Locally Advanced Inflammatory Myofibroblastic Tumor Treated With Targeted Therapy: A Case Report and Literature
Charis Durham1, Matthew Clemons2, Alwin Alias3
1Hematology and Medical Oncology, Baylor University Medical Center, part of Baylor Scott and White Health, Dallas, USA.
Cureus
|August 29, 2022
Summary
Anaplastic lymphoma kinase (ALK)-rearranged inflammatory myofibroblastic tumors show favorable responses to ALK-targeted tyrosine kinase inhibitors (TKIs). This case report highlights crizotinib
Area of Science:
- Oncology
- Molecular Pathology
Background:
- Inflammatory myofibroblastic tumors (IMTs) are characterized by genetic alterations, notably anaplastic lymphoma kinase (ALK) gene rearrangements.
- Other molecular targets in IMTs include ROS1, NTRK, and PDGFR, influencing therapeutic strategies.
Observation:
- This case report details a patient with locally advanced pulmonary IMT harboring an ALK rearrangement.
- The patient received neoadjuvant-intent crizotinib, an ALK-targeted tyrosine kinase inhibitor (TKI).
Findings:
- The patient exhibited a highly favorable response to crizotinib, leading to the decision to forgo surgery.
- A comprehensive review of published IMT cases treated with systemic therapy, including duration and outcomes, is presented.
Implications:
- ALK-targeted TKIs represent an effective treatment for advanced or metastatic ALK-rearranged IMTs.
- Further research is needed to establish optimal duration and sequencing of TKI therapy due to limited data.
Keywords:
adjuvant tyrosine kinase therapyalk fusionanaplastic lymphoma kinase (alk) tyrosine kinase inhibitorcrizotinibepithelioid inflammatory myofibroblastic tumorneoadjuvant tyrosine kinase inhibitor therapypulmonary inflammatory myofibroblastic tumor

