MDS + AML Flashcards
myelodysplastic syndrome
- <20% blasts
- bone marrow cells fail to create blood cells
- variable progression to CML
- 76yrs
Acute myeloid lymphoma
- heterogenous clonal malignancy
- Immature myeloid cell proliferation
- > 20% blasts
- Bone marrow failure
- 85-89yrs
MDS FBC
- low RBC
- Low WBC
- Low platelets
- Dysplastic features on peripheral blood film
AML FBC
- white cells can be anything
- RBC + platelets usually low
tests for MDA + AML
- blood - FBC + blood film
- bone marrow aspirate and trephine biopsy
Appearance of cells on bone marrow aspirate
MDS:
* 10% dysplasia in any cell line
* Blast 0-19%
AML:
* minimum 20% blasts
cause of MDS + AML
somatic gene mutations - not inherited so family history isn’t an indicator
No one persons MDS is the same as the next
- 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
Treatment of MDS how to decide what it is
- 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
treatment of MDS low blast % vs high blast %
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
MDS supportive treatments
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
European leukaemia net recommendations
recommendations for treatment with quality of life in mind
AML prognosis factors
baseline parameters which dictate survival
* type of AML - eg what mutation
* Age - worse if older
* Comorbidities
AML treatment first line if theyre not weak ect
- 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
other treatments if theyre frail
- 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