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A non-rhabdomyosarcoma soft tissue sarcoma (NRSTS) is a tumor that can develop in the body’s soft tissues. There are more than 50 types of NRSTS tumors. They are grouped together because they are rare and usually treated in a similar way.
NRSTS tumors commonly occur in the arms and legs. But they can occur anywhere in the body.
The subtypes of NRSTS together make up 4% of all childhood cancers.
Find out more about NRSTS on the Together by St. Jude™ online resource.
The most common types of NRSTS tumors in children include:
Other types of NRSTS tumors are:
Surgery is the most effective NRSTS treatment. Surgery is used to remove as much of the tumor as possible.
Radiation therapy may also be used with patients who have tumor remaining after surgery or for patients with more aggressive tumor types.
Chemotherapy may benefit certain patients with intermediate and high-risk NRSTS tumors.
Scientists are also studying targeted therapies to treat NRSTS.
St. Jude offers clinical trials and cancer research studies for children, teens, and young adults with NRSTS. Learn more about clinical trials at St. Jude.
Study goal:
The purpose of this clinical trial is to find better treatments for NRSTS patients who are intermediate- and high-risk. Our goal is to lower the risk of the tumor coming back after treatment, while using treatments with fewer risks of long-term side effects.
Age:
Up to 30 years old.
St. Jude provides the highest level of care for patients with NRSTS:
More reasons to choose St. Jude for care include:
Patients accepted to St. Jude must have a disease we treat and must be referred by a physician or other qualified medical professional. We accept most patients based on their ability to enroll in an open clinical trial.
Call: 1-888-226-4343 (toll-free) or 901-595-4055 (local) | Fax: 901-595-4011 | Email: referralinfo@stjude.org | 24-hour pager: 1-800-349-4334
The solid tumor coordinator is dedicated to helping you seek treatment or refer a patient.
Solid Tumor Coordinator