Locally Advanced Soft Tissue Sarcoma

2

Review clinical trials related to Locally Advanced Soft Tissue Sarcoma. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Superiority Trial Evaluating Digitalized Information Media for Patients With Advanced Sarcomas Receiving Systemic Treatment.

ePPS-2202 is a study designed to evaluate the benefits of a dematerialised personalised care plan (PCP) compared to standard information/PCP for patients with advanced sarcomas receiving systemic treatment. Participants will be randomised to an experimental group or a control group. Patients in the experimental group will receive the dematerialised PCP in addition to the standard PCP while patients in the control group will receive the standard PCP alone. All patients will be followed until the end of second-line treatment, the start of a new line of treatment, or until the 24-month follow-up.

Participants needed: 377
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Oscar LambretUpdated: Mar 18, 2026Locations: 11
Eligibility criteria

Sarcomas of soft tissues or viscera ; [+4]

Prior inclusion in ePPS trial for a prior systemic treatment ; [+5]

Status: Not yet recruiting

A Prospective, Single-arm, Multicenter Exploratory Clinical Study of Anlotinib Combined With Bempegaldesleukin and Conventional Chemoradiotherapy for the Treatment of Unresectable Locally Advanced or Metastatic Soft Tissue Sarcoma.

This study employs a multicenter, single-arm trial design. Participants will receive a treatment regimen consisting of "anlotinib plus bempegaldesleukin concurrent with radiotherapy," followed by a maintenance therapy phase of "anlotinib plus bempegaldesleukin concurrent with chemotherapy." The study aims to evaluate the clinical efficacy and safety of anlotinib in combination with bempegaldesleukin and conventional chemoradiotherapy for the treatment of unresectable locally advanced or metastatic soft tissue sarcoma.

Participants needed: 46
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital with Nanjing Medical UniversityUpdated: Sep 5, 2025Locations: 1
Eligibility criteria

Age: 18 to 80 years. [+7]

Prior treatment with PD-1/PD-L1/CTLA-4 antibodies, radiotherapy, or any targeted... [+8]