Loma Linda, California 92354

  • Soft Tissue Sarcoma

Purpose:

When treated with surgery alone, many soft-tissue sarcomas have a high chance of coming back. Radiation therapy is frequently used in addition to surgery to reduce the chances of the sarcoma coming back. However, radiation can have long-term side effects on the normal tissues surrounding the tumor, leading to problems such as swelling, scarring, and joint stiffness. Recently, there have been advances in the way that radiation therapy can be given. Proton radiation therapy is one of those advances. With proton radiation, it is possible to give radiation over a smaller area surrounding the tumor, resulting in less radiation to the surrounding normal tissues. The purpose of this study is to determine whether proton radiation decreases the long-term side effects of radiation on normal tissues and if smaller proton radiation fields reduce local recurrence compared to the larger radiation fields that have been used in prior studies.


Study summary:

Data support preoperative radiotherapy as one of the standard options in the management of large or high-grade extremity soft tissue sarcomas (STS). The advantages of preoperative radiotherapy are lower doses and smaller radiation volumes; these may be used to effect improvement of long-term side effects and extremity function. Another potential advantage is assisting surgery through tumor shrinkage and reduction of tumor cell seeding. The disadvantage of preoperative radiation is the higher likelihood of postoperative wound complications, but in a prospective phase III trial these complications were found to be generally temporary and without significant effect on long term function. Combined conservative surgery and radiotherapy has shown to achieve excellent local control in sarcoma patients following margin-negative surgery, but late radiation morbidity and reduced quality of life may result from adjuvant radiation. The dosimetric advantage of proton radiotherapy may translate into reduced acute and late effects due to improved normal-tissue sparing in the treatment of extremity and truncal STS. However, these potential advantages need to be validated in clinical trials. The investigators propose a phase II study to evaluate the effect of preoperative proton radiotherapy on the reduction of late radiation morbidity, patterns of failure, and impact of late radiation morbidity on general quality of life (QOL).


Criteria:

Inclusion Criteria: - Histologically proven primary soft tissue sarcoma of the upper extremity (including shoulder), lower extremity (including hip) or body trunk (excluding retroperitoneum). - No clinical evidence of distant metastatic disease - Evaluation by surgeon, with documentation that the tumor is resectable - ECOG performance status 0-1 - For females of childbearing potential, a serum pregnancy test within 4 weeks prior to registration - Patient must practice adequate contraception - Adequate bone marrow function Exclusion Criteria: - Patients with sarcoma of the head, neck, intra-abdominal or retroperitoneal region, hand or foot - Histopathology demonstrating rhabdomyosarcoma, extraosseous primitive neuroectodermal tumor (PNET), soft tissue Ewing's sarcoma, osteosarcoma, Kaposi's sarcoma, angiosarcoma, aggressive fibromatosis, dermatofibrosarcoma protuberans or chondrosarcoma - Clinical evidence of regional lymph node or distant metastatic disease - Prior invasive malignancy (except non-melanomatous skin cancer or early stage prostate cancer) unless disease free for a minimum of 3 years - Prior radiotherapy to the potential target anatomic region would result in overlap of radiation fields for current sarcoma - Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to used medically acceptable forms of contraception


NCT ID:

NCT01819831


Primary Contact:

Principal Investigator
Gary Yang, MD
gyang@llu.edu

Sandi or Miriam RN Coordinators, S Teichman RN or M Hernandez, RN
Phone: 909-558-4000 ext. 55240 / 88
Email: scteichm@llu.edu; mvhernandez@llu.edu


Backup Contact:

Email: gyang@llu.edu
Gary Yang, MD
Phone: 909-558-4000 ext. 15689


Location Contact:

Loma Linda, California 92354
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: September 23, 2021

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

If you would like to be contacted by the clinical trial representative please fill out the form below.