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Study identifier: NCT06738459 Synced from ClinicalTrials.gov · August 09, 2026
● Study status: RecruitingPRISM

Precision Retrospective Integrative Study for Metastatic Lymph Nodes in Breast Cancer

Condition: Breast Cancer  ·  Sponsor: Centro di Riferimento Oncologico - Aviano

PhaseN/A
Planned participants1500
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where4 locations · 2 countries

Interested? Contact the study team ↓

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Professional view of this study — listed sites, countries and recruiting context from the public registry. Everything below is written for patients and caregivers.See where this study is running →

About this study

Accurate assessment of axillary lymph nodes in patients with breast cancer is essential for prognosis and treatment planning. Staging and surgical management have evolved from axillary lymph node dissection to sentinel lymph node biopsy to minimize morbidity. However, sentinel lymph node biopsy has non-negligible morbidity, and more than 70% of biopsies are negative, calling into question its routine use. Magnetic resonance imaging (MRI) can be used to detect and stage lymph node metastases in situ, but its sensitivity and specificity are moderate to poor. Few studies have employed artificial intelligence to detect lymph node metastases on MRI images, and none have used an integrative multidata approach (IMA), defined as modeling the combination of clinical and laboratory data with multiparametric MRI. The primary objective of this retrospective observational study is to improve the accuracy of detecting lymph node involvement in breast cancer using IMA. The secondary objective is to allow longitudinal monitoring of the effects of neoadjuvant therapy on lymph node involvement

This description comes directly from the study's public registry record.

Talk to the study team

Fabio Del Ben, PhD  ·  0434659101  ·  fabio.delben@cro.it

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Patients diagnosed with breast cancer who underwent MRI and biopsy or surgery of axillary lymph nodes as part of their diagnosis and treatment * Patients of all genders, ages, and stage I-III of breast cancer * Patients who underwent neoadjuvant therapy and have longitudinal imaging data available for analysis (for secondary outcome analysis) Exclusion Criteria: * Patients whose MRI images were of insufficient quality for analysis * Patients who had a previous history of breast cancer * Patients with a history of axillary surgery or lymph node dissection prior to the current diagnosis of breast cancer * Patients who received neoadjuvant therapy at another institution

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (4)

Landeskrankenhaus VillachVillach, AustriaRecruiting
KI4LIFE, Fraunhofer Austria ResearchAustria, Austria, ItalyRecruiting
Klinikum Klagenfurt am Wörthersee Klagenfurt am WörtherseeVillach, Austria, ItalyRecruiting
Centro di Riferimento OncologicoAviano, Pordenone, ItalyRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

VillachAustriaAviano

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