Targeted FGFR inhibition results in a durable remission in an FGFR1-driven myeloid neoplasm with eosinophilia

Author:

Kasbekar Monica1,Nardi Valentina2,Dal Cin Paola3,Brunner Andrew M.4,Burke Meghan4,Chen Yi-Bin5,Connolly Christine4,Fathi Amir T.4,Foster Julia4,Macrae Molly4,McAfee Steven L.5,McGregor Kristin6,Narayan Rupa4,Ramos Aura Y.4,Som Tina T.4,Vartanian Meghan4,Friedman Robb S.6,Benhadji Karim A.7,Hobbs Gabriela S.4ORCID

Affiliation:

1. Department of Medicine and

2. Department of Pathology, Massachusetts General Hospital, Boston, MA;

3. Department of Pathology, Brigham and Women’s Hospital, Boston, MA;

4. Massachusetts General Hospital Cancer Center, Boston, MA;

5. Blood and Marrow Transplant Program, Massachusetts General Hospital, Boston, MA;

6. Cancer Center, Newton-Wellesley Hospital, Newton, MA; and

7. Taiho Oncology, Princeton, NJ

Abstract

Key Points A novel PCM1-FGFR1 gene rearrangement was identified in a patient with a myeloid neoplasm with eosinophilia. Futibatinib, an oral selective small molecule inhibitor of FGFR1-4, resulted in a durable complete hematologic and cytogenetic remission.

Publisher

American Society of Hematology

Subject

Hematology

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