Phase I/II Trial of Pre-Operative Image Guided Intensity Modulated Proton Radiation Therapy (IMPT) or Photon (IMRT) With Simultaneously Integrated Boost to the High Risk Margin for Retroperitoneal Sarcomas

Who is this study for? Adult patients with Primary Soft Tissue Sarcoma of the Retroperitoneum
Status: Recruiting
Location: See all (10) locations...
Intervention Type: Radiation
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

This research study is a Phase I clinical trial. Phase I clinical trials test the safety of an investigational intervention. Phase I studies also try to define the appropriate dose of the investigational therapy to use for further studies. Investigational means that the intervention is still being studied and that research doctors are trying to find out more about it. Retroperitoneal sarcomas are soft tissue tumors located at the far back of the abdomen. Typically, patients with retroperitoneal sarcomas either have surgery for the removal of their tumors alone, or have their tumors removed, followed by standard radiation therapy, or have pre-operative radiation followed by surgery. When conventional radiation therapy is delivered after surgery, it can damage normal tissue. In this study, you will undergo proton beam radiation therapy or IMRT before undergoing surgery for the removal of your tumor. Proton radiation and IMRT are FDA approved radiation delivery systems. Protons are tiny particles with positive charge that can be controlled to travel a certain distance and stop inside the body. In theory, this allows better control of where the radiation dose is delivered as compared to photons. Since proton radiation is more targeted, it may help to reduce unwanted side effects from radiation. In this study, a standard dose of radiation will be given to the majority of the tumor, while a simultaneously integrated boost of additional radiation will be given to certain areas of the tumor identified as higher risk. This means that a higher radiation dose will be given to the higher risk areas of the tumor. The purpose of this study is to determine the highest dose of radiation therapy with protons or IMRT that can be delivered safely in patients with retroperitoneal sarcomas and the effectiveness of proton beam radiation therapy as an intervention for patients with retroperitoneal sarcomas.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically proven primary soft tissue sarcoma of the retroperitoneum

• Measurable disease

• Life expectancy of greater than 2 years

Locations
United States
Illinois
Rush University Medical Center
RECRUITING
Chicago
Massachusetts
Dana-Farber Cancer Institute
RECRUITING
Boston
Massachusetts General Hospital
RECRUITING
Boston
Minnesota
Mayo Clinic
RECRUITING
Rochester
Missouri
Washington University School of Medicine Siteman Cancer Center West County
RECRUITING
Creve Coeur
Washington University School of Medicine Siteman Cancer Center South County
RECRUITING
Saint Louis
North Carolina
Duke University
RECRUITING
Durham
New York
Roswell Park Cancer Institute
RECRUITING
Buffalo
Texas
MD Anderson Cancer Center
RECRUITING
Houston
Utah
University of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Thomas DeLaney, MD
tdelaney@partners.org
617-726-6876
Time Frame
Start Date: 2012-12
Estimated Completion Date: 2025-08
Participants
Target number of participants: 80
Treatments
Experimental: Treatment Arm IMPT
IG-IMPT with SIB to the high risk margin
Experimental: Treatment Arm IMRT
IG IMRT with SIB to the high risk margin
Related Therapeutic Areas
Sponsors
Collaborators: Mayo Clinic, Washington University School of Medicine, Dana-Farber Cancer Institute, Roswell Park Cancer Institute, University of Utah, Duke University, National Cancer Institute (NCI), Rush University Medical Center
Leads: Massachusetts General Hospital

This content was sourced from clinicaltrials.gov

Similar Clinical Trials