Actively Recruiting
Observational Study for Quality Assessment of Sarcoma to Improve Diagnosis and Clinical Care Through a European and Latin American Multidisciplinary Network
Led by Grupo Espanol de Investigacion en Sarcomas · Updated on 2025-03-21
5000
Participants Needed
9
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are conducting an observational study to evaluate the quality of care for patients with soft-tissue sarcoma, gastrointestinal stromal tumor (GIST), and bone sarcoma. The study compares outcomes such as relapse-free survival, overall survival, and amputation rates between expert and non-expert centers. Expert pathology peer reviews and translational research on tumor samples from four sarcoma subtypes are included to explore biomarkers and develop preclinical models. The study includes both retrospective data from January 2012 to June 2019 and prospective data from July 2019 to January 2022. Data collected involves clinical and treatment information registered in a shared database. Quality indicators assessed include biopsy methods, imaging studies, multidisciplinary team discussions, surgical margins, re-resections, radiotherapy use, and molecular status assessments for GIST. Tumor samples will be analyzed by expert centers for diagnosis differences and biomarker research. Participants will provide informed consent and clinical data will be collected and analyzed over approximately three years. The study measures various quality and outcome indicators such as biopsy rates, imaging, surgical margins, survival rates, and amputation frequencies. Tumor tissue samples will be used for genetic and protein analyses, with some fresh samples used to create models for further research. Patients may withdraw consent at any time without affecting their care or participation in data collection.
CONDITIONS
Brief Title
Observational Study, for Quality Assessment, of Sarcoma in European and Latin American Multidisciplinary NETWORK
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histological diagnosis of soft-tissue sarcoma, gastrointestinal stromal tumor (GIST), or bone sarcoma (all subtypes) from January 2005 until June/September 2023
- Age 18 years or older
- Available clinical and treatment information
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 years
Participants' clinical data, diagnosis, treatment, and follow-up information are observed and recorded over time to assess quality of care and outcomes.
Regular clinical visits as per standard care
Trial Site Locations
Total: 9 locations
1
Alexander Fleming Sa
Buenos Aires, Argentina
Not Yet Recruiting
2
A C Camargo
São Paulo, Brazil
Actively Recruiting
3
Hospital San Vicente de Paúl
Heredia, Costa Rica
Not Yet Recruiting
4
Centre Leon Berard
Lyon, France
Actively Recruiting
5
Instituto Ortopedico Rizzoli
Bologna, Italy
Actively Recruiting
6
Insituto Nazionale Di Tumore
Milan, Italy
Actively Recruiting
7
Instituto Nacional de Cancerología
Mexico City, Mexico
Actively Recruiting
8
Instituo Nacional de enfermedades Neoplásicas
Surquillo, Peru
Actively Recruiting
9
Fundación Jiménez Díaz
Madrid, Madrid, Spain, 28040
Actively Recruiting
Research Team
M
Marta Martin
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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