Lung toxicity induced by anti-HER2 antibody - drug conjugates for breast cancer

Copyright © 2024 Elsevier B.V. All rights reserved..

Human epidermal growth factor receptor 2 (HER2) serves as both a prognostic indicator and a therapeutic target for breast cancer. Therefore, anti-HER2 therapy plays a crucial role in the treatment of HER2-positive cancer. Antibody-drug conjugates (ADCs) are composed of a monoclonal antibody, a chemical linker and a payload, wherein their aim is to reduce the toxicity associated with chemotherapy drugs by utilizing specific antibodies. Among the anti-HER2 ADCs currently approved for clinical use, trastuzumab emtansine(T-DM1) and trastuzumab deruxtecan (T-Dxd) have demonstrated remarkable efficacy in treating HER2-positive breast cancer. However, it is essential to emphasize the occurrence of lung toxicity during the treatment process, which can be life-threatening. In this review, we provide an overview of the new epidemiological features associated with interstitial lung disease (ILD) related to anti-HER2 ADCs in breast cancer. We also summarize the potential pathogenesis and explore the diagnosis and treatment strategies within this field.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - volume:195

Enthalten in:

Critical reviews in oncology/hematology - 195(2024) vom: 01. März, Seite 104274

Sprache:

Englisch

Beteiligte Personen:

Chai, Mengting [VerfasserIn]
Li, Li [VerfasserIn]
Wu, Huachao [VerfasserIn]
Liu, Yue [VerfasserIn]
Yi, Zongbi [VerfasserIn]
Yu, Haijun [VerfasserIn]

Links:

Volltext

Themen:

Ado-Trastuzumab Emtansine
Antibodies, Monoclonal, Humanized
Antibody-drug conjugate
Antineoplastic Agents
EC 2.7.10.1
HER2
Immunoconjugates
Interstitial lung disease
Journal Article
P188ANX8CK
Receptor, ErbB-2
Review
SE2KH7T06F
T-DM1
T-Dxd
Trastuzumab

Anmerkungen:

Date Completed 27.02.2024

Date Revised 18.04.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.critrevonc.2024.104274

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM368190374