Study of Propranolol in Newly Diagnosed Breast Cancer Patients Undergoing Neoadjuvant Chemotherapy

Phase

Condition

Breast Cancer

Cancer

Neoplasms

Treatment

N/A

Clinical Study ID

NCT01847001

AAAI9158

UL1TR000040

Ages > 18
Female

Study Summary

This study is being conducted in patients with newly diagnosed breast cancer that will be undergoing chemotherapy prior to surgery - neoadjuvant chemotherapy. The study involves treatment with standard chemotherapy and a commonly used, FDA-approved, blood pressure drug called propranolol (Inderal). The purposes of this study are to:

Determine the effect of propranolol plus chemotherapy on breast cancer cells as well as the growth of blood vessels surrounding breast cancer cells.
Determine the side effect profile of propranolol and chemotherapy in patients with breast cancer receiving neoadjuvant chemotherapy.

This research is being done because previous laboratory work has shown that propranolol may decrease the ability for the blood vessels around breast cancer cells to grow, which may be important in helping cancer cells grow. It also may reduce the likelihood for breast cancer cells to spread. If changes are seen in the breast cancer cells and surrounding blood vessels in this study, we will pan to evaluate whether propranolol decreases the likelihood of breast cancer from recurring in future, later studies. All chemotherapy regimens used in this study have been the standard of care for many years; however, the use of propranolol is being researched along with the chemotherapy regimens.

Eligibility Criteria

Inclusion

Inclusion Criteria:

English or Spanish speaking women age ≥18
Heart Rate > 60 bpm
Systolic Blood Pressure > 100 mm/Hg
Deemed eligible to receive neoadjuvant chemotherapy with 12 cycles of weekly taxanetherapy (paclitaxel 80mg/m2 or Abraxane 100 mg/m2 if there is a shortage ofpaclitaxel) followed by 4 cycles of Adriamycin (60mg/m2) and cyclophosphamide (600mg/m2) given every 2 weeks with growth-factor support.
Echocardiogram (ECHO) or multiple-gated acquisition scan (MUGA) with ejection fraction > 50%.
Patients with hormone receptor +/- and human epidermal growth factor receptor 2protein (HER2) +/- breast cancer are eligible
If a patient has HER2-positive breast cancer, Herceptin and Perjeta will be givenalong with taxane therapy
Any stage invasive breast cancer provided the primary breast tumor size is ≥ 1 cm
Agree to participate in research blood collection at 4 different time periods (20 ml = 4 teaspoons)
Agree to the evaluation of already collected core biopsy, as well as surgicalresection tissue, for predictive biomarkers. The biopsy prior to Taxol #1 is optional.

Exclusion

Exclusion Criteria:

Patients failing to meet the inclusion criteria
Corrected QT interval (QTc) prolongation as defined by > 470 milliseconds onelectrocardiogram (ECG)
First-degree Atrioventricular (AV) block on ECG in which P-R interval lengthened > 200milliseconds; Second Degree; or Third Degree
On beta-blocker treatment. If discontinued, patients must have been off beta-blockersfor at least 3 months.
History of asthma, given concern for β-blockade in this population

Study Design

October 01, 2012

October 16, 2019

Study Description

While a number of therapeutic options exist for patients with breast cancer (BC), breast tumor biology is differs across tumors and not all BCs respond to treatment. Identifying a marker predicting response could spare non-responders unnecessary side effects, cost, and time. A recent example in BC is bevacizumab, an expensive anti-angiogenic monoclonal antibody, for which the FDA revoked approval for patients with metastatic BC. While this targeted therapy may benefit some patients, no appropriate predictive marker has been identified in the drug development process. An ideal biologic marker would be easy to perform, reliable, low-cost and non-invasive. A limitation of assessing tumor-based markers in metastatic BC is the inability to procure tumor tissue at different treatment times. To circumvent this issue, anti-cancer agents can be assessed pre-operatively, where women with newly diagnosed BC receive a study drug, alone or with chemotherapy, between diagnostic breast biopsy and surgical resection. In addition, tumor changes can be directly compared to modulation of non-invasive markers, such as functional radiographs or blood, to identify a non-invasive marker predicting tumor response.

The investigators are conducting a neoadjuvant single-institution trial with the non-selective, inexpensive β -blocker propranolol with chemotherapy in locally advanced BC. β-blockade regulates angiogenesis in primary breast tumors. In these trials, the investigators plan to evaluate treatment-related microvascular response via changes in breast Diffuse Optical Tomography (DOT), a non-invasive, fast, safe, and inexpensive breast imaging tool. As the optical property contrast from endogenous chromophores (oxyhemoglobin, deoxyhemoglobin, water, and lipid) provides information on tissue vascularity, it can monitor response to anti-angiogenic agents. DOT changes occur as early as 1 week after starting pre-operative therapy. The dynamic DOT system incorporated in these trials is unique to Columbia University Medical Center (CUMC), as it has been designed by Columbia biomedical engineers. CUMC's laboratory collaborators have measured this DOT system with anti-angiogenesis agents in animal models, demonstrating the translational nature of this project. While non-dynamic DOT has been assessed in other neoadjuvant trials with small cohorts receiving heterogeneous chemotherapy agents, none have evaluated DOT response to anti-angiogenic agents.

Connect with a study center

Columbia University Irving Medical Center
New York, New York 10032
United States
Site Not Available

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