Pharmacy Services Chemotherapy Induced Nausea and Vomiting Haley Gill, BSP VCH-PHC Pharmacy Resident...

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Chemotherapy Induced Nausea and Vomiting

Haley Gill, BSPVCH-PHC Pharmacy Resident 2009-2010

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Outline

• Review the pathophysiology of chemotherapy induced nausea and vomiting (CINV)

• Review the different categories of CINV• Review the pharmacologic agents indicated

for CINV• Review the current guidelines for CINV

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Consequences of CINV

• medical complications– electrolyte imbalances– dehydration

• quality of life– impact daily functioning

• compliance with chemotherapy

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Pathophysiology of CINV

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Pathophysiology of CINV

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Classification of CINVAcute within 24 hours of chemotherapy

Delayed occurs > 24 hours after chemotherapy

Anticipatory prior to chemotherapy

Breakthrough while receiving prophylactic antiemetics

Refractory Not responsive to therapy

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Neurotransmitter Involvement

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Risk Factors

• Young age

• Female

• History of low alcohol intake

• Experience of emesis during pregnancy

• Emetogenic potential of chemotherapeutic agent

• History of motion sickness

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Antiemetic Agents

• Serotonin 5-HT3 Receptor Antagonists (5-HT3 RA)

• Corticosteroids• Dopamine-Serotonin Receptor Antagonists• Dopamine Receptor Antagonists• Neurokinin-1 Receptor Antagonists (NK-1

RA)• Benzodiazepines• Cannabinoids

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Serotonin 5-HT3 RA’s

• Block 5-HT3 receptors in the CNS and GI tract

• Equivalent in efficacy and toxicities

• More effective for acute CINV

• AE’s: headache, constipation, QTc interval prolongation

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Serotonin 5-HT3 RA’s

Available Agents Recommended Dose

Ondansetron (Zofran®) IV: 8 mg or 0.15 mg/kg

PO: 8 - 24 mg

dolasetron (Anzemet®) IV: 100 mg or 1.8 mg/kg

PO: 100 mg

granisetron (Kytril®) IV: 1 mg or 0.01 mg/kg

PO: 1 - 2 mg

**single-daily dose schedules are similar in efficacy to multiple-daily dosing**

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Corticosteroids

• Dexamethasone (Decadron®)

• Dose: 8 - 20 mg IV or PO

• Effective for both acute and delayed CINV

• MOA: unknown

• AE’s: Insomnia, hyperglycemia, heartburn

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Dopamine-Serotonin Receptor Antagonists

• Metoclopramide (Maxeran®) • 10-30 mg IV/PO Q4-6H ac

• Domperidone (Motilium®)• 10-20 mg PO Q4-6H ac

doses = dopamine antagonist effects doses = serotonin antagonist effects

• AE’s: sedation, EPS, diarrhea• Diphenhydramine (Benadryl®) may EPS

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Dopamine Receptor Antagonists

• prochlorperazine (Stemetil®)• 5 -10 mg IV/PO Q6H

• haloperidol (Haldol®)• 0.5 – 2 mg PO/SC Q6-12H

• MOA: block dopamine receptors in the CTZ

• AE’s: EPS, disorientation, sedation

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Neurokinin-1 Receptor Antagonists• Aprepitant (Emend®), Fosaprepitant (IV)

• Dose: 125 mg PO on day 1 then 80 mg PO daily on days 2 & 3

• MOA: blocks NK-1 receptor in brainstem emetic center & GI tract

• AE’s: fatigue, asthenia, hiccups

• Drug interactions: dose of dexamethasone by 50%

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Other AgentsAgent Dose Use

Lorazepam (Ativan ®)

0.5 - 2 mg IV/PO/SL Anticipatory N&V

Cannabinoids• dronabinol (Marinol®)• nabilone (Cesamet®)

2.5 – 10 mg PO TID - QID

Refractory & Breakthrough N&V

Olanzapine (Zyprexa®)

2.5 – 10mg PO hs Acute, Delayed & Refractory N&V

Gabapentin (Neurontin®)

Delayed

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Chemotherapy Emetic Risk GroupsHigh Risk in nearly all patients (>90%)

• Cyclophosphamide (high dose), cisplatin

Moderate Risk in 30% to 90% of patients• Daunorubicin, cytarabine (high dose), melphalan (high dose), azacitadine

Low Risk in 10% to 30% of patients• fludarabine, cytarabine (low dose)

Minimal Fewer than 10% at risk• bortezomib, vincristine, hydroxyurea

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Guidelines

• Multinational Association of Supportive Care in Cancer (MASCC)

• American Society of Clinical Oncology (ASCO)

• National Comprehensive Cancer Network (NCCN)

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Highly Emetogenic ChemotherapyAcute Delayed

MASCC 5-HT3RA + dexamethasone + aprepitant

Dexamethasone + aprepitant

ASCO 5-HT3RA + dexamethasone + aprepitant

Dexamethasone + aprepitant

NCCN 5-HT3RA + dexamethasone + aprepitant ± lorazepam

Dexamethasone + aprepitant ± lorazepam

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Moderately Emetogenic Chemotherapy

Acute Delayed

MASCC 5-HT3RA + dexamethasone

Dexamethasone or 5-HT3RA

ASCO 5-HT3RA + dexamethasone

Dexamethasone or 5-HT3RA

NCCN 5-HT3RA + dexamethasone ± lorazepam

Dexamethasone or 5-HT3RA ± lorazepam

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Low Emetogenic Chemotherapy

Acute Delayed

MASCC dexamethasone No Routine Prophylaxis

ASCO dexamethasone

NCCN dexamethasone ± lorazepam orprochlorperazine ± lorazepam ormetoclopramide ± lorazepam

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Minimal Emetogenic Chemotherapy

Acute Delayed

MASCC No Routine Prophylaxis

No Routine Prophylaxis

ASCO

NCCN

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Rescue Therapy

• Add an agent from another class

• phenothiazine, metoclopramide, or dexamethasone

• 5-HT3 RA unlikely to be beneficial if N & V developed with 5-HT3 RA prophylaxis

• Aprepitant NOT for established N & V

• Consider non-chemo causes

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Refractory Therapy

• Consider adjusting pre and post chemo regimen

• Little data

• Some evidence for aprepitant & palonosetron (not in Canada)

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Patient Education

• Very important!!

• Instruct patients to take their rescue drugs when nausea first begins

• May need to use regularly scheduled rescue drugs

• Additional doses of 5-HT3 RA not more effective than other rescue drugs

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CostDrug Cost/day

Aprepitant ~$33.00, $99.60 (tri-pack)

Ondansetron IV $1.80

PO $8.70

Dexamethasone IV $1.52

PO $1.64

Lorazepam IV $0.48

PO $0.05

Metoclopramide IV $11.60

PO $0.72

Prochlorperizine IV $4.68

PO $0.56

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Questions?

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References1. Kris MG, et al. American Society of Clinical Oncology Guideline for

Antiemetics in Oncology: Update 2006. J Clin Oncol 2006;24(18):2932-47

2. Hesketh PJ. Chemotherapy-Induced Nausea and Vomiting. N Engl J Med 2008;358:2482-94

3. Baker PD, et al. The Pathophysiology of Chemotherapy-Induced Nausea and Vomiting. Gastroenterology Nursing 2005;28(6):469-80

4. Navari RM. Pharmacological Management of Chemotherapy-induced Nausea and Vomiting: Focus on Recent Developments. Drugs 2009;69(5):515-33

5. Jordan K, et al. Guidelines for Antiemetic Treatment of Chemotherapy-Induced Nausea and Vomiting: Past, Present, and Future Recommendations Oncologist 2007;12;1143-1150

6. Multinational Association of Supportive Care in Cancer Antiemetic Guidelines (last update: March 2008). Available at www.mascc.org

7. National Comprehensive Cancer Network Antiemetic Guidelines 2007. Available at www.nccn.com

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Emetic Risk

Prophylaxis of acute CINV on day of chemo administration

Prophylaxis of delayed CINV

High 5-HT3RA + dexamethasone + aprepitant Days 2 & 3 after Chemotherapy: dexamethasone + aprepitant

Moderate Anthracycline + Cyclophosphamide:

5-HT3RA + dexamethasone + aprepitant Days 2 & 3 after chemotherapy: aprepitant

All other regimens of moderate emetic risk:

5-HT3RA + dexamethasone Days 2-4 after chemotherapy: dexamethasone or 5-HT3RA

Low Dexamethasone None

Minimal None None