Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06067347

Integration of Machine Learning and Genomics to Predict Outcomes for Newly Diagnosed, Relapsed and Refractory Mature T-cell and NK/T-cell Lymphomas: a Global Study of the PETAL Consortium

Led by Massachusetts General Hospital · Updated on 2026-04-09

1200

Participants Needed

14

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a global observational study to understand mature T-cell and NK-cell neoplasms (TNKL), which are types of lymphomas. The study aims to link molecular changes in the tumors to patient outcomes like overall survival and treatment response. It also explores how machine learning can help identify genetic factors that influence how patients respond or resist treatments, moving toward more personalized care. This study enrolls patients who are newly diagnosed or have relapsed/refractory TNKL from multiple institutions worldwide. Participants will be followed for up to four years during their clinical management. Researchers will collect data on demographics, clinical features, pathology, molecular tumor details, imaging, treatments, and quality of life. Genetic testing including whole exome and RNA sequencing will be done on tumor samples and other biological materials to provide a comprehensive molecular profile. Participants will have routine clinical visits where data and samples will be collected by research teams. The study will monitor key outcomes like overall survival, progression-free survival, response duration, and adverse events over four years. Data will be securely shared among sites, and advanced deep learning models will analyze the molecular information alongside clinical outcomes to predict patient responses and survival across different lymphoma subtypes and treatments.

CONDITIONS

Brief Title

A Global Study of the PETAL Consortium

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Histologically confirmed mature T-cell or NK-cell neoplasm that is untreated, relapsed, or refractory
  • All subtypes of peripheral T-cell lymphoma (PTCL) are eligible except T-cell large granular lymphocytic leukemia, cutaneous T-cell lymphoma (including mycosis fungoides and transformation), Sézary syndrome, and primary cutaneous CD30+ disorders
Not Eligible

You will not qualify if you...

  • Diagnosis of precursor T/NK neoplasms
  • Diagnosis of T-cell large granular lymphocytic leukemia
  • Diagnosis of cutaneous T-cell lymphoma such as mycosis fungoides, Sézary syndrome, or primary cutaneous CD30+ disorders
  • Individuals unable to provide informed consent
  • Individuals under 18 years old
  • Pregnant women
  • Prisoners

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 4 years

Participants are observed over the course of their clinical management with data collected on demographics, clinical features, pathology, molecular tumor information, radiology, treatment, and quality of life.

Regular visits as part of routine clinical care over 4 years

Trial Site Locations

Total: 14 locations

1

City of Hope

Duarte, California, United States, 91010

Actively Recruiting

2

University of Colorado

Denver, Colorado, United States, 80204

Actively Recruiting

3

Moffitt Cancer Center

Tampa, Florida, United States, 33612

Actively Recruiting

4

Massachusetts General Hospital

Boston, Massachusetts, United States, 02114

Actively Recruiting

5

Dana-Farber Cancer Institute

Boston, Massachusetts, United States, 02215

Actively Recruiting

6

Mayo Clinic

Rochester, Minnesota, United States, 55905

Actively Recruiting

7

Hackensack University Medical Center

Hackensack, New Jersey, United States, 07601

Actively Recruiting

8

OhioHealth

Columbus, Ohio, United States, 43214

Actively Recruiting

9

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

10

University of Virginia

Charlottesville, Virginia, United States, 22903-4

Actively Recruiting

11

Royal Adelaide Hospital

Adelaide, South Australia, Australia, 5000

Actively Recruiting

12

Peter MacCallum Cancer Centre

Melbourne, Victoria, Australia, 3000

Actively Recruiting

13

Kyoto University

Kyoto, Japan, 606-8501

Actively Recruiting

14

University of Cape Town

Cape Town, South Africa, South Africa, 7700

Actively Recruiting

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Research Team

S

Salvia Jain, MD

F

Forum Bhanushali

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

Frequently Asked Questions

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