Multifocal serous retinopathy with pemigatinib therapy for metastatic colon adenocarcinoma

Oleg Alekseev1, Effy Ojuok2, Scott Cousins2

  • 1Department of Ophthalmology, Duke University, 2351 Erwin Rd., Durham, NC, 27705, USA. oleg.alekseev@duke.edu.

Abstract

Insights

Pemigatinib, a fibroblast growth factor receptor (FGFR) inhibitor, can cause multifocal serous retinopathy. This condition, a potential class effect of FGFR inhibitors, typically resolves after discontinuing the medication.

Area of Science:

  • Ophthalmology
  • Oncology
  • Pharmacology

Background:

  • Pemigatinib is an approved fibroblast growth factor receptor (FGFR) inhibitor for cholangiocarcinoma treatment.
  • FGFR retinopathy is a newly identified condition, with limited reports linked to FGFR inhibitors.
  • This study presents the first documented case of multifocal serous retinopathy associated with pemigatinib.

Purpose of the Study:

  • To report a case of multifocal serous retinopathy in a patient treated with pemigatinib.
  • To characterize the clinical presentation and imaging findings of pemigatinib-induced retinopathy.
  • To discuss the implications for FGFR inhibitor class effects and management.

Main Methods:

  • A case report of a 67-year-old male with metastatic colon adenocarcinoma receiving pemigatinib.
  • Ophthalmic examination including fundus autofluorescence, fluorescein angiography, and indocyanine green angiography.
  • Assessment of retinopathy following pemigatinib discontinuation.

Main Results:

  • The patient developed bilateral multifocal serous retinopathy.
  • Fundus autofluorescence revealed multifocal hypoautofluorescent foci.
  • Angiography findings were unremarkable, and subretinal fluid resolved quickly after pemigatinib cessation.

Conclusions:

  • Multifocal serous retinopathy may be a class effect of fibroblast growth factor receptor (FGFR) inhibitors.
  • FGFR retinopathy shares clinical similarities with MEK retinopathy, including subretinal fluid and rapid resolution.
  • Further research is needed to fully characterize FGFR retinopathy and establish management guidelines due to the broader molecular targets of FGFR inhibitors compared to MEK inhibitors.