childhood cancer Flashcards

1
Q

how does the development of cancer typically differ in children than adults?

A
  • cancer arises from abnormal and unregulated cell growth, leading to crowding out of healthy cells
  • in children the cell of origin is typically an immature cell (where as in adult it is typically mature cells making replication errors)
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2
Q

what are predisposing factors to childhood cancers?

A
  • down syndrome, Li Fraumeni, Noonan’s Syndrome, NF1, p53 mutation
  • with down syndrome AML is more common
  • with p53 mutation increased risk of osteoblastoma, retinoblastoma
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3
Q

how prevalent is childhood cancer in Canada?

A
  • there are about 950 cases a year in Canada and about 40 per year in Saskatchewan
  • children make up less than 1% of all new cancer diagnosis in Canada
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4
Q

How is cancer in children diagnosed?

A
  • depends on type of cancer
  • first investigation is often a CBC (CBC often how leukemia is diagnosed)
  • bone marrow aspiration and biopsy
  • lumbar puncture
  • imaging (x-ray, MRI, CT, ultrasound)
  • surgical biopsy
  • urine and blood samples for tumor markers
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5
Q

treatment options for cancers

A
  • chemotherapy
  • surgery
  • radiation
  • biotherapy
  • allo or auto bone marrow transplant
  • some treatments are appropriate for certain types of cancers while others are not*
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6
Q

what is the difference between allo and auto bone marrow transfers?

A
  • both are a hemopoetic stemcell transplant (aka blood transfusion)
  • allo is when someone else’s bone marrow is used. this is done when bone marrow is where cancer is
  • auto is where bone marrow is taken, treatment done, then it is given back. sometimes called a rescue because bone marrow is rescued from destruction by the treatment
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7
Q

what are some types of biotherapies to treat cancer?

A
  • treatments using substances from living organisms: immunotherapy like vaccines, antibodies, or cytokines, genetherapy, or targeted therapies
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8
Q

Chemotherapy

A
  • a name for a group of medications that work by slowing or stopping growth of cancer cells, which grow and divide rapidly
  • often referred to as cytotoxic
  • can be used curatively or palliatively
  • lots of routes of administration
  • most not disease-targeted, meaning they have systemic side effects
  • each chemotherapy has a different mechanism of action - some target certain cell stages, why often given in combination and/or at different times
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9
Q

what are side effects of chemotherapy?

A
  • because chemotherapy targets rapidly growing and dividing cells, this often includes normal/healthy cells as well (like GI, hair, skin, etc)
  • bone marrow suppression
  • mouth sores
  • nausea and/or voiting
  • anorexia
  • hair loss
  • pain
  • lethargy
  • constipation
  • diarrhea
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10
Q

when do health care professionals need to take precautions when patients are receiving cytotoxic medications?

A
  • during drug preparation
  • during drug administration
  • management/contact with body fluids
  • spills (5mL is considered a large chemo spill)
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11
Q

what are chemotherapy handling precautions?

A
  • wear double gloves, gown, eye protection, possibly N95 mask
  • use special storage and disposal precautions of body fluids for at least 48 hours following last dosage
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12
Q

what is leukemia

A

a general term that refers to cancer of blood cells, which form and develop in the bone marrow

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13
Q

what is AML?

A

leukemia that occurs in the myeloid stem cells

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14
Q

what is ALL?

A

leukemia that occurs in lymphoid stem cells

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15
Q

what type of leukemia is the most common?

A

b lymphocytic (a form of ALL)

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16
Q

what type of leukemia is less responsive to chemotherapies?

A

t cell or t lymphocyte leukemia (a form of ALL)

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17
Q

what are signs and symptoms of leukemia?

A
  • mostly directly correlate to effects of leukemic cells crowding out healthy blood cells in bone marrow
  • recurrent or prolonged fever
  • lethargy/general malaise
  • anemia, pallor
  • therombocytopenia, ecchymosis and petechiae
  • hepatosplenomegaly
  • enlarged lymph nodes
  • recurrent infections
  • bone and joint pain
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18
Q

what age group has the highest incidence of leukemia?

A

-1-4 year olds

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19
Q

what type of leukemia is more common in older children and teenagers?

A

-AML

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20
Q

what type of therapy is standard, up-front therapy for all types of leukemia?

A
  • chemo
  • for ALL usually 4-5 cycles, followed by 2-2.5 years of maintenance therapy
  • for AML 3-4 cycles of intensive, in-patient chemo
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21
Q

when is a bone marrow transplant recommended for children with leukemia?

A

-when they have a high-risk disease at diagnosis or are not responding to standard treatment or if they experience relapse

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22
Q

which type of leukemia has a better survival rate?

A

ALL - it has a 5 year survival rate of 90%

while AML has a 5 year survival rate of 65%

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23
Q

what type of CNS tumour has a poor prognosis?

A

DIPG - a type of tumour in the PONS, this is because it occurs as part of normal tissue and can’t be removed
-though radiation can be used, it can only be given about 3 times

24
Q

what is an ependymoma?

A

a CNS tumour

-space occupying lesion in the brain

25
Q

what is lymphoma?

A
  • a general term for cancer of the immune system and lymphoid tissue
  • a blood cancer where dysregulation of immature white cells leads to crowding out of normal cells
  • is the third most common type of cancer in children
  • most cases occur in children over 5
26
Q

what are symptoms of lymphoma in children?

A

-painless, firm, mobile lymphadenopathy (often in cervical/supraclavicular region)

“b symptoms”

  • fever
  • night sweats
  • unexplained weight loss
  • fatigue
  • mediastinal mass (mass over the heart - a symptoms r/t non-hodgkin’s type)
27
Q

what types of cells can non-Hodgkin’s lymphoma affect?

A

– diffuse large B-cells, ALCL, white blood cells but differently than leukemia

28
Q

what can increase the risk of lymphoma?

A
  • mono infection (EBV)

- transplant recipients because of immunosuppressants

29
Q

where are neuroblastomas commonly found?

A

-solid tumour often found in spine, paraspinal nerve tissue, adrenal glands, kidney

30
Q

what are symptoms of neuroblastomas?

A
  • palpable abdominal mass
  • raccoon eyes
  • hypertension
  • other symptoms depend on location of space-occupying lesion
31
Q

what are soft-tissue sarcomas?

A

rare cancers arising in fat, muscle, or connective tissue

32
Q

what are the most common types of soft-tissue sarcomas?

A

rhabdomyosarcoma - develop from immature muscle cells

Wilm’s tumour - originate in kidney cells

33
Q

what are the two most common types of bone tumors?

A
  • osteosarcoma - develops from immature bone cells

- ewing sarcoma

34
Q

what is osteosarcoma

A

a bone tumor that develops from immature bone cells that would normally form new bone tissue, but instead destroy bone and lead to it weakening
-area affected must be extracted

35
Q

what are oncologic emergencies?

A
  • serious complications related to cancer patients
  • includes metabolic emergencies like tumor lysis syndrome, sepsis, hypercalcemia, and SIADH
  • hematologic - like bone marrow suppression, bleeding, coagulopathy, hyperleukocytosis
  • space-occupying lesions like mediastinal mass, brain tumors, neuroblastoma, lymphoma, spinal cord compression
36
Q

what is tumor lysis syndrome?

A
  • when cancer cells break down and release cytoplasmic materials into blood stream
  • this occurs in leukemia patients and much less commonly neuroblastitis patients
  • causes elevation of serum potasium, phosphorus, uric acid
  • causes decrease in serum calcium and urine output
  • can cause pain, cardiac changes, neurological changes, kidney failure, death
37
Q

what are possible symptoms of sepsis in children with cancer?

A
  • fever
  • low temperature
  • neutropenia
  • a positive blood culture for infection
  • hypotension
  • mottling
  • decreased LOC
  • reduced urine ouput
  • metabolic acidosis
38
Q

What are late effects of cancer?

A
  • a long-term or chronic effect as a result of their cancer treatment
  • approximately 2/3 of cancer survivors experience at least 1
  • common late effects: deficiencies of endocrine, sensory, neurocognitive, cardiopulmonary, reproductive, immunologic, and/or GI/GU systems; secondary malignancies, psychosocial impact
39
Q

What is a blast result in a CBC indicate

A
  • though less than 6% can mean nothing, higher values indicate leukaemia
  • normally theses aren’t reported on CBC results unless present - this is important to inform parents and children when being tested while in remission (otherwise they may think cancer isn’t being looked for and worry)
40
Q

what does AML stand for?

A

acute myeloid leukemia

41
Q

what does ALL stand for?

A

acute lymphoblastic leukemia

42
Q

what is bone marrow?

A

the spongy tissue inside bones that is responsible for hematopoiesis

-hematopoiesis also occurs secondarily in the spleen, lymph nodes, and thymus (in children)

43
Q

what kind of tumor is a neuroblastoma?

A

a solid tumor found outside the CNS

44
Q

what are some oncological emergencies?

A
  • metabolic emergencies like tumor lysis syndrom, sepsis, hypercalcemia, or SIADH
  • hematologic emergencies like bone marrow suppression, bleeding, coagulopathy, hyperleukocytosis
  • space-occupying lesions like mediastinal masses, brain tumors, neuroblastomas, lymphoma, or spinal cord compression
45
Q

what are symptoms that may indicate tumor lysis syndrome?

A
  • elevated serum potassium, phosphorous, uric acid

- decreased serum calcium and decreased urine output

46
Q

what are complications that tumor lysis syndrome can cause?

A
  • pain
  • cardiac changes/abnormalities
  • neurologic changes/abnormalities
  • kidney failure
  • death
47
Q

what is the treatment/prevention for tumor lysis syndrome?

A
  • IV fluids
  • diuretics
  • oral medications to eliminate serum uric acids (things to bind the toxic stuff)
  • dialysis
48
Q

a fever in a child with cancer should not be ignored, what should be done?

A
  • check a full set of vitals and perfusion
  • do a full systems assessment
  • notify the MRP
  • obtain blood cultures
  • if an antibiotic is indicated, ensure first dose is administered as soon as possible (this should really be within 60 minutes of first temperature spike - why antibiotics should be considered to be given to parents who live far from hospital)
49
Q

what are some advantages and disadvantages to a port-a-cath being placed for chemotherapy?

A
  • less pokes
  • can draw blood work from it
  • it is an inserted needle, which can be dislodged by kids through normal play
  • port access can be frightening for kids
50
Q

what are some side effects of dexamethasone treatment?

A
  • can cause irritability
  • can cause hunger
  • hunger can come on quickly and child can become “hangery” easily
  • sleep can be heavily impacted
51
Q

what are the three most common types of cancers in children?

A

leukemia (32%)
CNS tumors (19%)
lymphoma (11%)

52
Q

what type of cancer is the number 1 cause of cancer deaths in children?

A

CNS tumors (account for 1/3 of cancer-related deaths)

53
Q

what are ependymonas?

A

tumors that arise from ependyma, a tissue of the central nervous system

-they are space occupying lesions

54
Q

how are CNS tumors treated

A
surgery
radiation
chemotherapy
https://en.wikipedia.org/w/index.php?title=Ependymoma&oldid=772286118
note: chemo doesn't work for DIPG tumors
55
Q

what are the effects of space-occupying lesions on the brain or spinal cord?

A

increased ICP
invasive surgical interventions
immediate effects
long-term effects