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Updated: Dec 15, 2025

Acupoint Application Combined with Acupressure as an Adjunctive Therapy for Chemotherapy-Induced Nausea and Vomiting
Published on: June 21, 2024
Nausea and vomiting during post-transplantation cyclophosphamide administration
Toshihisa Nakashima1, Yoshihiro Inamoto2, Ayumu Ito3
1Department of Pharmacy, National Cancer Center Hospital, Tokyo, Japan.
Chemotherapy-induced nausea and vomiting (CINV) control is suboptimal with standard antiemetics during post-transplantation cyclophosphamide (PTCy). Additional antiemetic strategies are needed for patients undergoing PTCy to improve CINV management.
Area of Science:
- Hematology
- Oncology
- Pharmacology
Background:
- Post-transplantation cyclophosphamide (PTCy) is a key strategy for preventing graft-versus-host disease after allogeneic hematopoietic cell transplantation.
- Corticosteroids, commonly used for chemotherapy-induced nausea and vomiting (CINV) prophylaxis, are contraindicated during PTCy due to potential interference with T-cell depletion.
- This limitation poses a challenge for managing CINV in patients receiving PTCy.
Purpose of the Study:
- To evaluate the antiemetic efficacy of a combination regimen comprising a 5-hydroxytryptamine-3 receptor antagonist (5-HT3 RA) and a NK1 receptor antagonist (NK1 RA) in patients undergoing PTCy.
- To compare this efficacy against a similar antiemetic regimen that includes dexamethasone in patients conditioned with cyclophosphamide and total body irradiation (CY/TBI).
Main Methods:
- Retrospective analysis of 36 patients who received PTCy with 5-HT3 RA and NK1 RA combination therapy.
- Comparison with 27 patients who received CY/TBI conditioning with the same combination plus dexamethasone.
- Assessment of the proportion of patients experiencing no vomiting during the acute phase of PTCy administration.
Main Results:
- The proportion of patients who remained free of vomiting during acute PTCy administration was 81%.
- This rate was significantly lower compared to the 100% rate observed in the CY/TBI group (p=0.02).
- The findings indicate that CINV prevention with 5-HT3 RA and NK1 RA alone during PTCy is suboptimal.
Conclusions:
- The combination of 5-HT3 RA and NK1 RA provides suboptimal CINV control in patients undergoing PTCy.
- Additional antiemetic interventions are necessary to effectively manage CINV in this patient population.
- Further research into optimized antiemetic protocols for PTCy is warranted.
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