Association of Adjuvant Radiotherapy of Non-metastatic Breast Carcinoma With Immunomodulation and Circulating Tumor Cell Phenotype in Relation to Patient Age.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity of Jena

About this trial

In a prospective study, the influence of adjuvant radiotherapy in patients with non-metastatic breast carcinoma on the epithelial tumor cells (CETCs) circulating in the blood and their immunohistochemical characteristics depending on age will be investigated. In addition to a histopathological assignment of the CETCs as cells of the primary tumor, major trigger points of the immune system will be exploratively analyzed.

For this purpose, blood samples are taken from the patients at different time points after tumor resection and during adjuvant radiotherapy. In addition to the detection, isolation and genetic characterization of the CETCs, the determination of immunological biomarkers by immunophenotyping, among other methods, is planned. Furthermore, analyses of tissue from the primary tumor with respect to immunohistochemical features as well as tumor-infiltrating lymphocytes (TILs) are planned. The results will be classified and correlated especially with regard to patient age.

As there are insufficient data available for breast carcinoma regarding radiotherapeutic effects on the immune system depending on patient age, it is of great interest to better understand these molecular biological basics in order to identify potential prognostic biomarkers.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Primary diagnosis histologically confirmed invasive breast carcinoma pT1-4 pN0 or pN+ cM0

curative-intended breast-conserving therapy (BET) ± (neo-) adj. system therapy with subsequent adjuvant radiotherapy of the breast ± lymphatic drainage system planned

informed consent of the patient

Disqualifiers

DCIS, Inflammatory breast carcinoma

Recurrence situation

Presence of distant metastases

Second malignancies < 10 years prior to diagnosis of breast carcinoma

Trial population

Only female patients with non-metastatic breast carcinoma undergoing breast-conserving surgery (± neoadjuvant or adjuvant system therapy) at the Department of Gynecology and Reproductive Medicine Jena followed by adjuvant radiation therapy at the Department of Radiation Oncology and Radiotherapy Jena between June 1, 2021 and June 1, 2023 (recruitment period) will be studied.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Adjuvant radiotherapy

    Radiation

    Guideline-based therapy of primary non-metastatic early breast carcinoma

  • neoadjuvant and adjuvant chemotherapy

    Drug

    Guideline-based therapy of primary non-metastatic early breast carcinoma

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: premenopausal patients2 interventions
Group B: postmenopausal patients2 interventions

Trial outcomes

Primary outcomes

1

Age-dependent influence of radiotherapy on circulating epithelial tumor cell counts (CETC) and immunophenotype (PBMC).

Measurement of CETC count / µl blood in the course of therapy and correlation with patient age.

Time frame
observation period 2 years
2

Longitudinal quantification of CETCs as well as immunophenotype at specific time points during the course of therapy.

Measurement of CETC count / µl blood in the course of therapy and correlation with the cell count of detected T and B cells / µl blood.

Time frame
observation period 2 years
3

Comparison of immunohistochemical parameters of the primary tumor with the immunohistochemical and cytological parameters of CETC

Comparison of PD-L1 expression of primary tumor cells with CETC in percent. Comparison of hormone receptor status (estrogen, progesterone) values of primary tumor and CETC in percent.

Time frame
observation period 2 years

Secondary outcomes

1

Recurrence-free survival (RFS)

Recurrences as a function of time (analysis using Kaplan-Meier curves, log-rank test, and Cox regression).

Time frame
observation period 3 years follow up

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Jena

Lead sponsor

University Hospital Erlangen

Collaborator

Labor Prof. Pachmann

Collaborator