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NCT Number: NCT04219202

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

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital of Heidelberg, Radiation Oncology

Heidelberg, 69120, Germany

Location status: Recruiting

Location contact

Adriane Hommertgen

CONTACT

[email protected]

+49-6221-56 ext. 8202

Katharina Seidensaal, MD

SUB_INVESTIGATOR

Matthias Uhl, PD

CONTACT

[email protected]

+49-6221-56 ext. 8202

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Proton Radiation

Radiation

Therapeutic radiation Treatment with Protons

Carbon Ion radiation

Radiation

Therapeutic radiation Treatment with Carbon Ions

Primary outcomes

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

    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

Secondary outcomes

  1. local Tumor control

    Time frame: within 12 month after radiation treatment

    Number of patients without new arising Tumors at the treated Tumor site

  2. local Progression free survival

    Time frame: within 12 month after radiation treatment

    Number of patients without local Progression at the treated tumor site

  3. disease free survival

    Time frame: within 12 month after radiation treatment

    Number of Patients without relapse of treated disease

  4. Overall survival

    Time frame: within 12 month after radiation treatment

    Assesment of alive patients

  5. Quality of live

    Time frame: within 12 month after radiation treatment

    Assessed by EORTC QLQ-C30, Minimum value 0; Maximum value 6

Study contacts

Contact information is provided by the study sponsor or research team.

Juergen Debus, Prof.

CONTACT

[email protected]

+496221 ext. 8201

Katharina Kozyra, Dr

CONTACT

[email protected]

+496221 ext. 8201

Sponsors and collaborators

Lead sponsor

University Hospital Heidelberg

Other

Registry information

Official study title

Neoadjuvant Irradiation of Retroperitoneal Soft Tissue Sarcoma With Ions Retro-Ion Prospektive Randomisierte Phase-II-Studie

Acronym: Retro-Ion

Important dates

Study start
2019
Primary completion
2026
Study completion
2027
First posted
Jan 6, 2020
Registry last updated
Mar 10, 2026

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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