Standard Surveillance vs. Intensive Surveillance in Early Breast Cancer

Recruiting now · Not applicable

Conditions studied: Breast Cancer

In brief

The goal of this clinical study is to evaluate the potential benefits of intensified surveillance versus standard surveillance in medium-risk and high-risk early breast cancer patients. The main questions it aims to answer are: * Comparison of the 5-year ob´verall survival rates between patients in the Standard Surveillance arm versus patients in the liquid-biopsy guided Intensive Surveillance arm * Determination of the Overall Lead Time Effect generated due to tumor marker/CTC/ctDNA guided Intensive Surveillance compared to Standard Surveillance after primary therapy in early breast cancer patients. Participants will recieve regular blood drawals. Solely the blood samples of the intensive surveillance arm will be analysed for prospective tumor markers/CTCs/ctDNAs. Abnormal findings of either marker will trigger diagnostic imaging to search for possible metastases. The blood samples of the standard surveillance arm will solely be biobanked for future research purposes.

Key facts

Study ID: NCT05658172
Run by: Prof. Wolfgang Janni
People needed: 3500
Starts: 2022-12-07
Expected to finish: 2035-12-01
Last updated by the study team: 2025-05-02

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Written informed consent for all study procedures according to local regulatory requirements prior to beginning specific protocol procedures.
Unilateral or bilateral primary invasive carcinoma of the breast, confirmed histologically.
Patients with intermediate- to high-risk early breast cancer defined as either
an indication for (neo-)adjuvant chemotherapy (regardless whether performed or not), and/or
Large tumor (> 50 mm), and/or
Positive lymph nodes, and/or
High grade (>= G3). Indication to (neo-)adjuvant chemotherapy is seen as stated in the German S3 guideline for breast cancer as well as stated in the guidelines from the AGO.
A complete resection of the primary tumor, with resection margins free of invasive carcinoma.
Completion of primary anti-tumor therapy (adjuvant chemotherapy, surgery or radiotherapy, whichever occurs last) at least 4 weeks but no more than 24 months previously. Enrollment of patients during any kind of adjuvant therapy except chemotherapy (e.g., but not limited to endocrine therapy, antibody therapy, CDK4/6-inhibitors, PARP inhibitors, PI3K inhibitors, antibody-drug conjugates and other novel agents) is allowed.
Availability of primary tumor tissue from core biopsy or surgical removed tissue (FFPE Slide (≥ 6 mm³, min. 10 slides, thickness: 5 µm-10 µm, area >150 mm² and 1 H\&E stained slide, minimum 20% tumor content) or FFPE Block (≥ 6 mm³ thickness: 100 µm, area: >150 mm² and 1 H\&E stained slide, minimum 20% tumor content) or Genomic DNA extracted from FFPE slides or block (≥ 600 ng, Minimum volume: 25 µL, concentration: 20 ng/µL, buffer: 10 mM Tris pH 8, 1 mM EDTA)) at timepoint of enrollment.
Patients with primary systemic therapy: tissue from core biopsy
Patients receiving surgery as primary therapy: surgically removed cancer tissue.
No current clinical evidence for distant metastases.
Females or males ≥ 18 years and ≤ 75 years of age.
Performance status ≤ 1, Eastern Cooperative Oncology Group (ECOG) scale.
Patient must be willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.

You may not qualify if…

Patients with a history of any secondary primary malignancy are ineligible with the following exceptions:
in situ carcinoma of the cervix or
adequately treated basal cell carcinoma of the skin or
ipsi- or contralateral non-invasive carcinoma of the breast (DCIS).
Patients in pregnancy or breastfeeding. If a patient gets pregnant during the participation in the interventional phase of the study (Year 1-5), an end of intervention visit will be scheduled and the patient will enter the follow-up phase of the study. Pregnancy during the follow-up phase of the study is to be reported but does not lead to an exclusion of the study.
History of significant neurological or psychiatric disorders including psychotic disorders, dementia or seizures that would prohibit the understanding and giving of informed consent.
Renal insufficiency with GFR < 30 mL/min.
Previous or concomitant cytotoxic or other systemic antineoplastic treatment that is not used for treating the primary breast cancer.

Where it is running

University Hospital Ulm Gynecology/Obstetrics — Ulm, Germany (enrolling)

Full record on ClinicalTrials.gov

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