The dawn of targeted therapies for triple negative breast cancer (TNBC): a snapshot of investigational drugs in phase I and II trials.

Combination treatments RSK2 breast cancer clinical trials kinase inhibitors metastatic disease precision medicine targeted therapy tnbc triple negative breast cancer

Journal

Expert opinion on investigational drugs
ISSN: 1744-7658
Titre abrégé: Expert Opin Investig Drugs
Pays: England
ID NLM: 9434197

Informations de publication

Date de publication:
Nov 2020
Historique:
pubmed: 2 9 2020
medline: 5 3 2021
entrez: 2 9 2020
Statut: ppublish

Résumé

Triple negative breast cancer (TNBC) was once thought to be an insurmountable disease marked by a lack of targeted treatments. However, we are now witnessing the dawn of targeted therapies for TNBC in which progress has stemmed from an improved understanding of the components that make TNBC unique. The identification of biomarkers, such as BRCA1/2, PIK3CA and RSK2, have advanced the field remarkably and there is considerable interest in finding novel therapeutics for TNBC that offer durable clinical benefit with fewer adverse events. We discuss phase I/II trials of new and emerging targeted therapies for TNBC, according to ClinicalTrials.gov up to June 2020. Although the emphasis is on ongoing and completed early phase trials, we also highlight pivotal studies that have led to the approval of new targeted classes of drugs for TNBC, with a focus on outcomes and common adverse events of each class of therapy. The way forward for TNBC treatment is through precision medicine. The use of novel agents matched with biomarkers to identify patients with the best chance of sustainable response offers new hope. We now have great potential for improving the outcomes for patients with TNBC.

Identifiants

pubmed: 32869671
doi: 10.1080/13543784.2020.1818067
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers, Tumor 0
Drugs, Investigational 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1199-1208

Auteurs

My-My Huynh (MM)

Pre-clinical R&D, Phoenix Molecular Designs , Vancouver, BC, Canada.

Mary Rose Pambid (MR)

Pre-clinical R&D, Phoenix Molecular Designs , Vancouver, BC, Canada.

Aarthi Jayanthan (A)

Pre-clinical R&D, Phoenix Molecular Designs , Vancouver, BC, Canada.

Andrew Dorr (A)

Clinical Operations, Phoenix Molecular Designs , San Diego, CA, USA.

Gerrit Los (G)

Clinical Operations, Phoenix Molecular Designs , San Diego, CA, USA.

Sandra E Dunn (SE)

Pre-clinical R&D, Phoenix Molecular Designs , Vancouver, BC, Canada.
Clinical Operations, Phoenix Molecular Designs , San Diego, CA, USA.

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Classifications MeSH