Ocular toxicity associated with antibody-drug conjugates in cancer therapy: a comprehensive review

Junxiang Zhou1, Haoyue Wang1, Hua Xie2

  • 1Department of Pharmacy, Sichuan Clinical Research Center for Cancer, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, University of Electronic Science and Technology of China, Chengdu, China.

Insights

Ocular toxicity from antibody-drug conjugates (ADCs) is a growing concern, impacting patient quality of life. This review details ADC ocular side effects and strategies for mitigation.

Area of Science:

  • Oncology
  • Ophthalmology
  • Pharmacology

Background:

  • Ocular toxicity from anti-cancer drugs is often overlooked due to non-life-threatening nature.
  • Antibody-drug conjugates (ADCs) are potent oncology therapeutics with increasing reports of ocular toxicity.
  • ADC-induced ocular toxicity can severely impact visual function, quality of life, and treatment adherence.

Purpose of the Study:

  • To compile and analyze ocular toxicity data from approved ADCs.
  • To investigate mechanisms underlying ADC-associated ocular toxicity.
  • To explore strategies for mitigating ocular toxicity in ADC development and management.

Main Methods:

  • Systematic review of ocular toxicity data from clinical trials and postmarketing surveillance of approved ADCs.
  • Analysis of potential mechanisms of ADC-induced ocular toxicity.
  • Summary of reported ocular adverse events and their incidence.

Main Results:

  • Ocular toxicity is a significant concern across various approved ADCs, affecting visual function and patient well-being.
  • Identified potential mechanisms contributing to ADC-associated ocular toxicity.
  • Detailed incidence rates of ocular adverse events for different ADCs were compiled.

Conclusions:

  • Effective management, early detection, and monitoring are crucial for ADC-induced ocular toxicity.
  • Innovative approaches in drug development, including target selection, linker design, and payload optimization, are needed to reduce ocular toxicity.
  • A comprehensive understanding of ADC-tissue interactions is key to improving clinical outcomes and patient quality of life.

Related Concept Videos

Drug Toxicity: Allergic Reactions01:30

Drug Toxicity: Allergic Reactions

Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial exposure to a...
Drug Toxicity: Overview01:00

Drug Toxicity: Overview

Drug toxicity quantifies the harm a compound causes to an organism, varying by dose and potentially impacting whole systems or specific organs like the liver. Toxic reactions may arise from venomous insect or spider bites, with effects ranging from mild symptoms to severe outcomes such as brain damage or death. Common forms of acute poisoning include ethanol intoxication and overdose of pain or fever medications, with substances like GHB and heroin being particularly lethal at doses close to...
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
Hypersensitivity Reactions: Cytolytic Reactions01:01

Hypersensitivity Reactions: Cytolytic Reactions

Type II hypersensitivity involves IgG and IgM antibodies targeting cell surface antigens, leading to cell destruction. This can occur through complement activation, antibody-dependent cell-mediated cytotoxicity (ADCC), or acting as opsonins for phagocytosis. When excessive, these reactions cause significant tissue damage.Drug-induced hemolytic anemia is a common example, where drugs like penicillin or cephalosporins bind to red blood cells, forming drug-protein complexes. These complexes...
Cross-reactivity00:42

Cross-reactivity

Overview
Drug Toxicity: Dose-Dependent Reactions01:24

Drug Toxicity: Dose-Dependent Reactions

Drug toxicities can be stratified into pharmacological, pathological, or genotoxic based on their mechanisms. The incidence and severity of these toxicities generally increase with the drug's concentration in the body and exposure time.Pharmacological toxicity is evident when the therapeutic effects of drugs overshoot into adverse reactions in a predictable, dose-dependent manner. Central nervous system (CNS) depression from barbiturates is a classic example, with effects escalating from...