Chronic Lymphocytic Leukaemia Flashcards

1
Q

What is seen on blood film in CLL?

A

smudge cells

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2
Q

What is the immunophenotypic profile of CLL?

A

aberrant co expression of CD5, CD19 and CD23

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3
Q

What differentiates CLL from a leukaemic manifestation of mantle cell lymphoma?

A

CD23

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4
Q

What is the most common reason for diagnosis of CLL?

A

incidental finding on an FBE (60% of patients asymptomatic at diagnosis)

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5
Q

How is CLL staged?

A

Binet A = Hb > 100, plt > 100 and < 3 LN regions
Binet B = Hb > 100, plt > 100
Binet C = Hb < 100, plt < 100

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6
Q

What are the poor prognostic markers of CLL?

A

elevated beta 2 microglobulin
elevated LDH
certain molecular/chromosomal markers on FISH e.g. 17p deletion

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7
Q

What are the autoimmune complications of CLL?

A

autoimmune haemolytic anaemia

immune thrombocytopaniea purpura

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8
Q

What are the indications for commencing treatment in CLL?

A
worsening anemia/thrombocytopaenia
massive/symptomatic splenomegaly
massive lymphadenopathy
singificantly progressive lymphocytosis
AIHA or ITP unresponsive to steroids
symptomatic extranodal involvement
constitutional symptoms
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9
Q

What is the standard treatment for CLL?

A

rituximab, fludarabine and cyclophosphamide

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10
Q

Which patients should you use ibrutinib for in CLL?

A

17p deletion or p53 mutation

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11
Q

What is the mechanism of action of ibrutinib?

A

BTK inhibitor

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12
Q

What are the side effects of ibrutinib?

A

bruising, diarrhoea, fatigue, AF

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13
Q

What is the mechanism of action of venetoclax?

A

Bcl-2 inhibitor

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14
Q

Which patients get venetoclax in CLL?

A

relapsed or refractory CLL with 17p deletion

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