๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-07-30

Carboplatin and Paclitaxel With or Without Atezolizumab Before Surgery in Treating Patients With Newly Diagnosed, Stage II-III Triple-Negative Breast Cancer (NCT02883062)

Randomized Phase 2 Study of Neoadjuvant Chemotherapy, Carboplatin and Paclitaxel, With or Without Atezolizumab in Triple Negative Breast Cancer (TNBC)

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

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

This phase II trial studies how well carboplatin and paclitaxel with or without atezolizumab before surgery works in treating patients with newly diagnosed, stage II-III triple negative breast cancer. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving carboplatin and paclitaxel with or without atezolizumab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

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 (14 Sites)

  • Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona
  • Mayo Clinic in Arizona โ€” Scottsdale, Arizona
  • University of California Davis Comprehensive Cancer Center โ€” Sacramento, California
  • Mayo Clinic in Florida โ€” Jacksonville, Florida
  • Johns Hopkins University/Sidney Kimmel Cancer Center โ€” Baltimore, Maryland
  • Siteman Cancer Center at Saint Peters Hospital โ€” City of Saint Peters, Missouri
  • Siteman Cancer Center at West County Hospital โ€” Creve Coeur, Missouri
  • Washington University School of Medicine โ€” St Louis, Missouri
  • Siteman Cancer Center-South County โ€” St Louis, Missouri
  • Siteman Cancer Center at Christian Hospital โ€” St Louis, Missouri
  • UNC Lineberger Comprehensive Cancer Center โ€” Chapel Hill, North Carolina
  • Duke University Medical Center โ€” Durham, North Carolina
  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • UPMC Hillman Cancer Center โ€” Pittsburgh, Pennsylvania

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

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.

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†—