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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04219111
Other study ID # SCH-2181
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date October 1, 2017
Est. completion date May 4, 2018

Study information

Verified date January 2020
Source Sheffield Children's NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chronic myeloid leukaemia (CML) is a haematological malignancy primarily driven by the fusion oncogene BCR-ABL1, resulting in a constitutively expressed tyrosine kinase. CML is treated very effectively by the tyrosine kinase inhibitors (TKIs) resulting in almost undetectable levels of disease. However, some patients show resistance to first line treatment, requiring second and third generation TKIs. Such resistance is due to the presence of tyrosine kinase domain (TKD) mutations, however TKDs do not appear to be present in all patients who do not respond to treatment.

The aim of this project is to utilise gene expression arrays to identify transcriptomic profiles associated with resistance to TKIs in the absence of a demonstrable TKD mutation. The presence of such profiles may allow for a more targeted approach to treatment, if non-responders can be identified earlier in the disease management pathway. Being able to predict those that will not respond to first line treatment will allow for better stratification of patients.


Description:

The aim of this project is to use gene expression microarrays to detect expression profiles which may be associated with TKI resistance in order to better stratify CML patients and allow a more targeted approach to therapy. The project may also help elucidate the mechanism of resistance in those without a discernible TKD mutation. Ultimately it is hoped that this would lead to larger studies which could improve the clinical pathway for CML patients without TKD mutations.

Some previous studies have studied the gene expression profile of CML patients demonstrating resistance to TKIs, using Affymetrix arrays. However, none of these appear to have specifically investigated non-responders with and without a TKD mutation.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date May 4, 2018
Est. primary completion date May 4, 2018
Accepts healthy volunteers No
Gender All
Age group 17 Years to 85 Years
Eligibility Inclusion Criteria:

- CML patients with poor response to TKIs as identified through routine clinical testing at SDGS, either with or without a tyrosine kinase domain mutation as tested for by mutational analysis.

Exclusion Criteria:

- Any samples that do not meet the above inclusion criteria, but particularly not CML patients with an optimal response to TKIs.

Study Design


Related Conditions & MeSH terms

  • Gene Expression Profiles in CML Non-responders

Intervention

Genetic:
Clariom
Clariom S Assay

Locations

Country Name City State
United Kingdom Clinical Research Facility Sheffield South Yorkshire

Sponsors (1)

Lead Sponsor Collaborator
Sheffield Children's NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success identification of at least 5 markers of resistance in patients without a TKD mutation and confirmation of their expression levels using qPCR 2 months