Analyses of Exosomes in the Cerebrospinal Fluid for Breast Cancer Patients With Suspicion of Leptomeningeal Metastasis.
Primary Purpose
Breast Cancer, Leptomeningeal Metastasis
Status
Withdrawn
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Cerebrospinal fluid and blood sample collection at the initial diagnostic assessment
Cerebrospinal fluid and blood sample collection if conclusions of initial diagnostic assessment are "Lack of evidence" according to EANO-ESMO classification
Cerebrospinal fluid and blood sample collection if conclusions of initial diagnostic assessment are "confirmed", "probable" or "possible", leading to leptomeningeal metastase specific treatment
Sponsored by
About this trial
This is an interventional diagnostic trial for Breast Cancer focused on measuring Cerebrospinal fluid, Proteomic profile
Eligibility Criteria
Inclusion Criteria:
- Patient with histologically proven breast cancer
- Patient with suspected metastatic leptomeningitis
- Age ≥ 18 years
- Patient covered by the French social security regime
- Signed written informed consent
Exclusion Criteria:
- History of cancer other than the one being treated
- Contraindication to carrying out the lumbar puncture or cerebrospinal MRI
- Pregnant or breastfeeding patient
Sites / Locations
- Centre Oscar Lambret
- Centre Hospitalier Régional Universitaire de Lille
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Cerebrospinal fluid and Blood sample collection
Arm Description
Collection of cerebrospinal fluid and blood samples: At initial diagnostic assessment; 1 month and 3 months after initial diagnostic assessment, for patients classified "possible", "probable" or "confirmed" according to EANO-ESMO classification, leading to specific leptomeningeal metastase treatment; In case of symptoms leading to leptomeningeal metastase suspicion and at least 3 months after diagnostic assessment, for patients classified "lack of evidence" according to EANO-ESMO classification.
Outcomes
Primary Outcome Measures
Proteomic profiles issued from cerebrospinal fluid at diagnosis
Proteomic profile will be obtained by bioinformatic analysis of cerebrospinal fluid.
Cytology of cerebrospinal fluid at diagnosis
Results of cytological analysis of cerebrospinal fluid will be "Positive", "negative", "equivocal".
Secondary Outcome Measures
Proteomic profiles issued from cerebrospinal fluid
Proteomic profile will be obtained by bioinformatic analysis of cerebrospinal fluid:
1 month and 3 month after the start of a specific treatment of the leptomeningeal metastasis, if applicable,
3 months after the initial diagnosis of leptomeningeal metastasis if the likehood of leptomeningeal metastasis is "lack of evidence".
Histological subtype
Histological subtype will be subdivised as invasive ductal breast carcinoma, invasive lobular breast carcinoma, other brest carcinoma.
Hormonal receptors status
Hormonal receptors status will be subdivised as:
Positive hormonal receptors / Positive HER2
Positive hormonal receptors / Negative HER2
Negative hormonal receptors / Positive HER2
Triple negative
Likehood of leptomeningeal metastasis according to the EANO-ESMO classification.
EANO-ESMO classification is obtained by searching clinical symptoms, cancer cells in the cerebrospinal fluid (obtained by lumbar puncture), signs in RMI. The likehood of leptomeningeal metastasis is:
Lack of evidence,
Possible,
Probable,
Confirmed.
Overall survival
Overall survival is defined as time from date of registration to date of death regardless of the cause.
Proteomic profiles issued from blood
Proteomic profile will be obtained by bioinformatic analysis of blood.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03974204
Brief Title
Analyses of Exosomes in the Cerebrospinal Fluid for Breast Cancer Patients With Suspicion of Leptomeningeal Metastasis.
Official Title
Benefit of Analyzing Exosomes in the Cerebrospinal Fluid During the Medical Care of Breast Cancer Patients With Suspicion of Leptomeningeal Metastasis.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Withdrawn
Why Stopped
Modification of the care habits. We believe today that we are no longer able to carry out this study as initially described.
Study Start Date
July 2019 (Anticipated)
Primary Completion Date
October 2022 (Anticipated)
Study Completion Date
October 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Oscar Lambret
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a multicenter, interventional, prospective study among breast cancer patients with a suspicion of metastatic meningitis. The current study aims to assess the use of proteomic profile issued from cerebrospinal fluid microvesicles for diagnosis of leptomeningeal metastases.
Detailed Description
The aim of this study is to describe the association between the initial proteomic profile issued from cerebrospinal fluid microvesicles and the initial cytological analysis of the cerebrospinal fluid in breast cancer patients with a suspicion of metastatic meningitis.
Other objectives of the study include:
Describing the association between the initial proteomic profile and:
the histological types and hormonal receptors status of the breast cancer,
the likelihood of leptomeningeal metastasis according to the EANO-ESMO classification (Lack of evidence / possible / probable / confirmed) ,
the likelihood of leptomeningeal metastasis according to the EANO-ESMO classification, combined with histological type and hormonal receptors status.
Evaluate the prognostic value of the proteomic profiling for overall survival, according to the EANO-ESMO classification and other known prognosis factors, in patients classified "possible", "probable" or "confirmed" leading to leptomeningeal metastases specific treatment,
Evaluate the impact of the evolution of the proteomic profile a month after the start of this treatment on the overall survival, in patients with leptomeningeal metastases specific treatment,
Evaluate the association between the proteomic profile and the EANO-ESMO classification at least 3 months after the initial EANO-ESMO classification,
Evaluate the evolution of the proteomic profile 3 months after the initial EANO-ESMO classification, in patients initially classified "lack of evidence", broadly and according to the evolution of cytology, the administered treatments and to the EANO-ESMO response if applicable,
Compare the proteomic profiles issued from cerebrospinal fluid and blood
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Leptomeningeal Metastasis
Keywords
Cerebrospinal fluid, Proteomic profile
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cerebrospinal fluid and Blood sample collection
Arm Type
Experimental
Arm Description
Collection of cerebrospinal fluid and blood samples:
At initial diagnostic assessment;
1 month and 3 months after initial diagnostic assessment, for patients classified "possible", "probable" or "confirmed" according to EANO-ESMO classification, leading to specific leptomeningeal metastase treatment;
In case of symptoms leading to leptomeningeal metastase suspicion and at least 3 months after diagnostic assessment, for patients classified "lack of evidence" according to EANO-ESMO classification.
Intervention Type
Procedure
Intervention Name(s)
Cerebrospinal fluid and blood sample collection at the initial diagnostic assessment
Intervention Description
At the initial diagnostic assessment, 3mL of cerebrospinal fluid and 10 ml of blood sample will be collected in order to determine the proteomic profile. Cerebrospinal fluid will be collected during a lumbar puncture aiming to diagnose leptomeningeal metastases.
Intervention Type
Procedure
Intervention Name(s)
Cerebrospinal fluid and blood sample collection if conclusions of initial diagnostic assessment are "Lack of evidence" according to EANO-ESMO classification
Intervention Description
3mL of cerebrospinal fluid and 10 ml of blood sample will be collected:
When suspected metastatic meningitis symptoms arise and
at least 3 months after the initial diagnostic assessment, In order to determine the proteomic profile. Cerebrospinal fluid will be collected during a lumbar puncture aiming to diagnose leptomeningeal metastases.
Intervention Type
Procedure
Intervention Name(s)
Cerebrospinal fluid and blood sample collection if conclusions of initial diagnostic assessment are "confirmed", "probable" or "possible", leading to leptomeningeal metastase specific treatment
Intervention Description
3mL of cerebrospinal fluid and 10 ml of blood sample will be collected:
1 month after the beginning of the specific treatment,
3 months after the beginning of the specific treatment. Cerebrospinal fluid will be collected during a lumbar puncture aiming to assess treatment response or at intrathecal injection of treatment.
Primary Outcome Measure Information:
Title
Proteomic profiles issued from cerebrospinal fluid at diagnosis
Description
Proteomic profile will be obtained by bioinformatic analysis of cerebrospinal fluid.
Time Frame
Up to 1 week
Title
Cytology of cerebrospinal fluid at diagnosis
Description
Results of cytological analysis of cerebrospinal fluid will be "Positive", "negative", "equivocal".
Time Frame
Up to 1 week
Secondary Outcome Measure Information:
Title
Proteomic profiles issued from cerebrospinal fluid
Description
Proteomic profile will be obtained by bioinformatic analysis of cerebrospinal fluid:
1 month and 3 month after the start of a specific treatment of the leptomeningeal metastasis, if applicable,
3 months after the initial diagnosis of leptomeningeal metastasis if the likehood of leptomeningeal metastasis is "lack of evidence".
Time Frame
Up to 3 months
Title
Histological subtype
Description
Histological subtype will be subdivised as invasive ductal breast carcinoma, invasive lobular breast carcinoma, other brest carcinoma.
Time Frame
Before registration in study
Title
Hormonal receptors status
Description
Hormonal receptors status will be subdivised as:
Positive hormonal receptors / Positive HER2
Positive hormonal receptors / Negative HER2
Negative hormonal receptors / Positive HER2
Triple negative
Time Frame
Before registration in study
Title
Likehood of leptomeningeal metastasis according to the EANO-ESMO classification.
Description
EANO-ESMO classification is obtained by searching clinical symptoms, cancer cells in the cerebrospinal fluid (obtained by lumbar puncture), signs in RMI. The likehood of leptomeningeal metastasis is:
Lack of evidence,
Possible,
Probable,
Confirmed.
Time Frame
Up to 3 months after the intial diagnosis
Title
Overall survival
Description
Overall survival is defined as time from date of registration to date of death regardless of the cause.
Time Frame
Time from date of registration to date of death regardless of the cause, assessed up to 1 year
Title
Proteomic profiles issued from blood
Description
Proteomic profile will be obtained by bioinformatic analysis of blood.
Time Frame
Up to 3 months after the intial diagnosis
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with histologically proven breast cancer
Patient with suspected metastatic leptomeningitis
Age ≥ 18 years
Patient covered by the French social security regime
Signed written informed consent
Exclusion Criteria:
History of cancer other than the one being treated
Contraindication to carrying out the lumbar puncture or cerebrospinal MRI
Pregnant or breastfeeding patient
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emilie LE RHUN, MD
Organizational Affiliation
Centre Oscar Lambret
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre Oscar Lambret
City
Lille
State/Province
Hauts-de- France
ZIP/Postal Code
59020
Country
France
Facility Name
Centre Hospitalier Régional Universitaire de Lille
City
Lille
State/Province
Hauts-de-France
ZIP/Postal Code
59000
Country
France
12. IPD Sharing Statement
Learn more about this trial
Analyses of Exosomes in the Cerebrospinal Fluid for Breast Cancer Patients With Suspicion of Leptomeningeal Metastasis.
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