complications of N/V
limited
- dehydration
- electrolyte
- abnormalities
- fatigue
- depression
before 5-HT3 anti-emetics, it was expected to vomit 5-12 times per day
Types of N/V
anticipatory
- ___ response conditioned by severity and duration of previous emetic reactions from prior cycles of chemo
- non-PCOL like hypnosis helpful
- can be provoked by sight, sound, or smell
learned
cancer patients have hightened senses
Types of N/V
Acute
- emetic response correlating with the administration of chemo
- within __ hours of receiving chem
Delayed
- Related to chemotherapy occurring > ___ hours following completion of chemotherapy
– Mechanism is not fully understood, but there is ↑
evidence that substance P binding to ___ receptor may play a role
24
24
neurokinin 1
Types of N/V
Breakthrough
- occurs even if on scheduled anti-emetics ___ to chemotherapy
Refractory
- persists despite ___ anti-emetics
- Failed other therapies
Patho of CINV
Neurotransmitters implicated in CINV (5)
highly emetogenic chemo (level 5)
single agent
Combo Chemo
when considering combo chemo, need to consider emetogenicity
- level 1 or 2 agents do not contribute to the emetogenicity of the regimen
- adding level 3 or 4 ___ the emetogenicity of the combo by 1 level per agent
- add the different levels together to decide on which antiemetics to use
increasing
Oral Anticancer Agents
Moderate to high emetic risk:
(≥ 30% risk) Prophylaxis required on days of oral anticancer agent administration
Oral Anticancer Agents
Moderate to high emetic risk:
(≥ 30% risk) As needed dosing is initially appropriate on days of oral anticancer agent administration
risk factors for CINV
treatment guidelines
___ for acute N/V is based on the emetogenic potential of chemo
- ___ receptor antagonists may be substituted for each other
- oral efficacy = IV efficacy
prophylaxis
- 5HT3
highly emetogenic regimens
A) 4 drug
B) 3 drug
C) 3 drug
A) NK-1 antagonist, steroid, 5-HT3 antagonist, atypical anti-psychotic
B) atypical antipsychotic, 5HT-3 antagonist, steroid
C) NK-1 antagonist, steroid, 5-HT3 antagonist
These 3 agents can be added with any regimen and any emetogenicity if patients are experiencing these toxicities
+/- Lorazepam 0.5 mg to 2 mg PO or IV or sublingual either every 4 or 6 hours as needed
+/- H2 blocker or proton pump inhibitor
moderately emetogenic
A) 2 drug
B) 3 drug
C) 3 drugs
low emetogenic regimens
only 1 needed
- steroid ( ___ )
- metoclopramide
- prochlorperazine
- 5-HT3 (3)
Breakthrough Nausea and Vomiting
give an additional agent from a different drug class as needed
Depending on the severity of the N/V, you can schedule these agents
Delayed Nausea and Vomiting
typically involves use of one of the following (3)
Anticipatory N/V
___ - Use optimal antiemetic therapy during
every cycle of treatment
___ - 0.5 to 1 mg orally beginning the night before treatment and then again 1 to 2 hours prior to beginning of
chemotherapy
other prevention guidelines
Oral chemotherapy - High to moderate emetogenic risk
- Start ___ chemotherapy and continue daily
- ___ antagonists
Low to minimal emetogenic risk
- Start ___ chemotherapy and maybe given daily or prn
– ___
– ___
– ___ antagonists
Other Prevention Guidelines
Radiation Induced Emesis
- Start pretreatment for each day of radiation
therapy
- ___ PO +/- dexamethasone
- ___ PO +/- dexamethasone
Granisetron
Ondansetron
Radiopharmaceuticals
Recommendations for antiemetics include:
- ___ or ___ antagonists
- NOT ___ due to down regulation of somatostatin receptors
Common Toxicities Across Classes
Serotonin (5-HT3) antagonists
- Ondansetron
- Granisetron
- Dolasetron
- Palonosetron single agent or combination products (+/- netupitant
or fosnetupitant)
Common Toxicities Across Classes
Corticosteroids
- Dexamethasone
(Short term use):
- Anxiety
- euphoria
- insomnia
- hyperglycemia
- ↑’d appetite