CLL Flashcards
what is the epidemiology of CLL
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
What are the lab findings in CLL
Lymphocytosis, smear cells, normocytic normochromic anaemia, thrombocytopaenia, bone marrow lymphocytic replacement of normal marrow elements
Immunophenotyping of CLL
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
CLL prognostic factors
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)
worst case scenario CLL
Binet stage C, IgH unmutated, 17p del / p53 mutated
what is richter transformation
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)
why can CLL lead to autoimmune disease
deregulation of surviving normal b cell population
what is car-T therapy
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
CLL treatment
vaccinations for flue etc. antiinfective prophylaxis e.g. acyclovir, treat high grade richter transformation, must irradiate blood products, alloginic stem cells transplant if young
indication for treatment
- 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)