leukemia Flashcards

1
Q

AML characteristics

A

most common leukemia in older adults

most idiopathic, trisomy 21, or therapy-induced, myelodysplastic syndrome

DX: bmbx w 20% blasts

symptom onset < 3 months

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2
Q

heme malignancy symptomatology

A

fatigue, anorexia, weight loss, fever, bruising/bleeding

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3
Q

AML labs

A

anemia, reduced reticulocyte count
leukocytosis/leukopenia
thrombocytopenia, odd shapes

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4
Q

AML exam findings

A

fever
splenomegaly
hepatomegaly
lymphadenopathy

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5
Q

general supportive care

A

central venous access

transfusions (hgb >7, plt >10 unless bleeding then 20)

acute infection monitoring - filgrasim 24 hr after chemo

prophylaxis - antiviral (acyclovir), anti fungal (fluconazole), PJP (bactrim)

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6
Q

AML treatment

A

induction - 7+3 regimen = cytarabine and daunorubicin

evaluate for response w BMBx (<5% blasts)

SCT for <60 yrs

continued chemotherapy to prevent relapse in select patients

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7
Q

ALL characteristics

A

greatest risk in first 5 years of life

unknown cause, some genetic risks

DX: BMBX, peripheral blood smear, LP

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8
Q

ALL symptomatology

A

B symptoms - fever, chills, night sweats, weight loss

fatigue, easy bruising

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9
Q

ALL labs

A

pancytopenia

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10
Q

ALL treatment

A

pediatric-inspired regimens

induction, consolidation, maintenance phases

intense inpatient regimen for 3 months

SCT

4+years of therapy probable

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11
Q

CML characteristics

A

mean age at diagnosis 55-65
RF: radiation

Philadelphia chromosome 90% cases

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12
Q

CML symptomatology

A

fatigue, anemia, splenomegaly

weight loss if high cell burden

hyperviscocity events - MI, CVA, visual changes, dyspnea, confusion

blast phase - fever, weight loss, bone/joint pain, bleeding and thrombotic events, infections

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13
Q

CML physical exam

A

hepatomegaly
splenomegaly
lymphadenopathy
infection?
petechiae/purpura?

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14
Q

CML labs

A

leukocytosis w left shift
thrombocytosis
thrombocytopenia (rare)
anemia

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15
Q

CML diagnosis

A

BMBx- hyper cellular with myeloid hyperplasia & high myeloid-to-erythroid ratio

blasts <5%

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16
Q

CML treatment

A

BCR-ABL1 tyrosine kinase inhibitors
BCR-ABL1 oncoprotein synthesis inhibitor

SCT - 2nd/3rd line

17
Q

CLL characteristic

A

cancer of older adults

proliferation of mature B lymphocytes

can be very stable, many do not require treatment at time of dx

prognosis - IGHV

18
Q

CLL diagnosis

A

most incidental on CBC

flow cytometry

no BMBx!!!!

19
Q

CLL treatment

A

watchful waiting
criteria for starting treatment: bone marrow failure, splenomegaly, hepatomegaly, constitutional symptoms

chemo - FCR (fludarabine, cyclophosphamide, rituximab)

SCT only curative (but not many candidates)