Abstract

Background. Chronic myeloid leukemia is a hematological malignancy caused by expression of BCR-ABL tyrosine kinase oncogene, product of the t(9;22) Philadelphia translocation. Accelerated phase of this disease marks the onset of advanced rapidly progressive disease unresponsive to many therapies. Pregnancy limits broad number of therapies on patients because of their potential teratogenic effects. We report the case of a pregnant 34-year-old patient on accelerated phase successively managed by imatinib. She achieved a safe pregnancy and delivered at 39 weeks a healthy baby without congenital abnormalities. Our case is unusual because of the accelerated phase of the disease. Case Presentation. A 34-year-old African female with history of chronic phase of myeloid leukemia on imatinib, lost to follow-up for 4 months, presented to the hematological department for abdominal discomfort. Accelerated phase of chronic myeloid leukemia was diagnosed. Complete hematological response was achieved on high doses of imatinib. At the completion of 39 weeks, she delivered a healthy child without congenital anomalies. Conclusion. Despite its teratogenic and embryotoxic effects, front line imatinib is the only effective, well-tolerated treatment for patient on accelerated phase that can be offered to patients in sub-Saharan countries.

Highlights

  • Chronic myeloid leukemia is a hematological malignancy caused by expression of BCR-ABL tyrosine kinase oncogene, product of the t(9;22) Philadelphia translocation

  • Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder characterized by Philadelphia chromosome that results from a reciprocal translocation between chromosome 9 and chromosome 22

  • In our context, accelerated phase (AP) is usually diagnosed on chronic phase (CP) CML patients who progressed to AP because they discontinued imatinib

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Summary

Background

Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder characterized by Philadelphia chromosome that results from a reciprocal translocation between chromosome 9 and chromosome 22. This disease may follow biphasic or triphasic course that is usually diagnosed at chronic phase (CP). In our context, accelerated phase (AP) is usually diagnosed on CP CML patients who progressed to AP because they discontinued imatinib. Imatinib is available free of charge in the Congo since 2005 through nongovernmental organization It is the firstline treatment for CP CML. It had changed the natural history of chronic myeloid leukemia by showing overall survival benefits.

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