Extremity soft tissue sarcoma (ESTS) is a rare malignant nonepithelial disease, calling for combined modality treatments with surgery to further improve local control rates and long-term survival, especially in patients with multiple local recurrences with or without risk of amputation. In this double-arm, open-label, Phase II clinical trial, we will enroll 30 patients with pathologically confirmed ESTS without nodal involvement or distant metastases. Patients are randomly assigned to the combination treatment group or the radiation monotherapy group. Additionally, tumor and biological samples will be obtained directly before and after neoadjuvant therapy, allowing for studies of immune response and primary drug resistance mechanisms. ChiCTR2200060659 (http://www.chictr.org.cn) (ClinicalTrials.gov).

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11508951PMC
http://dx.doi.org/10.1080/14796694.2024.2385291DOI Listing

Publication Analysis

Top Keywords

extremity soft
8
soft tissue
8
tissue sarcoma
8
neo-adjuvant radiation
4
radiation intratumoral
4
intratumoral immunotherapy
4
immunotherapy surgery-
4
surgery- trial
4
trial extremity
4
sarcoma extremity
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!