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Expanding treatment options for patients with HER2+ metastatic breast cancer with margetuximab plus chemotherapy: a case report series.
Mahtani, Reshma; Harpalani, Natasha; Yan, Fengting; Phiel, Kristen; Kovalenko, Iuliia.
Afiliación
  • Mahtani R; Miami Cancer Institute - Medical Oncology, Baptist Health South Florida, Miami, FL, United States.
  • Harpalani N; Miami Cancer Institute, Baptist Hospital of Miami, Miami, FL, United States.
  • Yan F; Memorial Sloan Kettering Cancer Alliance, Miami Cancer Institute, Miami, FL, United States.
  • Phiel K; Miami Cancer Institute, Baptist Hospital of Miami, Miami, FL, United States.
  • Kovalenko I; Breast Medical Oncology, Swedish Cancer Institute, Seattle, WA, United States.
Front Oncol ; 14: 1419246, 2024.
Article en En | MEDLINE | ID: mdl-39220641
ABSTRACT

Background:

Human epidermal growth factor receptor 2 protein (HER2)-positive (+) metastatic breast cancer (MBC) is an aggressive disease and patients often undergo multiple lines of therapy following HER2 targeted therapies. The most recent National Comprehensive Cancer Network (NCCN) guidelines recommend margetuximab plus chemotherapy as fourth-line or later therapy for HER2+/hormone receptor (HR) + or negative (-) MBC. The aim of this case series is to provide information regarding margetuximab utilization in clinical practice as later-line therapy in women with HER2+ MBC. Case summaries Margetuximab plus chemotherapy was used as fourth- or later-line treatment in patients who had received multiple HER2-targeted agents, including trastuzumab, pertuzumab, ado-trastuzumab emtansine, trastuzumab deruxtecan, tucatinib, and neratinib. Patients responded to margetuximab plus chemotherapy with real-world progression-free survival (PFS) of 3, 4, and 7 months.

Conclusion:

Clinical outcomes from three heavily pretreated patients with metastatic HER2+/HR+ MBC demonstrated that margetuximab plus chemotherapy resulted in real-world PFS comparable to that reported in the controlled pivotal clinical trial and support use of this targeted therapy option in appropriately identified patients.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Oncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Oncol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza