Developing combination therapies with biologics in triple-negative breast cancer.

ADC PARP inhibitors TNBC Triple negative breast cancer antibody-drug conjugates immune checkpoints inhibitors new drugs

Journal

Expert opinion on biological therapy
ISSN: 1744-7682
Titre abrégé: Expert Opin Biol Ther
Pays: England
ID NLM: 101125414

Informations de publication

Date de publication:
03 Oct 2024
Historique:
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 3 10 2024
Statut: aheadofprint

Résumé

Novel compounds have entered the triple-negative breast cancer (TNBC) treatment algorithm, namely immune checkpoints inhibitors (ICIs), PARP inhibitors and antibody-drug conjugates (ADCs). The optimization of treatment efficacy can be enhanced with the use of combination treatments, and the incorporation of novel compounds. In this review, we discuss the combination treatments under development for the treatment of TNBC. The development of new drugs occurring in recent years has boosted the research for novel combinations to target TNBC heterogeneity and improve outcomes. ICIs, ADCs, tyrosine kinase inhibitors (TKIs), and PARP inhibitors have emerged as leading players in this new landscape, while other compounds like novel intracellular pathways inhibitors or cancer vaccines are drawing more and more interest. The future of TNBC is outlined in combination approaches, and based on new cancer targets, including many chemotherapy-free treatments. A large number of TNBC therapies have either proved clinically ineffective or weighted by unacceptable safety profiles. Others, however, have provided promising results and are currently in late-stage clinical trials, while a few have actually changed clinical practice in recent years. As novel, more and more selective drugs come up, combination strategies focusing the concept of synergy are fully warranted for the future.

Identifiants

pubmed: 39360776
doi: 10.1080/14712598.2024.2408756
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-20

Auteurs

Gilda Gaudio (G)

Department of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.
Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.

Enzo Martino (E)

Department of Radiological, Oncological and Pathological Science, Sapienza University of Rome, Rome, Italy.
Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.

Gloria Pellizzari (G)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Haemato-Oncology (DIPO), University of Milan, Milan, Italy.

Matteo Cavallone (M)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Haemato-Oncology (DIPO), University of Milan, Milan, Italy.

Grazia Castellano (G)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Haemato-Oncology (DIPO), University of Milan, Milan, Italy.

Abeid Omar (A)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Nuclear Medicine, Kenyatta University Teaching Referral and Research Hospital, Nairobi, Kenya.

Lika Katselashvili (L)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology, Caucasus Medical Centre, Tbilisi, Georgia.

Dario Trapani (D)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Haemato-Oncology (DIPO), University of Milan, Milan, Italy.

Giuseppe Curigliano (G)

Early Drug Development for Innovative Therapies, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Haemato-Oncology (DIPO), University of Milan, Milan, Italy.

Classifications MeSH