Evaluating and Monitoring Immune and Clinical Responses in Early-Stage Triple Negative Breast Can… (NCT05877859) | Clinical Trial Compass
RecruitingNot Applicable
Evaluating and Monitoring Immune and Clinical Responses in Early-Stage Triple Negative Breast Cancer Undergoing Neoadjuvant Chemo-immunotherapy With Pembrolizumab
United States10 participantsStarted 2023-05-30
Plain-language summary
This research study is a prospective, single arm, pilot study, designed to evaluate the correlation between the immune and clinical responses of subjects with untreated Stage II-III triple negative breast cancer (TNBC) undergoing standard of care neoadjuvant chemo- immunotherapy.
Who can participate
Age range18 Years
SexFEMALE
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Inclusion Criteria:
* Newly diagnosed, previously untreated, non-metastatic Stage II-III invasive breast cancer
* Estrogen receptor IHC expression ≤10%; progesterone receptor IHC expression ≤ 10%; HER2 negative
* HER2 negativity is defined as either of the following by local laboratory assessment:
* IHC 0, 1+, or 2+ and In situ hybridization (ISH) non-amplified (ratio of HER2 to CEP17 \<2.0 or single probe average HER2 gene copy number \<4 signals/cell)
* No prior chemotherapy, endocrine therapy, or immunotherapy
* Willingness and ability of the subject to comply with scheduled visits, standard of care drug administration plan, protocol-specified laboratory tests, other study procedures, and study restrictions.
* Evidence of a personally signed informed consent indicating that the subject is aware of the neoplastic nature of the disease and has been informed of the procedures to be followed, the experimental nature of the therapy, alternatives, potential risks and discomforts, potential benefits, and other pertinent aspects of study participation.
Exclusion Criteria:
An individual who meets any of the following criteria will be excluded from participation in this study:
* Pregnant, breastfeeding, or unwilling to practice birth control during participation in the study
* Patients who are receiving any other investigational agents or an investigational device within 21 days before administration of first dose of study drugs.
* Patients on steroid medications (i.e. prednison…
What they're measuring
1
Change in the cytokine milieu in the blood
Timeframe: From baseline within 24 hours of surgery