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B 细胞慢性淋巴细胞白血病中的血清免疫球蛋白。自然病史及预后意义。

Serum immunoglobulins in B-chronic lymphocytic leukemia. Natural history and prognostic significance.

作者信息

Rozman C, Montserrat E, Viñolas N

机构信息

Postgraduate School of Haematology Farreras Valentí, Hospital Clínic i Provincial, Universidad de Barcelona, Spain.

出版信息

Cancer. 1988 Jan 15;61(2):279-83. doi: 10.1002/1097-0142(19880115)61:2<279::aid-cncr2820610215>3.0.co;2-4.

Abstract

To investigate the prognostic significance of gammaglobulin and immunoglobulin levels in chronic lymphocytic leukemia (CLL), survival studies were performed in a series of patients with that disorder. The survival probability of patients with initial levels of gammaglobulin of less than 700 mg/dl was significantly lower (P = 0.03) than in patients with initial levels of 700 mg/dl or more. Decreased initial levels of IgG and IgA also were associated with reduced survival probability (P = 0.027 and P = 0.014, respectively), whereas hypo-IgM did not show any influence on survival. When the influence on survival of gammaglobulin and immunoglobulin concentration was analyzed by Cox's multivariate model, the only variable which entered the regression at significant level was IgA (P = 0.006). As shown by the same type of analysis, the prognostic value of hypo-IgA is independent from the clinical staging. The natural history of hypogammaglobulinemia and hypoimmunoglobulinemia was investigated by sequential analysis in a series of untreated patients. The appearance of decreased levels of these globulins was found to be a continuous process developing spontaneously during the untreated course of the disease. Among factors associated with the appearance of hypogammaglobulinemia during the evolution of CLL, initial lower levels of IgG and IgA, but not IgM, were found in a multivariate analysis.

摘要

为了研究γ球蛋白和免疫球蛋白水平在慢性淋巴细胞白血病(CLL)中的预后意义,我们对一系列患有该疾病的患者进行了生存研究。初始γ球蛋白水平低于700mg/dl的患者的生存概率显著低于(P = 0.03)初始水平为700mg/dl或更高的患者。初始IgG和IgA水平降低也与生存概率降低相关(分别为P = 0.027和P = 0.014),而低IgM对生存没有任何影响。当通过Cox多变量模型分析γ球蛋白和免疫球蛋白浓度对生存的影响时,进入回归的唯一显著变量是IgA(P = 0.006)。同类型分析表明,低IgA的预后价值独立于临床分期。通过对一系列未经治疗的患者进行序贯分析,研究了低γ球蛋白血症和低免疫球蛋白血症的自然病程。发现这些球蛋白水平降低的出现是在疾病未经治疗的过程中自发发展的一个持续过程。在CLL演变过程中与低γ球蛋白血症出现相关的因素中,多变量分析发现初始IgG和IgA水平较低,但IgM水平不低。

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