慢性淋巴细胞白血病
医学
不确定意义的单克隆抗体病
游戏病
免疫球蛋白M
单克隆抗体病
三体
抗体
免疫学
华登氏巨球蛋白血症
多发性骨髓瘤
内科学
单克隆
免疫球蛋白G
单克隆抗体
白血病
生物
淋巴瘤
遗传学
作者
Andrea Corbingi,Idanna Innocenti,Annamaria Tomasso,Raffaella Pasquale,Andrea Visentin,Marzia Varettoni,Elena Flospergher,Francesco Autore,Francesca Morelli,Livio Trentin,Gianluigi Reda,Dimitar G. Efremov,Luca Laurenti
摘要
Summary The relationship between chronic lymphocytic leukaemia (CLL) and qualitative/quantitative gammaglobulin abnormalities is well established. Nevertheless, in order to better understand this kind of connection, we examined 1505 patients with CLL and divided them into four subgroups on the basis of immunoglobulin (Ig) aberrations at diagnosis. A total of 73 (4·8%), 149 (10%), 200 (13·2%) and 1083 (72%) patients were identified with IgM monoclonal gammopathy (IgM/CLL), IgG monoclonal gammopathy (IgG/CLL), hypogammaglobulinaemia (hypo‐γ) and normal Ig levels (γ‐normal) respectively. IgM paraprotein was significantly associated with a more advanced Binet/Rai stage and del(17p)/ TP53 mutation, while IgG abnormalities correlated with a higher occurrence of trisomy 12. Patients with any type of Ig abnormality had shorter treatment‐free survival (TFS) but no significant impact affecting overall survival (OS) compared to those with normal Ig levels.
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