Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- M.D. Anderson Cancer Center
- Enrollment
- 111
- Locations
- 1
- Primary Endpoint
- Percentage of participants who have genomic test results available in <=7 days
Study Overview
Brief Summary
To learn more about the usefulness of molecular testing with the Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.
Detailed Description
Primary Objective:
• To determine the feasibility and turnaround of clinical WES and transcriptome sequencing
Secondary Objectives:
- To determine the frequency of actionable DNA and RNA alterations
- To determine the concordance of DNA and RNA alterations
- To determine the frequency of molecularly matched therapy
- To determine the feasibility of identifying mechanism(s) of acquired resistance with genomic profiling
- To determine the feasibility of molecularly matched therapy to acquired resistance alterations
Exploratory Objectives:
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Other
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Patient Eligibility:
- •Inclusion Criteria:
- •Male/female patients who are at least 18 years of age on the day of informed consent signing.
- •Patients must have a histologically documented diffuse large B-cell lymphoma requiring therapy.
- •Provision of written informed consent for the study.
Exclusion Criteria
- Not provided
Arms & Interventions
Molecular Testing
Molecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.
Intervention: Molecular Functional Portrait (Other)
Outcomes
Primary Outcomes
Percentage of participants who have genomic test results available in <=7 days
Time Frame: through study completion an average of 1 year
Secondary Outcomes
No secondary outcomes reported
