Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5618
DC FieldValueLanguage
dc.contributor.authorBou Zerdan, Marounen_US
dc.contributor.authorGhorayeb, Talaen_US
dc.contributor.authorSaliba, Faresen_US
dc.contributor.authorAllam, Sabineen_US
dc.contributor.authorBou Zerdan, Morganen_US
dc.contributor.authorYaghi, Maritaen_US
dc.contributor.authorBilani, Nadeemen_US
dc.contributor.authorJaafar, Rolaen_US
dc.contributor.authorNahleh, Zeinaen_US
dc.date.accessioned2022-05-19T07:02:18Z-
dc.date.available2022-05-19T07:02:18Z-
dc.date.issued2022-02-28-
dc.identifier.issn2072-6694-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5618-
dc.description.abstractBreast cancer (BC) is the most common malignancy affecting women. It is a highly heterogeneous disease broadly defined by the differential expression of cell surface receptors. In the United States, triple negative breast cancer (TNBC) represents 15 to 20% of all BC. When compared with other subtypes of BC, TNBC tends to present in younger women, and has a higher mortality rate of 40% in advanced stages within the first 5 years after diagnosis. TNBC has historically had limited treatment options when compared to other types of BC. The mainstay of treatment for TNBC remains cytotoxic chemotherapy despite the emergence of new biologic and targeted agents. Defining the specific tumor molecular profile including PDL-1 and androgen receptor testing is expanding treatment options in the clinical setting. Identifying more targetable, novel biomarkers that may better define therapeutic targets or prognostic markers is currently underway. TNBC nomenclature is expected to be updated in favor of other nomenclature which would help direct therapy, and further redefine TNBC's heterogeneity. Given the continuous advances in the field of TNBC, this review assesses the latest developments in basic characterization, subtyping, and treatment of TNBC, including novel drug developments with antibody-drug conjugates, immune checkpoint inhibitors, PARP inhibitors and androgen receptor targeted agents. Future trials are necessary in the face of these innovations to further support the use of new therapies in TNBC and the detection of the appropriate biomarkers.en_US
dc.language.isoengen_US
dc.subjectPoly (ADP-ribose) polymerase inhibitorsen_US
dc.subjectImmune checkpoint inhibitorsen_US
dc.subjectImmunoconjugatesen_US
dc.subjectTriple negative breast neoplasmsen_US
dc.titleTriple Negative Breast Cancer: Updates on Classification and Treatment in 2021en_US
dc.typeJournal Articleen_US
dc.identifier.doi10.3390/cancers14051253-
dc.identifier.pmid35267561-
dc.identifier.scopus2-s2.0-85125888654-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85125888654-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume14en_US
dc.description.issue5en_US
dc.date.catalogued2022-05-19-
dc.description.statusPublisheden_US
dc.identifier.openURLhttps://www.mdpi.com/2072-6694/14/5/1253/htmen_US
dc.relation.ispartoftextCancersen_US
dc.description.campusSGH campusen_US
Appears in Collections:Faculty of Medicine
Show simple item record

SCOPUSTM   
Citations

98
checked on Nov 23, 2024

Record view(s)

64
checked on Nov 25, 2024

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.