |
Beta-HCG |
| This hormone tumor marker is primarily associated with the following; Hydatidiform mole of the uterus, chriocarcinoma of the uterus, and germ cell tumors of the ovaries |
Beta-HCG |
| High levels of this hormone are almost always pathognomonic for germ cell neoplasm in men. |
Beta-HCG |
| This antigen is useful in diagnosis, evaluation of therapy, and sruveillance in patients with pancreatic and hepatobiliary cancer |
CA 19-9 |
| This antigen is elevated in 80-90% of women with ovarian cancer. |
CA 125 |
| This antigen is used in determining the extent of disease, prognosis, and response to therapy in patients with GI cancers. |
Carcinoembryonic Antigen (CEA) |
| Baseline for this antigen is elevated in smokers. |
Carcinoembryonic Antigen (CEA) |
| This antigen is used in screening for early detection of prostate cancer. |
Prostate Specific Antigen (PSA) |
| When combined with a digital rectal exam 90% of clinically significant cancers can be detected. |
Prostate Specific Antigen (PSA) |
| Not a tumor marker but a useful diagnostic tool for assessing risk of developing breast cancer in a woman in the general population |
The Gail model |
| This tool takes into acount these factors when assessing 5 year and lifetime risk of developing breast cancer; current age, age at menarche, previous breast biopsies, age at first live birth, family history of breast cancer. |
The Gail model |
| Breast cancer oncogenes |
BRCA 1, BRCA 2 |
| Men with this mutation carry a markedly increased risk of developing prostate cancer and or colorectal cancer, and may pass the mutation to their daughters. |
BRCA 2 |
| This tissue receptor indicates sensitivity to hormonal therapy. |
Estrogen Receptor (ER) assay, and Progesterone Receptor (PR) Assay |
| Tumors positive for this tissue receptor are more than twice as likely to respond to hormone therapy. |
ER assay |
| This tissue receptor is more often positive in postmenopausal breast cancer patients |
PR assay |
| An increased level of this antigen is associated with more aggressive breast cancers. |
HER 2 (neu) |
| Triple negative tumors have no hormonal target for therapy and are negative for which markers. |
ER, PR, HER 2 |
| This antigen is elevated in 70-80% of patients with metastatic disease, and is rarely elevated in early stage disease. |
CA 15-3 |
| This antigen is useful in monitoring response to therapy in metastatic breast cancer patients. |
CA 27.29 |
| This rare marker is associated with liquid tumors; lymphoma, leukemia, multiple myeloma. |
Beta2 microglobulin |
| This rare antigen is not a good screening tool b/c levels can be elevated in UTI, renal calculi, recent urinary surgery |
Bladder tumor antigen (BTA) |
| This rare marker is a good screening tool for patients at risk for bladder cancer |
Nuclear Matrix protein 22 (NMP22) |
| A sensitive marker for detection of bladder cancer across all disease stages and grades |
Survivin |
| This hormone is used to evaluat patients with at risk for/suspected medullary carcinoma of the thyroid. |
Human Calcitonin |
| This enzyme is associated with Neuroblastoma, carcinoid, and small cell lung cancer |
Neuron Specific Enolase (NSA) |
| This enzyme is primarily used to diagnose, stage, and monitor efficacy of treatment in prostate cancer |
Prostatic Acid Phosphatase (PAP) |
| This cancer has a 30% recurrence rate even decades after successful treatment |
Thyroid cancer |
| This protein is the primary marker for surveillance of well-differentiated thyroid cancers in postoperative patients. |
Thyroglobulin |
| Common tumor marker for ovarian cancer |
CA 125 |
| k-ras, c-myc, abl, Her2/neu are all examples of what |
Oncogenes |
| Genes that once mutated activates the growth pathway |
Oncogenes |
| Only one copy needs to be mutated to induce tumorogensis |
Oncogenes |
| Genes that normally inhibit growth |
Tumor suppressor genes |
| A mutation of these causes a loss of inhibition |
Tumor suppressor genes |
| Both copies need to be mutated to lose function |
Tumor suppressor genes |
| Classic presentation fo this type of cancer is painless jaundice |
Pancreatic cancer |
| Tumor marker for teratoma |
Alpha-Fetoprotein (AFP) |
| No meat |
No treat |
| Tissue |
Is the issue |
| In what scenario do you not need a pathological specimen to initiate treatment |
Pancreatic mass |
| A small needle is inserted into the mass and cells are removed for microscopic evaluation |
Fine needle aspiration |
| Can be done guided or unguided |
Fine needle aspiration |
| This type of biopsy is mainly applied to melanoma |
Punch biopsy |
| What type of biopsy is not indicated for suspected melanoma |
Shave biopsy |
| Once a tissue diagnosis positive for cancer is obtained what is the next step in treatment of the patient |
Radiographic staging |
| Based on the theory that lymphatic spread proceeds through a consistent anatomic network of ducts and nodes based on tumor location |
Sentinel lymph node biopsy |
| Looking for hot and blue nodes |
Sentinel lymph node biopsy |
| It is recommended that those with this disorder start haveing colonoscopies in their teens |
Familial adenomatous polyposis (FAP) |
| Should begin screening 10 years prior to the age of onset in the family member affected with what cancer. |
Hereditary Nonpolyposis Colorectal Cancer (HNPCC) |