Nintedanib-Induced Delayed Mucosal Healing after Adjuvant Radiation in a Case of Oropharyngeal Carcinoma

Abstract Since the launch of imatinib in 2001, tyrosine kinase inhibitors are being used in chemotherapy for a wide range of malignant tumors. Drugs that inactivate multiple molecular mechanisms are called multikinase inhibitors (MKIs). Nintedanib is a type of MKI that inhibits downstream cascades i...

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Published inCase reports in oncology Vol. 15; no. 2; pp. 776 - 782
Main Authors Takahashi, Satoru, Endo, Masashi, Fukuda, Yukiko, Ogawa, Kazunari, Nakamura, Michiko, Okada, Kohei, Kawahara, Masahiro, Akahane, Keiko, Nagatomo, Takafumi, Onaga, Ryutaro, Nishino, Hiroshi, Mori, Harushi, Shirai, Katsuyuki
Format Journal Article
LanguageEnglish
Published Basel, Switzerland S. Karger AG 30.08.2022
Karger Publishers
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Summary:Abstract Since the launch of imatinib in 2001, tyrosine kinase inhibitors are being used in chemotherapy for a wide range of malignant tumors. Drugs that inactivate multiple molecular mechanisms are called multikinase inhibitors (MKIs). Nintedanib is a type of MKI that inhibits downstream cascades in three systems: vascular endothelial growth factor receptor, fibroblast growth factor receptor, and platelet-derived growth factor receptor inhibitions. It was initially developed as an anticancer drug for non-small-cell lung carcinoma; however, it was also found to inhibit the proliferation of fibroblasts associated with chronic inflammation in the lungs. Therefore, it is being more widely used to treat idiopathic pulmonary fibrosis, a benign disease, than as an antineoplastic agent. Several studies have reported adverse events associated with the concurrent use of MKIs with surgery or radiotherapy. Specifically, there has been a report cautioning against delayed wound healing associated with the use of nintedanib in patients undergoing surgery. However, there is no specific mention of its concurrent use during irradiation. We describe a case of a 72-year-old man with severely delayed recovery from radiation mucositis when nintedanib was being administered for benign disease.
ISSN:1662-6575
1662-6575
DOI:10.1159/000526077