← Eichor
Study identifier: NCT03805022 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Benefit of Intensified Peri-operative Chemotherapy Within High-risk CINSARC Patients With Resectable Soft-tissue Sarcomas

Condition: Non-metastatic Soft-tissue Sarcoma · Resectable  ·  Sponsor: Institut Bergonié

PhasePhase 3
Planned participants351
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The primary objective of this trial is to investigate whether the addition of 3 additional neo-adjuvant cycles of chemotherapy (doxorubicin based chemotherapy) to standard management according to the ISG-STS 10-01 study (3 cycles of neoadjuvant doxorubicin based chemotherapy + surgery +/- radiotherapy) improves the outcome of high-risk CINSARC patients with resectable soft-tissue sarcoma (STS). Primary endpoint is metastatic progression-free survival (M-PFS, after 3 years of follow-up).

This description comes directly from the study's public registry record.

Talk to the study team

Antoine ITALIANO, MD, PhD  ·  +33 5.56.33.33.33  ·  a.italiano@bordeaux.unicancer.fr

Simone MATHOULIN-PELISSIER, MD, PhD  ·  m.mathoulin@bordeaux.unicancer.fr

Always discuss trial participation with your own doctor first.

Locations (10)

Institut BergonieBordeaux, FranceRecruiting
Centre Georges François LeclercDijon, FranceRecruiting
CHU DupuytrenLimoges, FranceRecruiting
Centre Léon BérardLyon, FranceRecruiting
Institut Paoli CalmettesMarseille, FranceRecruiting
Insitut du CancerMontpellier, FranceRecruiting
Institut de Cancérologie de l'Ouest - Site René GauducheauSaint-Herblain, FranceRecruiting
CHRU StrasbourgStrasbourg, FranceRecruiting
Institut Claudius RegaudToulouse, FranceRecruiting
Institut Gustave RoussyVillejuif, FranceNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT03805022