Summary
FGFR3-TACC3 fusion-positive IDH-wildtype (IDH-WT) glioblastoma (GB) is a rare GB subtype occurring in approximately 3% of cases. Its clinical behaviour and molecular profile are different from those of fusion-negative IDH-WT GBs. Evidence on the role of FGFR inhibitors in FGFR-altered gliomas is limited. We present the case of a patient with a FGFR3-TACC3 fusion-positive IDH-WT GB that at its second recurrence was treated with the FGFR inhibitor erdafitinib through a compassionate use program. Although no objective response was achieved, an overt deceleration in tumor growth was evidenced and the patient remained on treatment for 5.5 months.