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Programmed Death-Ligand1 Expression in Her-2 Positive and Triple Negative Breast Cancer

Correlation Between Programmed Death-Ligand1 Expression and Clinical Outcomes After Neoadjuvant Systemic Therapy in Her-2 Positive and Triple Negative Breast Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05169853
Enrollment
80
Registered
2021-12-27
Start date
2022-01-01
Completion date
2024-10-30
Last updated
2024-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HER2-positive Breast Cancer, Triple Negative Breast Cancer

Keywords

breast cancer, her-2 positive, triple negative, neoadjuvant therapy

Brief summary

Patients with Her-2 positive and triple negative breast cancer who received neoadjuvant chemotherapy will be included in the study. Paraffin blocks of preoperative core or tru-cut biopsies of the participants will be collected and tested for programmed death-ligand 1 (PD-L1) expression. The variation of PD-L1 expression among different breast cancer subtypes will be evaluated and the investigator will correlate between PD-L1 expression and pathological complete response to neoadjuvant systemic therapy.

Detailed description

Files of breast cancer patients attending breast cancer clinic at Ain Shams University Clinical oncology and nuclear medicine department will be viewed by the investigator and those who fit the selection criteria will be included in the study. Tru-cut or core tissue biopsies obtained from the participants for initial diagnosis will be collected and PD-L1 testing will be done on the specimens. Scoring of PD-L1 will be done using Combined positive score (CPS) score. PD-L1 expression will be evaluated among Her-2 positive and triple negative subtypes and will be correlated with pathological complete response after reviewing the postoperative pathology results of the patients.

Interventions

None listed

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients aged 18 years old or more * Histologically proven invasive breast cancer * Any T stage, any N Stage with no distant metastasis M0 as evident by clinical examination and sonomammography. * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of ≤ 2. * Patients with Her-2 positive Luminal B subtype, Her-2 enriched or triple negative breast cancer. * Patients who completed their systemic neoadjuvant therapy.

Exclusion criteria

* Second malignancy * Patients with early breast cancer clinicallyT1 (≤ 2 cm) N0 * Metastatic patients M1 * Patients with autoimmune diseases (Type I Diabetes mellitus, Systemic Lupus Erythematosus, Rheumatoid Arthritis, Sjogren's syndrome and Behcet disease) * Patients on systemic steroids or other immunomodulators (as Methotrexate, Tacrolimus and Cyclosporine) * Patients who started but didn't complete neoadjuvant systemic therapy * Patients who didn't undergo surgery after neoadjuvant systemic therapy

Design outcomes

Primary

MeasureTime frameDescription
Variation of PD-L1 expression in Her-2 positive and triple negative breast cancerthrough study completion, an average of 1 yearWe will compare between percentage of PD-L1 positive cases in the studied Her-2 positive and triple negative breast cancer subtypes
Correlation between pathological complete response and PD-L1 expressionthrough study completion, an average of 1 yearWe will correlate between PD-L1 expression and pathological complete response in the studied cases

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026