Actively Recruiting

Age: 18Years +
All Genders
NCT07377747

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

Led by Australia and New Zealand Sarcoma Association · Updated on 2026-01-30

100

Participants Needed

9

Research Sites

429 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older with first recurrent well-differentiated and/or dedifferentiated liposarcoma of the retroperitoneal space or pelvis after previous complete or near-complete surgery
  • No distant metastasis confirmed by chest, abdomen, and pelvis imaging within 1 month
  • Histologically confirmed well-differentiated or dedifferentiated liposarcoma only
  • Sarcoma not originating from bone, abdominal, or gynecological organs
  • Tumor must be deemed resectable with expected complete or near-complete removal and treatable by radiation therapy as confirmed by a multidisciplinary team
  • WHO performance status of 0 to 2
  • American Society of Anaesthesiologist (ASA) score of 1 to 3
  • No previous radiation therapy for retroperitoneal liposarcoma
  • Prior systemic therapy is allowed
  • No active concurrent malignancy except low-risk skin, prostate, or breast cancers including in situ
  • Women of childbearing potential must have a negative pregnancy test within 3 weeks before treatment
  • Able to comply with study requirements as judged by the investigator
  • Signed informed consent approved by the institutional review board
Not Eligible

You will not qualify if you...

  • Tumor is unresectable or likely to have incomplete removal as assessed by the multidisciplinary sarcoma team
  • Extent of recurrence prevents feasible preoperative radiation therapy to all visible disease
  • Contraindications to radiation therapy such as history of bowel obstruction, mesenteric ischemia, or severe chronic inflammatory bowel disease
  • Myxoid liposarcoma histology
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 9 locations

1

Emory Winship Cancer Institute

Atlanta, Georgia, United States, 30322

Actively Recruiting

2

OSU James Hospital

Columbus, Ohio, United States, 43210

Not Yet Recruiting

3

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

4

Chris O'Brien Lifehouse

Camperdown, New South Wales, Australia, 2050

Actively Recruiting

5

Prince of Wales Hospital

Randwick, New South Wales, Australia, 2031

Actively Recruiting

6

Peter MacCallum Cancer Centre

Melbourne, Victoria, Australia, 3000

Actively Recruiting

7

UZ Leuven

Leuven, Flemish Brabant, Belgium, 3000

Actively Recruiting

8

A.C.Camargo Cancer Center - Fundacao Antonio Prudente

Liberdade, São Paulo, Brazil, 01509-010

Actively Recruiting

9

The Netherlands Cancer Institute

Amsterdam, North Holland, Netherlands, 1066 CX

Actively Recruiting

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Research Team

J

Janina Chapman

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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