Actively Recruiting

Age: 5Years - 90Years
All Genders
Healthy Volunteers
ID06076226

A Retrospective Study on Donor Leukocyte Telomere Length and Prognosis in Acute Leukemia Patients Treated With Allogeneic Hematopoietic Stem Cell Transplantation

Led by Zhejiang University · Updated on 2023-10-10

2500

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying patients with acute leukemia who have undergone allogeneic hematopoietic stem cell transplantation (allo-HSCT) to understand how the length of donor leukocyte telomeres relates to patient outcomes. This observational study includes patients aged 5 to 90 years who achieved complete remission and full donor engraftment after transplantation. The study was conducted at Zhejiang University schools of medicine and complies with ethical standards. The study involves no interventions or treatments; it is an observational analysis. Donors' leukocyte telomere lengths were measured from blood samples collected before receiving granulocyte colony-stimulating factor (G-CSF) mobilization. Patients and donors were grouped by donor age (40 years or older versus younger than 40) to observe differences. Participants are followed after transplantation with assessments including overall survival up to 60 months, relapse-free survival, and cumulative incidence of relapse. Researchers evaluate survival outcomes from the date of transplant until death, relapse, or end of follow-up. The study collects clinical data and donor telomere measurements to analyze prognosis in acute leukemia patients post-transplant.

CONDITIONS

Brief Title

A Retrospective Study on the Relationship Between Donor Leukocyte Telomere Length and Prognosis of Acute Leukemia Patients Treated With Allogeneic Hematopoietic Stem Cell Transplantation

Who Can Participate

Age: 5Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 5 years or older
  • First allogeneic hematopoietic stem cell transplant from matched related, unrelated, or haploidentical donors
  • Achieved complete remission after allo-HSCT
  • Donor blood sample collected before granulocyte colony-stimulating factor mobilization
Not Eligible

You will not qualify if you...

  • Diagnoses other than acute leukemia, including acute myeloid leukemia, acute lymphocytic leukemia, and mixed phenotype acute leukemia
  • Failure to achieve engraftment with full donor chimerism after allo-HSCT
  • Inability to extract DNA for telomere length analysis

AI-Screening

AI-Powered Screening

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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)

Long-term Monitoring

Duration - Up to 60 months

Participants are observed following their allogeneic hematopoietic stem cell transplantation to assess survival and relapse outcomes.

Regular follow-up visits according to routine clinical care

Trial Site Locations

Total: 1 location

1

Clinical research ethics committee of the first affiliated hospital, college of medicine, zhejiang University

Hangzhou, Zhejiang, China

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Research Team

H

He Huang, PhD&MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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