Prediction of Response to Neoadjuvant Chemotherapy in Women With Operable Breast Cancer

TerminatedOBSERVATIONAL
Enrollment

134

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

October 31, 2012

Study Completion Date

October 31, 2012

Conditions
Breast Cancer
Interventions
OTHER

ChemoFX Assay

Test of an algorithm to predict pathologic response in patients treated with neoadjuvant chemotherapy for breast cancer.

Trial Locations (28)

10003

Beth Israel Medical Center, New York

15213

Magee Womens Hospital, Pittsburgh

18104

Breast Care Specialists, P.C., Allentown

23502

Virginia Oncology Associates, Norfolk

30060

Advanced Breast Care, Marietta

33176

Advanced Medical Specialties, Miami

37203

Advantage Clinical Research, Nashville

Tennessee Breast Specialists, Nashville

38138

Breast Clinic of Memphis, Germantown

53233

Aurora Sinai Medical Center, Milwaukee

65201

Missouri Cancer Associates, Columbia

73104

OU Medical Center, Oklahoma City

75230

Dallas Surgical Group, Dallas

Leading Edge Research, PA, Dallas

75231

Texas Oncology - Dallas Presbyterian Hospital, Dallas

75246

Texas Oncology - Baylor Charles A. Sammons Cancer Center, Dallas

75702

Texas Oncology - Tyler, Tyler

76022

Texas Oncology - Bedford, Bedford

76092

Southlake Oncology, Southlake

77024

Texas Oncology - Memorial City, Houston

78217

Cancer Care Centers of South Texas, San Antonio

89074

Comprehensive Cancer Centers of Nevada, Henderson

89106

Breast Care, Las Vegas

90033

USC/Norris Comprehensive Cancer Center, Los Angeles

90806

Breastlink Medical Group, Inc, Long Beach

97477

Willamette Valley Cancer Institute and Research Center, Springfield

07962

Morristown Memorial Hospital, Morristown

02905

Women & Infants Hospital, Providence

Sponsors
All Listed Sponsors
collaborator

United States Department of Defense

FED

lead

Precision Therapeutics

INDUSTRY