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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06375941
Other study ID # ProStars
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 29, 2024
Est. completion date April 1, 2034

Study information

Verified date April 2024
Source Italian Sarcoma Group
Contact Gianluca Ignazzi
Phone +393335359192
Email gianluca.ignazzi@italiansarcomagroup.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will be a multi-institutional, prospective, observational study of patients with localized primary AS of any site within ISG and RTR centers. Patients will be treated according to clinical practice of the center and according to ISG clinical recommendations on localized AS.


Description:

The management of localized AS remains a clinical challenge and needs to be better defined and standardized, especially with regards to the role of radiation-therapy and systemic treatment. Several questions about the best treatment approach to some clinical presentations remain open and would need to be answered by clinical studies. Unfortunately, the rarity of this histology among sarcomas makes it challenging to carry out clinical studies in all such presentations. Moreover, prognostic factors are lacking and differences in epidemiological, pathological and clinical aspects between primary AS and secondary AS need to be better characterized. These issues may be addressed with a prospective multi-institutional observational study, through the collection of clinical and pathological data of patients with localized AS. Involving all reference centres for sarcoma in Italy, the Italian Sarcoma Group (ISG) will be the ideal network for this study, with the collaboration of the Italian Rare Cancer Network (RTR), a 7collaborative network among Italian centres focusing on improving the quality of care of patients with rare tumors.


Recruitment information / eligibility

Status Recruiting
Enrollment 250
Est. completion date April 1, 2034
Est. primary completion date April 1, 2029
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - pathological diagnosis of AS; - any site of origin; - any age; - primary, localized, resectable disease. Exclusion Criteria: NA

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observational
Observational

Locations

Country Name City State
Italy IRCCS Istituto Nazionale Tumori - Milano Milano

Sponsors (1)

Lead Sponsor Collaborator
Italian Sarcoma Group

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Demographic characteristics Demographic data At the time of enrollment
Primary General characteristics Comorbidities At the time of enrollment
Primary Cancer data Previous cancer data At the time of enrollment
Primary Origin of Tumor Site of origin At the time of enrollment
Primary Tumor characteristics Multifocality At the time of enrollment
Primary Tumor size Size At the time of enrollment
Primary Tumor aspects Morphological aspects 10 years
Primary Pathological characteristics Proliferative index 10 years
Primary Tumor phenotype Tumor cell phenotype 10 years
Primary Molecular characteristics Molecular aspects 10 years
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