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NCT06067347RecruitingAccepts Healthy Volunteers

A Global Study of the PETAL Consortium

Massachusetts General Hospital

Start Date

1/5/2024

Completion Date

1/1/2028

Summary

The goal of this observational study is to correlate molecular alterations with outcomes including overall survival (OS), progression-free survival (PFS), response rates for patients with a new diagnosis, primary refractory or relapse, of mature T-cell and NK-cell neoplasms (TNKL). We hypothesize that machine learning can be leveraged to uncover distinct genetic vulnerabilities that underlie treatment response and resistance for patients with TNKL, thus moving towards personalized treatment solutions.

Detailed Description

This study is a prospective, longitudinal observational study of patients with newly diagnosed or relapsed/refractory T-cell and NK-cell neoplasms, conducted across multiple participating institutions globally. Patients will be enrolled during their initial visit as new patients and will be followed for up to four years through the course of their clinical management. Data for routine demographics, baseline clinical features, including pathology, molecular information related to the tumor, radiology, treatment characteristics and quality of life (QoL) associated with their lymphoma care will be collected over the course of 4 years by clinical research teams at every participating institution. The de-identified data will be securely shared through a password protected REDCap with other participating institutions under data usage agreements of the consortium. Next generation sequencing (NGS) including but not limited to whole exome sequencing and bulk RNA-sequencing will be performed on archived lymphoma specimens, mononuclear cells, cfDNA and saliva (when feasible) for a comprehensive molecular characterization of the tumor. Molecular data will be analyzed in correlation with patient outcomes. Advanced deep learning algorithms will be applied to predict responses and survival across lymphoma subtypes, heterogeneous clinical scenarios and various potential therapeutic approaches that the patient has not been exposed to.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Untreated, relapsed, or refractory histologically confirmed mature T-cell or NK-cell neoplasm. * All subtypes of PTCL are eligible except for T-cell large granular lymphocytic leukemia, cutaneous T-cell lymphoma such as but not limited to mycosis fungoides and transformation, Sézary syndrome, and primary cutaneous CD30+ disorders. Exclusion Criteria: * Precursor T/NK neoplasms, T-cell large granular lymphocytic leukemia, cutaneous T-cell lymphoma such as but not limited to mycosis fungoides and transformation, Sézary syndrome, and primary cutaneous CD30+ disorders. * Adults who are unable to consent, individuals who are not yet adults such as infants, children and teenagers, pregnant women, and prisoners.

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Conditions

T-Cell and NK-Cell Neoplasm

Locations

City of Hope

Duarte, California 91010

United States

University of Colorado

Denver, Colorado 80204

United States

Moffitt Cancer Center

Tampa, Florida 33612

United States

Massachusetts General Hospital

Boston, Massachusetts 02114

United States

Dana-Farber Cancer Institute

Boston, Massachusetts 02215

United States

Mayo Clinic

Rochester, Minnesota 55905

United States

Hackensack University Medical Center

Hackensack, New Jersey 07601

United States

OhioHealth

Columbus, Ohio 43214

United States

University of Pennsylvania

Philadelphia, Pennsylvania 19104

United States

University of Virginia

Charlottesville, Virginia 22903-4

United States

Royal Adelaide Hospital

Adelaide, South Australia 5000

Australia

Peter MacCallum Cancer Centre

Melbourne, Victoria 3000

Australia

Kyoto University

Kyoto, 606-8501

Japan

University of Cape Town

Cape Town, South Africa 7700

South Africa