MedPath

Farletuzumab

Generic Name
Farletuzumab
Drug Type
Biotech
CAS Number
896723-44-7
Unique Ingredient Identifier
2O09BG0OWA
Background

Farletuzumab (MORAb-003) is a fully humanized monoclonal antibody against the folate receptor alpha, for the potential treatment of epithelial ovarian cancer.

Indication

Investigated for use/treatment in ovarian cancer.

Datopotamab Deruxtecan's Role in HR+/HER2- Breast Cancer Treatment: Sequencing and Safety Considerations

• Datopotamab deruxtecan (Dato-DXd) is poised to become a standard treatment for metastatic hormone receptor-positive, HER2-negative breast cancer after prior systemic therapy. • Optimal sequencing of antibody-drug conjugates (ADCs) like Dato-DXd, sacituzumab govitecan, and trastuzumab deruxtecan remains uncertain, especially considering overlapping toxicities. • Real-world toxicity profiles suggest sacituzumab govitecan may cause more cytopenias and diarrhea, while Dato-DXd and trastuzumab deruxtecan are linked to interstitial lung disease. • The lack of overall survival difference in the TROPION-Breast01 trial raises questions about efficacy issues or the impact of crossover between treatment arms.

EU Approves AbbVie's Elahere for Platinum-Resistant Ovarian Cancer

• AbbVie's Elahere (mirvetuximab soravtansine) receives EU approval for folate receptor-alpha (FRα) positive, platinum-resistant ovarian cancer, marking a significant advancement in treatment options. • Elahere is the first antibody-drug conjugate (ADC) approved in the EU for this indication, demonstrating improved overall survival compared to chemotherapy in the MIRASOL trial. • The approval addresses a critical unmet need, as it ends a decade-long gap in new treatments for platinum-resistant ovarian cancer in the EU, offering hope for improved outcomes. • This approval, based on the MIRASOL trial, showed a 33% reduction in the risk of death and a 35% improvement in progression-free survival compared to chemotherapy.

Targeted Therapies Show Promise in High-Grade Serous Ovarian Cancer Treatment

• Traditional treatments for high-grade serous ovarian cancer, involving surgery and platinum-based chemotherapy, often lead to resistance, necessitating targeted therapies. • PARP inhibitors and anti-angiogenic agents like bevacizumab have improved upfront therapy, but other targeted approaches, including immunotherapy, have shown limited success. • Emerging therapeutic targets, such as tyrosine kinase inhibitors and lipid metabolism agents, are under investigation to combat this aggressive cancer. • Ongoing research explores gene therapy and ribosome-targeted drugs as potential modalities to enhance treatment outcomes for high-grade serous ovarian cancer.
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