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A Study for Tyrosine Kinase Inhibitors Discontinuation

An Observational Study for CML Patients Who Discontinued Tyrosine Kinase Inhibitors Intentionally After Achieving a Deep Molecular Response

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02897245
Acronym
A-STIM
Enrollment
200
Registered
2016-09-13
Start date
2012-12-31
Completion date
2022-12-31
Last updated
2018-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia

Keywords

Myelogenous, Chronic, BCR-ABL Positive

Brief summary

Treatment of Chronic Myeloid Leukemia (CML) has been revolutionized by the use of tyrosine kinase inhibitors including imatinib mesylate (Gleevec, Novartis Laboratories). Two other inhibitors of the BCR-ABL kinase are currently on the market in France, nilotinib (Tasigna®, Novartis Laboratories) in the first and second-line treatment and dasatinib (SPRYCEL®, Bristol-Myers Squibb Laboratories) in second line. Achieving a complete molecular response (CMR) in patients with Chronic Myeloid Leukemia (CML) treated with tyrosine kinase inhibitors may be currently regarded as the ultimate level of reduction of residual disease. The pilot Stop Imatinib study has opened the way for a french prospective study of stopping imatinib, the STIM study. The results of the STIM study showed that almost 60% of patients exhibited molecular relapse, most frequently within the first 6 months after discontinuation. The parameters that are statistically associated with the loss of complete molecular response are the Sokal score at diagnosis and the total duration of treatment with imatinib. Criteria to define molecular relapse in treatment free remission patients are not well defined and validated. The aim of the study is to validate the loss of major molecular response as a robust criteria for TKI resumption. The patient's population will be CML patients who are offered to discontinue therapy outside the STIM strial.

Interventions

OTHERNo intervention

Sponsors

Versailles Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient with Chronic Myelogenous leukemia * mors than 18 years old * intentionally stop treatment by tyrosine kinase inhibitor

Exclusion criteria

* inclusion in a prospective study * non intentionally stop (adverse event) * Stop for disease progression * Death patients

Design outcomes

Primary

MeasureTime frame
Survival without loss of molecular response major (RMM BCR-ABL / ABL IS ≤ 0.1%)2 years

Secondary

MeasureTime frame
Treatment free survival molecular evolution in treatment discontinuation2 years
Progression free survival2 years
Overall survival2 years
The rate of deep molecular response after restarting TKIs kinase2 years
Withdrawal syndrome2 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026