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Recruiting Observational

Prospective Study Evaluating the Treatment Outcomes for Localised Recurrent, Resectable Retroperitoneal Liposarcoma

NCT07377747 · tracked via the Priya Life Science France tracker
Sponsor
Australia and New Zealand Sarcoma Association
Phase
Observational
Started
2024-09-05
Last updated
2026-07-15

Condition(s) studied

Retroperitoneal Liposarcoma

Study summary

The aim of the study is to collect prospective data on the treatment outcomes in patients with first localized, resectable recurrent retroperitoneal well-differentiated and/or dedifferentiated liposarcoma undergoing curative intent treatment. Patients enrolled in this study will form a validation cohort of the TARPSWG recurrent RPS nomogram. The treatment decision (surgery alone, or preoperative RT +/- chemotherapy followed by surgery) is per the institutional multidisciplinary team recommendation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Adult age ≥ 18 presenting with first recurrent well-differentiated and/or dedifferentiated liposarcoma of retroperitoneal space or pelvis after previous macroscopically complete resection (R0/R1 resection) 2. No distant metastasis on cross-sectional imaging of chest/abdomen/pelvis (CT and/or MRI) within 1 month to confirm the absence of metastatic disease 3. Previous histologically proven well-differentiated or dedifferentiated liposarcoma histology only 4. Sarcoma not originating from bone or abdominal or gynecological viscera 5. Tumor confirmed to be resectable with likely R0/R1 resection, and all disease must be deemed to be treatable by RT (joint decision by surgeon and radiation oncologist at a sarcoma multidisciplinary team meeting) 6. WHO performance status 0-2 7. American Society of Anaesthesiologist (ASA) score 1-3 8. No prior RT for the retroperitoneal liposarcoma 9. Prior systemic therapy is allowed 10. No concurrent active malignancy (except for low risk skin malignancy, low risk prostate carcinoma, low risk breast carcinoma including in situ disease) 11. Women of childbearing potential must have a negative pregnancy test within 3 weeks prior to the first day of study treatment 12. Patient deemed able to comply with study requirements according to investigator evaluation 13. Signed, IRB-approved written informed consent Exclusion Criteria: 1. Unresectable disease or likely R2 resection as assessed by the multidisciplinary sarcoma team 2. Extent of recurrence where preoperative RT to all visible disease is not deemed to be feasible 3. Contradiction for RT such as history of bowel obstruction or mesenteric ischemia or severe chronic inflammatory bowel disease 4. Myxoid liposarcoma histology 5. Pregnancy

Primary outcome measure(s)

  • Abdominopelvic recurrence-free survival (ARFS). . — Up to 5 years.
    Defined as the time from the date of treatment start (either surgery, chemo or RT) for 1st recurrent LPS to the date of radiological abdominopelvic relapse or death whichever occurred first. Liver metastases will be regarded as distant metastatic events. rather than abdominopelvic relapse

Trial sites (13)

FacilityCityRegionStatus
Emory Winship Cancer Institute Atlanta Georgia Recruiting
Brigham and Women's Hospital Boston Massachusetts Not Yet Recruiting
OSU James Hospital Columbus Ohio Recruiting
MD Anderson Cancer Center Houston Texas Recruiting
Chris O'Brien Lifehouse Camperdown New South Wales Recruiting
Prince of Wales Hospital Randwick New South Wales Recruiting
Peter MacCallum Cancer Centre Melbourne Victoria Recruiting
UZ Leuven Leuven Flemish Brabant Recruiting
A.C.Camargo Cancer Center - Fundacao Antonio Prudente Liberdade São Paulo Recruiting
The Princess Margaret Cancer Centre Toronto Ontario Recruiting
Institut Curie Hospital Paris France Recruiting
The Netherlands Cancer Institute Amsterdam North Holland Recruiting
Maria Sklodowska-Curie National Research Institute of Oncology Warsaw Poland Not Yet Recruiting
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 NCT07377747 on ClinicalTrials.gov ↗ ← All trials in France