⭐️⭐️⭐️⭐️⭐️ "A total no brainer"

⭐️⭐️⭐️⭐️⭐️ "Love this, so easy."

Spots is the easy way to track your skin, mole and cancer changes.

Spots Global Cancer Trial Database for Trastuzumab in Treating Patients With Locally Advanced or Metastatic Synovial Sarcoma

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Trastuzumab in Treating Patients With Locally Advanced or Metastatic Synovial Sarcoma

Official Title: Phase II Study of Trastuzumab (NSC-688097) in Treatment of Locally Advanced or Metastatic Synovial Sarcoma

Study ID: NCT00104949

Conditions

Sarcoma

Interventions

trastuzumab

Study Description

Brief Summary: RATIONALE: Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Trastuzumab may also stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well trastuzumab works in treating patients with locally advanced or metastatic synovial sarcoma.

Detailed Description: OBJECTIVES: Primary * Determine the response rate (confirmed complete response and partial response) in patients with HER2/neu-overexpressing locally advanced or metastatic synovial sarcoma treated with trastuzumab (Herceptin\^®). Secondary * Determine the frequency and severity of toxic effects of this drug in these patients. * Determine overall survival and progression-free survival of patients treated with this drug. * Correlate, preliminarily, SYT-SSX translocation, HER2/neu expression, and monophasic and biphasic phenotype with clinical outcomes in patients treated with this drug. OUTLINE: This is a pilot, multicenter study. Patients receive trastuzumab (Herceptin\^®) IV over 90 minutes on day 1. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 6 weeks until disease progression and then every 6 months for up to 2 years from study entry. PROJECTED ACCRUAL: A total of 20-40 patients will be accrued for this study within 10-40 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Contact Details

Name: Ernest C. Borden, MD

Affiliation: The Cleveland Clinic

Role:

Name: Rashmi Chugh, MD

Affiliation: University of Michigan Rogel Cancer Center

Role:

Name: George D. Demetri, MD

Affiliation: Dana-Farber Cancer Institute

Role:

Name: Margaret von Mehren, MD

Affiliation: Fox Chase Cancer Center

Role:

Name: Vivien H.C. Bramwell, MB, BS, PhD, FRCP

Affiliation: Tom Baker Cancer Centre - Calgary

Role:

Name: Karen H. Albritton, MD

Affiliation: Dana-Farber Cancer Institute

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

Logo

Take Control of Your Skin and Body Changes Today.

Try out Spots for free, set up only takes 2 mins.

spots app storespots app store

Join others from around the world: