Cancer Clinical Trial
Official title:
A Pilot Study to Explore Serum and Imaging Biomarkers in Patients With Spinal Cord Compression
One of the complications of having cancer in the spinal vertebrae is that it can spread and
lead to compression of the spinal cord. Spinal cord compression is a serious event that needs
to be treated quickly in order to prevent permanent damage to the spinal cord and nerves.
- Researchers currently do not have the ability to accurately predict whether cancer of
the vertebrae will cause spinal cord compression. It is possible that accurate
predictions could allow doctors to treat patients even before they develop symptoms of
spinal cord compression, thereby preventing some of the long-term consequences.
Objectives:
- To compare patients with cancer of the spinal vertebrae with and without symptoms of
spinal cord compression by looking at markers in the blood and changes on novel magnetic
resonance imaging (MRI) techniques that might allow researchers to predict who will
experience spinal cord compression before they actually begin to have symptoms.
Eligibility:
- One group of healthy volunteers 18 years of age and older.
- One group of patients 18 years of age and older who have cancer that has spread to the
vertebrae without symptoms of spinal cord compression.
- One group of patients 18 years of age and older who have cancer that has spread to the
vertebrae with symptoms of spinal cord compression.
Design:
- Healthy volunteers:
- Blood will be drawn from each volunteer for initial tests and for more specific
biomarker tests.
- Comprehensive MRI of the spine, followed by a special type of MRI called diffusion
tensor imaging (DTI). It is believed that DTI may be even more sensitive in revealing
spinal cord abnormalities than regular MRI sequences.
- Patients with cancer of the vertebrae:
- Researchers will obtain information such as pathology reports, laboratory results,
diagnosis and treatment history, physical exam (PE) information, results of scans such
as x-rays, MRI, computerized tomography (CT), and positron emission tomography (PET),
and planned treatment details.
- Additional blood samples will be taken for specific biomarker tests.
- Questionnaire about pain, unusual sensations or numbness, bladder or bowel problems, and
mobility.
- Comprehensive MRI of the spine, followed by a DTI.
- Patients who appear to have symptoms of spinal cord compression will be offered standard
radiation treatment.
Background:
- Metastatic Epidural Spinal Cord Compression (MESCC) is an acute and common complication
with grave prognosis.
- Biomarkers for early detection and prediction of outcome in these patients may allow a
more objective treatment decision algorithm and hopefully change the unfortunate outcome
described.
- Serum S-100b, NSE and GFAP and Plasma NF-H are surrogates for neuronal damage in humans
and animal models.
- Diffusion tensor imaging (DTI) has been used in brain disorders, in predicting Spinal
Cord Injury outcome in animal models, and was found to be beneficial in detecting spinal
cord abnormalities in human subjects with acute and slowly progressive cord compression.
Objectives:
- To compare and evaluate the feasibility and reproducibility of DTI of the spinal cord in
healthy participants, to optimize the DTI Images and determine normal spine DTI values,
- To describe normal variations of serum/plasma and imaging biomarkers in healthy
participants and compare these with serum/plasma and imaging biomarkers values in
patients with vertebral metastases with and without spinal cord compression.
- To detect differences in the serum/plasma and imaging biomarkers in patients with
vertebral metastases with and without spinal cord compressions.
- To correlate serum/plasma and imaging biomarkers differences with clinical outcomes of
patients with vertebral metastases with spinal cord compression (pain, ambulation,
continence and survival at 1, 3, 6 and 12 months from radiotherapy).
Eligibility:
- Healthy volunteers with no prior history or concomitant central nervous system injury or
inflammatory disease, prior or planned brain or spinal cord radiation therapy or
surgical procedure and with no contraindication for MR scanning.
- Patients with metastatic cancer in the spinal vertebrae, with or without spinal cord
compression and with no prior history or concomitant central nervous system injury or
inflammatory disease, brain metastases, prior brain or spinal cord radiation therapy or
surgical procedure and with no contraindication for MR scanning.
Design:
- Preliminary DTI studies will be conducted for healthy volunteer participants to
determine normal spine DTI values, choose and optimize the scanning protocol, and
evaluate the presence of artifacts and reproducibility of the DTI Images. Normal values
and variability of serum and plasma biomarkers will be also determined.
- Patient participants with known vertebral bone metastases with or without spinal cord
compression will undergo a DTI study along with the standard MRI sequences, used to
evaluate MESCC patients. Blood samples for biomarkers will be also collected.
- Patients with documented MESCC, will be treated with standard radiotherapy fields, dose
and schedule. Steroid treatment will be used as clinically indicated. All study
procedures will be conducted prior to any therapy. Follow- up visits are planned at 1,
3, 6, and 12 months after radiotherapy completion with history and physical, DTI and
serum/plasma biomarker evaluations.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05346796 -
Survivorship Plan HEalth REcord (SPHERE) Implementation Trial
|
N/A | |
Recruiting |
NCT05094804 -
A Study of OR2805, a Monoclonal Antibody Targeting CD163, Alone and in Combination With Anticancer Agents
|
Phase 1/Phase 2 | |
Completed |
NCT04867850 -
Effect of Behavioral Nudges on Serious Illness Conversation Documentation
|
N/A | |
Enrolling by invitation |
NCT04086251 -
Remote Electronic Patient Monitoring in Oncology Patients
|
N/A | |
Completed |
NCT01285037 -
A Study of LY2801653 in Advanced Cancer
|
Phase 1 | |
Completed |
NCT00680992 -
Study of Denosumab in Subjects With Giant Cell Tumor of Bone
|
Phase 2 | |
Completed |
NCT00062842 -
Study of Irinotecan on a Weekly Schedule in Children
|
Phase 1 | |
Active, not recruiting |
NCT04548063 -
Consent Forms in Cancer Research: Examining the Effect of Length on Readability
|
N/A | |
Completed |
NCT04337203 -
Shared Healthcare Actions and Reflections Electronic Systems in Survivorship
|
N/A | |
Recruiting |
NCT04349293 -
Ex-vivo Evaluation of the Reactivity of the Immune Infiltrate of Cancers to Treatments With Monoclonal Antibodies Targeting the Immunomodulatory Pathways
|
N/A | |
Terminated |
NCT02866851 -
Feasibility Study of Monitoring by Web-application on Cytopenia Related to Chemotherapy
|
N/A | |
Active, not recruiting |
NCT05304988 -
Development and Validation of the EFT for Adolescents With Cancer
|
||
Completed |
NCT04448041 -
CRANE Feasibility Study: Nutritional Intervention for Patients Undergoing Cancer Surgery in Low- and Middle-Income Countries
|
||
Completed |
NCT00340522 -
Childhood Cancer and Plexiform Neurofibroma Tissue Microarray for Molecular Target Screening and Clinical Drug Development
|
||
Recruiting |
NCT04843891 -
Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis.
|
Phase 1 | |
Active, not recruiting |
NCT03844048 -
An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Venetoclax Clinical Trial
|
Phase 3 | |
Completed |
NCT03109041 -
Initial Feasibility Study to Treat Resectable Pancreatic Cancer With a Planar LDR Source
|
Phase 1 | |
Completed |
NCT03167372 -
Pilot Comparison of N-of-1 Trials of Light Therapy
|
N/A | |
Terminated |
NCT01441115 -
ECI301 and Radiation for Advanced or Metastatic Cancer
|
Phase 1 | |
Recruiting |
NCT06206785 -
Resting Energy Expenditure in Palliative Cancer Patients
|