News & Events

Clinical Trials to Optimize Outcomes in Early Breast Cancer: FDA Public Workshop

Organized by the:
U.S. Food & Drug Administration (FDA) Oncology Center of Excellence (OCE)
in collaboration with
the UCSF-Stanford Centers of Excellence in Regulatory Science and Innovation (CERSI)

Co-Chairs:

  • Tatiana Prowell, MD
  • Suparna Wedam, MD

Date: October 29, 2018

Time: 7:45 am to 4:15 pm

Location:

FDA White Oak Campus
Building 31, Room 1503 - Great Room
10903 New Hampshire Avenue
Silver Spring, MD 20993

FDA Campus Information, (e.g., local airports, directions, and local hotels)

Registration disclaimer icon

Background:

In 2018, many patients with early breast cancer will be cured of their disease.  While advances in genomic testing have enabled us to identify some patients with favorable prognoses who may be spared the toxicity of unnecessary treatment, it is likely that we continue to overtreat many patients, and we remain unable to identify patients at high risk of serious long-term toxicities of adjuvant therapy. De-escalation trials are therefore appropriate to change practice, but are often challenging to design and conduct. Simultaneously, there remains a high level of unmet need in patients who lack targeted therapy options, such as those with triple-negative breast cancer, and those whose disease is hormone receptor or HER2 positive but resistant to therapy. Some of these patients may be identified by the nature or extent of residual disease following neoadjuvant systemic therapy and others identified only by late relapses following adjuvant therapy. Targeted escalation trials conducted in the neoadjuvant setting provide the opportunity to identify patients at increased risk of breast cancer recurrence and test novel agents to improve clinical outcomes. The focus of this workshop is to gather stakeholders interested in early breast cancer to discuss strategies for successful escalation and de-escalation of therapy to optimize patient outcomes.

Workshop Objectives:

  • Provide a forum for open discussion between all stakeholders on strategies to optimize outcomes in early breast cancer
  • Discuss trials of de-escalation and targeted escalation of systemic therapy in early breast cancer
  • Discuss assessment of response in neoadjuvant trials in early breast cancer with a focus on endpoints that may support regulatory approval
  • Discuss feasibility challenges of conducting modern early breast cancer clinical trials and the need for robust evidence generation to satisfy regulatory/payer requirements

Webcast Information:

FDA will provide a free-of-charge, live webcast of this workshop. Further information regarding the webcast, including the web link for the webcast, will be made available closer to the workshop date.
FDA plans to post archived webcasts after the meeting, however, in cases where transmission was not successful, archived webcasts will not be available.

Meeting Information:

  • Agenda
  • Speakers list coming soon

Contact:

Sherwin Sapasap, MS, MBA, MHA
Center for Drug Evaluation and Research
Office of New Drugs
Office of Hematology and Oncology Products
Sherwin.Sapasap@fda.hhs.gov

Page Last Updated: 10/05/2018
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