2020
DOI: 10.1159/000510369
|View full text |Cite
|
Sign up to set email alerts
|

High Prevalence and Conservative Management of Acute Cholecystitis during Lenvatinib for Advanced Thyroid Cancer

Abstract: <b><i>Introduction:</i></b> Lenvatinib (LEN) is a multitarget tyrosine kinase inhibitor currently used for advanced, radioiodine refractory differentiated thyroid cancer (RAI-R DTC). Among adverse events (AEs), nausea, vomiting, and decreased appetite have been frequently described. We aimed to evaluate the prevalence, the clinical presentation, and the effectiveness of conservative treatment of gallbladder disorders in a consecutive series of patient treated with LEN. <b><i>… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(1 citation statement)
references
References 21 publications
0
1
0
Order By: Relevance
“…The onset of symptoms and the peak of γ-glutaryl transferase levels corresponded to the highest weight loss during the first months of treatment. When these disorders required surgical intervention, presurgical lenvatinib interruption was shorter than one week (at least 48 hours before) and the treatment was resumed immediately after wound healing ( 23 ); in other cases, supportive care with ursodeoxycholic acid, when appropriate, and TKI dose reduction were used ( 24 ). Few cases of fistula and tumor-related bleeding were described after 10 weeks of treatment with lenvatinib; individual dose adjustments should be considered to manage this adverse reaction ( 25 ).…”
Section: Safety Datamentioning
confidence: 99%
“…The onset of symptoms and the peak of γ-glutaryl transferase levels corresponded to the highest weight loss during the first months of treatment. When these disorders required surgical intervention, presurgical lenvatinib interruption was shorter than one week (at least 48 hours before) and the treatment was resumed immediately after wound healing ( 23 ); in other cases, supportive care with ursodeoxycholic acid, when appropriate, and TKI dose reduction were used ( 24 ). Few cases of fistula and tumor-related bleeding were described after 10 weeks of treatment with lenvatinib; individual dose adjustments should be considered to manage this adverse reaction ( 25 ).…”
Section: Safety Datamentioning
confidence: 99%