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Author
Murakami, Daizo Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Nishimoto, Kohei Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Takao, Soshi Department of Epidemiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences ORCID Kaken ID publons researchmap
Miyamaru, Satoru Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Kadowaki, Tomoka Department of Epidemiology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Saito, Haruki Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Takeda, Hiroki Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Ise, Momoko Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Suyama, Koichi Department of Medical Oncology, Toranomon Hospital
Orita, Yorihisa Department of Otolaryngology-Head and Neck Surgery, Kumamoto University Graduate School of Medicine
Abstract
The tyrosine kinase inhibitor lenvatinib has been confirmed as an effective treatment option for patients with unresectable thyroid carcinoma. We conducted a retrospective analysis of the significance of the effect of continued lenvatinib treatment for the longest duration possible at a reasonable daily dose and with a minimum discontinuation period in 42 patients with unresectable thyroid carcinoma treated with lenvatinib between 2015 and 2020. A Cox proportional hazard model-based analysis revealed that the overall survival of the patients treated with a <8 mg/day mean dose of lenvatinib was significantly better than that of the patients treated with 8-24 mg/day (hazard ratio [HR] 0.38 for 1.14-4.54 mg/day, and HR 0.01 for 4.56-7.97 mg/day) adjusted for various factors (e.g., sex, age, drug interruption period). The cumulative dose of lenvatinib administered tended to be higher in the patients treated with low doses (< 8 mg/day) than in the patients treated with relatively high doses (8-24 mg/day). Considering its adverse events, the continuation of lenvatinib treatment with an adequate daily dose and drug interruption may help prolong the survival of patients with unresectable thyroid carcinoma.
Keywords
thyroid carcinoma
lenvatinib
adverse effect
survival
Amo Type
Original Article
Publication Title
Acta Medica Okayama
Published Date
2024-02
Volume
volume78
Issue
issue1
Publisher
Okayama University Medical School
Start Page
63
End Page
70
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
Copyright Ⓒ 2024 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID