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原发性浆细胞白血病的死亡原因与多发性骨髓瘤不同:一项基于 SEER 数据库的符合 STROBE 准则的描述性研究。

Causes of death in primary plasma cell leukemia differ from multiple myeloma: A STROBE-compliant descriptive study based on SEER database.

机构信息

Department of Health Statistics, School of Public Health, Jinzhou Medical University, Jinzhou, Liaoning Province, P.R. China.

出版信息

Medicine (Baltimore). 2022 Jul 22;101(29):e29578. doi: 10.1097/MD.0000000000029578.

Abstract

The primary plasma cell leukemia (pPCL) is a rare but aggressive variant of multiple myeloma (MM). Few studies have focused on the differences in the causes of death between pPCL and MM. This study aimed to compare and evaluate the causes of death of patients with pPCL and MM. The data were collected from the Surveillance Epidemiology, and End Results (SEER) database. The demographic characteristics, survival, and causes of death in pPCL and MM patients were evaluated and compared. The competing risk regression model was performed to predict the cause of death. Between 1975 and 2009, the overall mortality rate was 96.13% and 88.71% for pPCL and MM, and the median survival was 9 and 26 months, respectively. In pPCL, leukemia caused 45.05% of the deaths, followed by myeloma (38.83%). In MM, myeloma was the leading cause of death, accounting for 74.89% of the deaths. Older age at diagnosis was a risk factor for dying of leukemia in pPCL patients (HR = 1.49, 95% CI: 1.16-1.91), while older age at death was associated with reduced risk (HR = 0.67, 95% CI: 0.52-0.86). Although the survival of pPCL patients increased with time periods of diagnosis since 1975 to 2009, the risk of dying of leukemia increased with the periods. For MM, most of the demographic characteristics were found to have independently predicting influence on the cause of death. Patients with pPCL and MM had distinct causes of death. Leukemia was the leading and the most serious cause of death in pPCL patients. The demographic factors could not predict the causes of death in pPCL. More large-scale and multi-center studies are needed to evaluate the effect of novel agents in pPCL patients, especially for patients who have progressed to leukemia.

摘要

原发性浆细胞白血病(pPCL)是多发性骨髓瘤(MM)的一种罕见但侵袭性变异型。很少有研究关注 pPCL 和 MM 患者死亡原因之间的差异。本研究旨在比较和评估 pPCL 和 MM 患者的死亡原因。数据来自监测、流行病学和最终结果(SEER)数据库。评估和比较了 pPCL 和 MM 患者的人口统计学特征、生存和死亡原因。使用竞争风险回归模型预测死亡原因。1975 年至 2009 年间,pPCL 和 MM 的总体死亡率分别为 96.13%和 88.71%,中位生存期分别为 9 个月和 26 个月。在 pPCL 中,白血病导致 45.05%的死亡,其次是骨髓瘤(38.83%)。在 MM 中,骨髓瘤是导致死亡的主要原因,占死亡人数的 74.89%。诊断时年龄较大是 pPCL 患者死于白血病的危险因素(HR=1.49,95%CI:1.16-1.91),而死亡时年龄较大与降低风险相关(HR=0.67,95%CI:0.52-0.86)。尽管随着 1975 年至 2009 年诊断时间的推移,pPCL 患者的生存率有所提高,但白血病死亡的风险随着时间的推移而增加。对于 MM,大多数人口统计学特征被发现对死亡原因有独立的预测影响。pPCL 和 MM 患者的死亡原因不同。白血病是 pPCL 患者的主要和最严重的死亡原因。人口统计学因素不能预测 pPCL 患者的死亡原因。需要更多的大规模、多中心研究来评估新型药物在 pPCL 患者中的疗效,特别是对于已经进展为白血病的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d458/9302293/57314f728844/medi-101-e29578-g001.jpg

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