CLL Flashcards

1
Q

what is the epidemiology of CLL

A

o Most common (UK = 4.2/100,000/year) leukaemia in West
o Tends to affect Caucasians
o Median age at presentation: 72 years (10% aged <55yo)
o Relatives have 7 x increased risk

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2
Q

What are the lab findings in CLL

A

Lymphocytosis, smear cells, normocytic normochromic anaemia, thrombocytopaenia, bone marrow lymphocytic replacement of normal marrow elements

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3
Q

Immunophenotyping of CLL

A
o	CD19 along Y axis and CD5 along X axis 
o	Normal Mature B Cells:
	CD19 POSITIVE
	CD5 NEGATIVE
o	Normal Mature T Cells:
	CD3 positive 
	CD4 or CD8 positive 
•	Th-cell 
•	CTL cell
	CD19 NEGATIVE
	CD5 POSITIVE
o	In CLL, the B cells continue to express CD5
o	This immunophenotyping assay shows a third population of lymphocytes co-expressing CD19 and CD5
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4
Q

CLL prognostic factors

A
o	Clinical (quantify burden of malignant cells)
	Rai staging
	Binet staging (see picture right)
o	Lab/malignant cell based:
	Cytogenetics (FISH panel)
	Immunoglobulin gene mutation status 
•	IgH mutated
•	IgH unmutated (BAD)
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5
Q

worst case scenario CLL

A

Binet stage C, IgH unmutated, 17p del / p53 mutated

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6
Q

what is richter transformation

A

o Although this is an indolent disease, there is a 1% chance every year that CLL can acquire more mutations and undergo a RICHTER TRANSFORMATION (become a high grade lymphoma)

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7
Q

why can CLL lead to autoimmune disease

A

deregulation of surviving normal b cell population

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8
Q

what is car-T therapy

A

o CAR-T are autologous T cells that are modified to contain chimeric antigen receptors
o The internal portion of these receptors = signalling molecules
o External portion has been engineered to target CD19 antigens on surface of B cells
o Reinfuse patient with autologous engineered T cells  target and kill the B cells
o Leads to complete B cell depletion  not a problem provided that you give IVIG

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9
Q

CLL treatment

A

vaccinations for flue etc. antiinfective prophylaxis e.g. acyclovir, treat high grade richter transformation, must irradiate blood products, alloginic stem cells transplant if young

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10
Q

indication for treatment

A
  • Progressive lymphocytosis (count doubling < 6 months)
  • Progressive bone marrow failure (Hb < 100; Platelets < 100; Neutrophils < 1)
  • Massive or progressive lymphadenopathy/splenomegaly
  • Systemic symptoms (B symptoms)
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