Myeloid malignancy Flashcards

1
Q

What are investigations for myeloid malignancies?

A
  • blood count + blood film
  • bone marrow aspirate/trephine
  • cytogenetics (karyotype) from leukamic blasts
  • immunophenotyping of leukaemic blasts
  • CSF examination if symptoms
  • targeted molecular genetics for associated aquired gene mutations
  • e.g. FLT, NPM1, IDH 1 + 2
  • inc. use of NGS myeloid gene panels in AML
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2
Q

What is the treatment for acute myeloid leukaemia?

A
  • supportive care
  • anti-leukaemic chemotherapy
  • daunorubicin + cytosine arabinoside (DA)
  • high dose cytosine arabinoside
  • gemtuzumab ozogamicin
  • CPX-351
  • allogeneic stem cell transplant
  • all-tran retinoic acid (ATRA) and arsenic trioxide (ATO) (in low risk acute promyelocytic leukaemia)
  • targeted treatments
  • e.g. midostaurin in FLT2 mutated AML
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3
Q

What is the mechanism of action of calicheomycin (mylotarg)- targeted antibody?

A
  1. CD33 expresion level
  2. CD33 saturation
  3. internalisation
  4. activation of calicheamicin
  5. new expression of CD33
  6. binding of GO
  7. efflux of calicheomycin
  8. induction of DNA breaks
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4
Q

What are features of chronic myeloid leukaemia (CML)?

A
  • anaemia
  • splenomegaly (often massive)
  • weight loss
  • hyperleukostasis
  • fundal haemorrage, venous congestion, altered conciousness, respiratory failure
  • gout
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5
Q

What are labratory features of chronic myeloid leukamia (CML)?

A
  • (very) high WCC
  • high platelet count
  • anaemia
  • blood film
  • all stages of white cell differentiation
  • inc. basophil
  • bine marrow hypercellular
  • bone marrow + blood cells, contain Philadelphia chromosome t(9;22)
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6
Q

What is the treatment for chronic myleoid leukaemia (CML)?

A
  • tyrosine kinase inhibitors (TKIs)
  • imatinab (Glivec)
  • dasatinib (Sprycel)
  • Nilotinib (Tasigna)
  • busitinib
  • ponatinib
    (direct inhibitors of BCR-ABL)
  • allogenic transplantation
    -only if TKI fails
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7
Q

What are features and treatment for myelodysplastic syndromes?

A
  • aquired clonal disorder of bone marrow
  • commonly old age
  • pre-leukaemic
  • macrocytic anaemia, pancytopenia
  • fatal- progression to bone marrow failure or AML
  • supportive treatment
  • stem cell transplantation (young)
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8
Q

What are different types of myeloproliferative neoplasms (MPN)?

A
  • polycythaemia vera (PC)
  • JAK2V617F mutation- 95%
  • essential thrombocythaemia (ET)
  • JAK2V617F mutation- 50%
  • CALR mutation- 25%
  • idiopathic myelofibrosis (IM)
  • JAK2V617F mutation- 50%
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9
Q

What are features of polycythaemia vera (PV)?

A
  • headaches
  • itch
  • vascular occlusion
  • thrombosis
  • TIA, stroke
  • splenomegaly
  • bone marrow failure- from secondary myelofibrosis
  • transformation to AML
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10
Q

What are labratory features of polycythaemia vera (PV)?

A
  • inc. haemoglobin concentration + haematocrit
  • inc. WCC + platelets
  • inc. uric acid
  • true inc. red cell mass when blood volume is measured
  • blood film
  • large + abnormal platelets
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11
Q

What is the treatment for polycythaemia vera (PV)?

A
  • venesection
  • keep haematocrit < 0.45 (men)/< 0.43 (women)
  • aspirin
  • hydroxycarbamide (HC)
  • ruxolitinib (JAK2 inhibitor)
  • if HC failure + systemic symptoms
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12
Q

What are features and treatment for essential thrombocythaemia (ET)?

A
  • inc. platelet count
  • arterial + venous thromboses, digital ischaemia, gout, headache
  • mild splenomegaly
  • progress to myelofibrosis, AML
  • aspirin + hydroxycarbamide
  • anagelide
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