Menu
Recruiting NCT04157569

CtDNA After Chemotherapy in Elderly Patients With Acute Leukemia

Observational Acute Leukemia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Acute Leukemia. Basic parameters: 60 years — 100 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Monitoring Circulating Tumor DNA After Chemotherapy in Elderly Patients With Acute Leukemia

Overview

This study will monitor CtDNA After Chemotherapy in Elderly Patients With AL

Detailed description

This study will use droplet digital PCR (ddPCR) method to quantify peripheral blood plasma mutant allele frequency (MAF) in elderly acute leukemia patients after chemotherapy to evaluate the clinical value of CtDNA .

Primary outcome measures

  • cumulative incidence of relapse(CIR) [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (1)
  • overall survival (OS) [Time frame: through study completion, an average of 2 years]

Eligibility criteria

Inclusion criteria

  • Written informed consent
  • Male
  • not pregnant female
  • patients >=60 years old
  • Diagnosis of acute leukemia

Exclusion criteria

  • Pregnancy
  • HIV positive
  • patients >=100 years old

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

China · 1 center
  • Navy General Hospital — Beijing

Identifiers

NCT: NCT04157569 · NavyGHB-006

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗