Development of a thrombus in the superior mesenteric artery associated with sequential therapy with tyrosine kinase inhibitors for hepatocellular carcinoma.
Aged
Carcinoma, Hepatocellular
/ drug therapy
Humans
Liver Neoplasms
/ drug therapy
Male
Mesenteric Artery, Superior
Phenylurea Compounds
/ adverse effects
Protein Kinase Inhibitors
/ adverse effects
Protein-Tyrosine Kinases
/ antagonists & inhibitors
Quinolines
/ adverse effects
Retrospective Studies
Thrombosis
/ chemically induced
Arterial thromboembolism
Hepatocellular carcinoma
Lenvatinib
Sequential therapy
Tyrosine kinase inhibitor
Journal
Clinical journal of gastroenterology
ISSN: 1865-7265
Titre abrégé: Clin J Gastroenterol
Pays: Japan
ID NLM: 101477246
Informations de publication
Date de publication:
Apr 2020
Apr 2020
Historique:
received:
11
03
2019
accepted:
11
07
2019
pubmed:
19
7
2019
medline:
21
1
2021
entrez:
19
7
2019
Statut:
ppublish
Résumé
Tyrosine kinase inhibitors (TKIs) are widely used for systemic chemotherapy of hepatocellular carcinoma (HCC). Arterial thromboembolism (ATE) has been reported to be an adverse event associated with TKI therapy, but its incidence is rare. Here, we report a case of an HCC patient who developed a thrombus in the superior mesenteric artery (SMA) while on TKI therapy. The patient was a 78-year-old Japanese man with hepatitis C virus-associated HCC with multiple nodules. Several sessions of transarterial chemoembolization therapy caused him to become refractory to the treatment. Sorafenib and regorafenib therapy had also been previously performed, but his disease continued to progress gradually. Therefore, we started lenvatinib therapy. When a contrast-enhanced computed tomography (CT) examination was performed 2 months later, we found a thrombus in the SMA. Retrospective analysis of the CT images revealed that the thrombus formed during the sorafenib-regorafenib sequential therapy and it developed rapidly, especially during the lenvatinib therapy. An HCC patient developed a thrombus in the SMA during TKI therapy. The incidence of ATE is rare in TKI treatment; however, long-term or sequential TKI therapy may increase the frequency of ATE. Further study is needed.
Identifiants
pubmed: 31317371
doi: 10.1007/s12328-019-01021-6
pii: 10.1007/s12328-019-01021-6
doi:
Substances chimiques
Phenylurea Compounds
0
Protein Kinase Inhibitors
0
Quinolines
0
Protein-Tyrosine Kinases
EC 2.7.10.1
lenvatinib
EE083865G2
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
247-251Références
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