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Clinical Trials/KCT0007901
KCT0007901
Not yet recruiting
未知

A Study of Treatment-free remission Evaluation in Real-world chronic myeloid leukemia-Prospective observational study

Gachon University Gil Medical Center0 sites200 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Gachon University Gil Medical Center
Enrollment
200
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Observational Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.\> 18\-year\-old male or female patient
  • 2\. ECOG execution status 0, 1 or 2
  • 3\. Patients diagnosed with BCR/ABL positive chronic\-phaseCML by bone marrow examination
  • 4\. Patients receiving TKI treatment for at least three years after initial diagnosis, including imatinib, dasatinib, nilotinib, radotinib, etc.
  • 5\. For qRT\-PCR follow\-up observation, patients with BCR/ABL1RQ\-PCR \< 0\.0069IS (MR4\.3 or higher) maintained for more than 2 years and had another confirmed response of 0\.0069IS or less at the central genetic testing institution that contracted for analysis.
  • 6\. Patients who agreed to participate in the study

Exclusion Criteria

  • 1\. Patients who had previously performed allografts
  • 2\. Patients who tried to interrupt TKI before
  • 3\. Past history of other active malignancies within 5 years prior to participation in clinical research, excluding fully cured or present basal cell skin cancer and past cervical endothelial cancer
  • 4\. Patients who have not recovered from previous surgery
  • 5\. Patients treated with other clinical research preparations within one to four weeks prior to the time of registration of the study
  • 6\. Pregnant or lactating women
  • 7\. Patients who may pose a risk to patient safety when determined by researchers
  • 8\. Patients who attempted TKI interruption for reasons other than TFR

Outcomes

Primary Outcomes

Not specified

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