[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Exceptional Response to Erdafitinib in FGFR2-Mutated Metastatic Pancreatic Ductal Adenocarcinoma

J Natl Compr Canc Netw. 2022 Oct;20(10):1076-1079. doi: 10.6004/jnccn.2022.7039.

Abstract

Despite advances in cancer therapeutics, pancreatic ductal adenocarcinoma (PDAC) remains among the deadliest malignancies, with a poor prognosis at time of diagnosis. Research in PDAC has suggested that adaptive signaling in the tumor microenvironment may promote tumor proliferation and survival. Several FGFR fusion genes-specifically FGFR2-are involved with the creation and progression of cancer. These mutations are found in a variety of cancer types. This report presents a unique case of a young patient with stage IV PDAC with a known FGFR2 fusion. This molecular alteration afforded a remarkable response to FGFR inhibitor therapy, erdafitinib, after the patient experienced disease progression on multiple chemotherapy regimens.

Keywords: FGFR2 mutations; Fusion genetics; KRAS WT PDAC; precision oncology.

Publication types

  • Case Reports

MeSH terms

  • Adenocarcinoma* / genetics
  • Carcinoma, Pancreatic Ductal* / drug therapy
  • Carcinoma, Pancreatic Ductal* / genetics
  • Humans
  • Pancreatic Neoplasms* / drug therapy
  • Pancreatic Neoplasms* / genetics
  • Pancreatic Neoplasms* / pathology
  • Pyrazoles
  • Quinoxalines
  • Receptor, Fibroblast Growth Factor, Type 2 / genetics
  • Receptor, Fibroblast Growth Factor, Type 2 / therapeutic use
  • Tumor Microenvironment

Substances

  • Pyrazoles
  • Quinoxalines
  • erdafitinib
  • FGFR2 protein, human
  • Receptor, Fibroblast Growth Factor, Type 2