Skip to content

Identification of BCR::ABL1 Mutations by Digital PCR in CML

Digital PCR for Deep Sensitivity BCR::ABL1 Mutation Screening in CML

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07158294
Acronym
DiP-in-CML
Enrollment
150
Registered
2025-09-05
Start date
2026-02-01
Completion date
2029-04-01
Last updated
2025-09-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Myeloid Leukemia (CML)

Keywords

Failure, Digital PCR, BCR:ABL1 mutation

Brief summary

The goal of this study is to asses the ability of digital PCR (ddPCR) to detect actionable mutations in adult CML patients with failure of TKI therapy. The main objective of the study is it aims to answer is to assess whether ddPCR is at least as effective as NGS in detecting actionable (2GTKI-resistant) mutations. To accomplish this aim, samples of participants treated according to clinical practice, will be taken and analyzed for the presence of BCR::ABL1 KD mutations by ddPCR.

Detailed description

This is a multicenter biological study addressing the efficiency of ddPCR in detecting actionable mutations in patients with failure of TKI therapy. The study will involve 4 reference laboratories for BCR::ABL1 KD mutation testing Italian hematological centers enrolling patients and collecting samples for analysis. Peripheral blood samples taken from patients treated according to clinical practice with resistance to imatinib or 2GTKI therapy according to the ELN recommendations will be shipped to one of the reference laboratories and analyzed by ddPCR using Bio-Rad ADS assays and reagents. Samples will be analyzed in batches of suitable size. ddPCR results will be compared with NGS results generated by reference laboratories belonging to LabNet CML network . In patients positive for mutations below 20% by ddPCR (low level mutations) peripheral blood sample(s) will be collected every 3 months at subsequent follow-up visits to monitor the kinetics of mutations in relation to therapy continuation or change. No modification of TKI type or TKI dose will be performed on the basis of ddPCR results.

Interventions

OTHERPeripheral blood withdrawal for BCR::ABL1 mutations testing

Peripheral blood samples taken from patients treated according to clinical practice with resistance to imatinib or 2GTKI therapy according to the ELN recommendations will be shipped to one of the reference laboratories and analyzed by ddPCR using Bio-Rad ADS assays and reagents. Samples will be analyzed in batches of suitable size. ddPCR results will be compared with NGS results. In patients positive for mutations below 20% by ddPCR (low level mutations) peripheral blood sample(s) will be collected every 3 months at subsequent follow-up visits to monitor the kinetics of mutations in relation to therapy continuation or change.

Sponsors

Gruppo Italiano Malattie EMatologiche dell'Adulto
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* molecularly confirmed diagnosis of BCR::ABL1+ CML; * positivity for either e13a2 or e14a2 transcript; * age ≥18 years; * chronic phase; * on therapy with imatinib or 2 GTKIs (dasatinib, nilotinib and bosutinib); * candidate to TKI switch because of resistance according to the ELN recommendations OR with a confirmed warning response to 2GTKI therapy according to the ELN recommendations; * Signed written informed consent according to ICH/EU/GCP and national local laws.

Exclusion criteria

* blastic phase; * Previous allogeneic transplant or candidate to allogeneic transplant; * on treatment with ponatinib or asciminib, investigational TKIs or non-TKI-therapy; * switch performed or planned due to intolerance and not to resistance.

Design outcomes

Primary

MeasureTime frameDescription
Mutations detected by ddPCRAt enrollmentThe rate of actionable (2GTKI-resistant) mutations detectable by ddPCR as compared to NGS in patients with failure of TKI therapy according to the current (2020) ELN recommendations.

Contacts

Primary ContactPaola Fazi
p.fazi@gimema.it00390670390528
Backup ContactEnrico Crea
e.crea@gimema.it00390670390514

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026