What the trials found
For clinicians
Chemotherapy-Induced Nausea and Vomiting: what the trials found
Several neurokinin-1 (NK1) receptor antagonists and combinations have demonstrated efficacy in managing chemotherapy-induced nausea and vomiting (CINV). NEPA (netupitant/palonosetron) showed a high probability of complete response over three cycles of chemotherapy (0.810) with significant results for acute, delayed, and overall CINV indicators 1. Similarly, the combination of netupitant and palonosetron demonstrated significantly higher rates of complete response at Cycle 1 compared to other treatments (74.3% vs 66.6%, p=0.001; 88.4% vs 85.0%, p=0.047) 14.
Rolapitant demonstrated significantly higher rates of complete response (no emesis and no rescue medication) compared to standard treatments in multiple trials, with results reaching statistical significance across different study populations [11, 12, 13]. Palonosetron showed high rates of complete response in both acute (186%) and delayed (170% or 165%) phases 10, while oral palonosetron also demonstrated high rates of no emesis and no rescue medication 15.
Other agents including aprepitant, casopitant, and fosaprepitant were evaluated for CINV. Aprepitant showed statistically significant improvements in complete response across acute (66.4% vs 52.0%, p<0.05), delayed (50.7% vs 26.0%, p<0.01), and overall phases 18, as well as higher numbers of patients reporting no vomiting 19. Casopitant demonstrated high rates of complete response in both acute and delayed phases for moderately emetogenic chemotherapy (MEC) regimens 5.
Olanzapine was evaluated in multiple trials, though results regarding its superiority over other medications were not statistically significant in some comparisons [3, 8, 22]. Other agents such as dexamethasone 9, fosnetupitant/palonosetron 7, and APF530 6 were also studied for CINV management.
Recent results — preliminary, needs further review
- Essential oils were investigated for CINVR symptoms and anxiety; however, results did not reach statistical significance (p=0.462; p=0.285) 21.
For the clinician treating this condition
- NK1 receptor antagonists like Rolapitant, Netupitant/Palonosetron, and Aprepitant have demonstrated statistically significant improvements in complete response rates for CINV.
- Palonosetron and Casopitant show high rates of complete response in both acute and delayed phases of chemotherapy.
- While multiple agents are available, specific combinations like NEPA show high probability of success across multiple cycles of chemotherapy.
AI synthesis of 11 cited trials,
updated Jun 20, 2026.
Informational only — not medical advice; trial data sourced from ClinicalTrials.gov.
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