CMML Flashcards

1
Q

Defining lab feature

A

absolute monocytosis for >3 months

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2
Q

CMML classification

A

overlap syndrome between MDS and MPN (Shared features of both)

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3
Q

what are the hypomethylating agents?

A

azacitidine or decitabine

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4
Q

Clinical behavior

A
  • among most aggressive chronic leukemias with a propensity to progress to AML
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5
Q

CMML patients are at risk for transformation to what + frequency of progression?

A
  • AML
  • 15-30 percent
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6
Q

Staging depends on

A

Percentage of blasts in peripheral blood and bone marrow

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7
Q

Management of higher risk CMML

A

IF medically fit, HSCT
IF not a transplant candidate, HMA or hydrea

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8
Q

Management of lower risk

A

Given asymptomatic and no indication for treatment, plan for active surveillance
Indications for treatment:
Constitutional/systemic symptoms (eg, fever, weight loss)
Organ involvement (eg, symptomatic splenomegaly, skin disease, renal dysfunction, pulmonary involvement)
Alterations in blood counts (eg, worsening cytopenias, increasing blast percentage, hyperleukocytosis, leukostasis)
Given indication for treatment, plan for HMA vs. hydrea

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9
Q

Monocyte threshold for CMML diagnosis

A

1000 monocytes/microliter

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10
Q

Monocyte threshold for CMML diagnosis if a mutation is present

A

500 monocytes/microliter

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11
Q

Most common CMML mutations

A

TET2
SRSF2
CBL

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