多发性骨髓瘤
医学
民族
种族(生物学)
人口学
流行病学
可能性
逻辑回归
监测、流行病学和最终结果
生存分析
子群分析
卫生公平
老年学
内科学
置信区间
公共卫生
病理
癌症登记处
植物
社会学
人类学
生物
作者
John X Wei,Aditi Shastri,R. Alejandro Sica,Ioannis Mantzaris,Noah Kornblum,Urvi A. Shah,Murali Janakiram,Kira Gritsman,Amit Verma,Mendel Goldfinger,Dennis Cooper,Nishi Shah
标识
DOI:10.3324/haematol.2023.283304
摘要
Over the past two decades, there have been significant advances in the treatment of multiple myeloma which has led to an improvement in overall survival (OS) (1,2). However, a notable proportion of patients continue to experience early mortality (EM), defined as two years from the time of diagnosis. This raises the possibility that improvements in myeloma survival have not extended equally to all groups. Using the latest data drawn from the Surveillance Epidemiology and End Results (SEER) database of patients in the United States spanning 2000-2019, we study impact of important sociodemographic factors on EM. Through regression modeling, we demonstrate that patients diagnosed from 2000-2005, of older age, male sex, and of certain racial minority status (non-Hispanic Black and Hispanic) have higher odds of EM. Of these factors, minority status contributed to worse 2-year overall survival as well. We evaluate whether income, as a surrogate to access to care, could potentially explain this finding, but find that race has a distinct relationship with EM that is not modified by income. This is further reinforced by subgroup analysis. After characterizing groups vulnerable to EM, we examine reasons for these disparities and potential avenues to address them.
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