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21 世纪初骨髓增生异常综合征患者的发病率和生存率估计:没有随时间改善的证据。

Incidence and survival estimates for patients with myelodysplastic syndrome in the early 21st century: no evidence of improvement over time.

机构信息

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DFKZ), Heidelberg, Germany.

Division of Preventive Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

出版信息

Leuk Lymphoma. 2022 Aug;63(8):1964-1969. doi: 10.1080/10428194.2022.2053529. Epub 2022 Mar 27.

Abstract

We examine changes in population level incidence and survival of patients diagnosed with myelodysplastic syndrome (MDS) in the United States in 2001-2016. Data were extracted from the Surveillance, Epidemiology, and End Results (SEER)-18 database. Period analysis was used to calculate one-, two-, and five-year survival. The incidence peaked at 5.6 per 100,000 in 2010 then decreased to 3.9 by 2016, with a decrease in the diagnoses of refractory anemia (RA) and RA with ringed sideroblasts (RARS) and a relative increase in RA with excess blasts (RAEB). Overall, one-, two-, and five-year relative survival decreased over time, going from 74.3%, 60.9%, and 42.3%, respectively, in 2008-2010 to 70.9%, 55.9%, and 37.6%, respectively, in 2014-2016. When survival was examined by histology, patients with RA/RARS and RAEB had similar survival expectations in 2008-2010 versus 2014-2016 and a decrease was observed for 5q-MDS. Our results highlight the need for new treatment options in MDS.

摘要

我们研究了 2001-2016 年美国骨髓增生异常综合征(MDS)患者人群发病率和生存率的变化。数据从监测、流行病学和最终结果(SEER)-18 数据库中提取。采用时期分析来计算一年、两年和五年生存率。发病率在 2010 年达到峰值,为每 10 万人 5.6 例,到 2016 年降至 3.9 例,难治性贫血(RA)和环形铁幼粒细胞性难治性贫血(RARS)的诊断减少,RA 伴原始细胞过多(RAEB)相对增加。总体而言,一年、两年和五年相对生存率随时间推移而下降,从 2008-2010 年的 74.3%、60.9%和 42.3%分别降至 2014-2016 年的 70.9%、55.9%和 37.6%。当按组织学检查生存情况时,RA/RARS 和 RAEB 患者在 2008-2010 年与 2014-2016 年的生存预期相似,并且观察到 5q-MDS 下降。我们的结果强调了 MDS 中需要新的治疗选择。

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