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An Observational Study on Epithelioid Sarcoma

Epithelioid Sarcoma. An Observational Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03099681
Acronym
EPISObs
Enrollment
100
Registered
2017-04-04
Start date
2017-08-22
Completion date
2030-03-31
Last updated
2025-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epithelioid Sarcoma

Brief summary

Prospective Italian study aimed to provide a description of the population affected by Epithelioid Sarcoma (ES)

Detailed description

The present prospective national study aims to provide a description of the population affected by ES, an insight into the natural history of the disease and an answer some on the outstanding questions on its management. Also, it will focus on enhancing any differences between the two ES variants (classical-type and proximal-type) in order gain a better understanding of the disease, tailor the treatment and lastly improve outcome.

Interventions

OTHERTreatment for Epitheloid Sarcoma

Treatment Epitheloid Sarcoma according the disease guideline

Sponsors

Italian Sarcoma Group
Lead SponsorNETWORK

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Histological diagnosis of epithelioid sarcoma according to 2014 World Health Organization (WHO) classification, performed on biopsy or surgical specimen 2. Signed informed consent 3. Adequate patient compliance to treatment or follow up 4. No age limit

Exclusion criteria

1. Other malignancies within past 5 years, with exception of carcinoma in situ of the cervix and basocellular skin cancers treated with eradicating intent 2. Impossibility to ensure adequate compliance

Design outcomes

Primary

MeasureTime frameDescription
Type of treatment given to patients with ESFrom diagnosis until the date of death from any cause assessed up to 60 monthsNumber of chemotherapy treatment received patients affected by ES

Secondary

MeasureTime frameDescription
Radiotherapy treatmentsFrom the time of diagnosis and then every 6 months up to 60 monthsNumber of patients affected by localized ES who received radiotherapy
Chemotherapy treatmentsFrom the time of diagnosis and then every 6 months up to 60 monthsNumber of patients affected by localized ES who received chemotherapy
Predictive biomarkers for responseAt time of diagnosis and at the time of any progression where a biopsy is performed up to 60 monthsTumor biomarkers expression in tumor tissue of patients affected by ES

Countries

Italy

Contacts

Primary ContactAnnamaria Frezza, MD
annamaria.frezza@istitutotumori.mi.it003902390

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026