Abstract

IntroductionImatinib mesylate (Glivec®/Gleevec®) is the standard first-line therapy for the treatment of chronic myeloid leukemia due to its high hematologic, cytogenetic, and molecular response rates and favorable long-term safety profile. A copy version of imatinib is currently available in several countries. We report on two cases of CML who were originally treated with Glivec in Egypt and subsequently switched to the copy drugCase presentationCase one was a 35-year old female with chronic myeloid leukemia in blast crisis who began treatment with combination chemotherapy and Glivec. The patient achieved and maintained a complete hematologic response and continued on Glivec 400 mg/day. In March 2007, she was switched to the copy drug In September 2007, the patient presented in hematologic relapse. At this time, treatment with chemotherapy in combination with Glivec 400 mg/day was resumed. The patient quickly achieved, and maintained, complete hematologic response on Glivec 400 mg/day. The second patient was a 64-year old male with chronic myeloid leukemia in blast crisis who began treatment with truncated chemotherapy in combination with Glivec 400 mg/day. After 6 months, the patient achieved a partial hematologic response and continued on alternating cycles of chemotherapy with continuous administration of Glivec 400 mg/day. The patient received Glivec from January 2006 to February 2007, after which time he was switched to the copy drug. In November 2007, he presented with upper gastrointestinal bleeding and multiple gastric erosions and died the same day.ConclusionThe safety and efficacy of the copy drug has not been established in randomized clinical trials. It is unknown whether patients, who respond to Glivec and then switch to copy versions of imatinib, will tolerate the copy drug and maintain their response.

Highlights

  • Imatinib mesylate (Glivec®/Gleevec®) is the standard first-line therapy for the treatment of chronic myeloid leukemia due to its high hematologic, cytogenetic, and molecular response rates and favorable long-term safety profile

  • Chronic myeloid leukemia (CML) is a clonal myeloproliferative disease characterized by the presence of the Philadelphia chromosome

  • CML progresses within several years from a chronic phase (CML-CP) to an accelerated phase, and to a blast crisis (CML-BC) which may be myeloid or lymphoid in origin and rapidly leads to death without intensive treatment [2]

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Summary

Introduction

Chronic myeloid leukemia (CML) is a clonal myeloproliferative disease characterized by the presence of the Philadelphia chromosome. On clinical exam she exhibited several skin bruises and subcutaneous bleeds, huge splenomegaly 4 cm below the costal margin hepatomegaly, and no palpable lymphadenopathy Her initial laboratory assessment revealed a total leukocyte count of 12.7 × 109/L, with 32% blast cells in the peripheral blood smear, hemoglobin (Hgb) concentration of 7.3 g/dL, and platelet count of 66 × 109/L. In November 2007, the patient presented with upper gastrointestinal bleeding, and endoscopy revealed multiple small gastric erosions His hematological profile showed a total leukocyte count of 188 × 109/L with 36% blast cells and marked absolute neutrophilia and monocytosis in the peripheral blood smear, Hgb concentration of 5.8 g/dL, and platelet count of 539 × 109/L.

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Sawyers CL
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