Breast Neoplasm Female Clinical Trial
— GEFPICS IHC4Official title:
Retrospective Study Assessing the Concordance of the IHC4 Score Performed in Local Pathology Laboratory or in a Central Laboratory to a Molecular Gold Standard Test Endopredict in Breast Cancer Infiltrating ER+ HER2-
Verified date | November 2023 |
Source | UNICANCER |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Retrospective observational, multicentric study assessing the immunohistochemistry (IHC) based test IHC4 score in infiltrating early breast cancer: comparison of the score performed in local laboratory vs in a central laboratory and concordance with a molecular gold standard classifier (EndoPredict).
Status | Completed |
Enrollment | 155 |
Est. completion date | November 1, 2023 |
Est. primary completion date | September 30, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Sample selection criteria: 1. Prior information of the patient. 2. Histologically proven invasive breast cancer, 3. ER-positive breast cancer, according to the following criteria: ER =10 % (local assessment) 4. HER2-negative tumor by IHC (score 0 or 1+) and/or fluorescent in situ hybridization (FISH)/chromogenic in situ hybridization (CISH) negative (local assessment) 5. IHC staining slides for ER, PR, KI67 and HER2 carry out on surgical resection according to local protocol available, 6. In situ hybridization (ISH) staining for HER2 carry out on surgical resection, in case of IHC 2+ for HER2 immunostaining 7. EndoPredict test results available (EPclin), 8. Formalin-fixed and paraffin-embedded (FFPE) block from surgical resection of the primary tumor available, 9. Patient =18 years old. |
Country | Name | City | State |
---|---|---|---|
France | Centre Antoine Lacassagne | Nice |
Lead Sponsor | Collaborator |
---|---|
UNICANCER | Roche Diagnostics |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To assess the reproducibility of the IHC4 score testing performed in local pathology laboratory (i.e. real life) to in a central laboratory. | Inter-laboratory concordance rate of IHC4 score performed in a local laboratory versus central laboratory. The equivalence of the two methods is defined as a =90% concordance rate. | Day 1 | |
Secondary | To assess the inter-observer reproducibility of IHC4 scoring carry out by different local pathologists on digitalised slides. | Inter-observer reproducibility of IHC4 scoring carry out by different local pathologists on digitalised slides. | Day 1 | |
Secondary | Reproducibility of IHC4+C score compare to the molecular gold standard EPclin (Endopredict). | To assess the consistency of IHC4+C score (IHC4 combined with nodal status and tumor grade) to the molecular gold standard EPclin (Endopredict). | Day 1 | |
Secondary | To assess the consistency of the IHC4 scoring performed by a pathologist to an automatic image recognition algorithm. | Inter-observer reproducibility of IHC4 scoring carry out by a pathologist to an automatic image recognition algorithm | Day 1 |
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