Abstract

Acute myeloid leukemia philadelphie positive (Ph+ AML) is a rare aggressive acute leukemia with poor prognosis. We report a patient with ph positive AML (FAB5), the transcript bcr/abl was not performed at diagnosis. She achieved complete remission after conventional induction chemotherapy. The consolidation therapy was based on Imatinib only due to infectious complications. She was in complete hematologic and cytogenetic remission for 19 months, and after she exhibited an isolated meningeal relapse. A second remission was achieved with intrathecal chemotherapy and cranial irradiation. Imatinib was switched to second generation Tyrosine kinase Inhibitor which had better diffusion into cerebrospinal fluid. She is in complete hematologic, cytogenetic and meningeal remission after 14 months of treatment. Imatinib monotherapy affords insufficient protection from CNS relapse. Second generation Tyrosine kinase Inhibitor seems to have better efficiency. Ph+ AML with monoblastic differentiation should be considered, like Ph+ ALL, at high risk of meningeal leukemia and should receive central nervous system prophylaxis.

Highlights

  • Acute myeloid leukemia philadelphie positive (Ph+AML) is a rare aggressive acute leukemia with a poor prognosis [1]

  • A high rate of meningeal relapse was reported in imatinib-treated patients with either lymphoid or bilineage chronic myeloid leukemia in blastic crisis (CML-BC) or Ph+ ALL [4,5], no data is available about Ph+ AML

  • This elevated risk of meningeal relapse is probably explicated by the poor penetration of Imatinib into the cerebrospinal fluid (CSF) [4,5,6]

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Summary

INTRODUCTION

AML) is a rare aggressive acute leukemia with a poor prognosis [1]. Imatinib mesylate a selective BCR-ABL tyrosine kinase inhibitor, has shown significant antileukemic activity in patients with chronic myeloid leukemia in blastic crisis (CML-BC), acute lymphoblastic leukemia philadelphie positive (Ph+ ALL) and few reported cases of de novo acute myeloid leukemia philadelphie positive (Ph+ AML) [2,3]. A high rate of meningeal relapse was reported in imatinib-treated patients with either lymphoid or bilineage CML-BC or Ph+ ALL [4,5], no data is available about Ph+ AML. This elevated risk of meningeal relapse is probably explicated by the poor penetration of Imatinib into the cerebrospinal fluid (CSF) [4,5,6]. We report a patient with de novo Ph+ AML who has received Imatinib as consolidation therapy and presents an isolate Meningeal Relapse

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