Could less radiation be just as good for sarcoma?
NCT ID NCT04288375
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study is testing whether giving a lower dose of radiation to a smaller area after surgery for soft tissue sarcoma works as well as the standard approach. The goal is to control the cancer while causing fewer long-term side effects. The trial includes 65 adults who had their tumor removed with clear margins and will receive 50 Gy of radiation over 25 sessions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- radiation therapy (IMRT)
- What this could lead to
- If successful, this could lead to a new standard of care that reduces long-term side effects from radiation while still controlling the sarcoma.
- What could go wrong
- This is a small Phase 2 study with only 65 participants, so results may not apply to everyone. Lowering the dose could also increase the risk of the cancer coming back.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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65 people
The number who actually took part.
- Started
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Feb 2020
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients must be diagnosed with a primary soft tissue sarcoma of the extremity, confirmed by MSKCC pathologic review * Age at the time of enrollment of ≥18 years * Patients must have undergone margin-negative oncologic resection of their primary tumor, as confirmed by MSKCC pathologic review * Patients must be able to start radiation within 3 months from time of surgery °If patient is receiving adjuvant chemotherapy, patient must start RT no longer than 3 months past their chemo treatment. * Female patients of childbearing potential must have a negative serum pregnancy test within 14 days of radiation start (or if urine test, within 24 hours of radiation start) * Sexually active patients of childbearing potential must agree to use effective contraception. * The use of chemotherapy will not be dictated by this trial. Patients are allowed to receive chemotherapy at the discretion of the disease management team (as is standard practice to make individualized decisions for each patient regarding the use of chemotherapy). Exclusion Criteria: * Patients with positive margins after surgical resection as indicated by MSKCC pathologic review * Patients with diagnosis of superficial myxofibrosarcoma with indistinct/infiltrative borders on preoperative MRI16 (see Appendix Figure 1 for reference figure) * Patients with multifocal disease in the extremity * Patients who have received prior radiotherapy at or adjacent to the primary tumor bed * Patients with a differentinvasive cancer requiring active treatment at the time of enrollment. * Patients with any concurrent medical or psychiatric condition or disease which, in the investigator's judgment, would make them inappropriate candidates for entry into this study
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Basking Ridge (All protocol activities)
Basking Ridge, New Jersey, 07920, United States
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Memorial Sloan Kettering Bergen (All protocol activities)
Montvale, New Jersey, 07645, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Commack (All protocol activities)
Commack, New York, 11725, United States
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Memorial Sloan Kettering Monmouth (All protocol activities)
Middletown, New Jersey, 07748, United States
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Memorial Sloan Kettering Nassau (All protocol activities)
Uniondale, New York, 11553, United States
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Memorial Sloan Kettering Westchester (All protocol activities)
Harrison, New York, 10604, United States
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Other studies related to the condition(s) this trial covers.
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