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Spots Global Cancer Trial Database for Palbociclib and Endocrine Therapy for LObular Breast Cancer Preoperative Study (PELOPS)

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Trial Identification

Brief Title: Palbociclib and Endocrine Therapy for LObular Breast Cancer Preoperative Study (PELOPS)

Official Title: Palbociclib and Endocrine Therapy for LObular Breast Cancer Preoperative Study (PELOPS): A Randomized Phase II Study of Palbociclib With Letrozole Versus Letrozole Alone for Invasive Lobular Carcinoma and Invasive Ductal Carcinoma

Study ID: NCT02764541

Conditions

Breast Cancer

Study Description

Brief Summary: This research study is evaluating how well Breast Cancer responds to preoperative treatment with Endocrine treatment in combination with a drug called Palbociclib or Endocrine treatment alone as possible treatments for Hormone Receptor Positive Breast Cancer.

Detailed Description: This is an open label phase II neoadjuvant clinical trial of Palbociclib in combination with endocrine therapy for hormone receptor positive early-stage breast cancer. The planned sample size is 180 participants. The study includes a "window treatment" phase followed by a treatment phase. In the window phase, participants will be treated with a two-week course of tamoxifen (Arm A) or letrozole (Arm B). In the treatment phase participants will be randomized to receive endocrine therapy in combination with palbociclib (Arm C) or endocrine therapy alone (Arm D) for a total duration of 24 weeks. Premenopausal patients with either invasive lobular or ductal carcinoma will be eligible to enroll directly into the treatment phase of the study. The study has two co-primary objectives: 1) To evaluate the difference in anti-proliferative activity of letrozole versus tamoxifen measured by changes in Ki67 from baseline to research biopsy (day 15) within cohorts of hormone receptor positive breast cancer for patients with invasive lobular and ductal carcinoma. 2) To evaluate the pathologic complete response (pCR) of endocrine therapy plus palbociclib and of endocrine therapy alone in breast cancer patients diagnosed with hormone receptor positive invasive breast cancer.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

Stamford Hospital, Stamford, Connecticut, United States

Eastern Maine Medical Center, Brewer, Maine, United States

Dana-Farber at St. Elizabeth's Medical Center, Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

DF/BWCC at Milford Regional Medical Center, Milford, Massachusetts, United States

DF/BWCC in clinical affiliation with South Shore Hospital, South Weymouth, Massachusetts, United States

Lifespan, Providence, Rhode Island, United States

Sarah Cannon Research Institute, Nashville, Tennessee, United States

Vanderbilt University Medical Center, Nashville, Tennessee, United States

MD Anderson Cancer Center, Houston, Texas, United States

Contact Details

Name: Otto Metzger, MD

Affiliation: Dana-Farber Cancer Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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