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OncoMatch/Clinical Trials/NCT05753384

Discontinuation of TyrosIne Kinase Inhibitors (TKI) in Chronic Myeloid Leukemia (CML) and Impact on the Immune System

Is NCT05753384 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies treatment of TKI in CML for tyrosine kinase inhibitors.

Phase 3RecruitingPoitiers University HospitalNCT05753384Data as of May 2026

Treatment: treatment of TKI in CMLTyrosine kinase inhibitors (TKI) have revolutionized the management and prognosis of chronic myeloid leukemia (CML). Daily treatment with TKI, which is necessary due to lack of cure, is frequently associated with moderate, chronic and sometimes severe adverse effects. The ability to permanently stop treatment with TKI has thus become a major goal in CML to prevent the occurrence of adverse events, improve quality of life and reduce the general cost of the treatment; we talk about Treatment Free Remission (TFR). It now remains to be demonstrated in a comparative prospective study that a strategy of de-escalation of the TKI treatment dose before treatment discontinuation optimizes TFR results. At the same time, it is possible to reduce adverse reactions and improve the quality of life of patients. In this context, the investigator propose to conduct a randomized clinical trial including CML patients, allowing to compare the results of TFR at 24 months between a sudden stop of treatment after a maintenance phase of dosage for 12 months and a de-escalation arm of dose (dosage reduced by 50%) for 12 months before stopping. A secondary immunological translational objective of this project will be to compare the quantitative and qualitative evolution of innate CD8 T cells between the 2 arms (abrupt cessation of ITK treatment versus progressive withdrawal) and look for a predictive innate CD8 T cells blood signature at the time of stopping treatment of a successful TFR in both arms.

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Extracted eligibility criteria

Cancer type

Chronic Myeloid Leukemia

Biomarker criteria

Required: BCR fusion with ABL1 (e13a2 or e14a2)

typical BCR::ABL1 rearrangement (e13a2 or e14a2)

Required: ABL1 fusion with BCR (e13a2 or e14a2)

typical BCR::ABL1 rearrangement (e13a2 or e14a2)

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: BCR-ABL inhibitor (imatinib)

Duration of treatment by Imatinib ≥ 4 years

Must have received: BCR-ABL inhibitor (dasatinib, nilotinib, bosutinib)

ITK2G ≥ 3 years

Must have received: BCR-ABL inhibitor (imatinib, dasatinib, nilotinib, bosutinib)

Imatinib and ITK2G ≥ 4 years

Cannot have received: BCR-ABL inhibitor

Exception: prior resistance to TKI

Prior resistance to TKI

Cannot have received: BCR-ABL inhibitor

Exception: prior attempt of TKI cessation

Patients who have already experienced an attempt of TKI cessation

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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