Back to Search
Start Over
INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models.
- Source :
-
PloS one [PLoS One] 2020 Apr 21; Vol. 15 (4), pp. e0231877. Date of Electronic Publication: 2020 Apr 21 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Alterations in fibroblast growth factor receptor (FGFR) genes have been identified as potential driver oncogenes. Pharmacological targeting of FGFRs may therefore provide therapeutic benefit to selected cancer patients, and proof-of-concept has been established in early clinical trials of FGFR inhibitors. Here, we present the molecular structure and preclinical characterization of INCB054828 (pemigatinib), a novel, selective inhibitor of FGFR 1, 2, and 3, currently in phase 2 clinical trials. INCB054828 pharmacokinetics and pharmacodynamics were investigated using cell lines and tumor models, and the antitumor effect of oral INCB054828 was investigated using xenograft tumor models with genetic alterations in FGFR1, 2, or 3. Enzymatic assays with recombinant human FGFR kinases showed potent inhibition of FGFR1, 2, and 3 by INCB054828 (half maximal inhibitory concentration [IC50] 0.4, 0.5, and 1.0 nM, respectively) with weaker activity against FGFR4 (IC50 30 nM). INCB054828 selectively inhibited growth of tumor cell lines with activation of FGFR signaling compared with cell lines lacking FGFR aberrations. The preclinical pharmacokinetic profile suggests target inhibition is achievable by INCB054828 in vivo with low oral doses. INCB054828 suppressed the growth of xenografted tumor models with FGFR1, 2, or 3 alterations as monotherapy, and the combination of INCB054828 with cisplatin provided significant benefit over either single agent, with an acceptable tolerability. The preclinical data presented for INCB054828, together with preliminary clinical observations, support continued investigation in patients with FGFR alterations, such as fusions and activating mutations.<br />Competing Interests: Holly Koblish, Liangxing Wu, Kevin Bowman, Sharon Diamond, Darlise DiMatteo, Yue Zhang, Michael Hansbury, Mark Rupar, Xiaoming Wen, Paul Collier, Patricia Feldman, Ronald Klabe, Krista A. Burke, Maxim Soloviev, Christine Gardiner, Xin He, Alla Volgina, Maryanne Covington, Richard Wynn, Timothy C. Burn, Swamy Yeleswaram, Wenqing Yao are employees of Incyte Corporationand own Incyte stock. Phillip C. C. Liu, Bruce Ruggeri, Peggy Scherle, Reid Huber, and Gregory Hollis were employees of Incyte employees Corporation at the time of this work and own Incyte stock.Our commercial affiliation does not alter our adherence to PLOS ONE policies on sharing data and materials.
- Subjects :
- Administration, Oral
Animals
Cell Line, Tumor
Female
Half-Life
Humans
Mice
Mice, Inbred C57BL
Mice, Nude
Mice, SCID
Morpholines chemistry
Morpholines pharmacokinetics
Neoplasms pathology
Protein Kinase Inhibitors chemistry
Protein Kinase Inhibitors pharmacokinetics
Pyrimidines chemistry
Pyrimidines pharmacokinetics
Pyrroles chemistry
Pyrroles pharmacokinetics
Rats
Rats, Nude
Receptor, Fibroblast Growth Factor, Type 1 metabolism
Receptor, Fibroblast Growth Factor, Type 2 metabolism
Receptor, Fibroblast Growth Factor, Type 3 metabolism
Xenograft Model Antitumor Assays
Morpholines therapeutic use
Neoplasms drug therapy
Protein Kinase Inhibitors therapeutic use
Pyrimidines therapeutic use
Pyrroles therapeutic use
Receptor, Fibroblast Growth Factor, Type 1 antagonists & inhibitors
Receptor, Fibroblast Growth Factor, Type 2 antagonists & inhibitors
Receptor, Fibroblast Growth Factor, Type 3 antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 15
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 32315352
- Full Text :
- https://doi.org/10.1371/journal.pone.0231877