5. Cancer case studies - chronic myeloid leukaemia Flashcards

1
Q

What is meant by a ‘myeloproliferative disorder’?

A

Where blood cells proliferate and develop with no control and they can accumulate

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2
Q

What is the cell of origin in CML?

A

Pluripotent stem cells

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3
Q

How can CML be recognised from a blood smear?

A

Increase in granulocytes

Hypersegmented nuclei

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4
Q

What are granulocytes?

A

WBCs with granules within them e.g. oesinophils and basophils

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5
Q

What are the two types of cell proliferation in CML?

A

Increased erythropoiesis - RBCs

Increased WBCs - leukaemia

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6
Q

Why is there hepatosplenomegaly in CML?

A

Because of the increased erythropoiesis - cell production shifts from the bone marrow to the spleen and the liver

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7
Q

What is the treatment for CML?

A

Chemotherapy (toxicity)
Stem cell transplant (risk of rejection)
Small molecule targeted therapy - tyrosine kinase inhibitors

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8
Q

What is the main TKI used to treat CML?

A

Imatinib

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9
Q

What are the three main TKIs used to treat CML?

A

Imatinib
Nilotinib
Dasatinib

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10
Q

What is the most common mutation responsible for CML?

A

Reciprocal mutation - chromosomes 9 and 22 - PHILADELPHIA CHROMOSOME

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