# Efficacy of 5-hydroxytryptamine 3 receptor antagonists versus metoclopramide for preventing nausea and vomiting during azacitidine chemotherapy in patients with myelodysplastic syndromes or acute leukemia: a retrospective observational study

**Authors:** Yoshinori Wakasugi, Yoshito Ikeda, Satoshi Noda, Makoto Murata, Shin-ya Morita

PMC · DOI: 10.1186/s40780-025-00444-3 · Journal of Pharmaceutical Health Care and Sciences · 2025-04-24

## TL;DR

This study found that 5-HT3 receptor antagonists are more effective than metoclopramide in preventing nausea and vomiting during azacitidine chemotherapy in patients with blood cancers.

## Contribution

A novel comparison of 5-HT3 receptor antagonists and metoclopramide for nausea prevention in azacitidine-treated patients.

## Key findings

- 5-HT3RAs showed significantly higher total, complete control, and complete response rates compared to metoclopramide.
- The time until first emetic episode or rescue medication was significantly longer with 5-HT3RAs.
- 5-HT3RAs appear more effective than metoclopramide for preventing chemotherapy-induced nausea and vomiting.

## Abstract

5-Hydroxytryptamine 3 receptor antagonists (5-HT3RAs) and dexamethasone are recommended to prevent azacitidine-induced nausea and vomiting. In clinical practice, 5-HT3RAs or metoclopramide is often used without dexamethasone. In this study, we aimed to determine whether 5-HT3RAs or metoclopramide is more effective for suppressing nausea and vomiting during azacitidine-based chemotherapy.

This study was a single-center retrospective observational study. Patients with myeloid malignancies receiving azacitidine-based regimens were treated with a 5-HT3RA (ramosetron or granisetron, n = 32) or metoclopramide (n = 18) for preventing nausea and vomiting. The occurrence of nausea and vomiting was assessed using total control (TC), complete control (CC), and complete response (CR) rates (chi-squared test), and the time to the first emetic episode or rescue medication (Cox proportional hazard regression analysis).

The 5-HT3RA group had significantly higher rates of TC, CC, and CR than the metoclopramide group (84% vs. 22%, 91% vs. 33%, and 91% vs. 33%, respectively). The time until the first emetic episode or rescue medication was also significantly longer in the 5-HT3RA group than in the metoclopramide group (p < 0.001).

5-HT3RAs may prevent azacitidine-induced nausea and vomiting more effectively than metoclopramide.

Retrospectively registered.

## Linked entities

- **Chemicals:** azacitidine (PubChem CID 9444), dexamethasone (PubChem CID 5743), ramosetron (PubChem CID 108000), granisetron (PubChem CID 5284566), metoclopramide (PubChem CID 4168)
- **Diseases:** myelodysplastic syndromes (MONDO:0018881), acute leukemia (MONDO:0010643)

## Full-text entities

- **Diseases:** myelodysplastic syndromes (MESH:D009190), acute leukemia (MESH:D015470), emetic (MESH:D020250), myeloid malignancies (MESH:D009369)
- **Chemicals:** dexamethasone (MESH:D003907), metoclopramide (MESH:D008787), ramosetron (MESH:C071315), azacitidine (MESH:D001374), granisetron (MESH:D017829)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12023488/full.md

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Source: https://tomesphere.com/paper/PMC12023488