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http://dx.doi.org/10.1016/j.cllc.2023.10.005 | DOI Listing |
Expert Opin Investig Drugs
December 2024
Department of Oncology, Case Western Reserve University, Cleveland, OH, USA.
Adv Sci (Weinh)
January 2025
Institute of Clinical Science, Zhongshan Hospital, Fudan University, Shanghai, 200032, China.
Intrahepatic cholangiocarcinoma (ICC) is a highly lethal malignancy that currently lacks effective clinical treatments. Eliminating stem cell-like cancer cells is an extremely promising but challenging strategy for treating ICC. A recently developed synthetic retinoid, sulfarotene, abrogates proliferation, and induces apoptosis of tumor-repopulating cells (TRCs) that exhibit stem cell-like properties, yet its effect and underlying mechanisms remain elusive in ICC.
View Article and Find Full Text PDFJ Adv Pract Oncol
February 2024
National Community Oncology Dispensing Association, Cazenovia, New York.
Oncologist
August 2024
Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, FL, United States.
Background: Pemigatinib demonstrated efficacy in fibroblast growth factor receptor (FGFR)-altered cholangiocarcinoma (CCA) in the FIGHT-202 trial. However, limited real-world evidence exists on treatment patterns and outcomes in this setting.
Patients And Methods: Patient characteristics, treatment patterns, and outcomes of US adults who received pemigatinib for unresectable, locally advanced or metastatic CCA were collected via retrospective physician-abstracted chart review.
Crit Rev Oncol Hematol
October 2024
Department of Experimental Medicine, Sapienza University of Rome, Viale Regina Elena, Rome 324 -00161, Italy.
Fibroblast Growth Factor Receptors (FGFRs) are emerging as key factors involved in tumorigenesis, tumor microenvironment remodeling and acquired resistance to targeted therapies. Pemigatinib is a Tyrosine-Kinase Inhibitor that selectively targets aberrant FGFR1, FGFR2 and FGFR3. Pemigatinib is now approved for advanced-stage cholangiocarcinoma (CCA) but data suggests that other tumor histotypes exhibit FGFR alterations, thus hypothesizing its potential efficacy in other cancer settings.
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