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Exam (elaborations)

BCPS - Oncology Supportive Care Exam Questions With Correct Answers

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BCPS - Oncology Supportive Care Exam Questions With Correct Answers ...

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BCPS - Oncology Supportive Care Exam Questions
With Correct Answers


Time frame for "acute" onset vomiting? - ANSWER 0-24 hours after chemo
administration



Time frame for "delayed" onset vomiting? - ANSWER >24 hours after chemo
administration



What "risk factor" actually decreases the incidence of emesis? - ANSWER History of
chronic alcoholism



What is the % cut-offs for ematogenicity of chemotherapy agents? - ANSWER Highly
emetic - >90% risk of emesis

Moderately emetic - >30 to 90% risk of emesis

Low emetogenicity - 10 to 30% risk of emesis

Minimally emetic - <10% risk of emesis



Recommended treatment regimen for CINV prevention for Cisplatin and other highly
emetogenic single agents - ANSWER DAY 1:

- NK1R antagonist PLUS

- 5-HT3 receptor antagonist PLUS

- Dexamethasone 12 mg IV/PO PLUS

- Olanazpine 10 mg



DAYS 2-4:

Dexamethasone and Olanzapine

, (if aprepitant used on Day 1, continue that on days 2 & 3. Otherwise NK1R antagonists
are just on Day 1)



Dexamethasone - 20 mg if used with rolipripitant or NO NK1R antagonist



Recommended treatment regimen for CINV prevention for Anthracycline combined with
cyclophosphamide in breast cancer - ANSWER Same as the Cisplatin regimen but no
dexamethasone on days 2-4 - not enough data to support it's use in this group.



DAY 1:

- NK1R antagonist PLUS

- 5-HT3 receptor antagonist PLUS

- Dexamethasone 12 mg IV/PO PLUS

- Olanazpine 10 mg



DAYS 2-4:

Olanzapine



Recommended treatment regimen for CINV prevention for Anthracycline combined with
cyclophosphamide in other cancers other than breast cancer? - ANSWER
Dexamethasone PLUS palonsetron



Recommended treatment regimen for CINV prevention for moderately-ematogenic,
carboplatin-based regimens - ANSWER ONCE doses of the following (ie no therapy past
day 1)

NK1R antagonist PLUS

5HT3 receptor antagonist PLUS

Dexamethasone



Recommended treatment regimen for CINV prevention for moderately-ematogenic,

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