作者: Roberto Marasca , Rossana Maffei , Silvia Martinelli , Stefania Fiorcari , Jenny Bulgarelli
DOI: 10.1002/HON.2028
关键词: Clone (cell biology) 、 Antibody 、 Lymph node 、 Fluorescence in situ hybridization 、 Chromosome 、 Chronic lymphocytic leukemia 、 Cancer research 、 Immunology 、 Hazard ratio 、 Beta-2 microglobulin 、 Biology
摘要: Deletion on the long arm of chromosome 11 occurs in 5-20% chronic lymphocytic leukaemia (CLL) patients. We analysed clinical-biological characteristics 131 CLL patients carrying 11q deletion documented before therapy (de novo deleted CLL). De were characterized by high frequencies unmutated immunoglobulin variable heavy genes, multiple fluorescence situ hybridization aberrations and lymph node involvement. Factors significantly associated with shorter time to first treatment (TTFT) advanced Binet stages, white blood cell count, increased ?2 -microglobulin levels, 17p addition, splenomegaly more extensive lymphadenopathy. found that <25% nuclei (n?=?22) experienced longer TTFT compared ?25% (n?=?87; median TTFT, 40 vs. 14?months, p?=?0.011) also showed better response treatments (complete response, 50% 21%, p?=?0.016). The variables identified multivariate analysis as independently reduced stages [hazard ratio (HR) 4.69; p?0.001] (HR 4.73; p?=?0.004). CLLs exhibit clinical outcome. percentage inside leukemic clone should be included prognostic definition therapy-naive