Localized Leiomyosarcoma Biomarker Protocol

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorUniversity of Michigan Rogel Cancer Center

About this trial

* 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.

Eligibility criteria

Qualifiers

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

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Blood and Tissue collection

Treatment groups

No treatment groups listed

Locations

3
University of Michigan48109, Ann ArborMichigan, United States
Mayo Clinic55901, RochesterMinnesota, United States
Vanderbilt University Medical Center37232, NashvilleTennessee, United States

Sponsors and collaborators

University of Michigan Rogel Cancer Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator