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Case Report
ALK Inhibition in a Patient with Inflammatory Myofibroblastic Tumor Harboring CARS1-ALK Fusion
Songji Choi1orcid , Miso Kim2orcid , Sheehyun Kim1, Taekeun Park2, Yoonjin Kwak4, Jeong Mo Bae4, Hongseok Yun1, Jee Hyun Kim3

DOI: https://doi.org/10.4143/crt.2024.1184 [Accepted]
Published online: December 18, 2024
1Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea
2Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
3Department of Internal Medicine, Department of Genomic Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea
4Department of Pathology, Seoul National University Hospital, Seoul, Korea
Corresponding author:  Miso Kim
Tel: 82-2-2072-4035 Fax: 82-2-2072-7379  Email: misokim@snu.ac.kr
Received: 10 December 2024   • Accepted: 14 December 2024
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Inflammatory myofibroblastic tumor (IMT) is a rare entity, primarily affecting young individuals, often involving the abdomen, pelvis, or lung. Approximately 50% of IMTs harbor ALK gene rearrangements, making ALK inhibitors a viable treatment. We report a case of a 40-year-old female with metastatic IMT harboring a CARS1-ALK fusion. Initial chemotherapy failed, but targeted therapy with alectinib through the KOrean Precision Medicine Networking Group Study of MOlecular profiling guided therapy based on genomic alterations in advanced Solid tumors (KOSMOS)-II study led to significant tumor regression and ongoing, durable clinical improvement of 19 months. This case highlights the importance of precision medicine and raises the reappraisal of targeted agents outside of approved indications for rare cancers with actionable genomic alterations.

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