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

Breast Cancer Clinical Trial

— PT-304  

Official title:

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

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01007890
• Other study ID #: PT-304
• Status: Terminated
• Phase: Phase 3
• First received: November 3, 2009
• Last updated: October 4, 2012
• Start date: November 2009
• Est. completion date: October 2012

Study information

• Verified date: October 2012
• Source: Precision Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Health authority: Department of Defense, U.S. Army Medical Research and Materiel Command, US:
• Study type: Observational

Clinical Trial Summary

The objective of this study is to develop a biomarker to predict pathological complete response in women treated with neoadjuvant chemotherapy for breast cancer. Such a biomarker would assist physicians in selecting the most effective chemotherapy for the individual patient.

Description:

The objective of this study is to develop a biomarker to predict pathological complete response in women treated with neoadjuvant chemotherapy for breast cancer. Such a biomarker would assist physicians in selecting the most effective chemotherapy for the individual patient. The anticipated biomarker will take into account clinical factors (such as tumor stage, tumor size, and age), phenotypic characteristics of the tumor (determined by pathological immunohistochemistry and ex vivo ChemoResponse assay), and genotypic characteristics of the tumor and patient (determined by genomic profiling via gene expression analysis of tumor RNA). It is expected that collective consideration of all of these factors will be more predictive of patient response to therapy than any of them alone.

Approximately 224 evaluable subjects will be recruited from approximately 30 US sites. Women with measurable operable invasive breast cancer diagnosed by core needle biopsy will be eligible for this study. Additional tumor specimens will be obtained prior to the start of chemotherapy via core needle biopsies to be used for the ex vivo ChemoResponse Assay and tumor genomic analysis (gene expression), respectively.

All subjects will receive neoadjuvant chemotherapy with one of two standard of care regimens that must consist of the following agents: doxorubicin (A), cyclophosphamide (C), and a taxane (T) such as docetaxel, paclitaxel, or Abraxane (nanoparticle albumin-bound paclitaxel [nab-paclitaxel]); or, docetaxel (T) and cyclophosphamide (C). These must be administered per NCCN guidelines by the treating physician.

Upon completion of chemotherapy treatment, women will undergo lumpectomy, modified radical mastectomy or other surgical procedure determined appropriate by the investigator and at that time will be evaluated for pathological response. At the time of lumpectomy, modified radical mastectomy, or other surgical procedure, additional tumor excess will be sent to Precision Therapeutics, Inc. (Precision) for exploratory analysis if there is no pathologic complete response (pCR), if there are sufficient tumor cells to send, and if the patient agrees to have her excess tumor cells sent to Precision for this purpose.

During the patient's course of participation on the study, the treating physician will remain blinded to the results of the ChemoResponse Assay and genomic analysis. If it is determined there is no pCR at the time of lumpectomy, modified radical mastectomy or other surgical procedure, Precision will make available a subsequent report to the physician containing additional information about chemotherapy drugs other than ACT that could benefit the further treatment decisions for the patient.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 134
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

Female subjects who satisfy the following conditions will be considered for enrollment into the study:

1. The subject must consent to be in the research study and must have signed an approved consent form conforming to institutional guidelines prior to study entry.

2. The diagnosis of breast cancer can be made by FNA or biopsy (other than incisional or excisional). The tumor specimen must demonstrate a diagnosis of invasive adenocarcinoma.

3. The primary breast cancer must be operable and measurable "greater than or equal to" 2.0 cm by use of physical exam and/or ultrasound, MRI, CT scan, or mammogram.

4. T1c, T2, T3, or T4 patients clinically staged as M0 (non-inflammatory) are eligible.

5. Patients with a prior diagnosis and treatment for DCIS are eligible.

6. Patients with multi-focal breast cancer are eligible.

7. The tumor must be confined to either the breast or to the breast and ipsilateral axilla.

8. The subject must be 18 years or older.

9. The interval between initial cytologic or histologic diagnosis of breast cancer and registration must be no more than 10 weeks.

10. ECOG Performance Status of 0 or 1 (see Appendix A) is required.

11. The subject must receive standard of care chemotherapy regimens consisting of either doxorubicin (A), cyclophosphamide (C), and a taxane (T) such as docetaxel, paclitaxel, or nab-paclitaxel administered in any sequence and combination the treating physician determines or docetaxel (T) plus cyclophosphamide (C).

Exclusion Criteria

Male subjects are not eligible for this study as the incidence of breast cancer in male subjects is significantly lower than female subjects. Those subjects who are strongly HER2-positive will be excluded as they will require treatment by biological agents for which the ChemoResponse Assay has not yet been validated. Subjects with evidence of distant metastatic disease are excluded as these subjects would not be good candidates for neoadjuvant therapy. Women who have had an excisional or incisional biopsy prior to entry would not have sufficient tumor sample to test or to be measured by physical exam for the study. Women who have nonmalignant comorbid conditions and diseases that would preclude them from being treated with doxorubicin (A), cyclophosphamide (C), and a taxane (T), and from completing the study are also excluded. Women with psychiatric or addictive disorders are excluded to protect those vulnerable subjects who may not be able to adequately give informed consent.

Women with one or more of the following conditions will be ineligible for this study:

1. Tumor determined to be strongly HER2-positive by immunohistochemistry (3+) or by fluorescent in situ hybridization (positive for gene amplification)

2. Definitive clinical or radiologic evidence of distant metastatic disease.

3. Excisional or incisional biopsy for this primary breast tumor.

4. Inflammatory breast cancer.

5. Synchronous contra-lateral breast cancer.

6. Multi-centric breast cancer.

7. Participation in the NSABP B-40 study.

8. Prior therapy for invasive breast cancer, including irradiation, chemo-, immuno-, and/or hormonal therapy.

a. Note: the only exception is hormonal therapy, which may have been given anytime after diagnosis and before study entry as long as the hormonal therapy is discontinued at or before registration. After surgery, hormonal therapy may be re-started, at the discretion of the treating physician.

9. Current therapy with any hormonal agent such as raloxifene, tamoxifen, or other selective estrogen receptor modulator (SERM), either for osteoporosis or breast cancer prevention, or sex hormonal therapy such as birth control pills, ovarian hormonal replacement therapy, etc. These patients are eligible IF these medications are discontinued prior to registration.

10. Surgical axillary staging procedure prior to study entry.

a. Note: exceptions include FNA of an axillary node and pre-neoadjuvant sentinel lymph node biopsy for patients with clinically negative axillary nodes.

11. Nonmalignant systemic disease (cardiovascular, renal, hepatic, etc.) that would preclude the woman from being treated with doxorubicin (A), cyclophosphamide (C), and a taxane (T), and from completing the study.

12. Psychiatric or addictive disorders that would preclude obtaining informed consent.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Other:
• ChemoFX Assay
Test of an algorithm to predict pathologic response in patients treated with neoadjuvant chemotherapy for breast cancer.

Locations

Country	Name	City	State
United States	Breast Care Specialists, P.C.	Allentown	Pennsylvania
United States	Texas Oncology - Bedford	Bedford	Texas
United States	Missouri Cancer Associates	Columbia	Missouri
United States	Dallas Surgical Group	Dallas	Texas
United States	Leading Edge Research, PA	Dallas	Texas
United States	Texas Oncology - Baylor Charles A. Sammons Cancer Center	Dallas	Texas
United States	Texas Oncology - Dallas Presbyterian Hospital	Dallas	Texas
United States	Breast Clinic of Memphis	Germantown	Tennessee
United States	Comprehensive Cancer Centers of Nevada	Henderson	Nevada
United States	Texas Oncology - Memorial City	Houston	Texas
United States	Breast Care	Las Vegas	Nevada
United States	Breastlink Medical Group, Inc	Long Beach	California
United States	USC/Norris Comprehensive Cancer Center	Los Angeles	California
United States	Advanced Breast Care	Marietta	Georgia
United States	Advanced Medical Specialties	Miami	Florida
United States	Aurora Sinai Medical Center	Milwaukee	Wisconsin
United States	Morristown Memorial Hospital	Morristown	New Jersey
United States	Advantage Clinical Research	Nashville	Tennessee
United States	Tennessee Breast Specialists	Nashville	Tennessee
United States	Beth Israel Medical Center	New York	New York
United States	Virginia Oncology Associates	Norfolk	Virginia
United States	OU Medical Center	Oklahoma City	Oklahoma
United States	Magee Womens Hospital	Pittsburgh	Pennsylvania
United States	Women & Infants Hospital	Providence	Rhode Island
United States	Cancer Care Centers of South Texas	San Antonio	Texas
United States	Southlake Oncology	Southlake	Texas
United States	Willamette Valley Cancer Institute and Research Center	Springfield	Oregon
United States	Texas Oncology - Tyler	Tyler	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Precision Therapeutics	United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary clinical endpoint pCR will be a dichotomous outcome variable with two levels: complete response and no complete response.		24 months	No
Secondary	Secondary clinical endpoint cOR will be an ordinal outcome variable with complete response (CR), partial response (PR), stable disease (SD) and progression disease (PD) four levels.		24 months	No

External Links

•   Precision Therapeutics Home Page