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This quadruple antiemetic regimen is a combination therapy consisting of the atypical antipsychotic olanzapine, a neurokinin-1 (NK1) receptor antagonist, a 5-hydroxytryptamine-3 (5-HT3) receptor antagonist, and the corticosteroid dexamethasone. It is specifically designed for the prevention of chemotherapy-induced nausea and vomiting (CINV) in patients receiving highly emetogenic chemotherapy (HEC), such as those with breast cancer. Olanzapine contributes to the antiemetic effect by blocking multiple receptors including dopamine D2 and serotonin 5-HT2C and 5-HT3. The NK1 receptor antagonist (e.g., aprepitant) inhibits substance P-mediated emesis, while the 5-HT3 receptor antagonist (e.g., palonosetron) blocks serotonin-induced emetic signals in the peripheral and central nervous systems. Dexamethasone acts as a synergistic adjunct, likely through anti-inflammatory mechanisms and modulation of the solitary tract nucleus. This specific combination is being evaluated in Phase 3 clinical trials led by Feixue Song, often as a pharmacological baseline to assess the adjunctive benefits of non-pharmacological interventions like electroacupuncture.
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