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RecruitingNCT06358625CRANIUMUpdated Aug 1, 2025

Identification of Risk Factors for Brain Recurrence in Patients With HER2-positive Localised Breast Cancer

An observational study in HER2-positive Breast Cancer, sponsored by Center Eugene Marquis. Recruiting at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-08-01.

Sponsored by Center Eugene Marquis · Observational

From the registry’s dates

  • Started Jun 2024; still recruiting 2 years 4 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
120
Ages
18 Years and older
Sex
Female
01

Study summary

HER2 gene amplification, detected in 20% to 30% of breast cancers, was a poor prognostic factor before the advent of anti-HER2 therapies. In the early 2000s, trastuzumab revolutionised the management of patients with HER2-positive (HER2+) breast cancer in the metastatic and localised stages of the disease.

At the time of diagnosis of metastatic disease, 7-11% of patients have brain metastases, with (70% of cases) or without symptoms (30% of cases). In the absence of brain metastases, 30% to 50% of patients will develop brain metastases within the first two years of treatment, depending on whether the disease is hormone receptor positive (HR+) or negative (HR-).

The presence of brain metastases is the most important prognostic factor. The neurological symptoms caused by the presence of these lesions, but also by the local treatments offered, affect patients' quality of life, although improvements in surgical and radiotherapy techniques have significantly reduced the need for particularly toxic whole brain radiotherapy.

International guidelines do not recommend systematic brain MRI in the absence of neurological symptoms, either in the adjuvant or metastatic stages of this disease. However, there may be a role for more systematic and earlier screening for cerebral recurrence, as single cerebral recurrences without extracranial involvement are common and the new anti-HER2 agents (i.e. tucatinib, an anti-HER2 tyrosine kinase inhibitor, and T-Dxd) have shown significant objective response rates in cerebral metastases.

To date, no clinical or histological prognostic factor (proliferation index, HR expression, etc.) has been used to identify a population of patients at high risk of cerebral relapse, allowing monitoring and treatment to be personalised.

New tools for these indications would significantly modify our clinical practice, allowing the identification of a subpopulation at high risk of cerebral recurrence, suitable for increased monitoring and therapeutic adjustment.

02

Conditions studied

  • HER2-positive Breast Cancer

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Keywords

  • Metastases
  • Central Nervous System
  • Biopsy
03

In context

Neoplasm Metastasis

3,517 studies on the registry are indexed under Neoplasm Metastasis; 885 are open to participants now.

This study's planned enrollment of 120 is close to the median of 121 across 594 observational studies indexed under Neoplasm Metastasis.

Browse Neoplasm Metastasis studies →

Lead sponsor

Center Eugene Marquis is the lead sponsor of 32 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

women with HER2+ non-metastatic breast cancer treated at the CRLCC Eugène marquis

Inclusion criteria

  • Age ≥ 18 years old
  • be a female patient
  • Patients with histologically proven HER2-positive invasive breast cancer (IHC 3+ or 2+ with positive SISH),
  • Neoadjuvant chemotherapy and intra-tumour clips indicated at the multidisciplinary consultation meeting (RCP).
  • Signed Informed Consent Form

Exclusion criteria

Exclusion Criteria:

  • pregnant or breast-feeding women
  • Have had a haematoma requiring level II analgesics at the time of the diagnostic biopsy.
  • Known coagulation disorders
  • Individual deprived of liberty or placed under the authority of a tutor, or a currator
  • Not be affiliated to a social security regimen
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
120 participants (estimated)
Patient registry
No

Groups and cohorts

  • HER positive

    The study will include an initial assessment and longitudinal and individual follow-up to identify the occurrence of clinical events of interest and to monitor the evolution of any tumour biomarkers on circulating tumour DNA.

    Other: Pre-treatment biopsy

Interventions

  • OtherPre-treatment biopsy

    A breast biopsy is performed just before the "clip" is placed in the tumour and additional blood samples are performed.

06

What researchers measure

Primary outcomes

  1. Transcriptomic profile change of HER2+ primary breast tumours before any treatment

    comparison of the transcriptomic profile of HER2+ primary breast tumours before any treatment of patients who will develop brain metastases within 5 years with patients who will not develop them

    Time frame: At inclusion

Secondary outcomes

  1. Transcriptomic profile change on circulating tumour DNA (ctDNA)

    High-throughput sequencing (NGS) of a panel of genes previously identified by transcriptomic analysis

    Time frame: At baseline, Year 1; Year2; Year3, Year4; Year 5, at relapse

07

Study locations

1 of 1 sites recruiting
  • Centre de lutte contre le cancer Eugène Marquis
    Rennes, 35 000, France
    • Fanny LE DU, Dr · Contact
    • Fanny LE DU, DR · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06358625
Lead sponsor
Center Eugene Marquis
Responsible party
Sponsor
First posted
Apr 10, 2024
Start date
Jun 6, 2024
Primary completion
Jun 6, 2031 (estimated)
Completion
Jun 6, 2031 (estimated)
Last update
Aug 1, 2025

Study contacts

Valérie JOLAINE, Dr
Contact
v.jolaine@rennes.unicancer.fr
(0)299253036 ext. +33
Marion TROCHET
Contact
m.trochet@rennes.unicancer.fr
(0)299253165 ext. +33
Fanny LE DU, Dr
principal investigator · Centre de lutte contre le cancer Eugène Marquis

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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