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A single-institutional cohort to determine the prevalence of new immunohistochemical panel in advanced triple-negative submitted to neoadjuvant chemotherapy and its association with response and survival.
Background/Rationale: Triple negative breast cancer (TNBC) is known to be a heterogeneous disease, and different molecular sub-classifications are proposed based in specific biomarkers as immunohistochemical (IHC) expression of the androgen-receptor (AR), Epidermal growth Factor Receptor (EGFR), Cytokeratin 5/6 (CK5/6), Cytokeratin14 (CK14), Cytokeratin 17 (CK17), clusters of differentiation 117 (CD 117), p53, Ki67 level, Programmed cell death-ligand 1 (PD-L1) and PD-L2 in tumor cell membrane and the pattern of tumor infiltrating mono-lymphocytes (PD-1+, FOXP3+, CD 4+ or cluster designation 8 (CD8 +), CD 3+, cluster of differentiation 56 (CD56+), cluster designation 68 (CD68+) or CD 14+). Predicting response and survival to neoadjuvant treatment of locally advanced triple-negative breast cancer remains a major challenge. Many doubts still prevail over the role of new biomarkers in predicting different outcomes for tumors with the same stage and morphological characteristics.
Objectives and Hypotheses:
Primary objective: To evaluate the association of the intratumoral lymphocytic infiltrate (TILs) status profile in the core biopsy with complete pathological response (CPR) outcomes to neoadjuvant chemotherapy and progression-free survival (PFS). Secondary objectives: To evaluate the association of the others biomarkers expression profile and the quality of TILs with PFS and CPR. To determine the prevalence of a large immunohistochemical panel (AR, EGFR, CK5/6, CK14, CK17, CD 117, p53, Ki67 level, PD-L1 and PD-L2 in tumor cell membrane and the pattern of tumor infiltrating mono-lymphocytes PD-1+, FOXP3+, CD 4+ , CD8 +, CD 3+, CD56+, CD68+ and/or CD 14+), before and after neoadjuvant chemotherapy. To determine if the negativation of biomarkers after the systemic treatment is associated with CPR and PFS.
Methods:
Study design: A cohort with retrospective data collection and sectional analysis of pathological material.
Data Source(s): Medical records and pathological material. Study Population: Women with locally advanced triple negative breast cancer consecutively enrolled at Brazilian National Cancer Institute (INCA) submitted to neoadjuvant treatment and subsequently operated.
Exposure(s): Status of specified biomarkers. Outcome(s): Complete Pathologic Response and Progression free Survival and Sample Size Estimations: With a type I error of 5% and study power of 80%, it is estimated that 155 patients are needed.
Statistical Analysis: Statistical analysis will be performed using SPSS (version 18.0 for windows, statistical package for social science (SPSS) Inc., Chicago, IL). Survival curves will be constructed using the Kaplan-Meier method.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Single-arm cohort | Initially, patients will be analyzed in a single group. After determining the status of the biomarkers, the patient sample will be divided into specific groups for comparative purposes. |
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| Measure | Description | Time Frame |
|---|---|---|
| Progression Free Survival (PFS) | The first event defined as local recurrence or distant relapse, or death, whichever come first. | Approximately 24 months: from diagnosis up to the first event defined as local recurrence or distant relapse, or death, whichever come first through study completion. |
| Measure | Description | Time Frame |
|---|---|---|
| Clinical Response Rate | To determine the clinical response rate in patients with palpable disease. | From date of first cycle of chemotherapy until completion of neoadjuvant treatment, approximately 16 weeks |
| Objective response rate |
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Inclusion Criteria:
Exclusion Criteria:
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Women who is biopsied and diagnosed with breast cancer in the public health system is referred to Brazilian National Cancer Institute (INCA) through a registry and screening performed by the Municipal Health Department of the city of Rio de Janeiro. Therefore, it becomes a great field for research of cancer patients by the large number of cases. Absolutely all patients enrolled in INCA for treatment have their biopsy material reviewed in DIPAT.
In this cohort, will be studied women with locally advanced TNBC consecutively enrolled at INCA between January 2010 and December 2014 that were submitted to neoadjuvant chemotherapy and subsequently operated.
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| Name | Affiliation | Role |
|---|---|---|
| Jesse L da Silva, MD | Instituto Nacional de Cancer | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Instituto Nacional do Cancer - CPQ | Rio de Janeiro | 20231050 | Brazil |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Mar 14, 2021 | |
| Reset | Apr 9, 2021 |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Mar 14, 2021 | Apr 9, 2021 |
| ID | Term |
|---|---|
| D064726 | Triple Negative Breast Neoplasms |
| D000095384 | Pathologic Complete Response |
| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
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Paraffin-embedded Hematoxylin & Eosin (H & E) core biopsy/early biopsy and surgical specimens previously analyzed in the Department of Patology of the Brazilian National Cancer Institute (INCA) will be doubly reviewed by two pathologists in our study for histological grade (Scarff-Bloom-Richardson method, modified by Elston and Ellis), histological type (according to World Health Organization, 2012), presence of carcinoma component "in situ", angiolymphatic invasion, perineural infiltration, presence of lymphocytic inflammatory infiltrate.
To compare overall objective response rate in both treatment groups.
| From date of first cycle of chemotherapy until completion of neoadjuvant treatment, approximately 16 weeks |
| Determine predictive markers | To determine predictive markers for sensitivity and resistance to chemotherapy. | Approximately 24 weeks: from diagnosis up to surgery. |
| Determine prognostic markers | To determine prognostic markers for progression free survival after neoadjuvant chemotherapy and surgery. | Approximately 24 months: from diagnosis up to the first event defined as local recurrence or distant relapse, or death, whichever come first through study completion. |
| D012871 |
| Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D018450 | Disease Progression |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |