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ID 70853
JaLCDOI
フルテキストURL
80_3_179.pdf 2.03 MB
著者
Morita, Ayako Center for Clinical Oncology, Okayama University Hospital
Katayama, Hideki Center for Clinical Oncology, Okayama University Hospital
Ichihara, Eiki Center for Clinical Oncology, Okayama University Hospital Kaken ID publons
Maeda, Yoshinobu Department of Hematology and Oncology, Okayama University Hospital Kaken ID researchmap
抄録
This retrospective study investigated whether eicosapentaenoic acid (EPA) reduces paclitaxel-associated chemotherapy-induced peripheral neuropathy (CIPN) and acute neuropathic pain in dyslipidemic cancer patients. The medical records of cancer patients treated with paclitaxel or nab-paclitaxel at Okayama University Hospital between January 2018 and December 2022 were reviewed. Patients receiving concomitant therapy for dyslipidemia were categorized as EPA users or non-EPA users. Numbness and pain severity were extracted from medical records. The primary endpoint was the change from baseline in Common Terminology Criteria for Adverse Events (CTCAE) grade for peripheral neuropathy and pain; groups were analyzed using the Mann–Whitney U test. Of 184 eligible patients, 18 received EPA. Bleeding events were more frequent in the EPA group; however, changes in numbness and pain did not differ significantly between groups at any time point. Overall, EPA did not show a preventive effect on paclitaxel-associated CIPN or acute neuropathic pain. Future studies should evaluate EPA in combination with other neuroprotective agents to better define its potential role in CIPN prevention.
キーワード
eicosapentaenoic acid
cancer patients
chemotherapy
peripheral neuropathy
cancer pain
Amo Type
Original Article
出版物タイトル
Acta Medica Okayama
発行日
2026-06
80巻
3号
出版者
Okayama University Medical School
開始ページ
179
終了ページ
184
ISSN
0386-300X
NCID
AA00508441
資料タイプ
学術雑誌論文
言語
英語
著作権者
Copyright Ⓒ 2026 by Okayama University Medical School
論文のバージョン
publisher
査読
有り
PubMed ID
Web of Science KeyUT