Evaluation of the effects and adverse drug reactions of low-dose dexamethasone premedication with weekly docetaxel
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kang, Rae Young | - |
dc.contributor.author | Yoo, Kyung Sook | - |
dc.contributor.author | Han, Hyeon Ju | - |
dc.contributor.author | Lee, Ju-Yeun | - |
dc.contributor.author | Lee, Se-Hoon | - |
dc.contributor.author | Kim, Dong-Wan | - |
dc.contributor.author | Lee, Yu Jeung | - |
dc.date.accessioned | 2022-07-14T20:03:39Z | - |
dc.date.available | 2022-07-14T20:03:39Z | - |
dc.date.created | 2021-05-11 | - |
dc.date.issued | 2017-02 | - |
dc.identifier.issn | 0941-4355 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153000 | - |
dc.description.abstract | Purpose A weekly docetaxel regimen had comparable efficacy with a tri-weekly schedule and caused significantly less severe neutropenia and febrile neutropenia. Therefore, a weekly docetaxel regimen has become increasingly common in cancer treatment. Premedication with corticosteroids can effectively prevent or reduce the severity of hypersensitivity and fluid retention. However, no recommended steroid dosage for a weekly docetaxel regimen has been established to date. The aim of this study is to compare the efficacy and complications of two different weekly docetaxel premedication protocols. Methods We retrospectively compared the hypersensitivity, hyperglycemia, and infection incidence associated with two weekly docetaxel premedication protocols. The control group (dexamethasone 10 mg intravenously and 4 mg orally every 12 h for four doses, starting 1 h before docetaxel administration) patients started weekly docetaxel chemotherapy between May 2012 and April 2013 at Seoul National University Hospital, and the experimental group (dexamethasone 10 mg intravenously 1 h prior to each docetaxel administration) patients started weekly docetaxel chemotherapy between May 2013 and April 2014. Results In total, 109 patients in the control group and 97 patients in the experimental group were included in this study, and there were no statistically significant differences in baseline characteristics between the two groups. The incidence of hypersensitivity and hyperglycemia were similar, but infections were observed significantly less in the experimental group (p = 0.020, OR = 0.408, 0.0190–0.0879). Conclusions A low-dose dexamethasone premedication protocol has comparable efficacy in the prevention of docetaxel hypersensitivity with fewer infection complications. Therefore, we recommend a low-dose dexamethasone premedication protocol for weekly docetaxel regimens. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | SPRINGER | - |
dc.title | Evaluation of the effects and adverse drug reactions of low-dose dexamethasone premedication with weekly docetaxel | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Ju-Yeun | - |
dc.identifier.doi | 10.1007/s00520-016-3420-y | - |
dc.identifier.scopusid | 2-s2.0-84989184592 | - |
dc.identifier.wosid | 000391615500013 | - |
dc.identifier.bibliographicCitation | SUPPORTIVE CARE IN CANCER, v.25, no.2, pp.429 - 437 | - |
dc.relation.isPartOf | SUPPORTIVE CARE IN CANCER | - |
dc.citation.title | SUPPORTIVE CARE IN CANCER | - |
dc.citation.volume | 25 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 429 | - |
dc.citation.endPage | 437 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Oncology | - |
dc.relation.journalResearchArea | Health Care Sciences & Services | - |
dc.relation.journalResearchArea | Rehabilitation | - |
dc.relation.journalWebOfScienceCategory | Oncology | - |
dc.relation.journalWebOfScienceCategory | Health Care Sciences & Services | - |
dc.relation.journalWebOfScienceCategory | Rehabilitation | - |
dc.subject.keywordPlus | CELL LUNG-CANCER | - |
dc.subject.keywordPlus | PHASE-II | - |
dc.subject.keywordPlus | HYPERSENSITIVITY REACTIONS | - |
dc.subject.keywordPlus | DIABETES-MELLITUS | - |
dc.subject.keywordPlus | DIAGNOSIS | - |
dc.subject.keywordPlus | PACLITAXEL | - |
dc.subject.keywordPlus | SCHEDULE | - |
dc.subject.keywordPlus | TRIAL | - |
dc.subject.keywordAuthor | Weekly docetaxel | - |
dc.subject.keywordAuthor | Dexamethasone | - |
dc.subject.keywordAuthor | Premedication | - |
dc.subject.keywordAuthor | Adverse drug reaction | - |
dc.identifier.url | https://link.springer.com/article/10.1007%2Fs00520-016-3420-y | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1365
COPYRIGHT © 2021 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.