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Updated: Jun 6, 2026

Validated Immunochemical Assay for Comprehensive Determination of the Human Epidermal Growth Factor Receptor 2 Released from and Bound to Cells
Published on: May 9, 2025
[Clinical usefulness of circulating ECD/HER-2 measurement for breast cancer patients' management]
Carole Mathelin1, Sabrina Croce, Sébastien Rault
1CHRU de Strasbourg, pôle de gynécologie-obstétrique, unité de sénologie, avenue Molière, 67200 Strasbourg cedex, France. Carole.Mathelin@chru-strasbourg.fr
Background:
About 15 to 20% of breast cancer cases overexpress human epidermal growth factor receptor-2 (HER-2). This overexpression is associated with poor clinical prognosis but therapeutic success of trastuzumab or lapatinib. HER-2 extracellular domain (ECD) undergoes a proteolytic cleavage and is shed into biologic fluid as a circulating antigen called ECD/HER-2, which can be detected by immunochemical assays.
Objective:
The aim of our review was to determine the clinical usefulness of ECD/HER-2 measurement in the management of breast cancer patients.
Material And Methods:
A Pubmed search for publications in English or French was carried out until March 31, 2010 (69 original articles and 8 reviews).
Results:
The measurement of ECD/HER-2 concentration does not exempt from the pathological determination of HER-2 expression in tumors; some HER-2 negative tumors are associated with high levels of ECD/HER-2, on the other hand, some HER-2 positive tumors present low levels of ECD/HER-2. The concentration of ECD/HER-2 is correlated to disease progression, since 10% of loco-regional breast cancers and more than a third of metastatic breast cancers have high levels of ECD/HER-2. The elevation of ECD/HER-2 levels generally occurs several months before the diagnosis of symptomatic metastases. The relevance of ECD/HER-2 measurements during chemotherapy, hormone therapy and trastuzumab treatment remains uncertain. Similarly, it is not commonly agreed that high levels of ECD/HER-2 before any treatment in the case of an early breast cancer, is an independent prognostic factor.
Discussion:
A close analysis of a variety of pathological, biochemical, clinical and methodological data may explain these discrepancies.
Conclusion:
New prospective studies using immunochemical measurements of ECD/HER-2 (with a consensual threshold) and based on both detailed pathological analyses and a comprehensive collection of clinical data are still required to establish the clinical usefulness of circulating ECD/HER-2 measurement for breast cancer patients' management.
