Kyle R A, Therneau T M, Rajkumar S V, Offord J R, Larson D R, Plevak M F, Melton L J
Division of Hematology and Internal Medicine, Section of Biostatistics, Mayo Clinic, Rochester, MN 55905, USA.
Semin Oncol. 2003 Apr;30(2):169-71. doi: 10.1053/sonc.2003.50062.
The current study was conducted to determine the risk of adverse outcomes among patients with monoclonal gammopathy of undetermined significance (MGUS) of the IgM class. Two hundred thirteen patients with IgM MGUS were identified in southeastern Minnesota from 1960 to 1994. The primary end point was progression to lymphoma or a related disorder assessed by the Kaplan-Meier method. Patients were followed for a total of 1,567 person-years (median, 6.3 years per subject). Seventeen patients developed lymphoma (relative risk [RR], 14.8) and six progressed to Waldenstrom's macroglobulinemia (RR, 262), while three developed primary amyloidosis (RR, 16.3) and three others had chronic lymphocytic leukemia (RR, 5.7). The relative risk of progression was 16-fold higher in the IgM MGUS patients compared to the white population of the Iowa Surveillance, Epidemiology, and End Results (SEER) program. The risk of progression of MGUS of IgM type to lymphoma or related disorders averaged 1.5% per year throughout the period of observation.
本研究旨在确定IgM型意义未明的单克隆丙种球蛋白病(MGUS)患者出现不良结局的风险。1960年至1994年期间,在明尼苏达州东南部确定了213例IgM MGUS患者。主要终点是通过Kaplan-Meier方法评估进展为淋巴瘤或相关疾病的情况。患者总共随访了1567人年(中位数为每位受试者6.3年)。17例患者发展为淋巴瘤(相对风险[RR],14.8),6例进展为华氏巨球蛋白血症(RR,262),3例发展为原发性淀粉样变性(RR,16.3),另外3例患有慢性淋巴细胞白血病(RR,5.7)。与爱荷华州监测、流行病学和最终结果(SEER)项目的白人人群相比,IgM MGUS患者进展的相对风险高16倍。在整个观察期内,IgM型MGUS进展为淋巴瘤或相关疾病的风险平均每年为1.5%。