University Hospital of Heidelberg, Radiation Oncology
Heidelberg, 69120, Germany
Location status: Recruiting
NCT Number: NCT04219202
The study is a randomized, open, prospective phase II study. The aim of the study is to evaluate the safety and feasibility of a hypofractionated, accelerated radiation approach based on the incidence of grade 3-5 NCI Common Terminology Criteria for Adverse Events (NCI-CTC-AE ) toxicity and / or termination of the planned therapy for any reason with neoadjuvant radiation with active beam guidance of the retroperitoneal Sarcomas using protons or carbon ions before a subsequent tumor resection.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Heidelberg, 69120, Germany
Location status: Recruiting
With retroperitoneal sarcomas, the patient benefits from neoadjuvant radiotherapy. Due to the special physical properties of particles (protons and C12 carbon ions), in particular the steep lateral dose drop, an improved protection of adjacent risk organs is e.g. Intestine, kidneys, liver etc. during the process of applying radiotherapy is possible.
The primary study objective is to demonstrate the safety and conduct of study treatment and the incidence of Grade 3-5 NCI-CTC-AE toxicity and / or termination of preferred therapy for any reason. Further target parameter is the proportion of applied therapies without the occurance of degree 3-5 NCI-CTC-AE(s).
The patients are randomized 1: 1 into the two arms (carbon ions vs. protons). Patients receive 39 Gy in (SD 3.0 Gy) in 6 fractions per week.
Secondary study objectives are local control (LC), local progression-free survival from the start of therapy (LPFS), disease-free survival (DFS), overall survival (OS) and quality of life (QoL) determined according to the EORTC-Quality of Life Questionaire (QLQ)- C30 questionnaire.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Therapeutic radiation Treatment with Protons
Therapeutic radiation Treatment with Carbon Ions
Time frame: within 12 month after radiation treatment
Evidence of the safety and practicability of the study treatment assessed for the incidence of grade 3-5 NCI-CTC-AE toxicity and / or termination of the planned therapy for any reason
Time frame: within 12 month after radiation treatment
Number of patients without new arising Tumors at the treated Tumor site
Time frame: within 12 month after radiation treatment
Number of patients without local Progression at the treated tumor site
Time frame: within 12 month after radiation treatment
Number of Patients without relapse of treated disease
Time frame: within 12 month after radiation treatment
Assesment of alive patients
Time frame: within 12 month after radiation treatment
Assessed by EORTC QLQ-C30, Minimum value 0; Maximum value 6
Interested in participating?
Request InfoUniversity Hospital Heidelberg
Other
Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion Prospektive Randomisierte Phase-II-Studie
Acronym: Retro-Ion
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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