
Unmet Needs in Early and Metastatic Breast Cancer
Panelists discuss how unmet needs in early and metastatic breast cancer include overcoming endocrine resistance, improving adverse effect management, ensuring guideline-concordant care, addressing long-term toxicities, and expanding the role of pharmacists in monitoring, clinical trial integration, and advancing the evolving CDK4/6 inhibitor pipeline.
Episodes in this series

Unmet Needs in Early and Metastatic Breast Cancer
Persistent Clinical Challenges and Emerging Solutions
Despite advances in CDK4/6 inhibitor therapy, significant unmet needs remain in hormone receptor-positive breast cancer management. Endocrine resistance continues to develop even with oral SERD combinations, necessitating novel therapeutic approaches beyond current targeted agents. Personalized therapy based on genomic profiling and circulating tumor DNA monitoring represents the next frontier, with pharmacists likely assuming primary responsibility for test interpretation and treatment guidance as these technologies become mainstream. Secondary malignancies, particularly therapy-related acute myeloid leukemia following chemotherapy exposure, remain devastating long-term complications requiring ongoing vigilance in survivorship care.
Treatment Access and Quality of Life Limitations
Guideline nonconcordance remains problematic, with eligible patients not receiving appropriate CDK4/6 inhibitor therapy due to identification gaps and knowledge disparities between practice settings. Despite improved toxicity management strategies, current adverse effect profiles continue limiting quality of life, particularly fatigue and gastrointestinal effects that impact daily functioning. As patient survival improves, the imperative for better tolerated therapies intensifies, requiring development of interventions that maintain efficacy while minimizing treatment burden. Patient follow-up and monitoring systems need strengthening to prevent treatment interruptions and ensure appropriate supportive care delivery.
Future Directions and Pharmacy Integration
Next-generation CDK4/6 inhibitors in clinical development show promise for reduced toxicity profiles while maintaining therapeutic efficacy, though larger confirmatory trials remain necessary. The expanding patient population requiring CDK4/6 inhibitor management—from metastatic to adjuvant to HER2-positive indications—creates substantial health care resource demands requiring systematic pharmacy integration. Early implementation of evidence-based toxicity mitigation strategies during clinical development phases could prevent postmarketing management challenges. Pharmacists represent essential team members for treatment selection, monitoring protocols, adverse effect management, and patient education across the expanding therapeutic landscape, with growing opportunities for specialized clinical pharmacy roles in breast cancer care delivery.
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