Value of MicroRNA30a in Philadelphia Positive Leukemic Patients
NCT ID: NCT05112653
Last Updated: 2021-11-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
70 participants
OBSERVATIONAL
2022-04-01
2024-12-01
Brief Summary
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Chronic myeloid leukemia is a myeloproliferative neoplasm, characterized by the unrestrained expansion of pluripotent bone marrow stem cells.The hallmark of the disease is the presence of a reciprocal t(9;22)(q34;q11.2), resulting in a derivative 9q+ and a small 22q-. The latter, known as the Philadelphia chromosome, results in a BCR-ABL fusion gene . The diagnosis requires fluorescent in situ hybridization (to demonstrate the BCR-ABL fusion gene or(PCR) to demonstrate the BCR-ABL mRNA transcript.
Detailed Description
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the study will dectect the possible value of microRNA30a as prognostic marker in Philadelphia positive acute leukemic patients(ALL, mixed-phenotype acute leukemia) on TKI therapy by assessment level of microRNA30a inpatients who achieved complete hematological remission(CHR) and who failed to achieve CHR.
The study goal has been taken through the role of microRNA30a in reducing ABL1 and BCR-ABL1 protein expression and microRNAs are capable of changing the levels of several key proteins at various steps of the autophagic pathway.
Conditions
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Study Design
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CASE_CONTROL
CROSS_SECTIONAL
Study Groups
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2
Group of Philadelphia positive leukemic patients will included in the study who divide into:
* patient newly diagnosed CML treated with first line of tyrosine kinase inhibitors therapy.
* Philadelphia positive acute leukemic patients(ALL, mixed-phenotype acute leukemia) on TKI therapy who achieved complete hematological remission(CHR) and who failed to achieve CHR.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2- Aged from 18- 60 years. 3-All eligible patients presenting at Clinical Haematology Unit Internal Medicine Department.
4- Without contraindication to receive TKIs therapy. 5-Must able to swallow tablet(TKI therapy).
Exclusion Criteria
2. patients who refuse to participate in the study.
18 Years
60 Years
ALL
No
Sponsors
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Assiut University
OTHER
Responsible Party
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Hager mohammed
assuit university
Other Identifiers
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AssiutU2021
Identifier Type: -
Identifier Source: org_study_id