Oncology Supportive Care Flashcards

1
Q

When should prophylactic antiemetics be used? ie emetogenic class of chemo and radiation

A

moderately or highly emetogenic chemo agents and highly emetogenic radiation

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2
Q

What chemo agents are best known for delayed N/V?

A

cisplatin
doxorubicin/cyclophosphamide

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3
Q

How many days should patients be protected for full period of risk for NV?

A

3 days if highly emetogenic and 2 days if moderately

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4
Q

What anti-emetogenic regimen is used for highly emetogenic chemo and radiation?

A

-Neurokinin (NK1) receptor antagonist
-Serotonin receptor antagonist
-Dexamethasone
+/- OLZ
+/- Lorazepam
+/- H2RA or PPI

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5
Q

What anti-emetogenic regimen is used for moderately emetogenic chemo and radiation?

A

-Serotonin receptor antagonist
-Dexamethasone
+/-Neurokinin (NK1) receptor antagonist

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6
Q

What are the most common serotonin-3 receptor antagonists?

A

dolasetron, granisetron, ondansetron, and palonosetron

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7
Q

What are some special considerations to take into account when prescribing palonosetron?

A

Half-life is ~40 hours, generally just give one dose
-PO can be given as combo product with NK1 antagonist

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8
Q

When should corticosteroid antiemetics be avoided?

A

-Immune checkpoint inhibitors when administered without cytotoxic chemo
-avoid for 3-5 days before and 90 days after CAR T-cell therapies

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9
Q

What are the most common NK1 receptor antagonists?

A

-aprepitant
-fosapripant
-rolapitant

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10
Q

When can NK1 receptor antagonists be used alone?

A

never, must be used in combo with serotonin receptor antagonists and dex

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11
Q

Common NK1 DDI?

A

Metabolized by CYP 3A4 and minor metabolism by CYP1A2 and CYP2C19
-oral contraceptives
-warfarin
-caution with R-CHOP

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12
Q

Common side effects of NK1 RAs?

A

Headachem asthenia, dyspepsia, constipation

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13
Q

What emesis treatment should be used for highly emetogenic oral chemo?

A

-Serotonin antagonist
+/- Lorazepam
+/- H2RA or PPI

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14
Q

What antiemetic should be used for low emetogenic risk oral chemos?

A

Metoclopramide OR prochlorperazine or serotonin RA

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15
Q

What is the MOA of benzamide analogs? What is the most common benzamide analog?

A

MOA -blockage of Dopamine receptors, stimulation of cholinergic activity in gut, increase gut motility
Ex: metoclopramide

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16
Q

What is the MOA of phenothiazines? What are the most common phenothiazines?

A

MOA: block dopamine receptors
Ex: prochlorperazine, chlorpromazine, promethazine

17
Q

When should bisphosphinates be started in patients with breast cancer?

A

Start in pts with evidence of bone metastases
-Give pamidronate or zolendronic acid every 3-4 weeks

18
Q

When does the nadir generally occur?

A

10-14 days after chemo administration

19
Q

How is the ANC calculated?
If the WBC is 4500 and 10% segmented neutrophils and 5% band neutorophils what is the ANC?

A

ANC= WBC x percentage of granulocytes or neutrophils
4500 (0.1+0.05)= 675

20
Q

What is the WBC, ANC, and platelet count cut off to determine if a PT should receive chemo?

A

WBC >3000, ANC >1500, platelet count >100,000

There are exceptions to these rules

21
Q

What is the definition of neutropenia?

A

ANC <500 or count of less than 1000 with a predicted decrease to less than 500 during the next 48 hours

22
Q

What ANC indicates a CSF should be used?

A

-As primary prophylaxis which chemo regs associated with 20% or greater risk of febrile neutropenia, continue until post-nadir ANC is >10,000
-Use as secondary prophy if post-nadir ANC is

23
Q

When should CSF be used for patients with established neutropenia?

A

PT who have febrile neutropenia and risk factors for complications

24
Q

How should macrocytic anemia be treated?

A

IM or PO vitamin B12 replacement

25
Q

What are common erythropoiesis-stimulating agents [ESAs]. When are they approved to be used?

A

Epstein and darbepoetin Alfa
-Can be used for chemo associated (not cancer associated) anemia once Hgb <10

26
Q

What is dexrazoxane?

A

Chelating agent to decrease anthracycline-induced free radical damage

27
Q

What are examples of anthracyclines?

A

-Suffix “rubicin”
Danorubicin, doxorubicin, idarubicin, epirubicin

28
Q

What is amifostine? Why is it not commonly used in clinical practice?

A

Prevents nephrotoxicity from cisplatin, can cause dangerous hypotension

29
Q

When is mesna used and why?

A

Used when acrolein is present in the bladder, Acrolein is a metabolite of cyclophosphamide and ifosfamide and mesna inactivates Acrolein and prevents its interaction with the bladder

30
Q

When does leucovorin need to be used?

A

may be used after methotrexate doses >100 mg/m2 and should be used in doses >500mg/m2,
-Continue until 24048 hour methotrexate level is <0.1mM

31
Q

What are factors that increase likelihood of methotrexate toxicity?

A

Renal dysfunction, third-space fluid

32
Q

What kind of toxicity does methotrexate cause?

A

Mucous membrane toxicity, renal and hepatic toxicity, CNS toxicity and myelosupprossion

33
Q

What is Glucarpidase?

A

Carboxypeptidase indicated for treating toxic methotrexate concentrations ( do not give leucovorin within 2 hours before or after a dose of glucarpidase)

34
Q

Should you use heat, cold, hyaluronidase, or sodium thiosulfate for doxorubicin, danorubicin, and epirubicin?

A

Cold

35
Q

Should you use heat, cold, hyaluronidase, or sodium thiosulfate for vincristine, vinblastine, and vinorelbine?

A

Heat

36
Q

Should you use heat, cold, hyaluronidase, or sodium thiosulfate for mecholrethamine?

A

Sodium thiosulfate

37
Q

Should you use heat, cold, hyaluronidase, or sodium thiosulfate for vinal alkaloids?

A

Hyaluronidase