Chemotherapy Induced Nausea
& Vomiting
Dhaval B. Joshi
Background
• Systemic chemotherapy – very frequently
causes nausea and vomiting
• Affects Patient’s Quality of life
• Leading to poor compliance
Factors affecting CINV
Specific therapeutic agents used
Dosage of the agents
Schedule and ROA of the agents
Target of the RT
Individual patient variability
Few imp. Points on NV
• More nausea than vomiting
• Younger r more likely to have Nausea than
older
• Younger women more prone than others
Types of NV
Acute
Delayed
Anticipatory
Breakthrough
Refractory
Classification of Emesis causing
Chemotherapeutic Agents
Moderate Emetic Risk
Anti-emetic Agents
• 5-hydroxytryptamine3 [5-HT3] receptor
antagonists
• Neurokinin 1 (NK-1) receptor antagonists:
Aprepitant
• Corticosteroids
Anti-emetic Agents
• Metoclopramide
• Butyrophenones
• Phenothiazines
• Cannabinoids
• Olanzapine
• Benzodiazepines
Management
• High emetogenic chemotherapy
• Moderate emetogenic chemotherapy
• Low/ Minimal emetogenic chemotherapy
Recommendations for preventing
Emesis for different conditions
• Multiday Chemotherapy: 5-HT3 Anta + steroid
• Combination Chemotherapy/ Concurrent
Chemotherapy and Radiation Therapy:
Combinations of anti-emetics
Paediatric Patients
• Combination of a 5-HT3 antagonist and
corticosteroid is suggested before
chemotherapy
Anticipatory CINV
• The NCCN guidelines provide
recommendations for additional medical
treatment, including the following:
• Alprazolam, PO: 0.5–2 mg TID, beginning the
night before treatment; or
• Lorazepam, PO: 0.5–2 mg, given the night
before and the morning of treatment
Delayed CINV
• NCCN considers intravenous palonosetron the
most effective 5-HT3 antagonist for preventing
delayed CINV and
• Recommends using aprepitant in patients
undergoing chemotherapy with an
anthracycline
Breakthrough CINV
General rule of thumb
• Cisplatin – Index agent used in clinical trials as
high emetogenic
• If you have mixture of varying levels of
emetogenic potential, err on the side of the
caution
General rule of thumb
• Make sure to wait at least for 30 minutes after
completion of IV anti-emetic pre-medications
before starting chemotherapy infusions
• Anti-emetics aren't for only Day-1
General rule of thumb
• Palanosatron and NK-1 antagonists are used
only for patients receiving high or moderate
emetogenic chemotherapy
• If patient develops breakthrough CINV, add
agent from different drug class that was not
used prophylactically
General rule of thumb
• Avoid trigger foods
• Recommend frequent snacking in between
meals
• Look towards patient’s hydration status
Case study
• AB is 35 yrs old F with newly diagnosed stage
III Large B cell Lymphoma. She has PMHx of
HTN, DM and severe motion sickness.
• Chemotherapy regimen ordered: R-CHOP
every 3 weeks for 6 cycles
Case study
• Rituximab 375 mg/m2
• Cyclophospahmide 750 mg/m2 IV on day 1
• Doxorubicin 50 mg/m2 IV on day 1
• Vincristine 1.4 mg/m2 IV on day 1
• Prednisone 100 mg PO daily day 1-5
Case study
Take home Medications:
• Prochlorperazine 10 mg PO q6-8 hrs as needed
for breakthrough nausea
• Docusate 100 mg PO daily as needed for
constipation
• Magic mouth wash QID as needed for mouth care
Questions
1. How would you classify the emetogenic
potential of R-CHOP regimen?
a.) Highly emetogenic
b.) Moderately emetogenic
c.) Low emetogenic
d.) Minimally emetogenic
e.) Not emetogenic
Questions
2. What risk factors does AB have for the
development of CINV?
a.) Age
b.) Gender
c.) Highly emetogenic chemotherapy
d.) Motion sickness history
e.) All of the above
Questions
3. Which is the appropriate anti-emetic
premedication regimen for AB?
????
THANK U

Chemotherapy induced Nausea and Vomiting (CINV) - Dhaval joshi

  • 1.
    Chemotherapy Induced Nausea &Vomiting Dhaval B. Joshi
  • 3.
    Background • Systemic chemotherapy– very frequently causes nausea and vomiting • Affects Patient’s Quality of life • Leading to poor compliance
  • 4.
    Factors affecting CINV Specifictherapeutic agents used Dosage of the agents Schedule and ROA of the agents Target of the RT Individual patient variability
  • 6.
    Few imp. Pointson NV • More nausea than vomiting • Younger r more likely to have Nausea than older • Younger women more prone than others
  • 7.
  • 8.
    Classification of Emesiscausing Chemotherapeutic Agents
  • 10.
  • 13.
    Anti-emetic Agents • 5-hydroxytryptamine3[5-HT3] receptor antagonists • Neurokinin 1 (NK-1) receptor antagonists: Aprepitant • Corticosteroids
  • 14.
    Anti-emetic Agents • Metoclopramide •Butyrophenones • Phenothiazines • Cannabinoids • Olanzapine • Benzodiazepines
  • 15.
    Management • High emetogenicchemotherapy • Moderate emetogenic chemotherapy • Low/ Minimal emetogenic chemotherapy
  • 16.
    Recommendations for preventing Emesisfor different conditions • Multiday Chemotherapy: 5-HT3 Anta + steroid • Combination Chemotherapy/ Concurrent Chemotherapy and Radiation Therapy: Combinations of anti-emetics
  • 17.
    Paediatric Patients • Combinationof a 5-HT3 antagonist and corticosteroid is suggested before chemotherapy
  • 18.
    Anticipatory CINV • TheNCCN guidelines provide recommendations for additional medical treatment, including the following: • Alprazolam, PO: 0.5–2 mg TID, beginning the night before treatment; or • Lorazepam, PO: 0.5–2 mg, given the night before and the morning of treatment
  • 19.
    Delayed CINV • NCCNconsiders intravenous palonosetron the most effective 5-HT3 antagonist for preventing delayed CINV and • Recommends using aprepitant in patients undergoing chemotherapy with an anthracycline
  • 20.
  • 21.
    General rule ofthumb • Cisplatin – Index agent used in clinical trials as high emetogenic • If you have mixture of varying levels of emetogenic potential, err on the side of the caution
  • 22.
    General rule ofthumb • Make sure to wait at least for 30 minutes after completion of IV anti-emetic pre-medications before starting chemotherapy infusions • Anti-emetics aren't for only Day-1
  • 23.
    General rule ofthumb • Palanosatron and NK-1 antagonists are used only for patients receiving high or moderate emetogenic chemotherapy • If patient develops breakthrough CINV, add agent from different drug class that was not used prophylactically
  • 24.
    General rule ofthumb • Avoid trigger foods • Recommend frequent snacking in between meals • Look towards patient’s hydration status
  • 25.
    Case study • ABis 35 yrs old F with newly diagnosed stage III Large B cell Lymphoma. She has PMHx of HTN, DM and severe motion sickness. • Chemotherapy regimen ordered: R-CHOP every 3 weeks for 6 cycles
  • 26.
    Case study • Rituximab375 mg/m2 • Cyclophospahmide 750 mg/m2 IV on day 1 • Doxorubicin 50 mg/m2 IV on day 1 • Vincristine 1.4 mg/m2 IV on day 1 • Prednisone 100 mg PO daily day 1-5
  • 27.
    Case study Take homeMedications: • Prochlorperazine 10 mg PO q6-8 hrs as needed for breakthrough nausea • Docusate 100 mg PO daily as needed for constipation • Magic mouth wash QID as needed for mouth care
  • 28.
    Questions 1. How wouldyou classify the emetogenic potential of R-CHOP regimen? a.) Highly emetogenic b.) Moderately emetogenic c.) Low emetogenic d.) Minimally emetogenic e.) Not emetogenic
  • 29.
    Questions 2. What riskfactors does AB have for the development of CINV? a.) Age b.) Gender c.) Highly emetogenic chemotherapy d.) Motion sickness history e.) All of the above
  • 30.
    Questions 3. Which isthe appropriate anti-emetic premedication regimen for AB? ????
  • 31.