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EXActDNA-003 / NSABP B-64: Study of Molecular Residual Disease Detection in Breast Cancer (MRD)

RecruitingObservational study

EXActDNA-003 / NSABP B-64: Breast Cancer Clinical Validation Study to Predict Recurrence of High-Risk Early Breast Cancer Treated With Neoadjuvant Therapy Using a Bespoke Circulating Tumor DNA Assay to Detect Molecular Residual Disease

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. The participant or a legally authorized representative must provide study-specific informed consent prior to study entry.
2. The participant must be ≥ 18 years of age.
3. ECOG performance status 0 or 1.
4. Histologically confirmed invasive carcinoma of the breast.
5. Planned neoadjuvant therapy which includes cytotoxic chemotherapy.
6. Tumor size ≥ 2.1 cm in greatest diameter.
7. Unifocal or multifocal cancer documented to be the same histologic clinical subtype.
8. Clinically node positive or if node negative, any one of the following:

   1. TNBC or HER2+ subtype
   2. HR+/HER2-negative with at least one of the following:

   i. High tumor grade (G3) ii. Ki67 index of 20% or higher iii. High genomic risk (Oncotype DX® (ODX) Breast Recurrence Score of \> 25, MammaPrint® High, etc.)
9. Willing and able to comply with the study requirements, which includes the collection of a total of 34 cc (2.5 Tablespoons) of blood for each research blood draw.
10. Available residual tissue from diagnostic biopsy from the breast or an involved ipsilateral lymph node for submission to create a bespoke ctDNA assay.

Exclusion Criteria:

1. Definitive clinical or radiologic evidence of metastatic disease.
2. Initiated neoadjuvant therapy for current breast cancer diagnosis.
3. Synchronous diagnosis of another invasive cancer, other than this breast cancer, except for non-melanoma skin cancers.
4. Completed all therapy (including endocrine therapy) \<5 years ago for any previous invasive solid organ malignancy (with exception of non-melanoma skin cancers) including prior breast cancer. Individuals with a prior history of noninvasive (in situ) carcinomas may participate if they have received definitive treatment.
5. Completed all therapy for any previous hematologic malignancy \< 5 years ago.
6. Multicentric or contralateral invasive breast cancers.
7. Known pregnancy at time of enrollment.
8. Prior solid organ transplant.
9. Prior allogeneic hematopoietic stem cell transplant.

About the study

The EXActDNA-003 study will prospectively enroll participants who are planning to undergo chemotherapy for high-risk, early breast cancer, who are willing to provide tissue and blood specimens for circulating tumor DNA (ctDNA) analysis.

Participants will be followed for up to 5.5 years.

What is being tested

Sponsor: Exact Sciences Corporation · Participants: 1,800 · Started: Jun 7, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06401421

Locations in the U.S.

AlaskaKatmai Oncology Group - Anchorage, Anchorage
CaliforniaStanford Cancer Institute, Palo Alto
Harbor-UCLA Medical Center - Hematology / Oncology, Torrance
Kaiser Permanente Medical Center, Vallejo
ColoradoUCHealth Cancer Care - Anschutz Medical Campus - University of Colorado Cancer Center, Aurora
FloridaAdventHealth East Altamonte Oncology and Hematology, Altamonte Springs
Mount Sinai Medical - Comprehensive Cancer Center, Miami Beach
Baptist Cancer Care - Plantation, Plantation
St. Joseph's Women's Hospital, Tampa
IllinoisRush Cancer Center, Chicago
IndianaDeaconess Chancellor Center for Oncology, Newburgh
KansasUniversity of Kansas Cancer Center, Westwood
KentuckySt. Elizabeth Edgewood Hospital, Edgewood
Baptist Health Louisville, Louisville
Norton Cancer Institute - Downtown, Louisville
MarylandGreater Baltimore Medical Center, Baltimore
MedStar Georgetown Cancer Institute, Baltimore
Sinai Hospital of Baltimore, Baltimore
Weinberg Center at Mercy, Baltimore
The Center for Cancer and Blood Disorders - Bethesda, Bethesda
James M Stockman Cancer Institute, Frederick
Tate Cancer Center at UM Baltimore Washington, Glen Burnie
Meritus Center for Clinical Research, Hagerstown
Holy Cross Hospital - Silver Spring, Silver Spring
University of Maryland St. Joseph Medical Center, Towson
MassachusettsLahey Hospital & Medical Center, Burlington
MinnesotaMetro Minnesota Community Oncology Consortium (MMCORC), Saint Louis Park
MissouriSaint Luke's Hospital of Kansas City, Kansas City
New JerseyJohn Theurer Cancer Center, Hackensack
Rutgers Cancer Institute of New Jersey, New Brunswick
New YorkStony Brook Medicine, Stony Brook
North CarolinaAtrium Health Levine Cancer Institute, Charlotte
Novant Health Cancer Institute - Elizabeth, Charlotte
FirstHealth Outpatient Cancer Center, Pinehurst
UNC Cancer Care at Nash, Rocky Mount
Atrium Health Wake Forest Baptist Medical Center, Winston-Salem
OhioAultman Timken Family Cancer Center, Canton
Cleveland Clinic Main Campus, Cleveland
PennsylvaniaPenn State Health Medical Group - Andrews Patel, Harrisburg
Penn State Cancer Institute, Hershey
UPMC Magee - Womens Hospital, Pittsburgh
Guthrie Sayre, Sayre
Rhode IslandWomen & Infants Hospital, Providence
South CarolinaSpartanburg Medical Center, Spartanburg
South DakotaAvera Cancer Institute, Sioux Falls
TennesseeBallad Health Cancer Center, Kingsport
TexasThe University of Texas MD Anderson Cancer Center, Houston
Joe Arrington Cancer Research & Treatment Center, Lubbock
VirginiaAlan B. Pearson Regional Cancer Center, Lynchburg
Bon Secours Cancer Institute at St. Francis, Midlothian
VCU Massey Comprehensive Cancer Center, Richmond
West VirginiaWVU Cancer Institute, Morgantown
WisconsinAurora Cancer Care - Wauwatosa, Wauwatosa

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.