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N/ARecruiting

A Registry for People With T-cell Lymphoma

Sponsored by Memorial Sloan Kettering Cancer Center

About this study

The purpose of this registry study is to create a database-a collection of information-for better understanding T-cell lymphoma. Researchers will use the information from this database to learn more about how to improve outcomes for people with T-cell lymphoma.

Where this study is enrolling (26)

  • Stanford University Medical Center (Data collection only)

    Stanford, California

    Call 650-725-5071

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  • City of Hope Cancer Center (Data collection only)

    Duarte, California

    Call 626-359-8111

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  • University of California San Francisco (Data collection only)

    San Francisco, California

    Call 415-353-2421

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  • UNIVERSITY OF CALIFORNIA SAN DIEGO (Data collection only)

    San Diego, California

    Call 858-822-6100

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  • University of Colorado (Data Collection Only)

    Aurora, Colorado

    Call 212-639-3983

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Show all 26 locations

  • Yale University (Data Collection Only)

    New Haven, Connecticut

    Call 203-200-4363

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  • Moffitt Cancer Center (Data Collection Only)

    Tampa, Florida

    Call 888-663-3488

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  • University of Miami (Data Collection Only)

    Miami, Florida

    Call 305-243-5302

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  • Emory University (Data Collection Only)

    Atlanta, Georgia

    I'm interested

  • Northwestern Medicine (Data Collection)

    Chicago, Illinois

    Call 312.926.3155

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  • Massachusetts General Hospital (Data Collection Only)

    Boston, Massachusetts

    Call 857-392-4495

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  • Dana Farber Cancer Institute (Data Collection Only)

    Boston, Massachusetts

    Call 877-442-3324

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  • Mayo Clinic (Data Collection Only)

    Rochester, Minnesota

    Call 507-284-2511

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  • Washington University (Data Collection Only)

    St Louis, Missouri

    Call 314-747-1171

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  • University of Nebraska (Data collection only)

    Omaha, Nebraska

    Call 402-559-4000

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  • Memorial Sloan Kettering at Basking Ridge (All protocol activities)

    Basking Ridge, New Jersey

    Call 646-608-2680

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  • Memorial Sloan Kettering Monmouth (All protocol activities)

    Middletown, New Jersey

    Call 646-608-2680

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  • Memorial Sloan Kettering Cancer Center (All Protocol Activities)

    New York, New York

    Call 646-608-2680

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  • Memorial Sloan Kettering Westchester (All protocol activities)

    Harrison, New York

    Call 646-608-2680

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  • Memorial Sloan Kettering Nassau (All protocol activities)

    Uniondale, New York

    Call 646-608-2680

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  • Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (All protocol activities)

    Commack, New York

    Call 646-608-2680

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  • Weill Cornell Medical Center (Data Collection Only)

    New York, New York

    Call 646-962-2064

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  • Ohio State University (Data Collection Only)

    Columbus, Ohio

    Call 614-293-8000

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  • University of Pennsylvania (Data Collection Only)

    Philadelphia, Pennsylvania

    I'm interested

  • Thomas Jefferson University Hospital (Data collection only)

    Philadelphia, Pennsylvania

    Call 215-955-8874

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  • MD Anderson Cancer Center (Data Collection Only)

    Houston, Texas

    Call 877-632-6789

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Who can participate

Inclusion criteria

  • ✓Written informed consent
  • ✓Adequate fresh or archival tumor biopsy or intent to obtain fresh tumor biopsy.
  • ✓Pathologically-confirmed mature T- or natural killer (NK)-cell lymphoma meeting one of the following diagnostic criterion (based on WHO classification and NCCN guidelines):
  • ✓T-cell prolymphocytic leukemia
  • ✓T-cell large granular lymphocytic leukemia
  • ✓Chronic lymphoproliferative disorder of NK cells
  • ✓Aggressive NK-cell leukemia
  • ✓Systemic Epstein-Barr virus (EBV)-positive T-cell lymphoma of childhood
  • ✓Chronic active EBV infection of T- and NK-cell type, systemic form
  • ✓Hydroa vacciniforme-like lymphoproliferative disorder
  • ✓Adult T-cell leukemia/lymphoma
  • ✓Extranodal NK/T-cell lymphoma, nasal type
  • ✓Enteropathy-associated T-cell lymphoma
  • ✓Monomorphic epitheliotropic intestinal T-cell lymphoma
  • ✓Intestinal T-cell lymphoma, not otherwise specified (NOS)
  • ✓Indolent T-cell lymphoproliferative disorder of the gastrointestinal tract
  • ✓Hepatosplenic T-cell lymphoma
  • ✓Subcutaneous panniculitis-like T-cell lymphoma
  • ✓Mycosis fungoides (limited to those with ≥ stage IB disease and those receiving active therapy)
  • ✓Sézary syndrome
  • ✓Primary cutaneous anaplastic large cell lymphoma (receiving systemic therapy)
  • ✓Primary cutaneous Gamma-Delta T-cell lymphoma
  • ✓Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
  • ✓Primary cutaneous acral CD8+ T-cell lymphoma (receiving systemic therapy)
  • ✓Peripheral T-cell lymphoma, not otherwise specified
  • ✓Angioimmunoblastic T-cell lymphoma
  • ✓Follicular T-cell lymphoma
  • ✓Nodal peripheral T-cell lymphoma with TFH phenotype
  • ✓Anaplastic large cell lymphoma, ALK-positive
  • ✓Anaplastic large cell lymphoma, ALK-negative
  • ✓Breast-implant associated anaplastic large cell lymphoma.
  • ✓NOTE: Patients with diagnoses of mycosis fungoides, primary cutaneous anaplastic large cell lymphoma, and/or primary cutaneous acral CD8+ T-cell lymphoma must be receiving systemic therapy.

Exclusion criteria

  • ✕Patients with of mycosis fungoides, primary cutaneous anaplastic large cell lymphoma, and/or primary cutaneous acral CD8+ T-cell lymphoma not receiving systemic therapy.
  • ✕Inability to collect prospective data, measure response, or perform adequate follow-up assessments in the clinical judgment of the treating physician. NOTE: Repository participation does not exclude participation in clinical trials, nor does existing clinical trial participation exclude enrollment in the study herein outlined.

Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.

Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.

Trial data sourced from ClinicalTrials.gov.