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

Status: Recruiting
Location: See all (9) locations...
Study Type: Observational
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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)

• 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

• Previous histologically proven well-differentiated or dedifferentiated liposarcoma histology only

• Sarcoma not originating from bone or abdominal or gynecological viscera

• 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)

• WHO performance status 0-2

• American Society of Anaesthesiologist (ASA) score 1-3

• No prior RT for the retroperitoneal liposarcoma

• Prior systemic therapy is allowed

⁃ No concurrent active malignancy (except for low risk skin malignancy, low risk prostate carcinoma, low risk breast carcinoma including in situ disease)

⁃ Women of childbearing potential must have a negative pregnancy test within 3 weeks prior to the first day of study treatment

⁃ Patient deemed able to comply with study requirements according to investigator evaluation

⁃ Signed, IRB-approved written informed consent

Locations
United States
Georgia
Emory Winship Cancer Institute
RECRUITING
Atlanta
Ohio
OSU James Hospital
NOT_YET_RECRUITING
Columbus
Texas
MD Anderson Cancer Center
RECRUITING
Houston
Other Locations
Australia
Chris O'Brien Lifehouse
RECRUITING
Camperdown
Peter MacCallum Cancer Centre
RECRUITING
Melbourne
Prince of Wales Hospital
RECRUITING
Randwick
Belgium
UZ Leuven
RECRUITING
Leuven
Brazil
A.C.Camargo Cancer Center - Fundacao Antonio Prudente
RECRUITING
Liberdade
Netherlands
The Netherlands Cancer Institute
RECRUITING
Amsterdam
Contact Information
Primary
Janina Chapman
janina.chapman@petermac.org
61414316490
Time Frame
Start Date: 2024-09-05
Estimated Completion Date: 2032-12
Participants
Target number of participants: 100
Treatments
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.
Sponsors
Leads: Australia and New Zealand Sarcoma Association

This content was sourced from clinicaltrials.gov