Chemotherapy-Induced Nausea and Vomiting Prophylaxis
CHEMOTHERAPY-INDUCED NAUSEA AND VOMITING PROPHYLAXIS | ||||
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The recommended approach for the prevention and management of chemotherapy-induced nausea and vomiting (CINV) varies by the emetic risk of the treatment regimen. Adherence to antiemetic guidelines has resulted in improved control of nausea and vomiting, and improved adherence to chemotherapy regimen. The ASCO guideline provides updated recommendations for the prevention and management of nausea and vomiting due to antineoplastic agents for cancer. | ||||
ANTIEMETIC REGIMENS | ||||
Emetic risk category1,2 | Drug regimen | |||
High emetic risk | NK1 receptor antagonist + 5-HT3 receptor antagonist + dexamethasone + olanzapine | |||
Moderate emetic risk3 | 5-HT3 receptor antagonist + dexamethasone | |||
Low emetic risk | 5-HT3 receptor antagonist OR dexamethasone | |||
Minimal emetic risk | No routine antiemetic prophylaxis | |||
Breakthrough / Refractory | Add to standard antiemetic regimen: olanzapine or drug of a different class or benzodiazepine or dopamine receptor antagonist or cannabinoids | |||
ANTIEMETIC DOSING | ||||
Drug | Day 14 | Day 2 | Day 3 | Day 4 |
HIGH RISK | ||||
NK1 receptor antagonist3 | ||||
Aprepitant OR | 125mg PO or 130mg IV | 80mg PO (if oral aprepitant on Day 1) | 80mg PO (if oral aprepitant on Day 1) | |
FosaprepitantOR | 150mg IV | |||
Rolapitant OR | 180mg PO | |||
Fosnetupitant-palonosetron5 | 235mg/0.25mg IV | |||
Netupitant-palonosetron5 | 300mg/0.5mg PO | |||
5-HT3 receptor antagonist5 | ||||
Granisetron OR | 2mg PO OR 1mg or 0.01mg/kg IV OR 1 patch OR 10mg SC | |||
Ondansetron OR | 24mg PO (tabs or soluble film) OR 8mg or 0.15mg/kg IV |
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Palonosetron OR | 0.25mg IV | |||
Dolasetron | 100mg PO | |||
Corticosteroid | ||||
Dexamethasone6 | 12mg PO or IV7 | 8mg PO or IV7,8,9 | 8mg PO or IV7,8,9 | 8mg PO or IV7,8,9 |
Atypical Antipsychotic | ||||
Olanzapine | 10mg or 5mg PO | 10mg or 5mg PO8 | 10mg or 5mg PO8 | 10mg or 5mg PO8 |
Moderate risk3 | ||||
5-HT3 receptor antagonist | ||||
Granisetron OR | 2mg PO OR 1mg or 0.01mg/kg IV OR 1 patch OR 10mg SC | |||
Ondansetron OR | 8mg PO twice daily OR 8mg soluble film twice daily OR 8mg or 0.15mg/kg IV | |||
Palonosetron OR | 0.50mg PO OR 0.25mg IV | |||
Dolasetron | 100mg PO | |||
Corticosteroid | ||||
Dexamethasone3 | 8mg PO or IV | 8mg PO or IV10 | 8mg PO or IV10 | |
LOW RISK | ||||
5-HT3 receptor antagonist | ||||
Granisetron OR | 2mg PO OR 1mg or 0.01mg/kg IV OR 1 patch OR 10mg SC | |||
Ondansetron OR | 8mg PO (tab or soluble film) OR 8mg IV | |||
Palonosetron OR | 0.25mg IV | |||
Dolasetron | 100mg PO | |||
Corticosteroid | ||||
Dexamethasone | 8mg PO or IV | |||
NOTES | ||||
Key: 5HT3 = 5-hydroxytryptamine-3 (serotonin); AUC = area under the curve; CINV = chemotherapy induced nausea and vomiting; IV = intravenous; NK1 = neurokinin 1; PO = oral; SC = subcutaneous 1 For emetic risk category of chemotherapeutic agents, see “Emetogenic Potential of Antineoplastic Agent” chart. 2 Adults treated with antineoplastic combinations should receive the antiemetic regimen appropriate for the component antineoplastic agent of greatest emetic risk. 3 For adults treated with carboplatin AUC ≥4mg/mL (emetic risk is at the higher end of the moderate-emetic risk category), add NK1 receptor antagonist for a 3-drug regimen. Dexamethasone dosing is Day 1 only: 20mg with rolapitant, and 12mg with aprepitant, fosaprepitant, or netupitant-palonosetron. 4 Give antiemetic regimen on the day of chemotherapy (single-day) before the dose of the antineoplastic agent. For multi-day chemotherapy, first determine the emetic risk of the agent(s) included in the regimen. Patients should receive the agent of the highest therapeutic index daily during chemotherapy and for 2 days thereafter. Granisetron transdermal patch or granisetron ext-rel inj, which deliver therapy over multiple days rather than a daily 5-HT3 receptor antagonist, can be given. 5 If netupitant-palonosetron or fosnetupitant-palonosetron is used, no additional 5-HT3 receptor antagonist is needed. 6 Dexamethasone dosing is for patients receiving the recommended 4-drug regimen for high-emetic risk. If NK1 receptor antagonist was omitted, the dexamethasone dose should be adjusted to 20mg on Day 1 and 16mg on Days 2–4. 7 If rolapitant is used, give with dexamethasone 20mg PO or IV on Day 1, and 8mg PO or IV twice daily on Days 2–4. 8 For cisplatin and other high-emetic-risk single agents, dexamethasone and olanzapine should be continued on Days 2–4. For anthracycline + cyclophosphamide regimens, only continue olanzapine on Days 2–4. 9 If fosaprepitant is used, give with dexamethasone 8mg PO or IV on Day 2, and 8mg PO or IV twice daily on Days 3–4. 10 For moderate-emetic risk agents that are known to cause delayed nausea & vomiting (eg, cyclophosphamide, doxorubicin, oxaliplatin), may continue dexamethasone on Days 2–3. |
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REFERENCES | ||||
Hesketh PJ, Kris MG, Basch E, et al. Antiemetics: ASCO Guideline Update. J Clin Oncol. 2020;38(24):2782-2797. doi:10.1200/JCO.20.01296.
(Rev 5/2023) |