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Study in Leptomeningeal Metastases of Breast Cancer

Cerebrospinal Fluid Biomarkers Value: Exploratory and Prospective Study in Leptomeningeal Metastases of Breast Cancer (LCS Bio Sein)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03252912
Acronym
LCS Bio Sein
Enrollment
51
Registered
2017-08-17
Start date
2017-01-06
Completion date
2020-09-15
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Brief summary

Breast cancer (BC) is the most frequent cause of leptomeningeal metastases (LM) .As for brain parenchymal metastases, the incidence of LM seems to be increasing, due to the growing incidence of metastatic BC, the improvement of survival and the poor diffusion of therapeutic agents into the central nervous system (CNS). Several prognostic factors have been identified, including the age at diagnosis, the functional and neurological status, the delay between the diagnosis of cancer and that of LM. The survival of patients is poor, less than 6 months in most published series. Several neuronal biomarkers could also be good candidates, such as the neurogranin CSF and/or serum levels or the CNS neurofilaments (NF), that seem to be a good reflect of axonal injury and neuronal loss. CNS NF have been investigated in several neurological diseases including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis and multiple sclerosis, but not yet in CNS metastases. Indeed, the creation of a clinico-biological collection seems to be of high value in order to investigate future biomarkers of interest

Detailed description

Breast cancer (BC) is the most frequent cause of leptomeningeal metastases (LM). As for brain parenchymal metastases, the incidence of LM seems to be increasing, due to the growing incidence of metastatic BC, the improvement of survival and the poor diffusion of therapeutic agents into the central nervous system (CNS). Several prognostic factors have been identified, including the age at diagnosis, the functional and neurological status, the delay between the diagnosis of cancer and that of LM. Other CSF biomarkers have been evaluated for the diagnosis of leptomeningeal metastases. Finally, the CellSearch® technique allows for the characterisation of proteins expressed by CSF tumors cells (E.G., HER2) and will make possible a better understanding of the physiopathology of tumor dissemination to the CS. Other neuronal biomarkers could be interesting for the diagnosis of LM in BC patients. Among them, the protein Tau (total-Tau or T-Tau) is involved in several neurological diseases. However, to date, no study has evaluated CSF or serum T-Tau in LM from solid tumors. Several neuronal biomarkers could also be good candidates, such as the neurogranin CSF and/or serum levels or the CNS neurofilaments (NF), that seem to be a good reflect of axonal injury and neuronal loss.

Interventions

BIOLOGICALblood samples

Two EDTA tubes (5 mL) and two dried tubes (5mL) will be will be taken the same day as the first lumbar .

Sponsors

Institut du Cancer de Montpellier - Val d'Aurelle
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female patient ≥ 18 years-old, no age limit; 2. Histologically confirmed diagnosis of BC; 3. Hormone receptors and HER2 statuses of the primary tumor available; 4. Suspected LM based on clinical symptoms or signs, or radiological abnormalities; 5. Indication of diagnosis lumbar puncture decided by the oncologist in charge of the patient; 6. Patients must be affiliated to a Social Security System; 7. Patient information and written informed consent form signed prior to any study specific procedures.

Exclusion criteria

1. History of other cancer(s) than the BC (except completely resected non-melanoma skin cancer or successfully treated in situ carcinoma). 2. Hormone receptors and/or HER2 statuses of the primary tumor not available; 3. Patients with a medical contra-indication to the realization of a lumbar puncture; 4. Patients with psychological, family, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; 5. Patients who are pregnant or breast-feeding. 6. Legal incapacity or limited legal capacity.

Design outcomes

Primary

MeasureTime frameDescription
Sensitivity of the CellSearch® technique on CSF samples in comparison with the conventional cytology on one to three CSF samplethrough study completion, an average of 2 yearsanalysis of result with the 2 technical procedure

Countries

France

Contacts

STUDY_DIRECTORmarc ychou

institut régional du Cancer de Montpellier

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026