PREDATOR: Neoadjuvant Gene Prediction for Breast Cancer

Breast Cancer Clinical Trial

Official title:

Prospective Study To Validate The Predictive Value Of Mammostrat Score, DDR Score And TLE3 Gene When A Taxane-Based Chemo Agents Or Anthracycline-Based Chemo Agent Is Used In The Neo-Adjuvant Setting

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02067416
• Other study ID #: Pro00007624
• Secondary ID: 0712-0127
• Status: Withdrawn
• Phase: Phase 2
• Start date: July 2012
• Est. completion date: June 2014

Study information

• Verified date: January 2023
• Source: The Methodist Hospital Research Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study of the assay, Mammostrat®. to verify its utility as a predictor or outcome tool to determine whom would benefit from chemotherapy prior to surgery. Also could be used as a clinical marker to identify patients with breast cancer who do not benefit from some preoperative chemotherapies.

Description:

The purpose of this phase II study is to find out if the test, Mammostrat® can be used as a predictor or outcome tool to determine who will best benefit from chemotherapy prior to surgery. This can be used to determine if Mammostrat assay may be used as a clinical marker to identify a subset of women with breast cancer who do not benefit from preoperative chemotherapy, either taxane/taxane-like (T) chemo agents or anthracycline-based chemotherapy and cyclophosphamide (AC).

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 2014
• Est. primary completion date: June 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients with histologic confirmation of invasive breast carcinoma.

2. Patients must have intact primary tumor.

3. =18 years of age.

4. Patients with bilateral breast cancer are eligible.

5. Patients with second primary breast cancers are eligible.

6. The primary breast tumor must be = 2 cm by physical exam or imaging.

7. The tumor must have been determined to be HER2-negative as follows:

• Fluorescent in situ hybridization (FISH)-negative (defined by ratio of HER2 to CEP17 must be < 2.2)
• Immunohistochemistry (IHC) 0-1+; or
• IHC 2+ and FISH-negative

8. ECOG PS of 0, 1, or 2.

9. Negative serum pregnancy test =7 days of treatment initiation and a serum or urine pregnancy test must be repeated = 3 days prior to starting treatment for women of childbearing potential (WOCBP). For WOCBP, adequate contraception must be used throughout the study. For this study, acceptable methods of contraception include a reliable intrauterine device or a spermicide in combination with a barrier method. Women who are already on hormonal forms of birth control may continue that treatment but must also use a barrier method.

10. Ability to understand the requirements of the study, provide written informed consent and authorization of use and disclosure of protected health information, and agree to abide by the study restrictions and return for the required assessments.

11. Patient must be willing to undergo breast biopsies as required by the study protocol.

12. Sufficient tissue must be available from the diagnostic core biopsies. If not, patients must undergo additional biopsies to perform Mammostrat.

Exclusion Criteria:

1. Patients with a history of other invasive malignancies diagnosed and treated within the previous 5 years, except non-melanoma skin cancer and non-invasive cervical cancer.

2. Prior treatment with any investigational drug within the preceding 4 weeks.

3. Evidence of New York Heart Association class III or greater cardiac disease.

4. History of myocardial infarction, stroke, ventricular arrhythmia, or symptomatic conduction abnormality within 6 months.

5. Concurrent severe or uncontrolled medical disease (i.e., active systemic infection, diabetes, hypertension, coronary artery disease, congestive heart Failure or major surgery) that, in the opinion of the Investigator, would compromise the safety of the patient or compromise the ability of the patient to complete the study.

6. Pregnant or nursing women.

7. Known allergic reaction to Cremophor or any of the chemo agents on this trial.

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Anthracycline based chemotherapy
standard of care neoadjuvant treatment with anthracycline based chemotherapy
• taxane-based chemotherapy
neoadjuvant taxane based chemotherapy given as standard of care

Locations

Country	Name	City	State
United States	Houston Methodist Hospital	Houston	Texas

Sponsors (3)

Lead Sponsor	Collaborator
Jenny C. Chang, MD	GE Healthcare, The Methodist Hospital Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Compare Mammostrat score clinical response rates to chemotherapy	The percentage of patients undergoing chemotherapy who have Mammostrat low risk scores will be calculated	2 years
Secondary	pathological complete response rate compare to predictors	The percentage of patients undergoing chemotherapy who have Mammostrat low risk scores will be calculated	2 years

External Links

•   Cancer-related options for clinical trial participation