🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Australia / NCT03838718
Recruiting Observational

REtroperitoneal SArcoma Registry: an International Prospective Initiative

NCT03838718 · tracked via the Priya Life Science Australia tracker
Phase
Observational
Started
2016-09-01
Last updated
2019-02-12

Condition(s) studied

Retroperitoneal Sarcoma

Study summary

Surgery is currently the only potentially curative treatment modality for localized retroperitoneal sarcoma (RPS). Available studies regarding oncologic outcomes are mainly retrospective in nature, and RPS are recognized as a rare disease. Therefore, prospective analysis of high quality data is a top priority.

Primary Objectives of this study are:

* to prospectively collect standardized clinical data and radiological and pathological material from primary RPS patients treated with surgery at reference centers.
* patient outcome will be evaluated in terms of overall survival (OS), disease-free survival (DFS), crude cumulative incidence (CCI) of local recurrence (LR) and distant metastasis (DM).

Secondary Objectives:

* to estimate the efficacy and safety of surgical treatment, including extended surgical approach to primary RPS;
* to prospectively evaluate the impact of multimodality therapy, including radiation therapy and chemotherapy;
* to identify clinical, radiological and pathological characteristics that may influence the oncological outcome or may be used as predictors of LR/DM/OS. These may be important biomarkers of disease;
* to utilize collected pathological material for research collaborations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * primary RPS operated on in the participating center; * age\>18 years at the time of the first treatment (pediatric patients can not be included) * histological confirmed diagnosis according to the WHO criteria done on biopsy or surgical specimen by dedicated sarcoma pathologist; * radiological examinations performed (contrast enhanced abdominal CT scan and/or MRI) prior to surgical resection; * signed informed consent form; * adequate compliance of the patients to the plan of follow-up Exclusion Criteria: * age\<18 years; * recurrent tumor; * benign retroperitoneal tumors; * serious psychiatric disease that precludes informed consent or limits compliance; * impossibility to ensure adequate follow-up

Primary outcome measure(s)

Trial sites (22)

FacilityCityRegionStatus
University of Southern California (USC) Los Angeles California Recruiting
Mayo Clinic Jacksonville Florida Recruiting
Moffitt Cancer Center Tampa Florida Recruiting
Winship Cancer Institute Emory Georgia Recruiting
Brigham and Women's Hospital/Dana-Farber Cancer Institute Boston Massachusetts Recruiting
The Ohio State University Columbus Ohio Recruiting
Peter MacCallum Cancer Center Melbourne Australia Recruiting
Maisonneuve-Rosemont Hospital / University of Montreal Montreal Canada Not Yet Recruiting
The Ottawa Hospital Ottawa Canada Recruiting
Mount Sinai / Princess Margaret Toronto Canada Recruiting
Institut Curie Paris France Recruiting
University Medical Center and Medical Faculty Mannheim, University of Heidelberg Mannheim Germany Not Yet Recruiting
Ludwig Maximilian University Munich Germany Recruiting
Fondazione IRCCS Istituto Nazionale dei Tumori Milan Italy Recruiting
Veneto Institute of Oncology Padova Italy Recruiting
Ospedale Borgo Roma Verona Italy Recruiting
Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology Warsaw Poland Recruiting
Institute of Oncology Ljubljana Ljubljana Slovenia Recruiting
Samsung Medical Center Seoul South Korea Not Yet Recruiting
Hospital Clinico Universitario "Virgen de la Arrixaca" Murcia Spain Not Yet Recruiting
University Hospital Birmingham (Queen Elizabeth) Birmingham United Kingdom Recruiting
Royal Marsden Hospital London United Kingdom Recruiting

Other trials for the same condition

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 NCT03838718 on ClinicalTrials.gov ↗ ← All trials in Australia