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Research · 03 of 05

HER2 antibody-drug conjugates commonly damage the ocular surface

Expect and monitor for ocular surface toxicity in patients on HER2 antibody-drug conjugates; manage with lubrication and oncology liaison rather than reflexive drug cessation.

Design
Prospective longitudinal cohort with corneal imaging
Population
21 patients with HER2-positive breast cancer on HER2-targeted antibody-drug conjugates
Primary outcome
Ocular surface and corneal structural toxicity over treatment
Effect
Toxicity in 86% (18/21), mean onset 28 days; dose- and time-dependent, partially reversible

HER2-targeted antibody-drug conjugates are increasingly used in breast cancer, and the eye is a frequent site of off-target toxicity. This prospective study followed 21 patients on HER2-ADC therapy with detailed ocular surface and corneal imaging.

Ocular surface toxicity developed in 86% (18 of 21), at a mean of 28 days. The hallmark was a vortex-like keratopathy progressing from subepithelial microcysts to a whorl pattern, with confocal imaging showing corneal nerve fibre fragmentation and loss and reduced corneal sensitivity. The changes were dose- and time-dependent and partially reversible, with corneal clarity trending back toward normal after 12 cycles.

For anyone sharing care of these patients, the message is to expect ocular surface disease, set a baseline, and monitor. Lubrication and dose discussion with oncology — rather than stopping effective cancer therapy reflexively — are the usual response, since most changes recover.

  • Prospective study of 21 patients on HER2-targeted antibody-drug conjugates.
  • Ocular surface toxicity in 86% (18 of 21), at a mean of 28 days.
  • Vortex-like keratopathy with corneal nerve loss and reduced corneal sensitivity.
  • Changes were dose- and time-dependent and partially reversible over 12 cycles.
  • Set a baseline ocular surface assessment and monitor patients starting these drugs.

Why it matters

It defines a common, recognisable and largely reversible toxicity, so eye symptoms need not trigger stopping an effective cancer drug.

Don't overread it

A small single-cohort study; it characterises the toxicity rather than comparing management strategies.

The statistics, in plain English

An 86% toxicity rate in a small prospective cohort shows the problem is common rather than rare; with 21 patients the exact rate is imprecise, but the consistent, reversible pattern is informative.

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