Ghobrial Irene M, Fonseca Rafael, Gertz Morie A, Plevak Matthew F, Larson Dirk R, Therneau Terry M, Wolf Robert C, Hoffmann Randi J, Lust John A, Witzig Thomas E, Lacy Martha Q, Dispenzieri Angela, Vincent Rajkumar S, Zeldenrust Stephen R, Greipp Philip R, Kyle Robert A
Division of Hematology, Internal Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Br J Haematol. 2006 Apr;133(2):158-64. doi: 10.1111/j.1365-2141.2006.06003.x.
We sought to define prognostic factors for survival in Waldenstrom macroglobulinaemia (WM). Of 585 patients diagnosed with WM and seen at Mayo Clinic between 1960 and 2001, 337 symptomatic patients met the inclusion criteria and were analysed for overall and disease-specific survival. The median survival from the time of diagnosis was 6.4 years. The median disease-specific survival was 11.2 years. Univariate analysis for overall survival identified the following adverse prognostic factors: age >65 years (P < 0.001), organomegaly (P < 0.001), elevated beta2-microglobulin (<0.001), anaemia (Hb < 10.0 g/dl) (P = 0.01), leucopenia (<4.0 x 10(9)/l) (P = 0.03), thrombocytopenia (<150 x 10(9)/l) (P = 0.01), serum albumin <40 g/l (P = 0.001), and quantitative IgM < 0.4 g/l (P = 0.04). On multivariate analysis, age >65 years and organomegaly were associated with poor prognosis. A prognostic model was built based on these two variables. Patients at high risk (1-2 risk factors, median survival 4.2 years) experienced worse survival than patients at low risk (0 risk factors, median survival 10.6 years), P < 0.001. The prognostic model was validated in 204 patients who were not included in the analysis cohort. Beta2-microglobulin > or =4 mg/l was associated with a threefold increase in the risk of death when added to the prognostic model. We describe a simple prognostic model for overall survival for newly diagnosed patients with WM.
我们试图确定华氏巨球蛋白血症(WM)患者生存的预后因素。在1960年至2001年间于梅奥诊所确诊并接受诊治的585例WM患者中,337例有症状的患者符合纳入标准,并对其总生存期和疾病特异性生存期进行了分析。从诊断时起的中位生存期为6.4年。疾病特异性中位生存期为11.2年。总生存期的单因素分析确定了以下不良预后因素:年龄>65岁(P<0.001)、器官肿大(P<0.001)、β2-微球蛋白升高(P<0.001)、贫血(血红蛋白<10.0 g/dl)(P=0.01)、白细胞减少(<4.0×10⁹/L)(P=0.03)、血小板减少(<150×10⁹/L)(P=0.01)、血清白蛋白<40 g/L(P=0.001)以及定量IgM<0.4 g/L(P=0.04)。多因素分析显示,年龄>65岁和器官肿大与预后不良相关。基于这两个变量建立了一个预后模型。高风险患者(1 - 2个风险因素,中位生存期4.2年)的生存期比低风险患者(0个风险因素,中位生存期10.6年)差,P<0.001。该预后模型在未纳入分析队列的204例患者中得到验证。当β2-微球蛋白≥4 mg/L加入预后模型时,死亡风险增加了两倍。我们描述了一种针对新诊断WM患者总生存期的简单预后模型。