Intro Flashcards

1
Q

Terminology:
1. Incidence
2. Incidence rate
3. Mortality Rate
4. Case fatality rate
5. Prevalence
6. Survival Rate

A
  1. Incidence: number of new cases identified in a specified population within a time period (e.g., 1 year)
  2. Incidence rate: number developing cancer per 100,000 population per year
  3. Mortality rate: number dying per 100,000/year (e.g., 2.6 per 100,000/year)
  4. Case fatality rate: percentage of people with specific cancer diagnosis that die from that cancer (e.g., 40% fatality rate)
  5. Prevalence: number of cases per population at a specific point in time (e.g., 50,234 documented cases in the United States)
  6. Survival rate: the percentage of people who are alive at certain stages after their diagnosis or the start of treatment, usually described as a five-year survival rate.
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2
Q

Cancer Age Ranges
<20

A

-brain/CNS/nerves (neuroblastoma = nerves)
-Eye - retinoblastotma
-blood/lymph (leukemia, lymphoma (hodgkin/nonhodgkin)
-Bone (Ewing sarcoma and osteosarcoma)
-skeletal muscles (rhabdomyosarcoma)

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3
Q

Age + Cancer: 21-49

A

-breast, cervix, uterine, ovarian
-testes (20-35)
-kidney
-bowel
lymph nodes (non-hodgkin)
-skin (melanoma)

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4
Q

Age + Cancer: 50-64

A

-lung
-Breast, cervix, uterine, ovarian
prostate
-kidney
-bowel + liver + Pancreas
-Skin

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5
Q

Age + Cancer > 65

A

-Oral cavity/pharynx/larynx/ lung
-GI: Esophagus, stomach, colorectal/rectal, pancreas
-breast, ovarian
-prostate
-bladder
-skin

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6
Q

Modifiable risk factors for cancer

A

-Tobacco + Alcohol
-High fat/low-fiber dietst
-High-risk occupations
-Sunscreen usage
-Sedentary life styles
-Cancer-related infecttions

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7
Q

Cancer-related infetions

A

-Helicopactor Hylori
-Hepatitis B and C
-Herpes
-HIV + HPV

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8
Q

Non-modifiable risk factors for cancer

A

-age, sex, race/etthnicity, genetics/family history

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9
Q

Healthcare disparities

A

-low income
-low health literacy
-rural
-lack of healthcare coverage

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10
Q

Occupational Cancer Hazards

A
  1. ABC - aspestos, biological agents, cleaning agents
  2. Radiation exposure
  3. Other (manufacturers, dry cleaners, jewlers, miners, etc
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11
Q

Cancer screening -
Skin

A

Yearly physical for everyon

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12
Q

Colorectal CA screening

A
  1. Colonoscopy Q10 yrs ≥ 45
  2. CT colonography or sigmoidoscopy Q5 years if NO colonoscopy
  3. Fecal Occult Blood or immunochemical test- yearly after 50
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13
Q

Cervical CA screenings

A

Pap smear 25-65 Q 3 years OR every 5 years with HPV screening concurrently

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14
Q

Breast

A

-Mammogram - yearly for average risk women >40 (30 for high risk)
-Clinical breast exam Q3 years 20-30, yearly for 40+
-MRI of breast for high-risk only

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15
Q

Endometrial cancer screening

A

-Yearly for high-risk only, no screening otherwise

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16
Q

Prostate cancer screening

A

-PSA: men over 50, discuss with provider. High-risk men (African American or with family hx) testing should occur at age 45. Further testing depends on PSA level (biopsy or Digital Rectal Exam

17
Q

Lung cancer screening

A

Annual Low-dose CT scan (LDCT): for at-risk adults ages 50 to 80 years old. Must be in fairly good health and currently smoke or have quit smoking in the past 15 years and have at least a 20 pack-year smoking history.

18
Q

Carcinogenesis

A

-process of cancer formation
-failure of cell repair and replication of cells with damage that no longer die

19
Q

what causes carcinogenesis

A

-Mutations in regulatory cells (proto-oncogenes, tumor suppressor genes, DNA repair genes)
-genomic instabilty
-inflammation

20
Q

oncogenes

A

stimulate or suppress normal apoptosis of cells

21
Q

P53 suppressor gene

A

produces a protein that detects DNA lesions and prevents cells from entering S phase to either induce rapirs or cell death
-most frequently mutated gene seen in cancer

22
Q

Cytogenetics

A

The structure and function of the chromosomes
-abnormalities are used to diagnose solid tumor and heme malignancies

23
Q

Common hereditary genes associated with cancer (6)

A

WT1: Wilms tumor
APC: familial colon polyposis, osteomas, thyroid cancer, hepatoblastoma
CDKN20: familial melanoma
BRCA-1/BRCA-2: familial breast and ovarian cancers
TP53 mutant: hereditary Li-Fraumeni syndrome
MLH1/MSH2/PMS1: hereditary Lynch Syndrome, which can cause colon, rectal, stomach, biliary, brain, endometrium, uterine and renal pelvis cancers

24
Q

Molecular testing and Genetics

A

BRAF, EGFR, ER receptor, PR receptor, KRAS, HER2/neu, Philadelphia chromosome (Ph+), CD-30

25
Q

What must studies have before participant enrollment?

A

-IRB approval or IEC approval (independent ethics committee)
-informed consent
-protection of vulnerable populations

26
Q

Clinical trial phase I and II

A

Phase Ia: studies how a drug acts in humans (FiH trial)
Phase Ib: studies interactions with other drugs (combination therapy)
Phase IIa: studies how a drug functions in disease types
Phase IIb: pivotal trials to evaluate safety and efficacy in humans

27
Q

Clinical trial Phase III and IV

A

Phase IIIa: trials to generate additional data for specific populations (e.g., patients with renal failure). Data assist in package insert and labeling of a drug.
Phase IIIb: trials done after submission of a New Drug Application (NDA) but before approval and launch
Phase IV: trials done after market launch; may include different formulations, dosages, age groups, and patient groups (aka: “post-marketing surveillance”)