How I treat endocrine-dependent metastatic breast cancer

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved..

Estrogen receptor-positive (ER+)/HER2-negative (HER2-), the so-called luminal-type breast cancer, is the most frequent subset, accounting for around 70% of all breast cancer cases. Endocrine therapy (ET) combined with cyclin-dependent kinases (CDK) 4/6 inhibitors is the standard first option in the management of advanced luminal breast cancer independently of disease extension. Classically, patients undergo multiple lines of ET ± targeted treatments until endocrine resistance occurs and palliative chemotherapy is proposed. Understanding endocrine resistance mechanisms and development of novel ET options is one of the main challenges in current clinical research. Another area of utmost interest is the improvement of post-endocrine therapeutic approaches. Among others, the development of antibody-drug conjugates (ADCs) is very promising, and some of these drugs will probably soon become a part of the therapeutic arsenal against this incurable disease. This review paper provides an overview of currently available treatment options in ER+/HER2- metastatic breast cancer and extensively discusses new approaches in late clinical development.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:8

Enthalten in:

ESMO open - 8(2023), 2 vom: 18. Apr., Seite 100882

Sprache:

Englisch

Beteiligte Personen:

Gombos, A [VerfasserIn]
Goncalves, A [VerfasserIn]
Curigliano, G [VerfasserIn]
Bartsch, R [VerfasserIn]
Kyte, J A [VerfasserIn]
Ignatiadis, M [VerfasserIn]
Awada, A [VerfasserIn]

Links:

Volltext

Themen:

Antibody–drug conjugate (ADC)
Antineoplastic Agents
CDK 4/6
Immunoconjugates
Journal Article
Luminal breast cancer
PIK3CA
Review
SERD
Selective Estrogen Receptor Modulators

Anmerkungen:

Date Completed 04.10.2023

Date Revised 04.10.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.esmoop.2023.100882

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM353127574