๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-06

IIT2023-09-Chung-UpfrontTAD: Upfront TAD/SNB in Patients With Breast Cancer With Nodal Metastases (NCT06092892)

IIT2023-09-Chung-UpfrontTAD: Upfront TAD/SNB in Patients With Clinical T1-2N0 ER+ Her2- Breast Cancer With Ultrasound Detected Nodal Metastases

๐ŸŸข Recruiting Phase2 ๐Ÿฉบ Clinical Procedure Protocol Sponsor: Alice Chung

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The purpose of the study is to determine the recurrence rates and survival of patients with clinical T1-2N0 ER+/Her2- invasive breast cancer who have biopsy proven image detected nodal disease treated with upfront lumpectomy or mastectomy with TAD followed by adjuvant therapy. This is a prospective, single arm phase II clinical trial. Patients will be screened and enrolled per eligibility criteria. Patient, tumor, and treatment data will be documented.

Who can join: Review the eligibility criteria below.

Location: Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute โ€” Los Angeles, California

Age range: 45 Years

๐Ÿงช Interventions in This Study

  • Breast Surgery (BCS or mastectomy) with TAD/SNB (PROCEDURE)
  • Adjuvant Radiation Therapy (RADIATION)

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (3 Sites)

  • Cedars-Sinai Medical Center, Samuel Oschin Comprehensive Cancer Institute โ€” Los Angeles, California
  • CS Cancer at Huntington Cancer Center โ€” Pasadena, California
  • CS Cancer at Valley Oncology Medical Group โ€” Tarzana, California

๐Ÿ“ž Contact the Study Coordinator

Phone: (310) 423-5842

Email: GroupCancerTrialInformation@cshs.org

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Breast Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—