Management of HER2-Low Metastatic Breast Cancer: A Comprehensive Statement by an Expert Group from the Middle East and Africa Region
نویسندگان
1 Department of Oncology, Mediclinic Hospital, Dubai, United Arab Emirates
2 Department of Oncology, Cairo University, Cairo, Egypt
3 The Medical Oncology Centre of Rosebank, Johannesburg, South Africa
4 Department of Medical Oncology, Bayindir Hospital, Ankara, Turkey
5 Department of Oncology, Chellah University, Rabat, Morocco
6 Department of Oncology, Almoosa Specialist Hospital, Oncology Center, Al Mubarraz, Saudi Arabia
7 Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
8 Department of Oncology, Sheikh Khalifa Specialty Hospital, Abu Dhabi, United Arab Emirates
9 Department of Oncology, Royal Preston Hospital, Sharoe Green Lane, Fulwood, Preston, United Kingdom
10 College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia
doi
10.30476/mejc.2024.103586.2143چکیده
Approximately 50 to 67% of breast cancers (BCs), traditionally categorized as human epidermal growth factor receptor 2 (HER2)-negative, but demonstrating low HER2 expression, are now being defined as a new HER2-low subset or HER2-low category of BC. For metastatic BC (mBC), standard therapy options include targeted approaches, such as cyclin-dependent kinase 4/6 inhibitors, phosphoinositide 3-kinase inhibitors, poly (adenosine diphosphate-ribose) polymerase inhibitors, and anti-programmed death-ligand 1 agents, depending on tumor type and its molecular profile. Recent clinical trials reported significant clinical benefits from novel anti‑HER2 antibody‑drug conjugates, such as trastuzumab deruxtecan in HER2‑low mBC. Novel treatment options have increased the complexity of the clinical decision‑making process, particularly for treatment sequencing for each clinical setting. A regional expert committee meeting was held to discuss the challenges, overcome limitations, and present recommendations to enhance HER2 reporting as well as treatment of patients with HER2‑low mBC in the Middle East and Africa region.
