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HER2-zero, HER2-low and HER2-positive Tumors Distribution Across HR Expression CategoriesNCT07561346

Clinico-pathological and Genomic Features of HER2-low Early Breast Cancer

An observational study of HER2-zero, HER2-low and HER2-positive Tumors Distribution Across HR Expression Categories, run by Hellenic Cooperative Oncology Group at 1 site in Greece.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Although breast cancer remains one of the most common and fatal cancer types among women worldwide, earlier diagnosis and improved therapeutic approaches have led to decreased mortality over last years. Read more about this study

Who is it for?
Ages 18 years and older, women only
How many people
3,648 participants
Where
1 siteGreece
Study dates
10 Dec 1996to 7 Jul 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Study population: patients with operable breast cancer treated with dds-CT including taxanes and anthracyclines. Adjuvant hormonal and radiation treatment were administered, as indicated

Who may be able to join

  • Age 18 and above
  • Histologically confirmed BC
  • All treated with adjuvant dose-dense sequential chemotherapy (dds-CT)
  • Tumor tissue specimen (FFPE) availability

Who cannot join

  • not adequate, and unsuitable tissue for IHC, FISH, NGS analysis

Trial locations and contacts

1 site in 1 country.

Greece1 site
  • Hellenic Cooperative Oncology Group (HeCOG)

    Athens, 11526

Other trials in Greece

About this study

Official title: Clinico-pathological and Genomic Features of HER2-low Early Breast Cancer (eBC). Results of Retrospective Analysis of Seven Adjuvant Trials by the Hellenic Cooperative Oncology Group (HeCOG)

Although breast cancer remains one of the most common and fatal cancer types among women worldwide, earlier diagnosis and improved therapeutic approaches have led to decreased mortality over last years. Indeed, the use of HER2-targeted drugs has improved clinical outcomes for patients with HER2 positive breast cancer, while, on the other hand, until recently, little progress has been made for HER2-negative (IHC score 0 and 1+) patients.

However, it seems that among these HER2-negative breast cancers, substantial heterogeneity exists regarding the expression of hormone receptors (HR) and HER2.

Read more

Biomarkers are critical for translating the biological heterogeneity of breast cancer into prognostically and therapeutically useful information. In recent years gene expression profiling and genomic analysis have shown utility in specific clinical scenarios, but immunohistochemistry (IHC) remains the cornerstone of biomarker testing in both early and advanced/metastatic disease.

In breast cancer, achieving efficacy with endocrine therapy or with HER2-blockade requires identifying patients whose tumors show significant survival dependency on the therapeutic target. This is achieved by using appropriate biomarkers cut-offs ensuring a favorable benefit-to-toxicity ratio for specific patients.

This paradigm has recently been challenged by a new class of HER2 drugs that use target expression not as a direct molecular lever but as a vehicle to deliver potent agents to cancer cells, breaking the straightforward link between the molecular target and the corresponding therapy. These drugs exhibit impressive activity at marker expression levels much lower than those required to effectively block HER2 signaling, shifting the diagnostic focus to the lower end of the staining spectrum, specifically distinguishing between HER2-zero and HER2-low expression.

Given the lack of a definitive molecular hallmark for cancers characterized by low HER2 expression, ongoing efforts aim to understand the biology of this heterogeneous group of tumors. This understanding is crucial to triage treatment, investigate resistance mechanisms, and inform potential combination strategies.

To enrich the available data, we perform a retrospective analysis of HER2-low patients in a large cohort of early breast cancer patients from Greece enrolled in 7 randomized and observational clinical studies.

Given the importance of the hormone receptors and the known differential distribution of ER/PgR status between HER2-zero, HER2-low and HER2-positive breast tumors, after analyzing the entire population cohort, ER/PgR status will be treated as a confounding variable in the analysis and the HER2 categories will be compared separately within ER/PR-positive and ER/PR-negative disease.

The study aims to investigate how HER2-zero, HER2-low and HER2-positive tumors are distributed across ER expression categories. Additionally, we will evaluate whether PgR positivity varies across ER expression categories, and if PgR identify heterogeneity within ER-low tumors.

As TP53 mutation is strongly linked to basal-like, high-grade, hormone receptor-negative and HER2-positive biology, we will examine if TP53 mutation frequency differs across ER categories and classic subtypes and if PIK3CA mutation frequency differs across ER categories and PgR-defined groups, as PIK3CA mutations are generally enriched in luminal breast cancer.

TIL biology is also strongly subtype-dependent. TNBC and HER2-positive disease are generally more immune-enriched than luminal disease, so we will examine if stromal TIL levels are associated with ER category, HER2 category and classic subtype in our study.

Summarizing, our aim is to evaluate if HER2-low status retains independent associations with clinicopathologic, immune or genomic features after adjustment for ER category and classic subtype, whether ER/HER2 matrix groups are associated with disease outcome, and associations remain after adjustment for standard prognostic factors and treatment.

Read the detailed description

From 1996 until 2020, 5,320 eligible patients with operable breast cancer were treated, within the context of 3 randomized and 4 observational clinical studies with dds-CT including taxanes and anthracyclines. Adjuvant hormonal and radiation treatment were administered, as indicated.

IHC and FiSH data from patients enrolled in the above randomized phase III trials conducted by the Hellenic Cooperative Oncology Group (HeCOG) will be retrospectively reviewed.

All patients have signed a study-specific written informed consent before randomization, consenting for the trial and permitting the use of their biological material for future research purposes. All studies were conducted in accordance with the Declaration of Helsinki.

Tumor material is examined mainly on tissue microarrays (TMA). Although, there is a HER2 assessment from local pathology laboratories, all tumors are re-evaluated centrally for ER, PgR and HER2 in the laboratory of Molecular Oncology according to ASCO/CAP guidelines. Tumors are subtyped with immunohistochemistry (IHC4) for ER, PgR, HER2 and Ki67. FISH is performed for the assessment of HER2 gene status. IHC for EGFR and CK5 is used for the classification of basal-like tumors; the expression of CD8 on TILs is also evaluated. Moreover, we investigate the mutational profile of Greek women with breast cancer, via the application of DNA Next Generation Sequencing (NGS) technologies, relative also to patient outcome.

Patient demographic, clinicopathological and treatment data are available in all cases.

Keywords
HER2 low breast cancer

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall Survival (OS)

    To investigate the long-term prognostic significance of HER2 positive, HER2 low and HER2 zero in terms of OS

    Measured: Time from study entry to death from any cause, assessed up to 120 months]

  2. Disease-Free Survival (DFS)

    To investigate the long-term prognostic significance of HER2 positive, HER2 low and HER2 zero in term of DFS

    Measured: Time from study entry to first recurrence (local, regional, distant) or death from any cause, whichever comes first, assessed up to 120 months]

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 May 2026
  2. Study start10 Dec 1996
  3. Primary completion7 Jul 2026
  4. Study completion7 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
3,648 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07561346
Sponsor's protocol ID
HE_10L/25
Status last verified
Apr 2026
First submitted
20 Mar 2026
Last updated
22 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Schettini F, Chic N, Braso-Maristany F, Pare L, Pascual T, Conte B, Martinez-Saez O, Adamo B, Vidal M, Barnadas E, Fernandez-Martinez A, Gonzalez-Farre B, Sanfeliu E, Cejalvo JM, Perrone G, Sabarese G, Zalfa F, Peg V, Fasani R, Villagrasa P, Gavila J, Barrios CH, Lluch A, Martin M, Locci M, De Placido S, Prat A. Clinical, pathological, and PAM50 gene expression features of HER2-low breast cancer. NPJ Breast Cancer. 2021 Jan 4;7(1):1. doi: 10.1038/s41523-020-00208-2.

    PubMed 33397968
  • Curigliano G, Dent R, Earle H, Modi S, Tarantino P, Viale G, Tolaney SM. Open questions, current challenges, and future perspectives in targeting human epidermal growth factor receptor 2-low breast cancer. ESMO Open. 2024 Apr;9(4):102989. doi: 10.1016/j.esmoop.2024.102989. Epub 2024 Apr 12.

    PubMed 38613914
  • Patel A, Unni N, Peng Y. The Changing Paradigm for the Treatment of HER2-Positive Breast Cancer. Cancers (Basel). 2020 Jul 28;12(8):2081. doi: 10.3390/cancers12082081.

    PubMed 32731409
  • Jokhadze N, Das A, Dizon DS. Global cancer statistics: A healthy population relies on population health. CA Cancer J Clin. 2024 May-Jun;74(3):224-226. doi: 10.3322/caac.21838. Epub 2024 Apr 4. No abstract available.

    PubMed 38572764

Questions about this trial

What is this clinical trial studying?

An observational study of HER2-zero, HER2-low and HER2-positive Tumors Distribution Across HR Expression Categories, run by Hellenic Cooperative Oncology Group at 1 site in Greece.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 22 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Greece. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall Survival (OS) (time frame: Time from study entry to death from any cause, assessed up to 120 months]). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07561346, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2026.

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