To Study the Impact of Stopping Therapy in Patients of CML With Molecular Remission
Primary Purpose
Chronic Myeloid Leukemia, Treatment Free Remission
Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Stopping the standard drug therpy
Quantitative bcrabl recording every month for first 6 months
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Myeloid Leukemia focused on measuring CML, treatment free remission
Eligibility Criteria
Inclusion Criteria:
- Patients of CML on TKI (Imatinib) therapy for more than 5 years
- Patients who have been in complete molecular response (MR 4.5 +) for at least three years
Exclusion Criteria:
- Patients who ever had blast crisis
- Patients achieving molecular response with second generation TKI due to failure of Imatinib
Sites / Locations
- Command Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Sustained molecular remission
Arm Description
Patients of CML who remain in sustained molecular remission at 12 months after Stopping the standard drug therapy
Outcomes
Primary Outcome Measures
Disease Recurrence
Re-appearance of bcr-abl transcripts by RQPCR at a level >0.01%
Secondary Outcome Measures
Full Information
NCT ID
NCT03062436
First Posted
February 20, 2017
Last Updated
July 22, 2019
Sponsor
Command Hospital, India
1. Study Identification
Unique Protocol Identification Number
NCT03062436
Brief Title
To Study the Impact of Stopping Therapy in Patients of CML With Molecular Remission
Official Title
Stopping Imatinib Therapy in CML Patients With Sustained Molecular Remission
Study Type
Interventional
2. Study Status
Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Command Hospital, India
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Patients with chronic myeloid leukemia (CML) are conventionally put on life long therapy with tyrosine kinase inhibitor drugs (Imatinib mesylate in India). Patients who achieve a deep molecular response which has been sustained for at least three years, can be taken off the drug therapy. Thereafter a close monitoring is required to monitor their disease relapse. In case there is evidence of disease recurrence on highly sensitive molecular assays, their drug therapy is restarted. The study aims to identify proportion of patients who can be kept off drug therapy in a state of sustained molecular remission.
Detailed Description
While a large number of studies which have stopped TKI therapy in similar patients exist in Europe and USA, no such study has been done on Indian or other south Asian population. Almost all studies done previously have noted that in relapsed patients, who show disease recurrence on stopping their TKI therapy, their remission state is regained once the TKI therapy is restarted.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Myeloid Leukemia, Treatment Free Remission
Keywords
CML, treatment free remission
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
27 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sustained molecular remission
Arm Type
Experimental
Arm Description
Patients of CML who remain in sustained molecular remission at 12 months after Stopping the standard drug therapy
Intervention Type
Other
Intervention Name(s)
Stopping the standard drug therpy
Intervention Description
Stopping the standard drug therapy of CML patients and monitoring their treatment free remission status
Intervention Type
Diagnostic Test
Intervention Name(s)
Quantitative bcrabl recording every month for first 6 months
Intervention Description
Monthly recording of quantitative bcrabl by RQPCR on patients peripheral blood derived RNA. RQPCR will have minimum sensitivity of log4.5
Primary Outcome Measure Information:
Title
Disease Recurrence
Description
Re-appearance of bcr-abl transcripts by RQPCR at a level >0.01%
Time Frame
12 months from cessation of the drug therapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients of CML on TKI (Imatinib) therapy for more than 5 years
Patients who have been in complete molecular response (MR 4.5 +) for at least three years
Exclusion Criteria:
Patients who ever had blast crisis
Patients achieving molecular response with second generation TKI due to failure of Imatinib
Facility Information:
Facility Name
Command Hospital
City
Pune
State/Province
Maharashtra
ZIP/Postal Code
411040
Country
India
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
To Study the Impact of Stopping Therapy in Patients of CML With Molecular Remission
We'll reach out to this number within 24 hrs