Kindler Thomas, Breitenbuecher Frank, Marx Andreas, Hess Georg, Gschaidmeier Harald, Gamm Heinold, Kirkpatrick Charles J, Huber Christoph, Fischer Thomas
Johannes Gutenberg University, Department of Hematology/Oncology, Mainz, Germany.
Blood. 2003 Apr 15;101(8):2960-2. doi: 10.1182/blood-2002-05-1469. Epub 2002 Dec 12.
Imatinib mesylate, a tyrosine kinase inhibitor targeting bcr-abl, platelet-derived growth factor receptor (PDGF-R), and c-Kit, effectively induces hematologic and cytogenetic remissions in bcr-abl(+) chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL) with only mild to moderate side effects. Here, we describe the successful treatment of a 64-year-old man with c-Kit(+) secondary acute myeloid leukemia (AML) refractory to standard chemotherapy. Upon 2 weeks of imatinib mesylate administration, the patient achieved a complete hematologic remission in peripheral blood. In addition, complete clearance of leukemic blasts in bone marrow and a significant cytogenetic response lasting for more than 5 months was observed. Sequence analysis of exons 2, 8, 10, 11, and 17 of the c-Kit receptor did not reveal structural alterations as previously described in a subset of AML cases. This is the first report of complete remission achieved upon administration of imatinib mesylate in a patient with highly refractory, secondary AML.