Clinical Outcomes of Patients With Newly Diagnosed Acute Myeloid Leukemia Receiving Treatment in a Safety-Net Hospital System.

IF 2.7 4区 医学 Q2 HEMATOLOGY Clinical Lymphoma, Myeloma & Leukemia Pub Date : 2024-12-21 DOI:10.1016/j.clml.2024.12.009
Jason Lu, Preeya Bhakta, Hyunsoo Hwang, Curtis Lachowiez, Effrosyni Apostolidou
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Abstract

Background: 'Standard of care' therapies for adult acute myeloid leukemia (AML) have yielded 5-year overall survival (OS) rates of 30%-45 %. Risk stratification and novel targeted therapies have improved 5-year OS rates to >75 % for certain groups in specialized centers.

Patients and methods: This is a retrospective cohort analysis of outcomes in patients ≥18 years with newly diagnosed AML treated between 2005 and 2019 in the Harris Health County, Safety-Net Hospital System in Houston, TX.

Results: 192 patients were identified. Median age was 52 years, 52 % were male and 57 % identified as Hispanic. Most patients were uninsured or indigent, receiving care under the county's financial assistance programs (62 %). Of the 184 response-assessable patients, 139 achieved composite complete remission (CRc) (76 %). 182 patients had indications for HCT and only 25 patients received HCT (14 %), with main reasons including noncitizenship status and financial/insurance constraints. The 5-year OS rate in the entire cohort was 30 % (35 % in patients <60 years and 16 % if ≥60 years), with 92 % of deaths attributed to AML-related complications. Early death (<4 weeks) rate was 2 %. Secondary, adverse-risk AML, and uninsured status all portended significantly worse OS rates, per multivariate analysis. Patients with indications for HCT who received this modality fared significantly better than those who did not receive it (5-year OS 54 % vs. 21 %).

Conclusions: Optimizing AML remission induction regimens, reducing medication costs, ensuring timely administration of AML directed therapies, enhancing equity and diversity in clinical trials, and addressing socioeconomic factors may improve leukemia care for underserved patients.

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新诊断急性髓系白血病患者在安全网医院系统接受治疗的临床结果。
背景:成人急性髓性白血病(AML)的“标准治疗”疗法的5年总生存率(OS)为30%- 45%。在专业中心,风险分层和新型靶向治疗将某些人群的5年总生存率提高到75%。患者和方法:这是一项回顾性队列分析,对2005年至2019年在德克萨斯州休斯顿的哈里斯健康县安全网医院系统中接受治疗的≥18岁新诊断的AML患者的结局进行了分析。中位年龄为52岁,52%为男性,57%为西班牙裔。大多数患者没有保险或贫困,在县财政援助计划下接受治疗(62%)。在184例可评估反应的患者中,139例达到了复合完全缓解(CRc)(76%)。182例患者有HCT指征,只有25例患者接受了HCT(14%),主要原因包括非公民身份和经济/保险限制。结论:优化AML缓解诱导方案,降低药物成本,确保及时给予AML定向治疗,增强临床试验的公平性和多样性,以及解决社会经济因素可能会改善服务不足患者的白血病治疗。
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来源期刊
CiteScore
2.70
自引率
3.70%
发文量
1606
审稿时长
26 days
期刊介绍: Clinical Lymphoma, Myeloma & Leukemia is a peer-reviewed monthly journal that publishes original articles describing various aspects of clinical and translational research of lymphoma, myeloma and leukemia. Clinical Lymphoma, Myeloma & Leukemia is devoted to articles on detection, diagnosis, prevention, and treatment of lymphoma, myeloma, leukemia and related disorders including macroglobulinemia, amyloidosis, and plasma-cell dyscrasias. The main emphasis is on recent scientific developments in all areas related to lymphoma, myeloma and leukemia. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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