Multidisciplinary Approach to Breast Cancer Through the Study of Altered Transcriptomic and Immune Accompanied by the Identification of Extractable Markers From the Radiodiagnostic Bioimaging

Sponsor
IRCCS SYNLAB SDN (Other)
Overall Status
Recruiting
CT.gov ID
NCT05809128
Collaborator
(none)
1,000
1
48
20.8

Study Details

Study Description

Brief Summary

Prospective observational study for onco-immunologic characterization and by bioimaging of breast neoplastic tissue of patients operated for breast cancer

Condition or Disease Intervention/Treatment Phase
  • Other: surgery for breast cancer and imaging test evaluations

Study Design

Study Type:
Observational
Anticipated Enrollment :
1000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Multidisciplinary Approach to Breast Cancer Through the Study of Altered Transcriptomic and Immune Accompanied by the Identification of Extractable Markers From the Radiodiagnostic Bioimaging
Actual Study Start Date :
May 29, 2019
Actual Primary Completion Date :
Jan 31, 2023
Anticipated Study Completion Date :
May 28, 2023

Outcome Measures

Primary Outcome Measures

  1. Multiparametric flow cytometry analyses of Custer of Differentiation (CD) proteins expression on tumor infiltrating lymphocytes [1-24 months]

    The following phase of the study aims to go to evaluate the immunology of breast cancer patients compared with the control. In particular we will perfome an accurate characterization in flow cytometry of the cells present in the peripheral blood and of the immune component infiltrating the tumor (tumor infiltrating lymphocytes). The different components of tumor infiltrating lymphocytes will be assessed using the following antibodies: CD45 , CD8, CD4,CD3, HLA-DR, CD19 , CD 326 (EpCAM) ,CD56 , CD14 and CD16.

  2. Analysis of gene expression profiles of cancer cells [1-24 months]

    The following area of study is focused on the study by molecular biology of samples of cancerous and healthy tissue that will be possible to obtain from the subjects participating in the study. For that phase, the type of instrumentation will be determined according to the amount of nucleic acids extracted from the tissues. In fact, samples that will allow recovery of high amounts of RNA and with a good degree of purity will be able to be used for studies carried out with next generation sequencing such as, for example, Ion Torrent S5. In the case of samples in which the RNA is difficult to extract or of low quality, methods such as real time polymerase chain reaction (PCR) in multiplex mode

  3. Extraction of features from radiological images to be used as biomarkers. [1-36 months]

    Radiological images from High-field MRI, multilayer CT, hybrid systems such as PET-CT and PET-MRI will be use to extract quantitative parameters of the lesion and the other structures of interest. An automatic segmentation , or alternatively, a manual segmentation by an experienced radiologist or experienced nuclear physician will be performe.

  4. Bioinformatics analysis [37-48 months]

    The correlations between the cytofluorimetric characterization of TILs and the quantitative parameters extracted from radiological images will be performed using different software such as Graphpad or ER softwares.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 80 Years
Sexes Eligible for Study:
Female
Inclusion Criteria:
  • Clinical diagnosis of breast cancer.

  • patients 25 to 80 years of age

Exclusion Criteria:
  • Patients who refuse to participate in the study;

  • Patients who do not fall within the age range mentioned above

Contacts and Locations

Locations

Site City State Country Postal Code
1 IRCCS Synlab SDN Naples Italy 80143

Sponsors and Collaborators

  • IRCCS SYNLAB SDN

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
IRCCS SYNLAB SDN
ClinicalTrials.gov Identifier:
NCT05809128
Other Study ID Numbers:
  • 3/19
First Posted:
Apr 12, 2023
Last Update Posted:
Apr 12, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 12, 2023