Durable benefit and slowdown in tumor growth dynamics with erdafitinib in a FGFR3-TACC3 fusion-positive IDH-wild type glioblastoma

Author:

Cabezas-Camarero Santiago12ORCID,Pérez-Alfayate Rebeca3,Polidura Carmen4,Gómez-Ruiz María Natividad4,Gil-Martínez Lidia4,Casado-Fariñas Isabel5,Bartolomé Jorge2,Pérez-Segura Pedro12

Affiliation:

1. Medical Oncology Department, IOB Institute of Oncology-Madrid , Madrid , Spain

2. Medical Oncology Department, Instituto de Investigación Sanitaria San Carlos (IdISSC), Hospital Clínico Universitario San Carlos , Madrid , Spain

3. Neurosurgery Department, Hospital Clínico Universitario San Carlos , Madrid , Spain

4. Radiology Department, Hospital Clínico Universitario San Carlos , Madrid , Spain

5. Pathology Department, Hospital Clínico Universitario San Carlos , Madrid , Spain

Abstract

FGFR3-TACC3 fusion-positive IDH-wild-type (IDH-WT) glioblastoma (GB) is a rare GB subtype occurring in approximately 3% of cases. It is clinical behavior and molecular profile is 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.

Funder

Grupo Español de Investigación en Neuro-Oncología

Johnson & Johnson Innovative Medicine

Erdafitinib

Astex Pharmaceuticals

Publisher

Oxford University Press (OUP)

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