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医疗保险受益人群中急性髓细胞白血病患者接受异基因造血细胞移植的利用趋势和未满足需求估计。

Trends in Allogeneic Hematopoietic Cell Transplantation Utilization and Estimated Unmet Need Among Medicare Beneficiaries with Acute Myelogenous Leukemia.

机构信息

National Marrow Donor Program/Be The Match, Minneapolis, Minnesota; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.

National Marrow Donor Program/Be The Match, Minneapolis, Minnesota; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.

出版信息

Transplant Cell Ther. 2022 Dec;28(12):852-858. doi: 10.1016/j.jtct.2022.09.015. Epub 2022 Sep 25.

DOI:10.1016/j.jtct.2022.09.015
PMID:36170959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10183994/
Abstract

Allogeneic hematopoietic cell transplantation (alloHCT) is a resource-intensive procedure and the sole potentially curative treatment available for patients with acute myelogenous leukemia (AML). Although Medicare coverage may help address a major financial barrier to accessing alloHCT, there remains an unmet need for alloHCT owing to sociodemographic disparities. This study examined trends and factors associated with the utilization of alloHCT and the estimated unmet need for alloHCT among Medicare beneficiaries with AML. This retrospective cohort study included patients (age 65 to 74 years) with a diagnosis of AML identified in Medicare claims data from 2010 through 2016. To study trends in utilization, transplantation rates were calculated as the number of patients who underwent alloHCT within 180 days and 1 year of diagnosis (numerator) divided by the total number of patients with AML within each diagnosis year (denominator). A multivariable logistic regression was used to identify factors associated with the likelihood of undergoing alloHCT within 1 year of diagnosis. Two approaches were applied to estimate the unmet need for alloHCT. The first approach used claims data to identify the potential need for alloHCT among patients who achieved complete remission for at least 90 days. The second approach used established National Marrow Donor Program (NMDP) methodology, which considers estimates of risk level, response to treatment, comorbidity, and early mortality, to identify the potential and unmet need for alloHCT. The overall estimated need and unmet need from 2010 to 2015 and over different time periods were evaluated for both approaches. The alloHCT rate within 180 days of diagnosis increased from 8% in 2010 to 15.8% in 2016 (P < .001), and the 1-year alloHCT rate also increased over time, from 11.9% in 2010 to 20.0% in 2015 (P < .001). The likelihood of undergoing alloHCT within 1 year of diagnosis was associated with diagnosis year, age, race, geographic region, Elixhauser Comorbidity Index, and population-level median household income. Between 2010 and 2015, the claims data approach estimated a lower potential need for alloHCT compared with the NMDP methodology estimate (27% versus 36%); both approaches estimated that 43% to 44% of patients with a potential need for alloHCT had an unmet treatment need. Despite the differences in estimated potential need between the 2 approaches, both showed a sustained unmet need but with a downward trend over time. Our data show that utilization of alloHCT has increased over time among Medicare beneficiaries with AML. Two approaches of need analysis were conducted for validation of estimated need and unmet need for alloHCT using claim-identified remission status, given the lack of cytogenetics and molecular information in claims data. Both approaches to estimating the unmet need for alloHCT found a downward trend over time; however, there are differences in utilization of alloHCT by age, race, geographic region, comorbidity, and socioeconomic status, indicating disparities in access to alloHCT among Medicare beneficiaries with AML. This suggests the need for policy efforts, research, and continued education to improve access to alloHCT and to close the gap between the actual utilization of alloHCT and the unmet need.

摘要

异基因造血细胞移植(alloHCT)是一项资源密集型的程序,也是急性髓细胞白血病(AML)患者唯一可能治愈的治疗方法。尽管医疗保险的覆盖范围可能有助于解决获得 alloHCT 的主要经济障碍,但由于社会人口差异,仍然存在 alloHCT 的未满足需求。本研究检查了 Medicare 受益人与 AML 患者接受 alloHCT 的趋势和相关因素,以及 alloHCT 的未满足需求估计。本回顾性队列研究纳入了 Medicare 索赔数据中 2010 年至 2016 年诊断为 AML 的年龄在 65 至 74 岁的患者。为了研究利用趋势,将移植率计算为在诊断后 180 天和 1 年内接受 alloHCT 的患者数量(分子)除以每年 AML 患者总数(分母)。使用多变量逻辑回归来确定与在诊断后 1 年内接受 alloHCT 的可能性相关的因素。应用了两种方法来估计 alloHCT 的未满足需求。第一种方法使用索赔数据来确定至少 90 天完全缓解的患者中 alloHCT 的潜在需求。第二种方法使用既定的国家骨髓捐赠者计划(NMDP)方法,该方法考虑了风险水平、治疗反应、合并症和早期死亡率的估计,以确定 alloHCT 的潜在和未满足需求。评估了这两种方法在 2010 年至 2015 年和不同时间段内的总估计需求和未满足需求。在诊断后 180 天内的 alloHCT 率从 2010 年的 8%增加到 2016 年的 15.8%(P<.001),1 年内的 alloHCT 率也随着时间的推移而增加,从 2010 年的 11.9%增加到 2015 年的 20.0%(P<.001)。在诊断后 1 年内接受 alloHCT 的可能性与诊断年份、年龄、种族、地理位置、Elixhauser 合并症指数和人口水平中位数家庭收入相关。在 2010 年至 2015 年期间,与 NMDP 方法估计值相比,索赔数据方法估计的 alloHCT 潜在需求较低(27%比 36%);两种方法均估计,有潜在 alloHCT 需求的患者中有 43%至 44%的患者存在未满足的治疗需求。尽管两种方法估计的潜在需求存在差异,但都显示出持续的未满足需求,但随着时间的推移呈下降趋势。我们的数据表明,随着时间的推移,医疗保险受益人与 AML 患者接受 alloHCT 的比例有所增加。由于索赔数据中缺乏细胞遗传学和分子信息,因此使用基于索赔确定的缓解状态进行了两种需求分析方法的验证,以估计 alloHCT 的潜在需求和未满足需求。两种估计 alloHCT 未满足需求的方法都发现随着时间的推移呈下降趋势;然而,年龄、种族、地理位置、合并症和社会经济地位对 alloHCT 的利用存在差异,这表明医疗保险受益人与 AML 患者获得 alloHCT 的机会存在差异。这表明需要采取政策措施、研究和持续教育,以改善 alloHCT 的获取,并缩小 alloHCT 的实际利用与未满足需求之间的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/32dfaedb4764/nihms-1852833-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/a1f88969308c/nihms-1852833-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/1a8ebc30ee7b/nihms-1852833-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/32dfaedb4764/nihms-1852833-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/a1f88969308c/nihms-1852833-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/1a8ebc30ee7b/nihms-1852833-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb11/10183994/32dfaedb4764/nihms-1852833-f0003.jpg

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