Acute Leukemia Flashcards

1
Q

What is leukemia, what are the two cancer types of leukemia

A

Cancer of the blood cell lines/ myeloid and lymphoid

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2
Q

T/F: Chronic leukemia need prompt treatment

A

False: Chronic is more indolent and sometimes doesn’t require treatment while acute needs prompt treatment

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3
Q

What are the risk factors for leukemia

A

genetic predisposition, acquired disease (MPD, aplastic anemia), occupational and enviornmental exposure, certain drugs

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4
Q

What therapies are associated with getting Acute myeloid leukemia (AML)

A

Alkylating agent (cyclophophamide, melaphalan, nitrogen mustard) causing abnormalities on chromosome 5 or 7/ Topoisomerase inhibitors (etoposide) causing abnormalities on 11q23 along with M4 and M5 morphologic features

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5
Q

How is acute leukemia differentiated from chronic leukemia

A

If a patient has blast percentage more than 20% it is acute leukemia, if a patient has a blast percentage less than 20% it is chronic leukemia

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6
Q

What are poor prognostic factors for leukemia

A

Advanced age (greater than 60), MDS or chemotherapy, cytogenetics and mutations, patients who do not have complete remission or remission less than 6 months, FAB subtype M6 and M7, elevated LDH

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7
Q

T/F: AML is easire to cure than ALL

A

True

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8
Q

What are the favorable cytogeneics for AML

A

t(15;17), inv(16), t(8;21)

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9
Q

How is AML diagnosed

A

Bone marrow biopsy

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10
Q

What are the two treatment stages for AML

A

Induction therapy (induce complete remission) and Post-remission therapy (eliminate undectable leukemia)

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11
Q

What is the Induction therapy for AML

A

Cytarabine 100-200 mg/m2 IVPB continous infusion over 24 hours for 7 days PLUS Daunorubicin 45-90 mg/m2 IV for 3 days (7 + 3)

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12
Q

T/F: Giving higher doses of Daunorubicin leads to higher outcomes of complete remission

A

True

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13
Q

What are the complications of Inductiion therapy for AML

A

Tumor lysis syndrome (prevent with hydration allopurinol and rasburicase), myelosupression

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14
Q

What is the post-remission therapy for AML with good to intermediate risk, low risk

A

High dose cytarabine 3g/m2 every 12 hours Day 1,3 and 5 for 3 to 4 cycles/ stem cell transplant

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15
Q

What are the two main complications of cytarabine

A

Neurotoxicity and Ocular toxicity (dexamethasone eye drops)

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16
Q

What is AML subtype with best prognosis and why

A

Acute promylegenous leukemia, has a clear mutation that defines it: t(15;17)

17
Q

What makes APL deadly if not treated

A

DIC due to promyelocytes packed with granules release tissue factors and acitivate the coagulation cascade

18
Q

What is the main medication that is given for APL, what is given if the patient has low to intermediate risk, high risk

A

All Trans Retinoic Acid (ATRA) 45mg/m2/day every 12 hours, arsenic trioxide, idarubicin

19
Q

What is given post remission for APL

A

ATRA PLUS Arsenic trioxide

20
Q

What is the MOA of ATRA

A

Induces proliferation of the abnormal clone of the maturation, differentiation and prognosis

21
Q

What patients should not get ATRA, other side effect

A

Not recommended to start in patients with WBC greater than 10,000 since retinoic acid syndrome is more likely/ QT prolongation

22
Q

What presentation of symptoms helps to differentiate between AML and ALL

A

CNS involvement (mental status changes, headaches)

23
Q

What are cytogenetics for ALL indicate a good prognosis, poor prognosis

A

Hyperploidy or del(9p)/ t(9;22), complex karyotype, t(8;14)

24
Q

What are the 4 stages for treating ALL

A

Induction, consolidation, delayed intensification, maintenance

25
Q

Why is CNS prophylaxis given to treat ALL, how is the CNS drugs given

A

Relapse in seen in Greater than 50% of patients surviving more than 2 years/ Intrathecal administration (methotrexate, cytarabine, hydrocortisone)

26
Q

What drugs are given for ALL induction

A

Anthracycline, vinicristine, corticosteroids, high dose cytarabine, methotrexate

27
Q

What is given for maintenance of ALL

A

6-MP, oral methotrexate, vinicristine, prednisone