Acu Leuk + MDS Flashcards

1
Q

what about cells in the bone marrow are indicative of acute leukaemia

A

1/5 bone marrow cells are primitive

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2
Q

what is the median age of onset of acute myeloid leukaemia (AML)

A

69

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3
Q

what is the diagnosis of AML

A

undifferentiated big nucleus of leukaemia cells

immune markers and cytogenetics

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4
Q

what are the clinical features of acute myeloid leukaemia

A

anaemia fatigue
infections - poor immune system
bruising
gum hypertrophy in acute monocytic leukaemia

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5
Q

what is a good prognosis marker in AML vs a bad one

A

NPM1 = good

FLT3ITD most common - bad = mutations mean resistance to chemotherapy

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6
Q

what are some risks of chemic IV treatment for tumours

A

tumour lysis = block kidneys with dead cells, sepsis and infertility

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7
Q

what syndrome would you want to start chemo for AML immediately

A

hyoperviscous syndrome

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8
Q

what does treatment of AML depend on

A

speed of relapse, subtype, physical state, comorbidity, patient wishes

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9
Q

what is an example of a low does chemo drug

A

cytarabine

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10
Q

what drugs are increasingly being used to treat AML in older patients

A

hypomethylating agents such as decitibine and azacytidine

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11
Q

what disease mutation occurs in 30% of AML cases

A

FLT3 ITD which is the poorer prognostic marker

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12
Q

give an example of FTL3 ITD inhibitors

A

midostaurin

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13
Q

what are the clinical presentations of ALL and who does it usually affect

A

sully children with 95% cure rate
fatigue, bruising, weight loss, night sweats
heptosplenomeglgy

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14
Q

what are the 4 components of ALL treatment

A

induction - chemo and steroids (8 weeks)
intensification - IV chemo - methotrexate (4 weeks)
consolidation (20 weeks) -
maintenance for 2 years - high risk patients have bone marrow transplant

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15
Q

when is ALL relapse most common

A

within 18 months stopping chemo

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16
Q

if disease of ALL relapses what are the more intensive drugs / techniques to treat it

A

Inotuzumab - CD22 traget
Chimeric antigen receptor (CAR) T cells = modify T cells
BMT

17
Q

what are the complications of ALL and AML

A

neutropenic sepsis and bleeding

18
Q

what is the definition of Myeloidysplasia and clinical features

A

several related disorders with common features reduced production of one or more of the peripheral blood cell lineages
fatigue infection bleeding

19
Q

what is the treatment of MDS

A

IPSS-R - stratify the disease - depends on neutrophils, platelets, Hb, primitive BM cells
may need BMt if severe