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A study of the incidence of molecular mutations in newly diagnosed acute lymphoblastic leukemia (ALL) patients by Next-generation sequencing technique

Recruiting
Conditions
Thai newly diagnosed ALL patients aged greater than 18 years.
Acute lymphoblastic leukemia, Next-generation sequencing ,Molecular mutations
Registration Number
TCTR20240409003
Lead Sponsor
Siriraj Hospital Mahidol University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
140
Inclusion Criteria

1.A retrospective cohort: Thai newly diagnosed ALL patients
2.A prospective cohort: Thai newly diagnosed ALL patients aged greater than 18 years who had genetic workup results by NGS study and signed informed consent OR

Exclusion Criteria

Poor quality specimen from a protocol number 388/2561(EC2)

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
incidence of molecular mutations in Thai adult newly diagnosed ALL patients by NGS technique 1 years Next-generation sequencing (targeted gene sequencing: Illumina machine)
Secondary Outcome Measures
NameTimeMethod
To evaluate the clinical outcome in Thai adult ALL patients considering molecular mutations 1 years Case record form comparing with genetic results by Illumina machine
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