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Radiation Therapy
Short-Course Radiotherapy + Surgery for Soft Tissue Sarcoma
Phase 2
Recruiting
Led By Eric Shinohara, MD
Research Sponsored by Vanderbilt-Ingram Cancer Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
ECOG performance status 0-2
Histologic diagnosis of a soft tissue sarcoma of extremity, pelvis, chest wall or trunk/abdominal wall (non-retroperitoneal location)
Must not have
History of prior radiation to the same area to be irradiated
Patients with planned neoadjuvant chemotherapy
Timeline
Screening 3 weeks
Treatment Varies
Follow Up approximately 2 years
Awards & highlights
No Placebo-Only Group
Summary
This trial uses a shorter, more intense course of radiation to treat soft tissue sarcomas. The hope is that it will allow patients to be treated more quickly with similar rates of controlling the cancer.
Who is the study for?
This trial is for individuals with a confirmed diagnosis of soft tissue sarcoma located in the limbs, pelvis, chest wall or non-retroperitoneal abdominal wall. Participants should be able to perform daily activities (ECOG status 0-2) and must be fit for radiation treatment and surgery. It's not open to those who've had prior radiation in the same area, have metastatic disease, are pregnant, will receive neoadjuvant chemotherapy, or have certain diseases that increase radiation side effects.
What is being tested?
The study is testing two shorter courses of hypofractionated radiotherapy (5 or 15 days) followed by surgical removal of the tumor in patients with soft tissue sarcoma. This approach is compared against the traditional longer course (5 weeks) to see if it can reduce treatment time without increasing wound complications or chances of cancer returning.
What are the potential side effects?
Potential side effects from hypofractionated radiotherapy may include skin irritation at the treatment site, fatigue, swelling due to fluid buildup (lymphedema), muscle stiffness around treated areas and delayed wound healing post-surgery.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I can take care of myself and am up and about more than half of the day.
Select...
My cancer is a type of soft tissue sarcoma located in my limbs, pelvis, chest wall, or abdominal wall.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had radiation treatment on the same area before.
Select...
I am scheduled for chemotherapy before surgery.
Select...
My cancer has spread to other parts of my body.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 2 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Local control rate
Secondary study objectives
Complication rate
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Group I: Group II (MH HRT)Experimental Treatment3 Interventions
Patients undergo HRT daily for a total of 15 fractions followed by surgery.
Group II: Group I (UH HRT)Experimental Treatment3 Interventions
Patients undergo HRT daily for a total of 5 fractions followed by surgery.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Resection
2023
Completed Phase 2
~420
Find a Location
Who is running the clinical trial?
Vanderbilt-Ingram Cancer CenterLead Sponsor
217 Previous Clinical Trials
63,516 Total Patients Enrolled
Eric Shinohara, MD5.02 ReviewsPrincipal Investigator - Vanderbilt Medical Center
Vanderbilt-Ingram Cancer Center
5Patient Review
Dr. Shinohara was very patient with me as we discussed the pros and cons of various treatment options for my prostate cancer. In the end, he recommended a course of action that he thought would be best for me. I would definitely recommend him to others.
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have had radiation treatment on the same area before.I am scheduled for chemotherapy before surgery.I have a genetic condition that increases my risk of side effects from radiation.You are pregnant.My cancer has spread to other parts of my body.I can take care of myself and am up and about more than half of the day.My cancer is a type of soft tissue sarcoma located in my limbs, pelvis, chest wall, or abdominal wall.I am able to undergo radiation treatment and surgery.
Research Study Groups:
This trial has the following groups:- Group 1: Group I (UH HRT)
- Group 2: Group II (MH HRT)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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