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Clinical Trials in France / NCT06022159
Recruiting Phase 2

A Study to Evaluate Pre-operative HYPOfractionated Radiation Therapy in Aged (≥ 70 Years Old) or "Fragile" (≥ 65 Years) Patients With Limb or Trunk Soft Tissue SARComa.

NCT06022159 · tracked via the Priya Life Science France tracker
Phase
Phase 2
Started
2023-11-28
Last updated
2026-06-02

Condition(s) studied

Soft Tissue Sarcoma

Investigational drug(s) / intervention(s)

Hypofractionated Radiation TherapyConservative treatment

Hypofractionated Radiation Therapy: The Hypofractionated Intensity-Modulated Radiation Therapy will be delivered in 5 fractions of 6 Gy each on the Planning Target Volume (PTV). The total dose of 30 Gy will be administered in approximately 1 week.

Conservative treatment: A wide en bloc resection is required (amputation is excluded) while ensuring the best functional preservation. The surgical procedure will take place about 1,5 to 2 months after the end of the radiation therapy.

Study summary

This is a phase II, multicenter, non-randomized study.

The main objective is to evaluate the treatment with hypofractionated radiation therapy in neo-adjuvant situations on wound healing in a population of aged patients (≥ 70 years old) or ≥ 65 years of age defined as "fragile" and treated for soft tissue sarcoma.

A maximum of 48 evaluable patients will be included in this study. The patients will receive an hypofractionated radiation therapy prior to conservative surgery.

Each patient will be followed for up to 3 years after the end of complete treatment (radiotherapy + surgery).

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patient with histologically confirmed soft tissue sarcoma of the limbs or trunk. 2. Indication for neo-adjuvant or adjuvant radiotherapy. 3. Patient aged ≥ 70 years with a performance status ECOG ≤ 2 and/or aged 65 to 70 years with an ECOG of 2 and identified by the investigator as "fragile". 4. Patient affiliated to a Social Health Insurance in France. 5. Patient able to participate and willing to give informed consent prior performance of any study-related procedures. Exclusion Criteria: 1. Retroperitoneal, ORL and visceral sarcomas. 2. Previous radiotherapy in the area. 3. Metastatic disease. 4. Concomitant or sequential chemotherapy. 5. Patient requiring total surgery (amputation). 6. Other cancer under treatment. 7. Any condition or pathology contraindicating MRI. 8. Any psychological, familial, geographic or social situation, potentially preventing the provision of informed consent or compliance to study procedure. 9. Patients included in another therapeutic interventional trial. 10. Patient who has forfeited his/her freedom by administrative or legal award or who is under legal protection (curatorship and guardianship, protection of justice).

Primary outcome measure(s)

Trial sites (11)

FacilityCityRegionStatus
Institut Bergonie Bordeaux France Recruiting
Centre Oscar Lambret Lille France Recruiting
Chu de Limoges Limoges France Recruiting
Centre Leon Berard Lyon France Recruiting
Institut Regional Du Cancer de Montpellier Montpellier France Recruiting
Institut Curie Paris France Recruiting
Chu de Poitiers Poitiers France Recruiting
Institut de Cancerologie de L'Ouest Saint-Herblain France Recruiting
Chu de Toulouse Toulouse France Recruiting
IUCT-O Toulouse France Recruiting
Institut Gustave Roussy Villejuif France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06022159 on ClinicalTrials.gov ↗ ← All trials in France