MedPath

Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma

Not Applicable
Recruiting
Conditions
Lymphoma
Interventions
Other: Molecular Functional Portrait
Registration Number
NCT05464823
Lead Sponsor
M.D. Anderson Cancer Center
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:

* To determine the feasibility of prioritizing targets with precision analytics

* To determine clinical outcomes in patients receiving molecularly matched therapy

* To determine the role of additional emerging diagnostic technologies

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
80
Inclusion Criteria
  1. Male/female patients who are at least 18 years of age on the day of informed consent signing.
  2. Patients must have a histologically documented diffuse large B-cell lymphoma requiring therapy.
  3. Provision of written informed consent for the study.
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Exclusion Criteria
  1. None
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Molecular TestingMolecular Functional PortraitMolecular Functional (MF) Portrait (a commercial test conducted by the sponsor of this study, BostonGene) in guiding lymphoma care.
Primary Outcome Measures
NameTimeMethod
Percentage of participants who have genomic test results available in <=7 daysthrough study completion an average of 1 year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

M D Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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