Immun Checkpoint Washout in Patients With Invasive Ductal Breast Cancer

NCT ID: NCT07003009

Last Updated: 2025-06-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-01

Study Completion Date

2025-10-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Invasive ductal carcinoma is the most common type of invasive breast cancer. In cases where axillary lymph node metastases are diagnosed through screening, they can be found in up to 25% of cases, and in symptomatic cases, up to 60% of cases. The clinical detection accuracy of axillary lymph node metastases is only 33%. Accurate staging of lymph nodes in breast cancer patients is crucial for both prognosis and treatment. Ultrasonography is much more sensitive than physical examination alone for determining axillary lymph node involvement in breast cancer staging. Fine needle aspiration biopsy or core biopsy is diagnostic in lymph nodes that cannot be clarified solely by ultrasonography or are suspicious. Although biopsy sampling yields high diagnostic rates, it requires an experienced pathologist and sometimes takes weeks to yield results. Therefore, there is a need for faster and less costly diagnostic methods for diagnosing axillary metastases. Among thyroid cancers, papillary thyroid carcinomas, a malignancy in which the lymph node washout method is used to determine lymph node metastasis, are the most common. In papillary thyroid cancer patients, washout sampling of neck lymph nodes by fine needle aspiration, searching for thyroglobulin, a protein normally found in thyroid tissue, is considered one of the most valid methods for detecting lymph node metastasis in this cancer. In recent years, immune checkpoint molecules associated with cancer have been widely used as biomarkers and agents in both diagnosis and treatment for cancer patients. There are numerous publications in the literature regarding the expression of immune checkpoint molecules such as Programmed cell death protein 1 (PD-1), Programmed death ligand 1 (PD-L1), and The cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) on the cell surface of breast cancer patients. Although the natural soluble forms of receptors and ligands of immune checkpoint molecules exist and they are important components of immune regulation, their exact mechanisms of action have not yet been determined. There are five studies in the literature evaluating the status of soluble immune checkpoint molecules in breast cancer patients, with one being a review article. It is highly likely that immune checkpoint molecules found on both the cell surface and soluble in blood and body fluids are also present in tumor metastatic regions. There is no study using these immunological biomarkers to determine metastasis in invasive ductal carcinoma patients with metastatic axillary lymph nodes ın the literature. In this study, the investigators will evaluate the soluble levels of immune checkpoint molecules in washout fluids obtained from metastatic axillary lymph nodes and benign lymph nodes in patients with invasive ductal breast carcinoma, and will assess the effectiveness of these immune checkpoint molecules and the washout method in diagnosing metastasis.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The most common cancer in women worldwide and the leading cause of death among those aged 20-59 is breast cancer. Invasive breast cancers are primarily classified as ductal and lobular. However, special types of invasive breast cancers, which constitute 10% of total cases, have been included in the current histological classification.

Invasive ductal carcinoma is the most frequently observed type among invasive breast cancers (80%) and is also defined as invasive ductal carcinoma of no special type. Macroscopic or microscopic axillary lymph node metastases have been detected in up to 25% of screening-diagnosed cases and up to 60% of symptomatic cases of invasive ductal carcinoma.

The clinical staging of breast cancer is primarily determined by the physical examination of the breast skin, breast tissue, and regional lymph nodes (axillary, supraclavicular, and internal mammary). However, the accuracy of clinically determining axillary lymph node metastases is only 33%. Proper lymph node staging in breast cancer patients is crucial for both prognosis and treatment.

Ultrasound is significantly more sensitive than physical examination alone in determining axillary lymph node involvement in breast cancer staging. For lymph nodes that remain indeterminate or suspicious on ultrasound, fine-needle aspiration biopsy or core biopsy provides a definitive diagnosis. The most commonly used staging system is the TNM staging system. The American Joint Committee on Cancer (AJCC) recently modified the TNM system. According to the latest TNM staging, the presence of macrometastases in ipsilateral level 1 and level 2 axillary lymph nodes classifies breast cancer as stage 2A or higher. Although biopsy sampling has a high diagnostic accuracy, it requires experienced pathologists, and the evaluation process can take weeks. Therefore, there is a need for faster and more cost-effective diagnostic methods for detecting axillary metastases.

The lymph node washout technique is used to determine lymph node metastasis in malignancies such as papillary thyroid carcinoma, the most common type of thyroid cancer. Papillary thyroid carcinomas generally do not exhibit aggressive clinical behavior and have favorable long-term prognoses. However, at the time of diagnosis, cervical and mediastinal lymph node involvement ranges from 27% to 46%, and the postoperative recurrence rate is between 3% and 30%. Thus, determining preoperative lymph node involvement and distinguishing it from benign reactive lymphadenitis is essential. For this purpose, fine-needle aspiration with thyroglobulin washout sampling has recently become widely used worldwide. In patients with papillary thyroid carcinoma, fine-needle aspiration of cervical lymph nodes and testing for thyroglobulin, a protein normally present in thyroid tissue, is considered one of the most reliable methods for detecting lymph node metastasis. A large-scale study by Moon et al. found that fine-needle aspiration thyroglobulin washout had a sensitivity of 93.2% and a specificity of 95.9% in detecting lymph node metastases in papillary thyroid carcinoma.

Immune checkpoints have gained attention, particularly after being awarded the Nobel Prize in 2018, as they play a crucial role in understanding the relationship between cancer and the immune system. PD-1 and its ligand PD-L1 function as immune checkpoints by inhibiting T-cell receptor signaling and co-stimulatory signals. T-cell immunoglobulin and mucin domain 3 (TIM-3) is expressed on interferon-γ-producing T cells, regulatory T cells (Tregs), dendritic cells, B cells, macrophages, natural killer (NK) cells, and mast cells. Dysregulation of TIM-3 expression has been linked to autoimmune diseases. High TIM-3 expression is associated with T-cell exhaustion and suppression of T-cell responses, particularly in chronic viral infections and tumor development. The clinical success of immune checkpoint inhibitors such as ipilimumab and nivolumab in melanoma and lung cancer has further increased interest in immune checkpoints.

Numerous studies in the literature have investigated the expression of immune checkpoints such as PD-1, PD-L1, and CTLA-4 on the cell surface in breast cancer patients. One study evaluating the genetic expression of immune checkpoints in breast cancer found a negative correlation between B7-H3 mRNA expression and survival, while a positive correlation was observed between survival and the expression of CTLA-4 and tyrosine-based inhibitory motif domain (TIGIT). Another study reported decreased Lymphocyte-activation gene 3 (LAG-3) expression in triple-negative breast cancer and human epidermal growth factor receptor 2 (HER2) positive breast cancers.

Natural soluble forms of immune checkpoint receptors and ligands also exist in body fluids and play a role in immune regulation, although their exact mechanisms remain unclear. Many studies are investigating the role of immune checkpoints in cancer patients. One study evaluated both tumor-associated and soluble levels of PD-L1 and CTLA-4 in the blood, finding that elevated levels of PD-L1 and CTLA-4 were associated with poor prognosis. There are five studies in the literature, including one report, evaluating soluble immune checkpoints in breast cancer patients.

Since immune checkpoints are present on the cell surface and in soluble form in blood and body fluids, they are also highly likely to be found in tumor-metastasized regions. In the literature there is no study using these immunological markers to determine metastasis in patients with invasive ductal carcinoma and metastatic axillary lymph nodes.

In this study, the investigators will evaluate the soluble levels of immune checkpoints commonly associated with cancer-sCD25 (IL-2Ra), 4-1BB, B7.2 (CD86), Free Active Transforming growth factor (TGF)-β1, CTLA-4, PD-L1, PD-1, Tim-3, LAG-3, and Galectin-9-in washout fluid samples obtained from metastatic axillary lymph nodes and benign lymph nodes in patients with invasive ductal breast carcinoma. The effectiveness of immune checkpoints and the washout technique in diagnosing lymphatic metastasis will be assessed as a rapid diagnostic method.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Breast Cancer Metastatic Breast Carcinoma

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

CROSSOVER

A washout sample will be obtained by axillary lymph nodes suspected to be metastatic which is not performed in routine lymph node biopsy procedure. Similarly, an axillary lymph node that is deemed non-metastatic based on imaging findings will be sampled under ultrasound guidance for the same patients.
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Metastatic axillary lymph nodes suspected

Group Type EXPERIMENTAL

Malign Lymph Node Washout

Intervention Type DIAGNOSTIC_TEST

During routine axillary lymph node sampling, which is performed as part of standard staging using imaging methods, a washout sample (which is not not routinely applied ) will be obtained by injecting 1 cc of 0.9% saline into axillary lymph nodes suspected to be metastatic. The aspirated washout sample will be placed in a biochemistry gel tube labeled as Sample 1.

Benign lymph nodes

Group Type OTHER

Benign Lymph Node Washout

Intervention Type DIAGNOSTIC_TEST

Description: During the biopsy performed to histopathologically confirm the benign nature of a radiologically presumed benign axillary lymph node, a washout sampling will also be conducted by injecting 1 cc of 0.9% saline into benign lymph node. The aspirated washout sample will be placed in a biochemistry gel tube labeled as Sample 2.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Malign Lymph Node Washout

During routine axillary lymph node sampling, which is performed as part of standard staging using imaging methods, a washout sample (which is not not routinely applied ) will be obtained by injecting 1 cc of 0.9% saline into axillary lymph nodes suspected to be metastatic. The aspirated washout sample will be placed in a biochemistry gel tube labeled as Sample 1.

Intervention Type DIAGNOSTIC_TEST

Benign Lymph Node Washout

Description: During the biopsy performed to histopathologically confirm the benign nature of a radiologically presumed benign axillary lymph node, a washout sampling will also be conducted by injecting 1 cc of 0.9% saline into benign lymph node. The aspirated washout sample will be placed in a biochemistry gel tube labeled as Sample 2.

Intervention Type DIAGNOSTIC_TEST

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Fine needle aspiration biopsy Washout Fine needle aspiration biopsy Washout

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Histopathologically proven invasive ductal carcinoma
* Patients who will have neoadjuvant therapy

Exclusion Criteria

* The fine-needle aspiration biopsy (FNAB) result of the suspected metastatic lymph node is negative.
* The FNAB result of the presumed healthy lymph node is malignant.
* They refuse to participate in the study.
* They have another primary malignancy.
* They are pregnant.
* They have a history of immunodeficiency.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Istanbul Training and Research Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ufuk Oguz Idiz

Chief of General Surgery, Principal Investigator, Clinical Associate professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Istanbul Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Ufuk Oguz Idiz, Assoc. Prof. MD. PhD

Role: CONTACT

+905062044714

Mert Ali Dolek, MD

Role: CONTACT

+905364310364

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Ufuk Oguz Idiz, Assoc.Prof. MD. PhD

Role: primary

+905062044714

References

Explore related publications, articles, or registry entries linked to this study.

Giuliano AE, Connolly JL, Edge SB, Mittendorf EA, Rugo HS, Solin LJ, Weaver DL, Winchester DJ, Hortobagyi GN. Breast Cancer-Major changes in the American Joint Committee on Cancer eighth edition cancer staging manual. CA Cancer J Clin. 2017 Jul 8;67(4):290-303. doi: 10.3322/caac.21393. Epub 2017 Mar 14.

Reference Type BACKGROUND
PMID: 28294295 (View on PubMed)

Moon JH, Kim YI, Lim JA, Choi HS, Cho SW, Kim KW, Park HJ, Paeng JC, Park YJ, Yi KH, Park DJ, Kim SE, Chung JK. Thyroglobulin in washout fluid from lymph node fine-needle aspiration biopsy in papillary thyroid cancer: large-scale validation of the cutoff value to determine malignancy and evaluation of discrepant results. J Clin Endocrinol Metab. 2013 Mar;98(3):1061-8. doi: 10.1210/jc.2012-3291. Epub 2013 Feb 7.

Reference Type BACKGROUND
PMID: 23393171 (View on PubMed)

Sallout L, Tashkandi M, Moqnas A, AlMajed H, Al-Naeem A, Alwelaie Y. Fine-needle aspiration biopsy of axillary lymph nodes: A reliable diagnostic tool for breast cancer staging. Cancer Cytopathol. 2024 Feb;132(2):103-108. doi: 10.1002/cncy.22770. Epub 2023 Oct 16.

Reference Type BACKGROUND
PMID: 37843531 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Breast lymph node

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.