淋巴浆细胞淋巴瘤
美罗华
华登氏巨球蛋白血症
医学
β-2微球蛋白
淋巴瘤
副蛋白
免疫学
抗体
免疫球蛋白M
免疫球蛋白A
多发性骨髓瘤
巨球蛋白血症
单克隆
内科学
病理
胃肠病学
免疫球蛋白G
单克隆抗体
作者
Xin Cao,L. Jeffrey Medeiros,Yi Xia,Xiaoxiao Wang,Sheeba K. Thomas,Sanam Loghavi,Xin Li,Jatin J. Shah,Steven A. Gustafson,Donna M. Weber,Roberto N. Miranda,Zijun Y. Xu‐Monette,Robert Z. Orlowski,Ken H. Young
标识
DOI:10.3109/10428194.2015.1096357
摘要
Lymphoplasmacytic lymphoma secreting IgG or IgA (non-IgM LPL) is rarely seen. Systematic studies of the clinical features and treatment outcomes are lacking in these patients. This study evaluated 17 patients with non-IgM LPL. The paraprotein secreted by these tumors was IgA (n=8; 47%) and IgG (n=9; 53%). The median serum level of paraprotein was 2,475 mg/dl (range=747-5260) for IgA and 2580 mg/dl (range=1900-7100) for IgG. The IgA-LPL group was more likely to present with B symptoms, a high beta2-microglobulin level and extramedullary involvement. Compared with patients with Waldenström macroglobulinemia (WM), patients with non-IgM LPL showed similar clinical and pathologic features, but a higher mortality within the first year after diagnosis (p<0.001) and worse overall survival (p=0.024), with no difference in progression-free survival and disease-specific survival. Rituximab alone or rituximab-based therapy was used frequently and was effective as either first-line or salvage therapy.
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