CLL Flashcards
What is the most common leukemia seen ?
most common form of leukaemia seen in adults.
What type of cell is CLL predominantly made out of ?
monoclonal proliferation of well-differentiated lymphocytes which are almost always B-cells
What are some of the clinical features of CLL?
Lymphadenopathy more than CML
weight loss
Investigation of CLL
full blood count:
lymphocytosis
anaemia: may occur either due to bone marrow replacement on autoimmune hemolytic anaemia (AIHA)
thrombocytopenia: may occur either due to bone marrow replacement on immune thrombocytopenia (AIHA)
blood film: smudge cells (also known as smear cells)
immunophenotyping is the key investigation
most cases can be identified using a panel of antibodies specific for CD5, CD19, CD20 and CD23
What type of AIHA is most commonly associated with CLL?
Warm autoimmune haemolytic anaemia occurs in around 10-15%
Indications for treatment of CLL?
worsening of anaemia and/or thrombocytopenia
massive (>10 cm) or progressive lymphadenopathy
massive (>6 cm) or progressive splenomegaly
progressive lymphocytosis: > 50% increase over 2 months or lymphocyte doubling time < 6 months
systemic symptoms: weight loss > 10% in previous 6 months,
fever >38ºC for > 2 weeks, extreme fatigue, night sweats
autoimmune cytopaenias e.g. ITP
Management
patients who have no indications for treatment are monitored with regular blood counts
fludarabine, cyclophosphamide and rituximab (FCR) has now emerged as initial treatment of choice for the majority of patients
ibrutinib may be used in patients who have failed a previous therapy
poor prognostic factors of CLL ?
deletions of part of the short arm of chromosome 17 (del 17p) are seen in around 5-10% of patients and are associated with a poor prognosis
CD38 expression positive
TP53 mutation
male sex
age > 70 years
lymphocyte count > 50
prolymphocytes comprising more than 10% of blood lymphocytes
lymphocyte doubling time < 12 months
raised LDH
CD38 expression positive
TP53 mutation
good prognosis of CLL
deletion of the long arm of chromosome 13 (del 13q) - most common abnormality, being seen in around 50% of patients. associated with a good prognosis