Purpose

- Leiomyosarcoma (LMS) is one of the more common soft tissue sarcomas (STS). - Patients presenting with large, high-grade, localized LMS are at significant risk of developing metastasis following curative surgery. - Clinical trials of neoadjuvant or adjuvant anthracycline and ifosfamide have suggested that patients with localized STS who are at high-risk of metastasis may benefit from chemotherapy, but the magnitude of benefit in unselected patient population is relatively small. - Currently, patient age, and tumor size and grade are used to assess risk of metastases and survival - Studies evaluating tumor response by imaging and histopathology have not established correlation between tumor characteristics as biomarkers for risk of metastasis or sarcoma recurrence. - Circulating tumor DNA (ctDNA) is present in blood of patients with advanced/metastatic LMS and may serve as biomarker of tumor response to chemotherapy. Blood samples will be collected prior to, during and after chemotherapy and analyzed for ctDNA and for mutations in genes that are associated with increased risk of developing sarcoma. Tumor tissue will be collected and analyzed for changes in genes. Digital images of the sarcoma from CT or MRI scans obtained during treatment will be obtained for advanced radiomic analysis. Patients will be followed for 2 years after study entry for signs of sarcoma recurrence. - A biomarker of tumor response and patient survival benefit from chemotherapy early in the course of chemotherapy would be of significant impact in treatment planning.

Condition

Eligibility

Eligible Ages
All ages
Eligible Sex
All
Accepts Healthy Volunteers
No

Criteria

Inclusion Criteria:

- Patients with localized leiomyosarcoma (LMS) of extremity, body wall or
retroperitoneum

- Grade 2 or 3, or high-grade LMS

- Tumor size >5 cm in greatest dimension

- Primary tumor amenable to complete resection

- There is no age requirement

- Participant agrees to receive neoadjuvant doxorubicin and ifosfamide combination
chemotherapy

- If pre-operative radiation is administered, it must be administered after
chemotherapy. Post-operative radiation may be administered

- Archival tumor tissue (either frozen sample, tissue block containing tumor, or
minimum of 4 unstained slides and 1 H&E stained slide) from diagnostic or
pre-treatment biopsy available for study research

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Recruiting Locations

University of Michigan
Ann Arbor, Michigan 48109
Contact:
Scott Schuetze, MD/PhD
734-647-8925

Mayo Clinic
Rochester, Minnesota 55901
Contact:
Brittany Siontis, MD

Vanderbilt University Medical Center
Nashville, Tennessee 37232
Contact:
Elizabeth J Davis, MD
615-322-5000

More Details

Status
Recruiting
Sponsor
University of Michigan Rogel Cancer Center

Study Contact

Scott Schuetze
7346478921
scotschu@med.umich.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.