# Exploring antiemetic strategies in hematologic malignancies: a comprehensive literature review and evaluation of antiemetic efficacy in patients receiving high-dose chemotherapy prior to hematopoietic stem cell transplantation

**Authors:** Karin Jordan, Berit Jordan, Jennifer Vanden Burgt, Franziska Jahn

PMC · DOI: 10.1007/s00520-025-09638-9 · Supportive Care in Cancer · 2025-06-24

## TL;DR

This paper reviews antiemetic strategies for patients with blood cancers undergoing high-dose chemotherapy before stem cell transplants, highlighting a lack of clear guidance and the need for more research.

## Contribution

The paper identifies a research gap in antiemetic efficacy for hematologic malignancies and evaluates existing literature to inform future studies.

## Key findings

- Most studies on antiemetics focus on solid tumors, leaving a gap in knowledge for hematologic malignancies.
- NK1 receptor antagonist regimens showed higher response rates, but were underutilized in reviewed studies.
- The heterogeneity of studies makes it difficult to draw clear conclusions about effective antiemetic strategies.

## Abstract

Most antiemetic studies have been conducted in patients with solid tumors receiving single-dose chemotherapy. A research gap leaves healthcare providers without clear guidance on effective antiemetic regimens and schedules for patients with hematologic malignancies undergoing high-dose multiday chemotherapy. This literature search identified antiemetic studies and assessed efficacy outcomes in the hematology setting, and specifically in patients receiving high-dose chemotherapy prior to hematopoietic stem cell transplantation (HSCT).

A literature review of both PubMed and Embase was performed for published studies evaluating antiemetic regimens including an NK1 receptor antagonist (RA) and/or a 5HT-3RA with/without dexamethasone in the hematology setting. Key features of all studies are reviewed, and antiemetic efficacy is summarized specifically for studies in which patients received high-dose chemotherapy prior to HSCT.

Twenty-two of an initial 926 identified publications met the predefined inclusion criteria. The studies were heterogenous, with varying characteristics pertaining to randomization, control groups, size, cancer types, chemotherapies, antiemetics, and assessments, making cross-study comparisons and conclusions difficult. The range of response rates was wide with numerous studies showing complete response, no emesis or no nausea rates of less than 50%. Response rates were highest when an NK1 RA regimen was administered; however, an NK1 RA was underutilized and only administered in two-thirds of the studies.

The results reflect a significant clinical problem in preventing chemotherapy-induced nausea and vomiting (CINV) in patients with hematologic malignancies. The scarcity and heterogeneity of studies highlight challenges inherent in this area. This underscores a pressing need for rigorous randomized trials in hematology and HSCT assessing treatment-related CINV and effectiveness of antiemetic regimens.

## Linked entities

- **Chemicals:** dexamethasone (PubChem CID 5743)

## Full-text entities

- **Genes:** TACR1 (tachykinin receptor 1) [NCBI Gene 6869] {aka NK1R, NKIR, SPR, TAC1R}
- **Diseases:** hematologic malignancies (MESH:D019337), cancer (MESH:D009369), nausea (MESH:D009325), emesis (MESH:D014839), CINV (MESH:D020250)
- **Chemicals:** dexamethasone (MESH:D003907)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12187819/full.md

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Source: https://tomesphere.com/paper/PMC12187819