Status:

COMPLETED

Minimal Residual Disease in Peripheral T-cell Lymphoma

Lead Sponsor:

Washington University School of Medicine

Collaborating Sponsors:

Invivoscribe, Inc.

National Cancer Institute (NCI)

Conditions:

Peripheral T Cell Lymphoma

Eligibility:

All Genders

18+ years

Brief Summary

As T-cell receptor sequencing by LymphoTrack is an assay with high sensitivity that can be performed in peripheral blood, the investigators wish to evaluate the ability of this assay to predict which ...

Eligibility Criteria

Inclusion

  • At least 18 years of age.
  • Histologically-confirmed peripheral T-cell lymphoma being treated with curative intent. Eligible histologies include, but are not limited to: peripheral T-cell lymphoma, not otherwise specified; angioimmunoblastic T-cell lymphoma; anaplastic large cell lymphoma, ALK negative; and anaplastic large cell lymphoma, ALK positive.
  • Plan for treatment with frontline multi-agent anthracycline containing chemotherapy for curative intent (for example, CHOP, CHOEP, EPOCH). A frontline therapy program can include different sequential phases of treatment, including high-dose therapy and autologous stem cell transplantation.
  • Availability of pre-treatment test specimen from bone marrow, blood, lymph node, or alternate site to identify tumor-specific clonotype, or willingness to undergo biopsy if sufficient tissue is not available at time of enrollment (e.g. 15 slides from fixed formalin-fixed paraffin embedded tumor tissue
  • \*Patients who have less than 15 slides of fixed formalin-fixed paraffin embedded tumor tissue may be considered for enrollment after discussion with the study principal investigator
  • Able to understand and willing to sign an IRB approved written informed consent document.

Exclusion

  • Receiving second line of therapy or greater.
  • Diagnosis of primary cutaneous T-cell lymphoma, extranodal NK-cell lymphoma, acute T-cell lymphoma/leukemia, hepatosplenic T-cell lymphoma.

Key Trial Info

Start Date :

July 31 2017

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

November 30 2023

Estimated Enrollment :

44 Patients enrolled

Trial Details

Trial ID

NCT03297697

Start Date

July 31 2017

End Date

November 30 2023

Last Update

May 16 2024

Active Locations (3)

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Page 1 of 1 (3 locations)

1

Dana Farber Cancer Institute

Boston, Massachusetts, United States, 02215

2

Washington University School of Medicine

St Louis, Missouri, United States, 63110

3

Memorial Sloan Kettering Cancer Center

New York, New York, United States, 10065