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Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion (Retro-Ion)

Primary Purpose

Sarcoma,Soft Tissue

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Proton radiation
Carbon Ion radiation
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sarcoma,Soft Tissue

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically confirmed retroperitoneal soft-tissue sarcoma which is resectable or marginally resectable
  • Karnofsky index of ≥ 70%
  • Age from 18 years
  • Completed patient information and written consent
  • ability to give consent

Exclusion Criteria:

  • Stage IV (distant metastases)
  • Lymphogenic metastasis
  • Metal implants at the level of the sarcoma, which influence the treatment planning
  • Previous radiation therapy in the treatment area
  • Desmoid tumors, peritoneal sarcomatosis, GIST
  • Simultaneous participation in another clinical study that could influence the results of the respective study
  • Active medical implants for which there is no license for ion irradiation at the time of treatment (e.g. pacemaker, defibrillator)
  • Pregnant women

Sites / Locations

  • University Hospital of Heidelberg, Radiation OncologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Proton Treatment

Carbon Ion Treatment

Arm Description

Patient receive 39 Gy (in 13 fractions (SD 3,0 Gy) Proton Treatment

Patient receive 39 Gy (in 13 fractions (SD 3,0 Gy) Carbon Ion Treatment

Outcomes

Primary Outcome Measures

Incidence of grad 3-5 NCI-CTC-AE toxicities
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

Secondary Outcome Measures

local Tumor control
Number of patients without new arising Tumors at the treated Tumor site
local Progression free survival
Number of patients without local Progression at the treated tumor site
disease free survival
Number of Patients without relapse of treated disease
Overall survival
Assesment of alive patients
Quality of live
Assessed by EORTC QLQ-C30, Minimum value 0; Maximum value 6

Full Information

First Posted
January 3, 2020
Last Updated
June 21, 2021
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT04219202
Brief Title
Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion
Acronym
Retro-Ion
Official Title
Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion Prospektive Randomisierte Phase-II-Studie
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Recruiting
Study Start Date
May 9, 2019 (Actual)
Primary Completion Date
May 9, 2023 (Anticipated)
Study Completion Date
May 9, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoma,Soft Tissue

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Proton Treatment
Arm Type
Active Comparator
Arm Description
Patient receive 39 Gy (in 13 fractions (SD 3,0 Gy) Proton Treatment
Arm Title
Carbon Ion Treatment
Arm Type
Experimental
Arm Description
Patient receive 39 Gy (in 13 fractions (SD 3,0 Gy) Carbon Ion Treatment
Intervention Type
Radiation
Intervention Name(s)
Proton radiation
Intervention Description
Therapeutic radiation Treatment with Protons
Intervention Type
Radiation
Intervention Name(s)
Carbon Ion radiation
Intervention Description
Therapeutic radiation Treatment with Carbon Ions
Primary Outcome Measure Information:
Title
Incidence of grad 3-5 NCI-CTC-AE toxicities
Description
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
Secondary Outcome Measure Information:
Title
local Tumor control
Description
Number of patients without new arising Tumors at the treated Tumor site
Time Frame
within 12 month after radiation treatment
Title
local Progression free survival
Description
Number of patients without local Progression at the treated tumor site
Time Frame
within 12 month after radiation treatment
Title
disease free survival
Description
Number of Patients without relapse of treated disease
Time Frame
within 12 month after radiation treatment
Title
Overall survival
Description
Assesment of alive patients
Time Frame
within 12 month after radiation treatment
Title
Quality of live
Description
Assessed by EORTC QLQ-C30, Minimum value 0; Maximum value 6
Time Frame
within 12 month after radiation treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically confirmed retroperitoneal soft-tissue sarcoma which is resectable or marginally resectable Karnofsky index of ≥ 70% Age from 18 years Completed patient information and written consent ability to give consent Exclusion Criteria: Stage IV (distant metastases) Lymphogenic metastasis Metal implants at the level of the sarcoma, which influence the treatment planning Previous radiation therapy in the treatment area Desmoid tumors, peritoneal sarcomatosis, GIST Simultaneous participation in another clinical study that could influence the results of the respective study Active medical implants for which there is no license for ion irradiation at the time of treatment (e.g. pacemaker, defibrillator) Pregnant women
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juergen Debus, Prof.
Phone
+496221
Ext
8201
Email
juergen.debus@med.uni-heidelberg.de
First Name & Middle Initial & Last Name or Official Title & Degree
Katharina Seidensaal, MD
Phone
+496221
Ext
8201
Email
katharina.seidensaal@med.uni-heidelberg.de
Facility Information:
Facility Name
University Hospital of Heidelberg, Radiation Oncology
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matthias Uhl, PD
Phone
+49-6221-56
Ext
8202
Email
Matthias.uhl@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Adriane Hommertgen
Phone
+49-6221-56
Ext
8202
Email
adriane.hommertgen@med.uni-heidelberg.de
First Name & Middle Initial & Last Name & Degree
Katharina Seidensaal, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33579340
Citation
Seidensaal K, Kieser M, Hommertgen A, Jaekel C, Harrabi SB, Herfarth K, Mechtesheimer G, Lehner B, Schneider M, Nienhueser H, Frohling S, Egerer G, Debus J, Uhl M. Neoadjuvant irradiation of retroperitoneal soft tissue sarcoma with ions (Retro-Ion): study protocol for a randomized phase II pilot trial. Trials. 2021 Feb 12;22(1):134. doi: 10.1186/s13063-021-05069-z.
Results Reference
derived

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Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion

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