Study of a Cohort of Cases of Synovial Sarcoma Treated in the Orthopedic Surgery and Traumatology Department of the Hospital de Sant Pau Between 1983 and 2016
NCT ID: NCT03833037
Last Updated: 2020-02-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
102 participants
OBSERVATIONAL
2019-02-01
2019-12-31
Brief Summary
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Detailed Description
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To analyze exhaustively a series of cases of synovial sarcoma (as an example of classic subtype of soft tissue sarcoma) to analyse the complementary tests performed and their evolution over time.
To analyse the results of surgical treatment and adjuvant therapies in synovial sarcoma and its evolution over time.
To study the prognostic factors dependent on the patient and the applied therapeutics.
To establish a results-based treatment and follow-up algorithm for patients diagnosed with synovial sarcoma.
To describe the epidemiological characteristics of the group of patients in the study.
To evaluate the overall survival and disease-free survival as well as the mortality of the disease.
To assess the rate of local recurrence and remote dissemination of synovial sarcomas in the series.
To demonstrate the influence of neoadjuvant chemotherapy and radiotherapy in the treatment of the tumor.
Conduct a study by age group with respect to the influence on patient survival. To carry out a study by tumor-sized groups with respect to the influence on the survival of the patients.
To carry out a chronological study on the influence of the advances in the treatments on the survival of the patients.
Compare the results obtained with the published literature.
Conditions
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Study Design
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COHORT
OTHER
Interventions
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Soft tissue sarcomas in adults
Adult sinovial sarcoma
Eligibility Criteria
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Inclusion Criteria
The inclusion criteria were: diagnosed cases of synovial sarcoma by the service of pathological anatomy and treated by unit orthopedic surgery oncology, in location of limbs, paravertebral trunk and/or pelvis. We studied the complete medical history of the cases available for the analysis and with a minimum follow-up of 12 months.
Exclusion Criteria:
10 Years
100 Years
ALL
No
Sponsors
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Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
OTHER
Responsible Party
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Principal Investigators
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Claudia Lamas
Role: STUDY_DIRECTOR
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Locations
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Hospital de la Santa Creu i Sant Pau
Barcelona, , Spain
Countries
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Other Identifiers
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IIBSP-SAR-2018-100
Identifier Type: -
Identifier Source: org_study_id
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