Proton or Photon RT for Retroperitoneal Sarcomas

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Massachusetts General Hospital
Study ID
NCT01659203
Phase
PHASE1/PHASE2
Status
Recruiting

Conditions

  • Retroperitoneal Sarcoma

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • IG-IMPT — RADIATION
    Daily, Monday-Friday for about 6 weeks
  • IG IMRT — RADIATION
    Daily, Monday-Friday for about 6 weeks

Study Details

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.

Key Dates

Start date
Dec 31, 2012
Status verified
Mar 2026
Primary completion
Jun 30, 2027
Completion
Dec 31, 2027

Study Design

Enrollment
80 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • 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

Primary Outcome Measure

Phase I: Determine MTD [ Time Frame: 2 years ]

Central Contacts

Locations (10)

FacilityCityStateZIPSite coordinators
Rush University Medical CenterChicagoIllinois60612
Dian Wang, MD
Dana-Farber Cancer InstituteBostonMassachusetts02115
Elizabeth Baldini, MD, MPH
6177326310
Elizabeth Baldini, MD, MPH (PRINCIPAL_INVESTIGATOR)
Massachusetts General HospitalBostonMassachusetts02114
Thomas DeLaney, MD
6177266876
Thomas DeLaney, MD (PRINCIPAL_INVESTIGATOR)
Mayo ClinicRochesterMinnesota55902
Ivy Peterson, MD
Washington University School of Medicine Siteman Cancer Center West CountyCreve CoeurMissouri63141
Jeff Michalski, MD
Washington University School of Medicine Siteman Cancer Center South CountySt LouisMissouri63129
Jeff Michalski, MD
Roswell Park Cancer InstituteBuffaloNew York14263
Varun Chowdhry, MD
Varun Chowdhry, MD (PRINCIPAL_INVESTIGATOR)
Duke UniversityDurhamNorth Carolina27710
Trey Blazer, MD
MD Anderson Cancer CenterHoustonTexas77030
Andrew Bishop, MD
Andrew Bishop, MD (PRINCIPAL_INVESTIGATOR)
University of UtahSalt Lake CityUtah84112
Ying Hitchcock, MD

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