Nanochip Technology in Monitoring Treatment Response and Detecting Relapse in Participants With Diffuse Large B-Cell Lymphoma
Status: | Recruiting |
---|---|
Conditions: | Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/4/2018 |
Start Date: | September 26, 2018 |
End Date: | December 31, 2021 |
Contact: | Ohio State University Comprehensive Cancer Center |
Email: | OSUCCCClinicaltrials@osumc.edu |
Phone: | 800-293-5066 |
A Pilot Study of Nanochip Technology for Monitoring Treatment Response and Detection of Relapse in Patients With Diffuse Large B-Cell Lymphoma
This trial studies how well nanochip technology (immuno-tethered lipoplex nanoparticle [ILN]
biochip) works in monitoring treatment response and in detecting relapse in participants with
diffuse large B-cell lymphoma. Finding genetic markers for diffuse large B-cell lymphoma may
help identify participants with this disease and help predict the outcome of treatment. It is
not yet known how well ILN biochip-based testing monitors treatment response or detects
relapse in participants with diffuse large B-cell lymphoma.
biochip) works in monitoring treatment response and in detecting relapse in participants with
diffuse large B-cell lymphoma. Finding genetic markers for diffuse large B-cell lymphoma may
help identify participants with this disease and help predict the outcome of treatment. It is
not yet known how well ILN biochip-based testing monitors treatment response or detects
relapse in participants with diffuse large B-cell lymphoma.
PRIMARY OBJECTIVES:
I. Determine whether ILN biochip can be used to detect molecular marker(s) to monitor
treatment response in patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL).
II. Determine whether ILN biochip can promote early detection of disease relapse in patients
with DLBCL.
OUTLINE:
Participants' blood samples undergo ILN biochip testing at diagnosis, before and after every
course of chemotherapy, every 3 months for 2 years, and at relapse.
I. Determine whether ILN biochip can be used to detect molecular marker(s) to monitor
treatment response in patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL).
II. Determine whether ILN biochip can promote early detection of disease relapse in patients
with DLBCL.
OUTLINE:
Participants' blood samples undergo ILN biochip testing at diagnosis, before and after every
course of chemotherapy, every 3 months for 2 years, and at relapse.
Inclusion Criteria:
- Histologically confirmed treatment naive DLBCL. Subtypes including high grade B-cell
lymphoma, not otherwise specified (NOS) and de-novo DLBCL including germinal center
B-cell type (GCB) and non-GCB subtypes.
- Intent to receive entire care (treatment and follow-up) at Ohio State University
(OSU).
- Receiving treatment with curative intent.
- Receiving planned 6 cycles of chemotherapy.
- Ability to consent.
Exclusion Criteria:
- Transformed lymphomas.
- DLBCL with leukemic presentation.
- Primary central nervous system (CNS) lymphoma.
- Participating in other clinical trial/ receiving experimental therapy.
- Patients with a "currently active" second malignancy that, in the opinion of the
principal investigator, will interfere with patient participation, or confound data
interpretation.
- Pregnancy (positive serum or urine pregnancy test) or breast feeding.
We found this trial at
1
site
Columbus, Ohio 43210
Principal Investigator: Narendranath Epperla, MD
Phone: 614-293-6191
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