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Original Research

Open Access

The effect of aprepitant and dexamethasone combination on paclitaxel-induced hypersensitivity reaction

  • T. Yamamoto1,*,
  • M. Naito1
  • S. Hara1
  • T. Kudo2
  • Y. Miwa1

1Department of Pharmacy, Osaka University Hospital, Suita, Osaka, Japan

2Department of Frontier Science for Cancer and Chemotherapy Graduate School of Medicine Osaka University, Suita, Osaka, Japan

DOI: 10.12892/ejgo3362.2016 Vol.37,Issue 6,December 2016 pp.833-836

Published: 10 December 2016

*Corresponding Author(s): T. Yamamoto E-mail: yamatomo@hosp.med.osaka-u.ac.jp

Abstract

Purpose of investigation: Dexamethasone (DEX) is often administered to prevent paclitaxel (PTX)-induced hypersensitivity reactions (HSR). The DEX dose is reduced when administered in combination with aprepitant (APR). However, the influence of that dose reduction on PTX-induced HSR has not been thoroughly studied. The present authors aimed to investigate the effects of the combined administration of APR and DEX on PTX-induced HSR. Materials and Methods: Fifty-one patients who received a three-week PTX regimen in combination with APR and DEX were retrospectively analysed. The authors compared the dose of DEX with the incidence of HSR and other toxicities. Results: Patients were stratified into two groups depending on the DEX dose, > 20 mg (group D, 33 patients), and < 12 mg (group reD, 26 patients). The incidence of HSR in Groups D and reD were 51.5% (17/33) and 53.8% (14/26), respectively. The frequencies of other toxicities between the groups were comparable. Conclusion: The findings suggest that although a reduction in DEX dose is possible when APR is co-administered, this does not affect the PTX-induced HSR. However, adverse effect should be closely monitored.

Keywords

Paclitaxel; Hypersensitivity reactions; Aprepitant; Dexamethasone.

Cite and Share

T. Yamamoto,M. Naito,S. Hara,T. Kudo,Y. Miwa. The effect of aprepitant and dexamethasone combination on paclitaxel-induced hypersensitivity reaction. European Journal of Gynaecological Oncology. 2016. 37(6);833-836.

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