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http://www.scirp.org/journal/PaperInformation.aspx?PaperID=50793#.VE8SF1fHRK0
Author(s)
Background: Patients with stem cell
myeloproliferative disorders have a particularly poor prognosis and
limited treatment options, i.e. mainly aggressive chemotherapy or
allogeneic stem cell transplantation. In 2004, Chen et al. reported a
patient presenting a t(8;13) (p11;q12) cytogenic anomaly who responded
positively to treatment with PKC412 (midostaurin), an oral
multi-targeted tyrosine kinase inhibitor. Here, we report a second case
treated with the above-mentioned drug. Patient: A 71-year-old woman was
diagnosed as having chronic myelogenous leukaemia with eosinophilia
secondary to t(8;13) with FGFR1 involvement. Due to her age, an
allogeneic stem cell transplantation was not possible. Treatment: A
treatment combining aggressive chemotherapy and midostaurin was
explored. The patient received one cycle of hyper-CVAD chemotherapy
followed by maintenance therapy with midostaurin. A relapse occurred
after six months, and she was treated with four more cycles of
hyper-CVAD chemotherapy. The patient entered a complete clinical,
haematological and cytogenetic remission. A maintenance therapy with
midostaurin continued for four months until she developed a
chemoresistant relapse followed by acute leukaemia. Conclusion: This is
the second case of a t(8;13) myeloid and lymphoid neoplasm with FGFR1
abnormalities treated successfully with midostaurin. Midostaurin is
administered orally, allows for outpatient care and in this case showed
only occasional and minimal side effects. The combination of hyper-CVAD
and midostaurin extended survival by 21 months without allogeneic
transplantation. This case further supports the possibility of using
midostaurin for the treatment of other diseases with FGFR1
dysregulations; however, specific clinical trials are needed to confirm
this hypothesis.
KEYWORDS
Cite this paper
Beris, P. , Nagy, M. , Robert, D. , Samii, K. ,
McKee, T. and Schuler, J. (2014) Compassionate Use of Midostaurin in
Myeloid and Lymphoid Neoplasia with FGFR1 Abnormality. Case Reports in Clinical Medicine, 3, 560-565. doi: 10.4236/crcm.2014.310122.
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