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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05422547
Other study ID # Immunoscore®
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 1, 2022
Est. completion date December 30, 2023

Study information

Verified date June 2022
Source D'Or Institute for Research and Education
Contact Camila M Moniz, PhD
Phone 55 11 2109-8855
Email camila.venchiarutti@idor.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The proposed study is a bidirectional analytical study, composed of a retrospective and a prospective cohorts. Patients with stage II - III colorectal cancer undergoing oncological surgery will be analyzed. The study will include a convenience sample of 100 individuals. Fifty cases will be included retrospectively and fifty prospectively. The study aims to evaluate the benefit of using the Immunoscore test as a predictor of recurrence in patients with operated stage II-III colon tumors. It will also be evaluated the impact on oncologic decision and costs.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 30, 2023
Est. primary completion date December 30, 2022
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Anatomopathological diagnosis of colorectal adenocarcinoma 2. Stage II - III (AJCC 8th edition) 3. Patient undergoing surgery with curative intent Exclusion Criteria: 1. Current or previous diagnosis (within the last 5 years) of another invasive primary malignant neoplasm, with the exception of non-melanoma skin neoplasm 2. Presence of distant metastatic disease evidenced in imaging tests

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Immunoscore Colon Test
Immunoscore® is a tissue-based immune test that measures the host's immune response at the site of the tumor. It is performed on formalin-fixed paraffin-embedded (FFPE) tumor tissue samples from resections of localized colon cancer. The test uses whole slide imaging and artificial intelligence algorithms for assessment of the type, density, and location of T cells in FFPE tumor sections to determine an individual Immunoscore® for each patient.

Locations

Country Name City State
Brazil Instituto D'Or de Pesquisa e Ensino - Brasília Brasília Distrito Federal
Brazil Instituto D'Or de Pesquisa e Ensino - Rio de Janeiro Rio De Janeiro

Sponsors (3)

Lead Sponsor Collaborator
D'Or Institute for Research and Education Diagnosticos da America SA, HalioDx

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Tumour recurrence Impact of Immunoscore stratification on tumor recurrence at 2 years 2 years
Secondary Disease-free survival (DFS) Impact of Immunoscore stratification on DFS at 5 years 5 years
Secondary Overall survival (OS) Impact of Immunoscore stratification on OS at 5 years 5 years
Secondary DFS acoording tumor side Impact of Immunoscore stratification on DFS in right and left tumors at 3 years 3 years
Secondary OS acoording tumor side Impact of Immunoscore stratification on OS in right and left tumors at 3 years 3 years
Secondary Indication of adjuvant therapy Percentage of patients who had an indication for adjuvant therapy through the evaluation of medical prescriptions 6 months
Secondary Biomarker measurements Correlation of Immunoscore stratification with the KRAS, NRAS and BRAF status 6 months
Secondary Possible economic impact Difference in monetary value due to Immuno Score stratification and chemotherapy indication 5 years
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