Recruiting

Curative Intent Treatment

Sponsor:

Australia and New Zealand Sarcoma Association

Code:

NCT07377747

Conditions

Retroperitoneal Liposarcoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Study Details

Brief 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.

Conditions

Retroperitoneal Liposarcoma

Study ID

NCT07377747

Start date

Sep 5, 2024

Status verified date

Jul, 2026

Completion date

Dec, 2032

Anticipated

Primary completion date

Dec, 2032

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Surgery with preoperative radiotherapy

This includes patient who have had any chemotherapy.

Surgery without preoperative radiotherapy

This includes patients who had surgery alone, surgery with postoperative radiotherapy and/or any chemotherapy.

Primary outcome measure

  • Abdominopelvic recurrence-free survival (ARFS). . [ Time Frame: Up to 5 years. ]

Central Contacts and Locations

Central contacts

Locations

Emory Winship Cancer Institute

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

Principal Investigator:

Kenneth Cardona

OSU James Hospital

Recruiting

Columbus, Ohio, United States, 43210

Contacts

Principal Investigator:

David Konieczkowski

MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77030

Contacts

Principal Investigator:

Christina Roland

The Princess Margaret Cancer Centre

Recruiting

Toronto, Ontario, Canada, M5G 2C4

Contacts

Principal Investigator:

Charles Catton

More Information

Sponsor

Australia and New Zealand Sarcoma Association

Last update posted

Jul 15, 2026

Last verified

Jul, 2026

Keywords

  • Sarcoma
  • liposarcoma
  • retroperitoneal

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Australia and New Zealand Sarcoma Association on 2026-07-15.