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NCT07727083Recruiting

Clinical and Biological Cohort Study of EBV-Positive T/NK-Cell Lymphoproliferative Diseases

A Multicenter Ambidirectional Clinical and Biological Cohort Study of Epstein-Barr Virus-Positive T/NK-Cell Lymphoproliferative Diseases

Source: ClinicalTrials.gov · Last updated 13 Aug 2026

Brief summary (registry, in English)

This is a multicenter, non-interventional, ambidirectional cohort study of Epstein-Barr virus-positive T/NK-cell lymphoproliferative diseases. The study consists of a retrospective clinical cohort of 500 consecutively diagnosed patients with extranodal NK/T-cell lymphoma and a prospective clinical-biological cohort of 1,000 newly diagnosed patients with extranodal NK/T-cell lymphoma, aggressive NK-cell leukemia, systemic chronic active Epstein-Barr virus disease of T/NK-cell type, or Epstein-Barr virus-positive nodal T/NK-cell lymphoma. The study will characterize clinical features, treatment pathways, response, relapse or progression patterns, and long-term survival. The prospective cohort will additionally undergo standardized collection of peripheral blood and optional tumor tissue specimens at predefined clinical time points. Clinical, molecular, viral, and immune biomarkers will be evaluated for their associations with treatment response, treatment failure, disease progression, and survival. No treatment is assigned by the study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
1500 (estimated)
First submitted
19 Jul 2026
Start date
11 Aug 2026
Primary completion date
31 Dec 2035
Lead sponsor
Rong Tao
NCT number
NCT07727083

What you commit to

  • Study type: Observational
  • Planned participants: 1500
  • From 11 Aug 2026 to the primary completion date, 31 Dec 2035
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • For the retrospective cohort: no usable survival follow-up information, inability to confirm survival status, or inability to calculate the principal survival outcomes.
  • For the prospective cohort: unwillingness or inability to participate in protocol-defined longitudinal clinical follow-up.

Who the study is looking for

  • Age 18 years or older.
  • Newly diagnosed Epstein-Barr virus-positive T/NK-cell lymphoproliferative disease meeting World Health Organization diagnostic criteria.
  • For the retrospective cohort: diagnosis of extranodal NK/T-cell lymphoma between January 1, 2017 and December 31, 2025 at a participating center.
  • For the prospective cohort: diagnosis between June 1, 2026 and December 31, 2030 of one of the following:
  • Extranodal NK/T-cell lymphoma;
  • Aggressive NK-cell leukemia;
  • Systemic chronic active Epstein-Barr virus disease of T/NK-cell type; or Epstein-Barr virus-positive nodal T/NK-cell lymphoma.
  • Availability of essential diagnostic, staging, and treatment information.
  • For the prospective cohort: written informed consent and successful collection of the protocol-required baseline peripheral blood specimen.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan University Shanghai Cancer Center
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ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.