- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04991532
Dasatinib Down-regulates the Expression of PD-1 and Enhances Killing pH + Leukemia Stem Cells
August 4, 2021 updated by: Dan Xu, Nanfang Hospital of Southern Medical University
Research on the Mechanism of Dasatinib Down-regulates the Expression of PD-1 in CMV-activated NKG2C+NK Cells and Enhances Killing pH + Leukemia Stem Cells.
Research on the mechanism of dasatinib down-regulates the expression of PD-1 in CMV-activated NKG2C+NK cells and enhances killing pH + leukemia stem cells.
Study Overview
Detailed Description
Some patients with CML can withdraw from TKIs after treatment, and the mechanism might be related to the effect of memory NK cells on anti-Ph+ leukemic stem cells (LSCs).
Dasatinib affects immune through several pathways including the expression of PD1 in immune cells.
Our previous work showed increased NKG2C+ NK cells were found in cases with CMV-DNA+ who suffered Ph+ leukemia and received Dasatinib, and these memory NK cells have anti-LSCs activity.
We hypothesize that: CMV infection activates NKG2C+ memory NK cells proliferation; Dasatinib down-regulates the expression of PD1 in PD1+NKG2C+ NK cell subsets and then enhances anti-LSCs activity of these cells.
In this study, the effect of Dasatinib on CMV-activated NKG2C+ cell subsets and its mechanism will be studies.
Besides, the different NKG2C+ cell subsets on LSCs will be compared.
This study might be helpful to clarify the mechanism of TKI withdrawal and to offer foundation for CMV and Ph+ ALL treatment strategies
Study Type
Observational
Enrollment (Anticipated)
324
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dan Xu
- Phone Number: +86-20-61641615
- Email: 522111156@qq.com
Study Contact Backup
- Name: weixiang lu
- Phone Number: +86-20-61641615
- Email: 522111156@qq.com
Study Locations
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Guangdong
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Guangzhou, Guangdong, China, 510515
- Recruiting
- Department of Hematology,Nanfang Hospital, Southern Medical University
-
Contact:
- Dan Xu
- Phone Number: +86-20-61641615
- Email: 522111156@qq.com
-
Contact:
- weixiang lu
- Phone Number: +86-20-61641615
- Email: 522111156@qq.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
CML-CP patients treated with TKIs
Description
Inclusion Criteria:
- Age >18 years old, gender is not limited
- CML-CP patients treated with TKIs
- No pregnancy was planned during the treatment
Exclusion Criteria:
1.The researcher judged that it was not suitable to participate in this study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Dasatinib group
the CML patient treated with dasatinib
|
|
Imatinib group
the CML patient treated with imatinib
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NK cells and T cell activation subsets in CML-CP patients treated with TKI for 2 years
Time Frame: 2 years
|
NK cells and T cell activation subsets in CML-CP patients treated with TKI for 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Dan Xu, Nanfang Hospital of Southern Medical University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 20, 2021
Primary Completion (Anticipated)
October 1, 2022
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
August 3, 2021
First Submitted That Met QC Criteria
August 4, 2021
First Posted (Actual)
August 5, 2021
Study Record Updates
Last Update Posted (Actual)
August 5, 2021
Last Update Submitted That Met QC Criteria
August 4, 2021
Last Verified
August 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NFEC-2021-130
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.