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Imatinib Mesylate Effectiveness in Chronic Myeloid Leukemia with Additional Cytogenetic Abnormalities at Diagnosis among Black Africans
Author(s) -
Tolo Aissata,
Duni Sawadogo,
Clotaire Danho Nanho,
Boidy Kouakou,
N’Dogomo Meité,
N’Dhatz Emeuraude,
Roméo Ayémou,
Sekongo Yassongui Mamadou,
Paul Kouéhion,
Konan Mozart,
Gustave Koffi,
Ibrahima Sanogo
Publication year - 2013
Publication title -
advances in hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.371
H-Index - 31
eISSN - 1687-9112
pISSN - 1687-9104
DOI - 10.1155/2013/901589
Subject(s) - medicine , imatinib mesylate , philadelphia chromosome , imatinib , myeloid leukemia , trisomy , hematology , trisomy 8 , cytogenetics , gastroenterology , chromosome , chromosomal translocation , biochemistry , chemistry , genetics , biology , gene
Imatinib mesylate provides good results in the treatment of CML in general. But what about the results of this treatment in CML associated with additional cytogenetic abnormalities at diagnosis among black Africans? For this, we retrospectively studied 27 cases of CML associated with additional cytogenetic abnormalities, diagnosed in the department of clinical hematology of the University Hospital of Yopougon in Côte d'Ivoire, from May 2005 to October 2011. The age of patients ranged from 13 to 68 years, with a mean age of 38 years and a sex ratio of 2. Patients were severely symptomatic with a high Sokal score of 67%. CML in chronic phase accounted for 67%. The prevalence of additional cytogenetic abnormalities was 29.7%. There were variants of the Philadelphia chromosome (18.5%), trisomy 8 (14.8%), complex cytogenetic abnormalities (18.5%), second Philadelphia chromosome (14.8%), and minor cytogenetic abnormalities (44.4%). Complete hematologic remission was achieved in 59%, with 52% of major cytogenetic remission. The outcome was fatal in 37% of patients. Death was related in 40% to hematologic toxicity and in 30% to acutisation. The median survival was 40 months.

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