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Crizotinib-induced erosive esophagitis in a pediatric patient with neuroblastoma
Nicole Lubcke1, Kevin Van Camp2
11 University of Wisconsin Hospitals and Clinics, American Family Children's Hospital, Madison, WI, USA.
Abstract:
Crizotinib is an oral tyrosine kinase inhibitor, approved by the FDA in 2011, for use in anaplastic lymphoma kinase positive, metastatic, non-small cell lung cancer. Crizotinib inhibits oncogenic protein expression and impairs cellular proliferation in tumors with an overexpressed anaplastic lymphoma kinase gene. Currently used most frequently in the adult patient population, pediatric use is becoming more prominent, specifically in disease states exhibiting anaplastic lymphoma kinase-positive, metastatic disease, such as neuroblastoma. Approximately 8% of neuroblastomas have activating anaplastic lymphoma kinase-mutations, making this a promising target for a difficult-to-treat disease. Studies in the pediatric population are limited. However, targeted anaplastic lymphoma kinase-inhibitor therapies have shown improved outcomes at both one-year and two-year marks in both overall survival and progression free survival in anaplastic lymphoma kinase-positive adult patients with non-small cell lung cancer. One Children's Oncology Group phase I trial examined toxicities associated with anaplastic lymphoma kinase inhibitor therapy in pediatric patients. Results revealed varying grades in severity of neutropenia, dizziness, and liver function test elevation. In the adult population, severe toxicities reported by the manufacturer include effects on liver, cardiac and lung function. Additionally, several cases of severe, erosive, pill-esophagitis due to crizotinib therapy have been documented in the adult population. Erosive esophagitis is common in the pediatric population due to a variety of factors. Ingestion of medications or other corrosive agents accounts for approximately 3-5% (5000-10,000 cases per year) of esophagitis presentation in the pediatric population. Common causative medications include non-steroidal anti-inflammatory drugs, antibiotics such as doxycycline and tetracycline, and ferrous sulfate. Presented here is the first reported case of crizotinib-induced pill esophagitis in a pediatric patient.
Insights
Crizotinib, used for ALK-positive cancers, is now being studied in children. This report details the first pediatric case of crizotinib-induced pill esophagitis, a rare but serious side effect.
Area of Science:
- Oncology
- Pharmacology
Background:
- Crizotinib is an FDA-approved oral tyrosine kinase inhibitor for ALK-positive metastatic non-small cell lung cancer.
- Pediatric use of crizotinib is increasing for ALK-positive metastatic diseases like neuroblastoma, where it targets activating mutations.
Observation:
- While crizotinib shows promise in pediatric oncology, data on its use and toxicities in children are limited.
- Adult studies report severe toxicities including liver, cardiac, and lung dysfunction, as well as pill esophagitis.
- Pill esophagitis is a known issue in pediatrics, often caused by medications like NSAIDs, antibiotics, and ferrous sulfate.
Findings:
- This case presents the first documented instance of crizotinib-induced pill esophagitis in a pediatric patient.
- The patient experienced severe esophagitis, highlighting a potential adverse drug reaction in the pediatric population.
Implications:
- This case underscores the importance of monitoring for gastrointestinal toxicities, specifically pill esophagitis, in pediatric patients receiving crizotinib.
- Further research is needed to understand the incidence and management of crizotinib-induced esophagitis in children.
- Clinicians should be aware of this potential adverse effect when prescribing crizotinib to pediatric patients.
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