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A Study for Tyrosine Kinase Inhibitors Discontinuation (A-STIM)

V

Versailles Hospital

Status

Unknown

Conditions

Leukemia

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT02897245
12/22_aSTIM

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

200 participants in 1 patient group

Patient with intentionally stop
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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