Clinical Trial: Sporadic Angiomyolipomas (AMLs) Growth Kinetics While on Everolimus

Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Interventional

Official Title: A Phase II Study of Sporadic Angiomyolipomas (AMLs) Growth Kinetics While on Everolimus Therapy

Brief Summary: The purpose of this research study is to see if oral everolimus is tolerable and effective in the treatment of sporadic Angiomyolipomas (AMLs). AMLs are the most common non-cancerous tumor of the kidney. They are composed of blood vessels, muscle cells and fat cells.Everolimus is already an approved drug for several other diseases like kidney cancer, but is being studied now specifically to see if it is helpful for people with AML.

Detailed Summary:

Primary Objective

1. To evaluate the efficacy and tolerability of everolimus in reducing tumor volume in sporadic AMLs as measured by dynamic contrast enhanced magnetic resonance imaging (DCE MRI), in patients who might otherwise be considered for active surgical or percutaneous intervention.

Secondary Objectives

  1. To evaluate health-related quality of life (HRQoL) in subjects treated with everolimus for sporadic AMLs.
  2. To assess the growth kinetics of sporadic AMLs in patients who have been treated with everolimus as part of the study and demonstrate an objective response as well as those who have been treated with everolimus during the study with a suboptimal or no response.
  3. To measure the rate of surgical or percutaneous (embolization) intervention at 1 year from day 1 of study.
  4. To assess the safety and tolerability of everolimus in patients with sporadic AML.

Sponsor: Fox Chase Cancer Center

Current Primary Outcome: The efficacy and tolerability of everolimus in reducing tumor volume in sporadic AMLs as measured by DCE MRI [ Time Frame: 1 year from start of treatment ]

Original Primary Outcome: Same as current

Current Secondary Outcome:

  • Health-related quality of life (HRQoL) [ Time Frame: 4-6 months ]
  • Rate of surgical or percutaneous (embolization) intervention [ Time Frame: 1 year from Day 1 ]
  • Number of Participants With Treatment-Related Adverse Events as Assessed by Common Toxicity Criteria for Adverse Effects (CTCAE v4.0) [ Time Frame: 1 year from start of treatment ]


Original Secondary Outcome: Same as current

Information By: Fox Chase Cancer Center

Dates:
Date Received: August 20, 2015
Date Started: September 2015
Date Completion: July 2017
Last Updated: November 22, 2016
Last Verified: November 2016