TFR(Treatment-Free Remission)
OtherWithdrawal TKIs(Tyrosine kinase inhibitors: Imatinib or Flumatinib or Nilotinb or Dasatinib)
NCT Number: NCT05440747
Improving the quality of life and achieving Treatment-Free Remission(TFR) is a long-term goal of treatment in CML-CP patients, and deep molecular response (DMR) is necessary to achieve TFR. Cording to the historical literature, it is reported that patients with CML-CP take MMR as the therapeutic target, and the acquisition rate of DMR under long-term TKI treatment is 50%. The 2-year success rate of TFR patients was 50%. Therefore, maybe only 25% of patients with CML can successfully stop the drug for a long time. It cannot meet the withdrawal needs of patients with long-term drug survival.
This study is to design a real-world observational registration study for optimal effect. On the premise of taking DMR as the target decision, through initial treatment intervention, improve the DMR rate, which will promote clinical practice, so as to improve the 2-year TFR rate of cml-cp patients. This study is a multicenter, observational, prospective registry to identify the optimal treatment for achieving TFR in CML patients. In this study, the investigators will assess the deep molecular response after 12 months of treatment and the 2-year treatment-free remission rate (TFR 2y) after drug discontinuation.
Eligible participants with CML-CP can be enrolled. The observation period of all participants is at least 60 months, of which the first 36 months is the shortest treatment period, and the last 24 months is the TFR observation period after TKIs (Imatinib/Flumatinib/Nilotinb/ Dasatinib) withdrawal. During the treatment phase, participants can receive TKIs ± IFN (or other treatments) as first-line/second-line treatment, and the treatment plan will be adjusted according to the molecular response. Patients should accept TKI treatment for at least 3 years or more, and MR4/MR4.5 should achieve at least 2 years before discontinuation.
Trial opening soon.
Get Notified14 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All Patients with TFR requeirement should provid written informed consent before enrollment.
Exclusion criteria
Withdrawal TKIs(Tyrosine kinase inhibitors: Imatinib or Flumatinib or Nilotinb or Dasatinib)
Time frame: The 12th month
DMR is defined by IS BCR-ABL/ABL achieve MR4.0(≤0.01%)
Time frame: The second year
The proportion of drug withdrawal
Time frame: The 6months、12months
TFR rate of 6/12months,Median duration of TFR
Time frame: The 24/36/48/60 months
DMR rate of 24/36/48/60 months, Median duration of DMR, DMR is defined by IS BCR-ABL/ABL achieve MR4.0
Time frame: 2 years
DMR is defined by IS BCR-ABL/ABL achieve MR4.0
Time frame: The whole study, up to 7 years
Time and proportion from diagnosis to disease progression to AP or BC
Time frame: TFR phase in the study, up to 2 years
Time and proportion from discontinuation to loss of MMR in TFR phase up to 2 years.
Time frame: The TFR phase, up to 2 years
Time and proportion from restarting therapy after MMR-lose to obtain MMR through TFR phase.
Time frame: The whole study , up to 7 years
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time frame: Every 3 months in the whole enrollment period, up to 7 years
EORTCQLQ-CML-24 survey every 3 months in the whole enrollment period
Time frame: After participants loss optimal efficacy in milestone,and once a years after that, up to 7 years
Bone marrow karyotype analysis once a year in the patients without optimal efficacy in milestone through study completion
Time frame: The whole study, up to 7 years
Molecular Mutation Examination(qPCR) once a year in patient without optimal efficacy through study completion.
Contact information is provided by the study sponsor or research team.
Jianyu Weng, PhD
CONTACT
Lisi Huang
CONTACT
Guangdong Provincial People's Hospital
Other
A Multicenter, Observational Register Study of Treatment Free Remission in Patients With Chronic Myeloid Leukemia (CML-CP)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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