CML Pediatric ITK Response According to Molecular Identification at Diagnosis

Trial Title: CML Pediatric ITK Response According to Molecular Identification at Diagnosis

NCT ID: NCT05605379

Condition: Chronic Myeloid Leukemia

Conditions: Official terms:
Leukemia, Myeloid
Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Conditions: Keywords:
Chronic Myeloid Leukemia
Children
Molecular landscape
TKI response
Expression profile

Study type: Observational

Overall status: Recruiting

Study design:

Time perspective: Retrospective

Intervention:

Intervention type: Biological
Intervention name: Next Generation Sequencing (DNA and RNA)
Description: Targeted Next Generation Sequencing (DNA and RNA)
Arm group label: No responders (without CCR at 1 year)
Arm group label: Responders (with CCR at 1 year)

Summary: Treatment of chronic myeloid leukemia (CML) has been revolutionized by tyrosine kinase inhibitor (TKI). Nevertheless, case of failure and suboptimal response are still observed even in children. Pediatric CML is a rare disease and differs from adult in terms of disease presentation and treatment response underlying a likely different CML biology. Molecular mechanisms that induce resistance to TKI are still poorly characterized except mutations in the tyrosine kinase domain of BCR::ABL1. We propose to search for a molecular signature to predict the response to TKI in the pediatric population.

Detailed description: Commonly mutated genes associated with myeloid malignancies have been described in acceleration phase and blastic phase but also at diagnostic in adult chronic phase-CML (CP-CML). The impact of these mutations on treatment response is still debated but several studies observed a worse outcome in adult patients with some mutations. In children only one study explored the molecular status of 30 genes in 21 children and young adults. They found a higher proportion of ASXL1 mutations in children than in adult They did not observed any significant difference in overall survival of ASXL1 mutated versus non-mutated patients but probably due the small size of the cohort. We propose here, to investigate retrospectively on DNA at diagnosis of 88 CP-CML children the mutation status of 64 genes by next generation sequencing and to see if there is an association with the response to TKI treatment. We will complete the molecular signature by analyzing the differentially genetic expression profile by RNA-seq on peripheral blood RNA of 8 patients with CCR at 12 months (and/or a BCR ::ABL1 IS ≤1%IS) and 8 patients with no CCR at 12 months.

Criteria for eligibility:

Study pop:
Pediatric CML patients

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Age at diagnosis less than or equal to 18 years - Presence of a Philadelphia chromosome detected by cytogenetic analysis (conventional karyotype or Fluorescence In Situ Hybridization (FISH)) and a BCR ::ABL1 transcript e13a2 ou e14a2 - Diagnosis in chronic phase according to the European Leukemia Net (ELN) criteria - First-line treatment with TKIs - Possible pre-treatment with hydroxyurea - DNA available at diagnosis - RNA available for a sub-group patients (8 responders vs 8 no responders) Exclusion Criteria: - Age at diagnosis more than 18 years - Diagnosis in accelerated phase or blastic phase - First line treatment other than TKI

Gender: All

Minimum age: 6 Years

Maximum age: 18 Years

Healthy volunteers: No

Locations:

Facility:
Name: CHU de Bordeaux, Service Hématologie Biologique

Address:
City: Bordeaux
Country: France

Status: Recruiting

Contact:
Last name: Stéphanie DULUCQ
Email: stephanie.dulucq@chu-bordeaux.fr

Start date: February 27, 2023

Completion date: March 2025

Lead sponsor:
Agency: University Hospital, Bordeaux
Agency class: Other

Source: University Hospital, Bordeaux

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05605379