Side effect management Flashcards

1
Q

Interventions being investigated to prevent chemo induced peripheral neuropathy

A

Cryotherapy (some evidence but no proof)
Compression therapy (tight gloves, some evidence)
Exercise (some evidence)

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2
Q

Interventions being investigated to treat chemo induced peripheral neuropathy

A

1) Stop chemo short (decide on risk/benefit of further chemo)
2) Duloxetine (cymbalta) (proven efficacy)
3) Some data for acupuncture

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3
Q

Neuropathy caveat

A

Neuropathy can continue to worsen even after you stop chemo

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4
Q

Management of cancer cachexia

A
  • Refer to nutrition
  • Shift from 3 meals a day, to frequent high calorie, nutrient dense snacks
  • No parenteral or tube feeding
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5
Q

Definition of cancer cachexia

A

Loss of appetite, weight, and skeletal muscle

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6
Q

pharmacologic management of cancer cachexia supported by evidence

A

There are no FDA approved drugs to treat cancer cachexia but there is data for the following:

  • progesterone analogs (megestrone acetate or megace). Associated with modest weight gain (but its fat, not skeletal muscle) and will increase QOL.
  • corticosteroids (improved appetite + weight gain (fat, not muscle) wellbeing)
  • Optimal dosing and timing unknown
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7
Q

pharmacologic management of cancer cachexia NOT supported by evidence

A

dronabinol/cannabinoids (insufficient data per ASCO and high fall risk in elderly)

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8
Q

Checkpoint inhibitors and emetogenic potential?

A

little to none

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9
Q

Are steroids contraindicated with checkpoint inhibitors?

A

No, still have demonstrated efficacy (this is an issue in combination studies with emetogenic chemo)

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10
Q

primary classes (mechanisms) of drugs used for chemo induced nausea

A

NK1, 5-Ht3 receptor antagonists, steroids

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11
Q

pulmonary side effect now being associated with CPI’s

A

ILD

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12
Q

Definition of GCSF for primary prophylaxis

A

Primary prophylaxis refers to the initiation of G-CSFs during the first cycle of myelosuppressive chemotherapy, with the goal of preventing neutropenic complications throughout all of the chemotherapy cycles.

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13
Q

Neulasta formulation

A

One time injection

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14
Q

neupegen vs neulasta in terms of MOA and formulation

A

neupegen – binds to GCSF receptor, which you continue until counts recover
neulasta – binds irreversibly to receptor until it leaves the marrow, so you only need to give it once. (either sc injection or on body injector that automatically gives injection).

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15
Q

RF’s for severe emesis

A

Age and gender (young females get the worst, older men do better, especially alcoholics)

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16
Q

Timeline of emesis with chemo

A
  • typically within first few hours
  • some highly emetogenic chemo, you can have delayed reaction
  • some patients get anticipatory emesis but less common these days with better antiemetics
17
Q

risk stratification of chemo emetogenesis

A

low, medium, or high risk

18
Q

what is asthenia

A

decreased muscle strength

19
Q

2 major categories of drugs that can be used to treat neutropenia

A

1) recombinant human granulocyte colony stimulating factor (G-CSF; filgrastim and pegylated filgrastim)
2) granulocyte-macrophage colony stimulating factor (GM-CSF; sargramostim)

20
Q

next step after diagnosing mucositis

A

Ask patient if it interferes with eating/oral intake

21
Q

Management of immune therapy Grade III myocarditis

A
  • permanently discontinue immunotherapy

- Start high dose steroids

22
Q

Cetuximab mechanism

A

EGFR inhibitor

23
Q

Steroid sparing agent for immunotherapy related hepatotoxicity

A

ATG or mycophenolate (depending on severity) (NOT INFLIXIMAB, which can cause LFT elevations)

24
Q

Antiemetics for patients receiving a highly emetogenic chemo

A
3 drug combination:
*NK-1 receptor antagonist
5-HT3 receptor antagonist
Dexamethasone
**Many also give olanzapine
25
Q

Aprepitant MOA

A

Neurokinin 1 receptor antagnist

26
Q

How antiemetics are determined

A

Emetogenic risk category of chemo:
High
Moderate
Low

27
Q

Antiemetics for moderately emetogenic chemo

A

Two-drug combination:
Palonosetron
Dexamethasone

28
Q

Antiemetics for low emetogenic chemo

A

5-HT3 receptor antagonist

29
Q

Chemo regimens and drugs with high emetic risk

A
  • Adriamycin/cyclophosphamide
  • Cisplatin
  • Cyclophosphamide
  • Dacarbazine
  • Ifosfamide
  • Streptozocin