Sarcoma survival: does guideline care make the difference?
NCT ID NCT07864870
First seen Oct 08, 2026 · Last updated Oct 09, 2026 · Updated 1 time
Summary
Researchers at a French hospital are reviewing medical records of about 900 adults treated for soft tissue sarcoma to see how closely their care matched international guidelines. The study compares patients treated between 2010 and 2016 with those treated between 2017 and 2024. It asks whether better adherence to recommended practices is linked to longer overall survival.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If guideline adherence tracks with longer survival, this could strengthen the case for standardizing sarcoma care at hospitals everywhere.
- What could go wrong
- This is a retrospective look at records from one hospital, so it can show patterns but cannot prove that following guidelines causes better survival. Findings may not apply to other centers or patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 900 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients with suspected or confirmed soft tissue sarcoma presented at multidisciplinary tumor boards in Strasbourg between 2017 and 2024
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient aged 18 years or older at first multidisciplinary tumor board presentation * Presented for multidisciplinary tumor board evaluation for soft tissue or visceral tumor * First presentation between 01/01/2017 and 31/12/2024 * Absence of opposition to reuse of medical data for research purposes Exclusion Criteria: * Presence of opposition to reuse of medical data for research purposes * Patient younger than 18 years at first presentation * Bone tumors, gastrointestinal stromal tumors (GIST), or Kaposi sarcoma * First presentation outside the study period * Management outside Alsace-Moselle * Duplicate records
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Service d'hématologie-oncologie pédiatrique - CHU de Strasbourg - France
RECRUITINGStrasbourg, 67091, France
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