MDS + AML Flashcards

1
Q

myelodysplastic syndrome

A
  • <20% blasts
  • bone marrow cells fail to create blood cells
  • variable progression to CML
  • 76yrs
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2
Q

Acute myeloid lymphoma

A
  • heterogenous clonal malignancy
  • Immature myeloid cell proliferation
  • > 20% blasts
  • Bone marrow failure
  • 85-89yrs
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3
Q

MDS FBC

A
  • low RBC
  • Low WBC
  • Low platelets
  • Dysplastic features on peripheral blood film
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4
Q

AML FBC

A
  • white cells can be anything
  • RBC + platelets usually low
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5
Q

tests for MDA + AML

A
  • blood - FBC + blood film
  • bone marrow aspirate and trephine biopsy
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6
Q

Appearance of cells on bone marrow aspirate

A

MDS:
* 10% dysplasia in any cell line
* Blast 0-19%

AML:
* minimum 20% blasts

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7
Q

cause of MDS + AML

A

somatic gene mutations - not inherited so family history isn’t an indicator

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8
Q

No one persons MDS is the same as the next

A
  • genetically and clinically heterogenous
  • Effect on blood counts and function of blood cells
  • How a person feels and their ability to function day to day
  • Huge interplay between MDS and the individuals other heath problems
  • Disease behaviour and how it affects an individual can evolve over time
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9
Q

Treatment of MDS how to decide what it is

A
  • base depends on their life, comorbidities, severity, symptoms etc
  • Got to make that decision w the patient
  • Aims are to reduce symptoms, reduce progression to AML, improve QOL
  • depends on % of blast as to what it is
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10
Q

treatment of MDS low blast % vs high blast %

A

Low blast:
* stimulate marrow to inc blood cells production
* Alleviate symptoms due to low blood counts
* Low toxicity

High blast %
* reduce leukaemia cell burden with chemo / chemo-like medications
* High toxicity

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11
Q

MDS supportive treatments

A

Anaemia:
* red cell transfusions
* Reduce / treat any associated bleeding contributions to anaemia
* Agents to stimulate erythropoietin

Neutropenia:
* treat infections with antibiotics
* G-CSF injections
* Also used to stimulate stem cell production in healthy stem cell donors

Thrombocytopenia:
* platelet infusions
* Tranexamic acid (improve the ability of platelets to reduce bleeding)
* Drugs to stimulate the bone marrows ability to produce platelets

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12
Q

European leukaemia net recommendations

A

recommendations for treatment with quality of life in mind

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13
Q

AML prognosis factors

A

baseline parameters which dictate survival
* type of AML - eg what mutation
* Age - worse if older
* Comorbidities

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14
Q

AML treatment first line if theyre not weak ect

A
  • chemo - combo of drugs
    Need to support fertility
    Clinical trial availability
  • IV administered
  • Anthracycline (daunorubicin)
  • Cytabine
  • Potential for targeted therapy in some patients eg tyrosine kinase inhibitors in philidelphia gene
  • Hickman / PICC line / portacath insertion
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15
Q

other treatments if theyre frail

A
  • less intensive but non-curative
  • For older / less fit
  • Azacytide
  • Low dose subcutaneous cytarabine
  • Trial drugs eg targeted therapy
  • Also supportive measures like transfusions and antibiotics for infection
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