Clinical trial Recruiting at 7 sites Observational Ages 18 to 120

Quality assessment of sarcoma care in Europe and Latin America

Official title: Observational Study, for Quality Assessment, of Sarcoma As a Model to Improve Diagnosis and Clinical Care of Rare Tumors Through a European and Latin American Multidisciplinary NETWORK

Run by Grupo Espanol de Investigacion en Sarcomas · NCT04181970 · Data updated 2026-11-12

This study looks at how well patients with different types of sarcoma are treated in Europe and Latin America to see if care is better at expert centers and to find ways to improve outcomes.

More Soft Tissue Sarcoma trials

Quick facts

Study typeObservational
Ages18 Years to 120 Years
SexAll
Enrollment5000 (estimated)
SponsorGrupo Espanol de Investigacion en Sarcomas
Academic / other
Locations9 sites (Buenos Aires and 8 other locations)
StatusRecruiting
StartedJune 30, 2019
Main results expectedSeptember 30, 2026
Study endsSeptember 30, 2026
Registry record updatedMarch 21, 2025
Trial IDNCT04181970 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 and older with a histological diagnosis of soft-tissue sarcoma, gastrointestinal stromal tumor, or bone sarcoma.

Probably not a fit

Patients with sarcomas diagnosed before January 2005 or those without available clinical and treatment information may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to evaluate the quality of care for patients with soft-tissue sarcoma, gastrointestinal stromal tumors, and bone sarcoma across expert and non-expert centers. It involves both retrospective and prospective data collection, analyzing various quality indicators and patient outcomes such as survival rates and treatment efficacy. The study also includes a translational research component, utilizing tumor samples to identify biomarkers and develop preclinical models. The goal is to enhance the understanding of treatment differences and improve patient prognosis in sarcoma care.

Why it matters

Potential benefit: If successful, this study could lead to improved treatment protocols and outcomes for sarcoma patients.

How similar studies have gone: Previous studies have shown positive outcomes in sarcoma management when patients are treated at expert centers, supporting the relevance of this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Histological diagnosis of soft-tissue sarcoma, GIST or bone sarcoma (all subtypes) from January 2005 until Juny/September 2023.
* ≥ 18 years
* Available clinical and treatment information

Exclusion Criteria:

There is no exclusion criteria

Where it's running

  • A C Camargo
    São Paulo, Brazil
    Recruiting
  • Centre Leon Berard
    Lyon, France
    Recruiting
  • Instituto Ortopedico Rizzoli
    Bologna, Italy
    Recruiting
  • Insituto Nazionale Di Tumore
    Milan, Italy
    Recruiting
  • Instituto Nacional de Cancerología
    Mexico City, Mexico
    Recruiting
  • Instituo Nacional de enfermedades Neoplásicas
    Surquillo, Peru
    Recruiting
Show 3 more locations
  • Fundación Jiménez Díaz
    Madrid, Madrid, Spain
    Recruiting
  • Alexander Fleming Sa
    Buenos Aires, Argentina
    Not yet recruiting
  • Hospital San Vicente de Paúl
    Heredia, Costa Rica
    Not yet recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.