Assessing the Ontogeny of P-glycoprotein Expression in Blood of Pediatric Leukemic Patients

Sponsor
Tanta University (Other)
Overall Status
Completed
CT.gov ID
NCT05021159
Collaborator
(none)
20
3
17
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Study Details

Study Description

Brief Summary

Determine P-glycoprotein expression in blood samples of Acute Lymphocytic leukemia (ALL) pediatric patients receiving MTX treatment and trace its ontogeny and compare it with its expression in pediatric healthy subjects. In addition, to determine the correlation of P-glycoprotein expression and Methotrexate concentration at steady state.

Condition or Disease Intervention/Treatment Phase
  • Other: MTX, (but the investigator is not using any intervention, the participants are already taking it in their treatment protocol and the investigator is just analyzing p-gp expression)

Detailed Description

The 20 leukemic patients will be classified into three age groups according to the ages that will be available at the time of sample collection.

  • All patients will be recruited from Tanta Oncology Center, Tanta University.

  • The study will be approved by the Research Ethics Committee of Tanta University and college of Pharmacy ethical committee.

  • An informed consent will be obtained from parents of all patients in this research before enrollment.

  • All patients' data will be private and confidential. Any unexpected risks that may appear during the course of the research will be reported to patients and the ethical committee on time.

Blood Samples will be obtained from healthy pediatric subjects of the same ages of the diseased group subjects (Samples will be obtained from subjects from a primary care center during their routine blood analysis excluding patients of chronic diseases, patients receiving any medications, and patients of impaired kidney or liver functions).

P-glycoprotein expression will be estimated in all samples using Permeability glycoprotein (P-gp), ELISA Kit, and its expression will be traced with development from the youngest till the oldest age available, this will also be compared with normal healthy pediatric subjects.

Study Design

Study Type:
Observational
Actual Enrollment :
20 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Assessing the Ontogeny of P-glycoprotein Expression in Blood of Pediatric Leukemic Patients
Actual Study Start Date :
Mar 1, 2020
Actual Primary Completion Date :
Jun 1, 2021
Actual Study Completion Date :
Aug 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Methotrexate Group

20 acute lymphocytic leukemia patients receiving MTX treatment (3- 5 mg/ cm2)

Other: MTX, (but the investigator is not using any intervention, the participants are already taking it in their treatment protocol and the investigator is just analyzing p-gp expression)
the investigator is not using any intervention, the participants are already taking it in their treatment protocol and the investigator is just analyzing p-gp expression

Healthy control group

20 healthy pediatric subjects not receiving any treatment

Outcome Measures

Primary Outcome Measures

  1. P-gp expression in blood samples [42 hours]

    P-gp expression in blood samples

  2. Methotrexate concentration in blood samples [42 hours]

    Methotrexate concentration in blood samples

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pediatric Acute Lymphocytic Leukemia Patients

  • aged < 18 years old

  • who are already taking the ALL MTX protocol.

Exclusion Criteria:
  • Severe renal impairment (eGFR< 30 mL/min/1.73 m2 at screening)

  • Critically ill patients.

  • Other types of cancer

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of Pharmacy, Tanta University Tanta Gharbiya Egypt 31111
2 Tanta Cancer Center Tanta Gharbiya Egypt 31111
3 Tanta University Tanta Gharbiya Egypt 31111

Sponsors and Collaborators

  • Tanta University

Investigators

  • Principal Investigator: Yasmine M Elmorsi, Msc, Assistant lecturer in Clinical Pharmacy Dept., Faculty of pahrmacy, Tanta University
  • Study Chair: Osama M Ibrahim, Professor, Professor in Clinical Pharmacy Dept., Faculty of pahrmacy, Tanta University
  • Study Chair: Tarek M Mostafa, Professor, Assistant Professor in Clinical Pharmacy Dept., Faculty of pahrmacy, Tanta University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Yasmine Elmorsi, Principal Investigator, Tanta University
ClinicalTrials.gov Identifier:
NCT05021159
Other Study ID Numbers:
  • 141052
First Posted:
Aug 25, 2021
Last Update Posted:
Sep 2, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 2, 2021