Ji Mengmeng, Shih Yi-Hsuan, Huber John H, Wang Mei, Feuer Eric J, Etzioni Ruth, Wang Shi-Yi, Chang Su-Hsin
Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.
Department of Electrical and Systems Engineering, Washington University in St. Louis, St. Louis, Missouri.
Cancer Epidemiol Biomarkers Prev. 2024 Dec 2;33(12):1690-1697. doi: 10.1158/1055-9965.EPI-24-0490.
Monoclonal gammopathy of undetermined significance (MGUS) is the premalignant condition of multiple myeloma. Given a lack of population-based screening for MGUS and its asymptomatic nature, the epidemiology of MGUS remains unknown. This study estimated age- and race/ethnicity-specific MGUS incidence and preclinical duration from MGUS to multiple myeloma in the United States.
A previously published modeling approach was used to calculate national MGUS incidence using estimates of MGUS prevalence, multiple myeloma incidence, multiple myeloma-specific and all-cause mortality, and population age distribution from the National Health and Nutrition Examination Survey, 1999 to 2004, and Surveillance, Epidemiology, and End Results, 2000 to 2021. The estimated MGUS prevalence was divided by MGUS incidence to obtain preclinical duration of multiple myeloma.
MGUS incidence for non-Hispanic White (NHW) populations was 52, 86, 142, and 181 and for non-Hispanic Black (NHB) population was 110, 212, 392, and 570 per 100,000 person-years at ages 50, 60, 70, and 80 years, respectively. The average preclinical duration was 20.5 (95% confidence interval, CI, 16.5-26.1) years for the NHW population and 14.2 (95% CI, 11.5-17.6) years for the NHB population. The cumulative risk of developing MGUS in age 50 to 85 was 2.8% (95% CI, 1.7%-4.2%) for the NHW population and 6.1% (95% CI, 3.8%-10.0%) for the NHB population.
NHB populations had a higher MGUS incidence rate at all ages and a shorter preclinical duration of multiple myeloma compared to their NHW counterparts.
This study provides insights into the epidemiology of MGUS and enhances our understanding of the natural history of multiple myeloma. See related In the Spotlight, p. 1547.
意义未明的单克隆丙种球蛋白病(MGUS)是多发性骨髓瘤的癌前病变。鉴于缺乏基于人群的MGUS筛查及其无症状的特性,MGUS的流行病学情况仍不明确。本研究估计了美国不同年龄和种族/族裔的MGUS发病率以及从MGUS发展到多发性骨髓瘤的临床前期持续时间。
采用先前发表的建模方法,利用1999年至2004年国家健康与营养检查调查以及2000年至2021年监测、流行病学和最终结果中的MGUS患病率、多发性骨髓瘤发病率、多发性骨髓瘤特异性死亡率和全因死亡率以及人群年龄分布估计值,计算全国MGUS发病率。将估计的MGUS患病率除以MGUS发病率,以获得多发性骨髓瘤的临床前期持续时间。
50岁、60岁、70岁和80岁时,非西班牙裔白人(NHW)人群的MGUS发病率分别为每10万人年52例、86例、142例和181例,非西班牙裔黑人(NHB)人群的发病率分别为每10万人年110例、212例、392例和570例。NHW人群的平均临床前期持续时间为20.5年(95%置信区间,CI,16.5 - 26.1年),NHB人群为14.2年(95%CI,11.5 - 17.6年)。50至85岁人群中发生MGUS的累积风险,NHW人群为2.8%(95%CI,1.7% - 4.2%),NHB人群为6.1%(95%CI,3.8% - 10.0%)。
与NHW人群相比,NHB人群在所有年龄段的MGUS发病率更高,且多发性骨髓瘤的临床前期持续时间更短。
本研究为MGUS的流行病学提供了见解,并增强了我们对多发性骨髓瘤自然史的理解。见相关“聚焦”,第1547页。