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Successful Crizotinib-targeted Therapy of Pediatric Unresectable ERC1::ALK Fusion Sarcoma
Journal article   Open access   Peer reviewed

Successful Crizotinib-targeted Therapy of Pediatric Unresectable ERC1::ALK Fusion Sarcoma

Megan L. Wood, Julie C. Fanburg-Smith, James M. Brian, Jason C. White, Jonathan L. Powell and Andrew S. Freiberg
Journal of pediatric hematology/oncology, v 46(2), pp e184-e187
Mar 2024
PMID: 38099690
url
https://doi.org/10.1097/MPH.0000000000002777View
Published, Version of Record (VoR) Open

Abstract

Online : Clinical and Laboratory Observations
Anaplastic lymphoma kinase (ALK)-fusion sarcomas are rare part of the emerging theoretically targetable tyrosine kinase RAS::MAPK pathway fusion myopericytic-ovoid sarcomas. We report our clinicopathologic and treatment experience with an ALK fusion sarcoma. A novel ELKS/RAB6-interacting/CAST family member 1–unaligned ALK fusion infiltrative nonmetastatic low-grade sarcoma of the right hand of a 15-month-old male was treated with crizotinib, an ALK tyrosine kinase inhibitor as oral monotherapy, inducing complete radiographic and clinical resolution by 10 months and sustained response now over 12 months after elective discontinuation. Crizotinib can successfully be used to treat unresectable novel ALK fusion sarcomas.

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Web of Science research areas
Hematology
Oncology
Pediatrics
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