
Novel Endocrine Therapy for Breast Cancer: What Lies Ahead?
Panelists discuss the rapidly evolving endocrine treatment landscape in oncology, emphasizing the shift toward personalized therapy guided by tumor biomarkers such as ESR1, PI3K, and HER2-low, with excitement about new targeted agents and combination strategies expected over the next 5 years; they highlight challenges in treatment sequencing and resistance but remain optimistic that ongoing research and emerging data will enable more effective, tailored care that improves survival, delays toxicity, and potentially enhances cure rates.
Episodes in this series

The conversation centered on the rapidly evolving landscape of novel endocrine treatments in oncology, particularly focusing on where the field might be heading over the next five 5 years. The pace of development has been described as a marathon, with numerous new agents and mechanisms of action emerging on the horizon. There is clear excitement about the influx of targeted therapies that are nearing clinical adoption, driven by a deeper understanding of tumor biology and mutation profiles. This approach of personalized therapy based on genetic markers is seen as a fundamental shift that will persist, enabling clinicians to tailor treatment plans more precisely.
Monitoring the emergence of specific mutations and biomarkers, such as ESR1, PI3K, AKT, HER2-low status, and BRCA, will become increasingly important. These markers help guide treatment choices, including when to integrate antibody-drug conjugates (ADCs) or PARP inhibitors, reflecting a more nuanced strategy in managing patient care. The future of treatment will likely involve combining targeted therapies with optimal endocrine therapy backbones, administered earlier in the treatment sequence. Novel agents with unique mechanisms are expected to fit into later lines of therapy to delay the need for more aggressive treatments like such as ADCs, potentially improving patient outcomes by extending progression-free survival and delaying toxicities.
Finally, the conversation acknowledged the ongoing challenges in sequencing these new treatments and understanding resistance mechanisms. The field is marked by optimism as upcoming major oncology conferences are anticipated to unveil additional data that will inform clinical practice. The ultimate goals remain to provide more effective, personalized care that prolongs survival, reduces side adverse effects, and potentially increases cure rates. This dynamic period of innovation promises a future where therapies are increasingly targeted, and treatment paradigms continue to evolve in response to emerging scientific insights.





































