Clinical trial · Observational
A Therapy Treatment Response Trial in Patients With Leptomeningeal Metastases ((LM) Using CNSide
A Longitudinal Therapy Response Monitoring Study in Subjects With Leptomeningeal Metastases Using CNSide (CSF Tumor Cells) Compared to Standard of Care (CSF Cytology, Clinical Evaluation, and Imaging).
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): The sponsor can no longer financially support the trial.
Summary
Brief summary (as posted)
The FORESEE Study is a multi-center, prospective clinical trial enrolling patients with Breast or Non-Small Cell Lung Cancer (NSCLC) who have suspicious or confirmed Leptomeningeal Metastases (LM). Standard of Care methods to diagnose, or assess the treatment response of LM (Clinical Evaluation, MRI and Cytology) have limited sensitivity and specificity. This creates challenges for physicians to manage LM or determine the best course of treatment. CNSide, is a Laboratory Developed Test (LDT ) that is used commercially at the Physician's discretion in Biocept's CLIA certified, CAP accredited laboratory. CNSide can detect and quantify tumor cells in the CSF from patients with Breast Cancer or NSCLC having a suspicious or confirmed LM. The goal of the FORESEE Study is to evaluate the performance of CNSide in monitoring the LM's response to treatment and to assess the impact of CNSide on treatment decisions made by Physicians.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Leptomeningeal Disease | Leptomeningeal Neoplasm | ALIAS | 0.90 |
| Leptomeningeal Metastasis | — | UNRESOLVED | — |
| Leptomeningeal Neoplasms | Leptomeningeal Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Non-Small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CNSide | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- label
- Breast Cancer
- description
- Subjects with Breast Cancer of all subtypes and independent of Hormone status who have a confirmed or suspicious Leptomeningeal Metastasis by Investigator assessment of radiographic image and clinical evaluation and cytology
- interventionNames
- Device: CNSide
- label
- Non-Small Cell Lung Cancer
- description
- Subjects with Non-Small Cell Lung Cancer of all subtypes who have a confirmed or suspicious Leptomeningeal Metastasis by Investigator assessment of radiographic image and clinical evaluation and cytology
- interventionNames
- Device: CNSide
Primary outcomes (1)
- measure
- Assess the impact of CNSide on treatment decisions
- timeFrame
- 1 year
- description
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. Subjects =\> 18 years of age 2. All genders, races, or ethnic groups, 3. Diagnosed with Breast Cancer or NSCLC who present with clinically suspected LM based on Investigator assessment of radiographic image, cytology, and clinical evaluation. 4. Cytology positive and negative subjects will be included. 5. Subjects willing to provide an Informed Consent. 6. Subjects willing and able to undergo CSF or blood collection via Lumbar Puncture and Ommaya Reservoir as well as veni-puncture and shunt. 7. Both patients with and without parenchymal brain metastases will be eligible as long as leptomeningeal metastases are suspected 8. Subjects who previously had a diagnosis of Leptomeningeal Disease by Investigator assessment of radiographic image and clinical evaluation and cytology. Exclusion Criteria: 1. Subjects who do not have cancer, 2. Subjects with other types of tumors than breast or lung cancer 3. Subjects diagnosed with a primary brain tumor 4. Subjects who are unable to undergo lumbar puncture, a shunt or veni-puncture. 5. Lack of suspicious LM based in imaging or clinical evaluation. 6. Ordering the Commercial CNSide test while subject is on study 7. Pregnant women and adults lacking capacity to consent for themselves
References
Publications (0)
Data not yet available