T315I clone selection in a Ph+ all patient under low-dose ponatinib maintenance.

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info:eu-repo/semantics/altIdentifier/doi/10.1002/ccr3.1032

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info:eu-repo/semantics/altIdentifier/pmid/28781850

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info:eu-repo/semantics/altIdentifier/pissn/2050-0904

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info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_F5940E9F0C9D2

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J. Noetzli et al., « T315I clone selection in a Ph+ all patient under low-dose ponatinib maintenance. », Serveur académique Lausannois, ID : 10.1002/ccr3.1032


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We report here the clinical course of a Ph+ ALL patient who was treated with ponatinib 15 mg/day, as maintenance therapy, and developed a BCR-ABL T315I mutation leading to ALL relapse. This clonal evolution was reversed, without adverse effects, by increasing ponatinib to 45 mg/day. To our knowledge, we have been confronted with the first clinical case of a T315I clonal selection of ALL caused by subeffective therapeutic level of the drug. This single patient experience highlights the risk of T315I clone selection in Ph+ ALL treated with reduced dose ponatinib.

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