First-line pemigatinib in a myeloid/lymphoid neoplasm with FGFR1 rearrangement: shifting the current treatment paradigm

Myeloid/lymphoid neoplasms with FGFR1 rearrangement (MLNFGFR1) are rare, aggressive hematologic malignancies with limited treatment options. Although pemigatinib is approved for relapsed/refractory disease, evidence supporting its role in the frontline setting remains limited. We report a 69-year-old female with newly diagnosed MLNFGFR1 in blast phase, presenting with concurrent myeloproliferative neoplasm and T-lymphoblastic lymphoma. As the patient declined intensive chemotherapy, frontline pemigatinib was initiated in combination with intrathecal chemotherapy for central nervous system prophylaxis. A rapid hematologic response was achieved, followed by complete metabolic and cytogenetic responses. At 17 months after pemigatinib initiation, she remains in complete remission, with treatment-related toxicity being manageable through dose modifications and temporary interruptions. This case illustrates the potential of FGFR1 inhibition as a frontline therapeutic option in selected patients with MLNFGFR1, while highlighting the importance of careful toxicity management and the need for further studies to establish its role in this setting.

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Publication Details

Journal
Leukemia & lymphoma/Leukemia and lymphoma
Published
2026-11-02
DOI
https://doi.org/10.1080/10428194.2026.2757354
Primary Topic
Acute Myeloid Leukemia Research
Type
article
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article

First-line pemigatinib in a myeloid/lymphoid neoplasm with FGFR1 rearrangement: shifting the current treatment paradigm

Eleni Variami, Penelope A. Korkolopoulou, Konstantinos Sideris, Panagiotis Theodorou Diamantopoulos et al.
Leukemia & lymphoma/Leukemia and lymphoma
Acute Myeloid Leukemia Research
article

First-line pemigatinib in a myeloid/lymphoid neoplasm with FGFR1 rearrangement: shifting the current treatment paradigm

Eleni Variami, Penelope A. Korkolopoulou, Konstantinos Sideris, Panagiotis Theodorou Diamantopoulos, Eleftheria Lakiotaki, Stavroula Syriopoulou, Christos Stafylidis, Elena E. Solomou, Marina Mantzourani, Dimitra Vlachopoulou, Christina‐Nefeli Kontandreopoulou, Iraklis Patsialos, Michaela Plaka, Nikos Georgakopoulos, Sofia Stouggioti
article en

Abstract

Myeloid/lymphoid neoplasms with FGFR1 rearrangement (MLNFGFR1) are rare, aggressive hematologic malignancies with limited treatment options. Although pemigatinib is approved for relapsed/refractory disease, evidence supporting its role in the frontline setting remains limited. We report a 69-year-old female with newly diagnosed MLNFGFR1 in blast phase, presenting with concurrent myeloproliferative neoplasm and T-lymphoblastic lymphoma. As the patient declined intensive chemotherapy, frontline pemigatinib was initiated in combination with intrathecal chemotherapy for central nervous system prophylaxis. A rapid hematologic response was achieved, followed by complete metabolic and cytogenetic responses. At 17 months after pemigatinib initiation, she remains in complete remission, with treatment-related toxicity being manageable through dose modifications and temporary interruptions. This case illustrates the potential of FGFR1 inhibition as a frontline therapeutic option in selected patients with MLNFGFR1, while highlighting the importance of careful toxicity management and the need for further studies to establish its role in this setting.

Leukemia & lymphoma/Leukemia and lymphoma
University of Patras (GR), National and Kapodistrian University of Athens (GR), Laiko General Hospital of Athens (GR), Andreas Sygros Hospital (GR), HistoGenetics (United States) (US)
Openalex Percentile: Top 13%
Acute Myeloid Leukemia Research
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