Hematological, immunophenotypic, and cytogenetic characteristics of acute myeloblastic leukemia with trisomy 11
Autor: | Jesús F. San Miguel, Jesús M. Hernández, José M. Hernández, Fernando Ramos, Norma C. Gutiérrez, Juan Luis García, Josefina Galende, M. Belén González, José J. Pérez, Mercedes Romero, M. Belén Vidriales, Magdalena Sierra |
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Rok vydání: | 2005 |
Předmět: |
Male
Cancer Research medicine.medical_specialty Acute myeloblastic leukemia Trisomy Biology Trisomy 8 Gastroenterology Immunophenotyping hemic and lymphatic diseases Internal medicine Genetics medicine Humans Molecular Biology In Situ Hybridization Fluorescence Aged Aged 80 and over CD117 Chromosomes Human Pair 11 Incidence (epidemiology) Cytogenetics Karyotype Middle Aged medicine.disease Leukemia Myeloid Acute Immunology biology.protein Female |
Zdroj: | Cancer Genetics and Cytogenetics. 160:68-72 |
ISSN: | 0165-4608 |
DOI: | 10.1016/j.cancergencyto.2004.11.008 |
Popis: | We evaluated the incidence of trisomy 11 in acute myeloblastic leukemia (AML) and its correlation with the most relevant clinical, biological, and immunophenotypic disease characteristics in a total of 399 consecutive AML patients. Trisomy 11 was found in 15 patients (3.8%), in 3 of them as the sole abnormality. Median age was 68 years (range 48-87); 87% of patients were older than 60 years. Seven patients displayed multilineage dysplasia. Cytogenetics showed an association with trisomy 8 in six patients, and in five cases with a del(5q); nine patients had complex karyotypes. In all cases, in situ hybridization studies revealed three copies of the MLL gene, but no rearrangements or tandem duplications of MLL. Immunophenotypic analysis of blast cells showed a constant immature immunophenotypic profile with CD34 or CD117 expression (or both) in all cases analyzed. The complete remission rate was 43%; median survival time was only 2 months. |
Databáze: | OpenAIRE |
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