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Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma

Feasibility of Combined Genomics/Transcriptomics for Patients With Lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05464823
Enrollment
111
Registered
2022-07-19
Start date
2022-07-07
Completion date
2027-05-12
Last updated
2026-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lymphoma

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

Interventions

OTHERMolecular Functional Portrait

Participants will be asked to allow previously-collected tumor tissue to be used for the MF Portrait test

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patient Eligibility: 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.

Exclusion criteria

1\. None

Design outcomes

Primary

MeasureTime frame
Percentage of participants who have genomic test results available in <=7 daysthrough study completion an average of 1 year

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORJason Westin, MD

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026