Evaluation of Prophylactic Corticosteroid Eye Drop Use in the Management of Corneal Abnormalities Induced by the Antibody-Drug Conjugate Mirvetuximab Soravtansine

Clin Cancer Res. 2019 Mar 15;25(6):1727-1736. doi: 10.1158/1078-0432.CCR-18-2474. Epub 2018 Nov 9.

Abstract

Purpose: Reversible, low-grade ocular adverse events (AE) are associated with administration of mirvetuximab soravtansine, a folate receptor alpha (FRα)-targeted antibody-drug conjugate undergoing phase III clinical evaluation in platinum-resistant ovarian cancer. This study investigated the underlying mechanisms of ocular toxicity and evaluated primary prophylactic use of corticosteroid eye drops in patients receiving mirvetuximab soravtansine.

Patients and methods: Target expression in the human eye was determined by IHC. The ocular toxicity profile of mirvetuximab soravtansine was assessed preclinically using Dutch-Belted rabbits. In a phase I clinical study, patients with ovarian cancer were treated with 6 mg/kg mirvetuximab soravtansine intravenously once every 3 weeks, including one expansion cohort with corticosteroid eye drops administered daily for the first 10 days of each treatment cycle.

Results: FRα expression was absent from human corneal tissues. Ocular abnormalities in the rabbit eye appeared phenotypically consistent with off-target effects on the cornea. Forty patients were enrolled in the expansion cohort. Reversible grade 1 or 2 blurred vision and keratopathy occurred in 16 (40%) and 12 (30%) patients, respectively; no grade 3/4 ocular events were observed. Compared with those patients who did not receive primary prophylaxis, corticosteroid eye drop use resulted in fewer dose reductions (5% vs. 15%) and none discontinued due to ocular AEs.

Conclusions: Preclinical modeling was predictive of the corneal-related symptoms seen in some patients dosed with mirvetuximab soravtansine. Primary prophylactic use of topical corticosteroid eye drops resulted in a trend toward symptomatic improvement and a reduction in ocular AE-related dose modifications in patients treated with mirvetuximab soravtansine.

Publication types

  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Antibodies, Monoclonal, Humanized / administration & dosage
  • Antibodies, Monoclonal, Humanized / adverse effects*
  • Cornea / drug effects
  • Cornea / pathology
  • Corneal Diseases / chemically induced
  • Corneal Diseases / pathology
  • Corneal Diseases / prevention & control*
  • Drug Administration Schedule
  • Drug Evaluation, Preclinical
  • Drug Resistance, Neoplasm
  • Female
  • Folate Receptor 1 / antagonists & inhibitors
  • Folate Receptor 1 / metabolism
  • Glucocorticoids / administration & dosage*
  • Humans
  • Immunoconjugates / administration & dosage
  • Immunoconjugates / adverse effects*
  • Infusions, Intravenous
  • Male
  • Maytansine / administration & dosage
  • Maytansine / adverse effects
  • Maytansine / analogs & derivatives*
  • Middle Aged
  • Ophthalmic Solutions / administration & dosage
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / pathology
  • Rabbits
  • Toxicity Tests, Subacute
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal, Humanized
  • FOLR1 protein, human
  • Folate Receptor 1
  • Glucocorticoids
  • Immunoconjugates
  • Ophthalmic Solutions
  • Maytansine
  • mirvetuximab soravtansine