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Spots Global Cancer Trial Database for Phase II Trial of Sunitinib (SU011248) in Patients With Recurrent or Inoperable Meningioma

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Trial Identification

Brief Title: Phase II Trial of Sunitinib (SU011248) in Patients With Recurrent or Inoperable Meningioma

Official Title: Phase II Trial of Sunitinib (SU011248) in Patients With Recurrent or Inoperable Meningioma

Study ID: NCT00589784

Interventions

Sunitinib

Study Description

Brief Summary: The purpose of this study is to find out what effects, good and/or bad, sunitinib has on patients and their tumors. At this time, no drugs are routinely used to treat meningioma, hemangioblastoma or hemangiopericytoma. Only surgery and radiation therapy are known to be useful. Sunitinib is a drug approved for advanced kidney cancer. Sunitinib is also being studied for other tumors. It may be useful in the treatment of brain tumors because it can prevent formation of new blood vessels that allow tumor cells to survive and grow.

Detailed Description: This is a phase II study of Sunitinib in patients with recurrent or inoperable meningiomas. An exploratory study will be performed for patients with recurrent hemangiopericytoma or hemangioblastoma. There will be approximately 50 patients enrolled on this study (40 meningiomas and 10 hemangiopericytomas/hemangioblastomas). The treatment plan is to use daily SU11248 at a dose of 50 mg, using the established schedule of 4 weeks of treatment followed by two weeks of rest period, forming a six-week treatment cycle. A medical professional will see each patient at least every six weeks while on the medication for toxicity assessment and physical examination. Extent of disease evaluations will occur at baseline, two weeks, twelve weeks, 24 weeks, and every twelve weeks thereafter. These evaluations will include MRI of the brain (or CT head if a patient cannot undergo MRI) and MR perfusion.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Dana Farber Cancer Institute, Boston, Massachusetts, United States

Memoral Sloan Kettering Cancer Center, Basking Ridge, New Jersey, United States

Memorial Sloan-Kettering Cancer Center at Commack, Commack, New York, United States

Memorial Sloan-Kettering Cancer Center, New York, New York, United States

University of Pittsburgh Medical Center, Pittsburg, Pennsylvania, United States

University of Virginia Health Science Center, Charlottesville, Virginia, United States

Contact Details

Name: Thomas Kaley, MD

Affiliation: Memorial Sloan Kettering Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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