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Spots Global Cancer Trial Database for Study of Efficacy of Ribociclib After Progression on CDK4/6 Inhibition in Patients With HR+ HER2- Advanced Breast Cancer

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Trial Identification

Brief Title: Study of Efficacy of Ribociclib After Progression on CDK4/6 Inhibition in Patients With HR+ HER2- Advanced Breast Cancer

Official Title: A randoMized phAse II trIal of fulvestraNt wiTh or Without Ribociclib After Progression on AntI-estrogeN Therapy Plus Cyclin-dependent Kinase 4/6 Inhibition in Patients With Unresectable or Metastatic Hormone Receptor +, HER2 - Breast Cancer (MAINTAIN Trial)

Study ID: NCT02632045

Study Description

Brief Summary: This is a randomized trial for patients with metastatic hormone receptor (HR)-positive human epidermal growth factor receptor 2 (HER2)-negative breast cancer who have progressed on an aromatase inhibitor plus a CDK4/6 inhibitor (either palbociclib or ribociclib) to either fulvestrant alone or fulvestrant with ribociclib (LEE-011). The purpose of the trial is to determine whether there is continued benefit for patients to remain on a CDK4/6 inhibitor at the time of switching anti-estrogen therapy. As ribociclib and palbociclib have a similar toxicity and drug profile and mechanism of action, we feel that it is appropriate for patients to receive either drug with an aromatase inhibitor prior to randomization.

Detailed Description: Despite advances in early detection and therapeutic options, unresectable or metastatic breast cancer remains incurable and is one of the leading causes of cancer-related mortality. Breast cancer is a molecularly heterogeneous disease. This study will be evaluating estrogen receptor (ER) expression positivity and/or progesterone receptor (PgR) positivity of breast cancer with the absence of over-expression or amplification of HER2. Inhibitors of the cyclin dependent kinases 4 and 6 (CDK4/6) have been developed and demonstrated impressive activity in patients with ER-positive HER2-negative breast cancer with marked improvements in progression free survival. This question is asking whether CDK 4/6 inhibition should be continued with hormone therapy in patients who will be switching their hormone therapy in the metastatic breast cancer setting.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham (UAB), Birmingham, Alabama, United States

Northside Hospital, Inc., Atlanta, Georgia, United States

Northwestern Medical Hospital, Chicago, Illinois, United States

The University of Kansas Cancer Center, Westwood, Kansas, United States

Albert Einstein University / Montefiore Medical Center, Bronx, New York, United States

Northwell Health/Monter Cancer Center, Lake Success, New York, United States

NYU Langone Medical Center, New York, New York, United States

Mount Sinai Medical Center, New York, New York, United States

Columbia University Medical Center, New York, New York, United States

Weill Cornell Medical Center, New York, New York, United States

Stony Brook Cancer Center, Stony Brook, New York, United States

Vanderbilt-Ingham Cancer Center, Nashville, Tennessee, United States

University of Wisconsin School of Medicine, Madison, Wisconsin, United States

Contact Details

Name: Melissa Accordino, MD

Affiliation: Columbia University

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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