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Summary Oncology and Public Health | VU Amsterdam

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Summary from Oncology and Public Health (AB_1184) at VU Amsterdam covering the foundational concepts of cancer epidemiology and public health approaches to oncology. Topics include the global burden of cancer, the Big 5 cancer types, public health functions and achievements, cancer prevention strategies (primary and secondary), geographic variation in cancer incidence, and European networks for rare cancer care including the hub-and-spoke model. I achieved an 8.5/10 for the exam

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Lecture 1: Introduction
Big 5 > breast, squamous cell carcinoma (skin), lung, prostate, colon
In total, 216 different cancer types. 86% are rare (1 in 5 diagnosed per year has a rare cancer).


Lecture 2: Public health issues in oncology
Definition public health
 = the science and art of preventing disease, prolonging life and promoting health through the
organized efforts of society.
o Health is a state of complete physical, mental and social well-being and the absence of
disease.

Public health vs medicine
 Public health
o Population based
o Disease prevention
o Health promotion
o Interventions are environmental and human behavior (lifestyle, nutrient score, etc)
 Medicine
o Focusses on individual patients
o Diagnosis
o Treatment
o Intervention is medical care

Application of public health
 Population: from local areas to the world population (organize sports day in neighborhood to
promote physical activity).
 Causes of disease: from behavior to broader environments (e.g. why someone starts smoking
can be dependent on the environment).
 Prevention of disease: from individual patients to national policies (vaccination).
 General health outcomes: form quality of life to healthy life expectancy.

3 fields of public health research
 Epidemiology and community diagnosis
 Collective prevention and health promotion
 Health care organization and performance

Public health functions
 Assessment and monitoring health
 Formulation of policies
 Focus on cos-effective care, etc.

Public health achievements
 Since 1900: vaccination, safer workplaces, control of infectious diseases.
 Since 1920: safer/healthier food, healthier mothers and babies, family planning.
 Since 1965: fluoridation of drinking water, motor-vehicle safety, recognition of tobacco as a
health hazard, decline in deaths of CAD and stroke.

Biggest success in public health > improved sewage disposal and clean water.

,Global burden of cancer
 Cancer is leading cause of death. Expected to rise enormously. 1 in 8 deaths worldwide.
o Getting older, earlier diagnostics, lifestyle, population is increasing.
 Geographic variation
o Stomach cancer > 7x increased risk in Japan and Korea
o Breast & prostate > less in Asia, more in Caucasian people
o Melanoma > more in Australia and sunny parts
o Liver cancer more in south-east Asia and east Africa
o Thyroid cancer: deficiency of iodine in local food and water supplies (swiss alps)

Cancer prevention
 Primary prevention
o Prevent people from getting the disease (e.g. healthier lifestyle)
o In cancer: HPV vaccination, encourage healthy lifesyle
 Secondary prevention
o Try diagnosing in early stage of disease (e.g. mammograms, pap smear, etc)
o In cancer: screening for breast, cervical or colon cancer
 Tertiary prevention
o Preventing the disease from getting worse or slow it down (e.g. relieving side effects
of chemo)
o In cancer: survivorship care (improve HRQoL), prevention cancer reoccurrence

How much of your cancer risk can be reduced by living healthy?
a. 20-25%
b. 30-35%
c. 40-45%
d. 50-55%
B > about a third.

How do we study risk factors
 Cant do RCT. Do retrospective cohort or case-control study (basically same thing).
o End up with an WCRF matrix
 How much variables are related to different kinds of cancer.

What lifestyle improvement will reduce your cancer risk the most?
a. Start being physically active
b. Stop consumption of alcohol
c. Overweight > healthy weight
d. Stop smoking
D

,Lecture 3: Introduction into oncology
Patient case
 CT scan
o Black = lung
o White in the middle is heart
o White on the right corner (next to the heart) is a tumor
 Biopsy is taken > diagnosis lung cancer.
 PET-scan to be able to stage patient (how far has the cancer spread).
o Glucose taken in before the scan. Tracer accumulates in the tumor (takes it up) > can see
where exactly it is.
o See metastasis

What is cancer
 Can arise in any cell of the body.
 Cancer comprises a large group of diseases characterized by abnormal cells, which:
o Continuously proliferate
o Invades local tissue
o Can spread to other organs.

Difference benign and malignant
 Benign does respect normal borders (even though it can grow quite big). Will never form
metastasis and wont kill you.
 Malignant tumors have an irregular shape, do metastasize.

How many cancer cells are needed to form a tumor as big as a grape?
a. 10.000
b. 100.000
c. 1.000.000
d. 100.000.000
D
1.000.000 cancer cells > head of a pin
1.000.000.000 cancer cells > small grape.
Patient usually has had cancer for several years before it is detected or causes symptoms.

Types of cancer
 Carcinoma (85%, most common)
o Squamous cell carcinoma
 Comes from the lining (surface)
o Adenocarcinoma
 Comes from glandular tissue (underneath the surface). Responds differently to
treatment
 Sarcoma
o From bone and soft tissue
 Glioma
o From glial cells in CNS (often brain tumors)
 Melanoma
o From melanocytes in the skin
 Leukemia
o From blood-forming tissue of the bone marrow
 Lymphoma and myeloma

, o From lymph node tissue
How does cancer arise
 DNA replication is complex and vulnerable to damage (especially by toxins (e.g. smoke,
asbestos)).
o Can be direct (due to the toxin) or indirect (increased cell replication)
o Can also have random errors
 Normally cells repair the damage or undergo apoptosis
o Some cells survive

Types of genomic alterations
 Point mutation > 2 bases switched around. Leads to different protein
 Deletion > get smaller/shorter protein
 Insertion > extra bases inserted into the DNA. Leads to larger protein
 Translocation > DNA of 2 chromosomes are exchanged, leading to abnormal protein

Consequences of genomic alterations
 Type and location of the alteration are important > determine the consequence.
 2 types of genes that can be mutated
o Tumor suppressor gene (break system)
 Normally block cell cycle progression
 E.g. non-functional p53. Cant target it yet. See in almost all cancers.
 Normally activated when there is DNA damage > binds > hold replication
process > DNA repair > if not work > cell suicide (so damage isn’t passed on)
 E.g. tumor suppressor
 BRCA1/2 > hereditary breast cancer
o (proto-)oncogene (accelerator)
 Normally, codes for protein involved in cell growth
 Mutation > more active protein > increased cell growth
 Ras is on continuously (stimulates Raf, causing cell devision)
 E.g. oncogenes
 HER2 > breast cancer (can be targeted)
 B-RAF and MEK > important in development melanoma (also can be targeted)

Hallmarks of cancer (multi-hit model) (first 3 most important)
 Stimulate their own growth (self-sufficiency)
 Resist inhibitory signal
 Resist programmed cell death
 Multiply indefinitely (limitless replicative potential)
 Stimulate growth of new blood vessels (sustained angiogenesis)
 Invade local tissue and metastasis
 Abnormal metabolic pathways allow them to survive
 Evade immune system
 Show genome instability and mutation
 Show tumor promoting inflammation

How many genes altered
 In common solid tumors (e.g. colon, breast) > 33-66 genes display mutations
o Outliers > lung and melanoma (+-200 mutated genes).
 Led to immunotherapy being used in these types (more foreign, easier to be
removed by immune system)

Table of contents

  1. 01 Lecture 1: Introduction 1
  2. 02 Lecture 2: Public health issues in oncology 1
  3. 03 Lecture 3: Introduction into oncology 3
  4. 04 Lecture 4: Tumor diagnosis and treatment 6
  5. 05 Lecture 5: Targeted therapy and immunotherapy (incl patient) 9
  6. 06 Lecture 6: Late effects of diagnosis and treatment 12
  7. 07 Lecture 7: Neoplasia 15
  8. 08 Lecture 8: psycho oncology research 18
  9. 09 Lecture 9: Cancer epidemiology 20
  10. 10 Lecture 10: Risk communication and population cancer screening decisions 22
  11. 11 Lecture 11: Cancer and work 26
  12. 12 Lecture 12: Pain management 28
  13. 13 Lecture 13: E-health in oncology 31
  14. 14 Lecture 14: Shared decision making (video) 34
  15. 15 Lecture 15: Prevention and screening 37
  16. 16 Lecture 16: Nutrition 41
  17. 17 Lecture 17: Netherlands Cancer Registry 43
  18. 18 Lecture 18: End-of-life and palliative care 45
  19. 19 Lecture 19: Distress (video) 49
  20. 20 Lecture 20: AYAs 50
  21. 21 Lecture 21: CNS, chemo and neurocognitive function 53
  22. 22 Lecture 22: Rare cancers 57

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September 1, 2026
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