Actively Recruiting

Age: 0 - 18Years
All Genders
NCT06452732

Using Multiparametric Flow Cytometry to Detect Peripheral Blood and Bone Marrow Leukaemia Stem Cells for Relapse Prediction in P-AML

Led by Peking University People's Hospital · Updated on 2025-12-31

283

Participants Needed

2

Research Sites

86 weeks

Total Duration

On this page

Sponsors

P

Peking University People's Hospital

Lead Sponsor

T

The First Affiliated Hospital of Zhengzhou University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Leukaemia is a major disease that seriously endangers human health, the long-term survival rate of acute myeloid leukaemia receiving conventional chemotherapy is only 10% to 45%, haematological relapse is the main cause of treatment failure in acute myeloid leukaemia, reducing the relapse rate is the key to improving the efficacy of acute leukaemia, biomarker-guided preemptive therapy is an effective way to reduce the recurrence of leukaemia, existing markers to predict the recurrence has a high false Existing markers have high false-negative and false-positive rates for predicting relapse, and improving the accuracy of leukaemia relapse prediction is a major clinical problem that needs to be solved urgently. The group has found that circulating leukaemia stem cells remaining after chemotherapy are the key to relapse, therefore, we propose to conduct a multicentre prospective clinical study on the prediction of acute leukaemia relapse by circulating leukaemia stem cells.

CONDITIONS

Official Title

Using Multiparametric Flow Cytometry to Detect Peripheral Blood and Bone Marrow Leukaemia Stem Cells for Relapse Prediction in P-AML

Who Can Participate

Age: 0 - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Newly diagnoses candidates with acute myeloid leukemia.
  • Lower than or equal to 18 years-old;
  • Subjects are able to provide written informed consent.
Not Eligible

You will not qualify if you...

  • Subjects who cannot comply with the study;
  • Subjects with severe cardiac disease (ejection fraction<50% ), liver disease (total bilirubin >34umol/L, ALT and AST>1.5×upper limit normal) or kidney disease (Serum creatinine>130umol/L).
  • Subjects with severe infection.
  • Subjects with other conditions that cannot receive chemotherapy or transplantation.

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Peking University People's Hospital

Beijing, Beijing Municipality, China, 100044

Actively Recruiting

2

People's Hospital of Peking University

Beijing, Beijing Municipality, China, 100044

Actively Recruiting

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Research Team

Y

Yingjun Chang Y Prof. Ying-Jun Chang Chang

CONTACT

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

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