17. Oncology Flashcards

1
Q

Oncology

A

Dealing with the study and treatment of cancer (malignant tumours)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Onocologist

A

A physician who practices oncology

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Neoplasm

A

A mass of tissue that grows faster than normal in an uncoordinated manner

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Tumour

A

Literally mean ‘swelling’ (Latin) but is now primarily used to describe a mass/growth of tissue. This growth can be either malignant or benign
A tumour no longer responds to normal growth factors, grwoing faster than normal in an uncoordinated manner

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Cancer

A

Cancer is the second leading cause of death globally and is responsible for nine million deaths per year.
• The most common causes of cancer death in the world are: Lung, liver, colorectal, stomach and breast.
• Globally, the number of people with cancer is projected to double by 2030.
• More developed countries have higher cancer rates. This emphasises the link to environment, lifestyle, diet, medications and drugs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Cancer Environments

A

Acidic environment
Anaerobic environment
Glucose rich

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Acidid environment

A
Red meats
Processed foods
Dairy
Sugar
Salt 
Smoked Foods
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Anaerobic environment

A

Lacking oxygen

Consider stress, breathing, diet, exercise

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Glucose rich

A

Malignant cells are dependent on glucose for their own metabolism. These cells have many more glucose receptors on their membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Cell cycle

A
  • Proteins are normally produced by cells which give it contact inhibition.
  • Contact inhibition prevents cells dividing beyond the space available.
  • Cancerous cells lose contact inhibition.
  • Together with contact inhibition, cells have a programmed number of reproductive cycles.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Mutation

A

The change in the genetic information (change in DNA sequence / number).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Mutagen

A

An agent that changes the genetic information. Mutagens can be:
• Environmental hazards.
• Chemicals (environmental, household, drugs, vaccines).
• Radiation (x-rays, microwaves, mobile phones).
• Viruses.
• Inflammation.
• Defective immunity.
• Stress / emotional trauma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Carcinogen

A
  • A carcinogen is any cancer-causing agent.

* For example: Nitrosamines, heavy metals, asbestos, x-rays, UV-rays

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Carcinogenesis

A
  • Carcinogenesis is the process by which normal cells are transformed into cancer cells.
  • Only 5–10% of cancers are attributed to inherited genetic defects, whilst the remaining 90–95% are attributed to the environment and lifestyle.
  • Generally, causative factors can be difficult to establish because many cancers take many years to develop. Some tumours take 20–40 years.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Risk Factors

A
  • Genetic factors (e.g. BRCA) / family history.
  • Chronic inflammation — inflammatory bowel diseases, gastro-oesophageal reflux disease, gastritis, etc. Chronic inflammation promotes proliferation of cancer cells.
  • Radiation — environmental, medical, microwaves, phones.
  • Smoking — causes one mutation every 15 cigarettes.
  • Drugs and cosmetics — (e.g. parabens).
  • GIT dysfunction — liver (detoxifies substances), intestines (excrete body wastes, absorb nutrients and immune function).
  • Vitamin D deficiency and thyroid disease.
  • Chronic stress — suppresses the immune system.
  • Sexual behaviour (e.g. cervical cancer, HIV, etc.)
  • Compromised immunity.
  • Excess alcohol (e.g. for mouth, oesophageal, breast and colorectal).
  • Obesity; e.g. breast cancer in post-menopausal women (excess body fat changes hormone metabolism  higher oestrogen  drives oestrogen-positive tumours).
  • Excessive exposure to sunlight.
  • Metal toxins (i.e. aluminium. mercury).
  • Medications e.g. immunosuppressants, HRT, antibiotics (altering flora and immunity).
  • Vaccine ingredients e.g. aluminium, formaldehyde, mercury, human / animal DNA, etc.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Dietary Risk Factors

A
  • Red meats (especially for colorectal, prostate, bladder, breast, gastric and pancreatic cancers). Higher risk if charcoal cooked / smoked and at high temperatures.
  • Burnt food (produces ‘acrylamides’).
  • Low fibre — high in phytochemicals and clears toxins and hormones such as oestrogen through the bowel.
  • N-nitroso compounds (e.g. cured meats).
  • Refined sugars — feed cancer cells and promote growth (and increase acidity).
  • Dairy — pro-inflammatory and contains IGFs (insulin- like growth factors) that promote tumour growth.
  • Table salt, pesticides and aspartame.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Cancer and Host Immunity

A

Chronic immunodeficiency can increase the risk for cancer.
• Cytotoxic T-lymphocytes, natural killer cells and macrophages are needed to destroy abnormal cells.
• HIV targets CD4 cells (T-helper cells and macrophages), which, therefore, compromises the host immune system.
• Even chronic stress, which would elevate cortisol levels, would suppress the immune system.
• A healthy, functioning immune system is essential to providing support against malignant cell development.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Benign Tumours

A

Benign tumours usually consist of differentiated cells which appear similar to normal cells so may be functional.
• Reproduce at a higher rate than normal.
• A benign tumour is very often encapsulated -> no metastasis.
• It grows very slowly and does not spread; systemic effects rarely seen.
• Not life-threatening but damage can result from compression of tissues (e.g. brain -> raised intracranial pressure).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Malignant Tumours

A

Usually made of undifferentiated, non-functional cells with varied shapes and sizes and large nuclei.
• The cells reproduce much faster than normal.
• Not encapsulated -> infiltrate other tissues (metastasise).
• Often systemic — can spread very quickly to other organs.
• Life-threatening due to tissue destruction and spread of tumour.
• Oncology is the study of malignant tumours.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Grades

A

Grading is the measure of the degree of cell differentiation / abnormality.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Grade 1

A

Tumour cells still similar to original. Cells are differentiated and specialised (i.e. benign tumour).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Grade 4

A

Tumour cells undifferentiated / many abnormal cells varying in size and shape.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

Staging

A

Staging is the classification of malignant tumours according to the extent of the disease at the time of diagnosis.
• Staging helps to identify treatment approaches, disease progression and prognosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Stage 0

A

Pre-cancerous cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Stage I

A

Cancer limited to tissue of origin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Stage II

A

Limited local spread of cancerous cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Stage III

A

Extensive local and regional spread

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

Stage IV

A

Distant metastasis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

TNM Staging System

A

There are several types of staging methods.
•The ‘tumour, node, metastasis’ (TNM) system classifies cancer by:
•T (1–4): Size of primary tumour; e.g. 4 is largest.
•N (0–3): Degree of lymph node involvement.
•M (0–1): Metastasis (1 indicates metastasis).
•(X = cannot be assessed).

30
Q

Cancer: Local Effects

A

A tumour with no function damages the ‘space’ it occupies.
• Tumours can compress blood vessels leading to necrosis of surrounding tissues. In larger tumours, it occurs within tumour (i.e. calcification -> on x-ray).
• Malignant cells do not adhere to each other — they metastasise.
• Pain is not usually an early symptom of cancer. If it occurs, it is caused by pressure or inflammation.
• Obstruction may occur in tubes or ducts in the body.
• Tissue ulceration / necrosis may produce infection (more likely with chemo / radiotherapy because of compromised immunity).

31
Q

Cancer: Systemic Effects

A
  1. Weight loss and cachexia
  2. Anaemia
  3. Infection
  4. Para-neoplastic syndromes
32
Q

Weight-loss and cachexia

A
  • Cachexia is weight loss and muscle atrophy (hence fatigue and weakness).
  • Cancer patients can still have a strong appetite.
33
Q

Anaemia

A

This can occur due to malnutrition, chronic bleeding from an ulcerated tumour, bone marrow suppression.

34
Q

Infection

A

Host resistance compromised, giving way to infections; e.g. pneumonia.

35
Q

Para-neoplastic syndromes

A
  • Symptoms that occur at site distant from a tumour or metastases.
  • E.g. lung cancers may produce ACTH leading to Cushing’s syndrome (excess corticosteroids produced by lung tumour cells).
36
Q

Metastasis

A

Metastasis describes the spread of a malignant tumour.
• Malignant tumours spread via blood or lymph and produce secondary tumours.
• Often first metastases appear in regional lymph nodes.
• Venous and lymphatic flow usually endangers mostly the lungs and liver.
• Cells in the secondary tumour are similar to the parent tumour.
• Common sites of metastasis include: Bone, liver, lungs and brain.

37
Q

Cancer Presentation

A
Initially very few, vague symptoms in cancer:
• Unexplained weight loss.
• Anaemia and fatigue.
• Night sweats.
• Unusual bleeding or discharge (e.g. vaginal).
• Persistent indigestion / heartburn.
• Difficulty swallowing.
• Change in bowel or bladder habits.
• A change in appearance of a wart or mole.
• Persistent cough or hoarseness.
• A solid lump.
• Swollen lymph nodes.
38
Q

Diagnostic Tests

A
  1. BLOOD TESTS.
  2. TUMOUR MARKERS.
  3. IMAGING.
  4. BIOPSIES.

Diagnostic tests:
• Diagnostic tests enable detection of malignant growths.
• Testing also supports better monitoring of progress.
• No diagnostic test is 100% reliable and false positive or false negative results are possible.

39
Q

Blood tests

A
  • These include: haemoglobin, erythrocytes, leukocytes (leukaemia), platelets.
  • Liver, thyroid, renal function tests.
40
Q

Tumour Markers

A
  • Substances (usually proteins) produced by tumours (malignant cells). Can be found in the blood, urine, stools or tissues.
  • Some markers are found in non-cancerous conditions, whilst other tumour markers might indicate a malignancy.
  • Tumour markers must be used within the context of the patient presentation and other clinical findings.
  • Some tumour markers are more sensitive / more indicative of some types of cancer; e.g. CA-125 and ovarian cancer.
41
Q

Tumour Markers: CEA

A

Carcinoembryonic antigen (CEA) is a glycoprotein that is present within normal mucosal cells, but is often undetectable in the blood after birth.
• CEA is a blood-borne marker.
• CEA can be elevated in certain types of cancer, especially colorectal cancer.
• CEA has a low sensitivity and specificity and so is used more for monitoring than screening or diagnosing (blood test).
• May also be elevated in ulcerative colitis, pancreatitis and liver cirrhosis.

42
Q

Tumour Markers: PSA

A

Prostate specific antigen (PSA) is a protein produced by prostatic cells.
• PSA is normally present in small quantities in the serum (blood) of healthy men.
• May be elevated in the presence of prostate cancer and in other prostate disorders such as benign prostatic hyperplasia.
• PSA is used to assist in the diagnosis of prostate cancer, although it often produces false positives.
• PSA testing can be used to monitor tumour progression and metastasis (particularly post-treatment).

43
Q

Tumout Markers: hCG

A

human chorionic gonadotropin:
• Males do not naturally produce β-hCG.
• Can test for cancer in some locations — testicles, pancreas, pituitary, placenta.
• Also elevated in pregnancy (should only be produced at this time).

44
Q

Tumour Marker: M2-PK

A
  • Not an organ-specific tumour marker, so it may be elevated in many tumour types.
  • Increased stool levels are being investigated as a screening method for colorectal tumours and levels may be used for follow-up screenings in various other cancers.
45
Q

Tumour Marker: CA-125

A
  • CA-125 is a protein that may be elevated in many cases of ovarian cancer and tested in a blood test.
  • CA-125 can be monitored to see whether treatment might be destroying the cancerous cells.
  • Normal blood ranges are less than 35 U/mL.
46
Q

Tumour Marker: 15-3

A

• CA 15-3 is a tumour marker that may be elevated in breast cancer patients in a blood test.
• CA 15-3 can be useful in monitoring metastatic breast cancer.
• Normal blood ranges are less than 30 U/mL.
31

47
Q

Imaging

A
  • X-rays -> harmful (induce mutation).
  • MRI: Magnetic resonance imaging.
  • CT: Computed tomography.
  • Radioisotopes.
48
Q

Biopsies

A
  • Fine needle, core or surgical biopsies.
  • A small sample of tissue is removed and examined histologically.
  • Malignant cells have an undifferentiated cell structure.
  • Speculation that taking the biopsy may cause cancer cells to break off and spread.
49
Q

Treatment

A

Basic conventional treatments: (combined or single).
• Surgery
• Chemotherapy
• Radiation

50
Q

Curative

A

Treatment that is used in an attempt to resolve the malignancy.

51
Q

Palliative

A
  • Care that focuses on reducing symptom severity rather than ‘curing’. This is seen in late stages where symptomatic management and preventing complications is vital.
  • Palliative care focuses on quality of life.
52
Q

Surgery

A

Removal of the tumour, surrounding tissue and lymph nodes. Some examples include:
• MASTECTOMY: Removal of the breast.
• PROSTATECTOMY: Removal of the prostate gland with a very high rate of adverse effects!
• ORCHIECTOMY: Removal of the testes.

53
Q

Radiotherapy

A
  • Radiotherapy can be administered with curative or palliative intentions.
  • Affects those cells which divide most rapidly (both cancer cells and healthy cells which divide regularly).
  • Causes loss of reproduction and induces apoptosis.
54
Q

Radiotherapy: Types

A
  • There are three different types of radiotherapy:
  • External beam radiation
  • Internal beam radiation
  • Systemic beam radiation
55
Q

External Beam Radiation

A

Beams are generated from outside the patient.

56
Q

Internal Beam Radiation

A

A higher dose of radiation released from within a body cavity.

57
Q

Systemic Beam Radiation

A

Radioactive material enters the blood to reach cells all over the body (very toxic!).

58
Q

Radiotherapy adverse effects

A
  • Bone marrow depression (leading to aplastic anaemia with pancytopenia)  immunocompromised.
  • Inflammation / ulceration of skin exposed to beams.
  • Hair loss and gut ulceration (diarrhoea and bleeding).
  • Sterility.
  • General fatigue / weakness. Fibrosis of tissue.
59
Q

Support during radiation

A
  • Exercise reduces the fatigue during radiation therapy.
  • Adequate rest and relaxation is essential (reduces stress).
  • Acupuncture, herbs, homeopathy; e.g. radiation burns: Calendula, Rad. brom. / Sol / Sulphur.
  • Creams, gels and oils applied to skin irritation, etc.
60
Q

Chemotherapy

A

Specific chemical agents that are destructive to malignant cells.
• Targets rapidly dividing cells (cannot distinguish between normal and cancer). Healthy cells that have high rate of growth -> adverse effects.
• It interferes with protein synthesis and DNA replication.
• Different drug combinations are chosen for different cancers.

61
Q

Chemotherapy: Adverse effects

A
Often develops 7–14 days post treatment.
• Bone marrow depression; (opportunistic infections, fatigue, bruising, etc.).
• Diarrhoea, vomiting, nausea.
• Hair loss.
• Organ damage and cancer!
62
Q

Other Cancer Drugs

A

HORMONES:
•Oestrogens or anti-androgen drugs for prostate cancer.
•Tamoxifen to block oestrogen receptors -> adverse effects (effectively induces menopause).
•Glucocorticoids (for example, in lymphomas).
BIOLOGIC RESPONSE MODIFIERS:
•Interferon
ANALGESICS:
•Opioid analgesics such as morphine (act on the CNS) can be given to assist with symptomatic management (common in palliative medicine).

63
Q

Nutritional Therapy

A
  • Phytonutrients (essential also in cancer prevention), high level of antioxidants, high fibre, whole plant foods, adequate protein and omega-3; support immunity; anti-inflammatory foods.
  • Diet rich in fruit and vegetables (7–9+ portions).
  • Anti-tumour substances; e.g. antioxidants, plant-based diet, folate (prevents DNA damage), beta glucans (e.g. mushrooms), amygdalin.
  • Medicinal mushrooms (immunomodulators and adaptogenics); e.g. chaga, cordyceps, reishi, shiitake
64
Q

Herbal Medicine

A
  • There are numerous herbs that have been shown as effective in supporting cancer patients; for example:
  • Chemo- and radiotherapy protective adaptogens.
  • Anti-tumour adaptogens.
  • Herbs protective against oxidative stress.
65
Q

Other Complementary Treatments

A
  • Acupuncture.
  • Homeopathy.
  • Other therapies; e.g. Ayurveda, TCM, reflexology.
66
Q

Prognosis

A

A ‘cure’ for cancer is generally defined by orthodox medicine as a five-year survival without reoccurrence.
• It is essential to recognise that cancer reoccurrence after this period is common.
• In some cases, several periods of remission may occur before the cancer becomes terminal.
• Death rates vary for different types of cancer and are dependent on the individual.
• Some malignancies are more aggressive and metastasise more rapidly than others.
• Some cancers only present clinically once the disease is very advanced.

67
Q

Types of Cancer

A

Carcinomas
Sarcomas
Leukaemias

68
Q

Carcinomas

A

Cancers which form in epithelial tissue lining skin, mouth, nose, throat, respiratory tract, lung, breast, prostate, stomach, intestines.

69
Q

Sarcomas

A

Cancers which develop in connective tissue

 bone, cartilage, muscles, tendons.

70
Q

Leukaemias

A
  • Cancers which evolve in blood and bone marrow.
  • Abnormal leukocytes produced travel throughout the bloodstream.
  • They do NOT form solid tumours, but invade other cells.