Abstract |
There is an increasing interest for anaplastic lymphoma kinase (ALK) inhibitors in pediatric oncology for specific entities such as ALK-driven inflammatory myofibroblastic tumor (IMT). IMT treatment can be challenging due to localization of the tumor and in rare cases of metastasis. When standard surgical treatment is not feasible, ALK inhibitors may play an important role, as recently reported for the first-generation ALK inhibitors ( crizotinib). However, data on the second-generation ALK inhibitors are limited. We report two emblematic cases of IMT in pediatric patients, treated with the second-generation ALK inhibitor ceritinib in the context of a clinical trial (NCT01742286).
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Authors | Erica Brivio, C Michel Zwaan |
Journal | Pediatric blood & cancer
(Pediatr Blood Cancer)
Vol. 66
Issue 5
Pg. e27645
(05 2019)
ISSN: 1545-5017 [Electronic] United States |
PMID | 30697903
(Publication Type: Case Reports, Journal Article)
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Copyright | © 2019 The Authors. Pediatric Blood & Cancer Published by Wiley Periodicals, Inc. |
Chemical References |
- Protein Kinase Inhibitors
- Crizotinib
- ALK protein, human
- Anaplastic Lymphoma Kinase
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Topics |
- Adolescent
- Anaplastic Lymphoma Kinase
(antagonists & inhibitors)
- Child
- Crizotinib
(therapeutic use)
- Humans
- Inflammation
(drug therapy, pathology)
- Male
- Myofibroblasts
(drug effects, pathology)
- Neoplasms, Muscle Tissue
(drug therapy, pathology)
- Prognosis
- Protein Kinase Inhibitors
(therapeutic use)
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