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Crit Rev Oncol Hematol. 2022 Dec;180:103862. doi: 10.1016/j.critrevonc.2022.103862. Epub 2022 Nov 1.
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Treating Anemic Patients With Myelofibrosis in the New Janus Kinase Inhibitor Era: Current Evidence and Real-world Implications.在新的 Janus 激酶抑制剂时代治疗骨髓纤维化贫血患者:当前证据及现实意义
Hemasphere. 2022 Sep 30;6(10):e778. doi: 10.1097/HS9.0000000000000778. eCollection 2022 Oct.
4
Overall survival in the SIMPLIFY-1 and SIMPLIFY-2 phase 3 trials of momelotinib in patients with myelofibrosis.SIMPLIFY-1 和 SIMPLIFY-2 期临床试验中,芦可替尼治疗骨髓纤维化患者的总生存情况。
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Oncologist. 2022 Mar 11;27(3):228-235. doi: 10.1093/oncolo/oyab058.
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A prognostic model to predict survival after 6 months of ruxolitinib in patients with myelofibrosis.预测芦可替尼治疗骨髓纤维化患者 6 个月后生存的预后模型。
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Leuk Lymphoma. 2022 Mar;63(3):694-702. doi: 10.1080/10428194.2021.1992756. Epub 2021 Oct 25.
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基于输血状态和贫血严重程度评估骨髓纤维化患者的估算医疗资源利用和成本:对医疗保险按服务收费索赔数据的回顾性分析。

Evaluating estimated health care resource utilization and costs in patients with myelofibrosis based on transfusion status and anemia severity: A retrospective analysis of the Medicare Fee-For-Service claims data.

机构信息

Cleveland Clinic Taussig Cancer Institute, Cleveland, OH.

Inovalon, Bowie, MD.

出版信息

J Manag Care Spec Pharm. 2024 Dec;30(12):1395-1404. doi: 10.18553/jmcp.2024.24050. Epub 2024 Oct 3.

DOI:10.18553/jmcp.2024.24050
PMID:39360964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11607217/
Abstract

BACKGROUND

Myelofibrosis (MF) is a rare but aggressive myeloproliferative neoplasm that commonly affects older patients, with a mean age of onset of older than 60 years. At least a third of patients with primary MF are anemic at diagnosis, and nearly all patients become anemic over time; approximately half require red blood cell transfusions within a year of diagnosis. Anemia and transfusion dependence are leading negative prognostic factors for overall survival and are associated with diminished quality of life and increased health care-related economic burden in patients with MF.

OBJECTIVE

To describe baseline characteristics, health care resource utilization (HCRU), and costs as a function of transfusion status and anemia severity in patients diagnosed with MF among the US Medicare Fee-For-Service (FFS) population.

METHODS

This retrospective cohort study included patients diagnosed with MF appearing in the 100% Medicare FFS database enrolled between January 1, 2012, and December 31, 2020. Patients were segmented into hemoglobin level cohorts (no, mild, moderate, and severe anemia) and transfusion status cohorts (transfusion independent [TI], transfusion requiring [TR], or transfusion dependent [TD]). Across cohorts, demographics and disease characteristics were assessed at baseline; per patient per month all-cause HCRU and medical and pharmacy costs were reported during follow-up. All results were summarized descriptively.

RESULTS

The transfusion status cohort (N = 1,749) included TI (n = 980), TR (n = 559), and TD (n = 210) patients; the anemia severity cohort (N = 365) included patients with no (n = 100), mild (n = 128), moderate (n = 99), and severe (n = 38) anemia. On average, TR and TD patients or those with moderate or severe anemia had numerically higher Deyo-Charlson Comorbidity Index scores than those who were TI or had mild or no anemia. TR and TD cohorts reported numerically greater all-cause outpatient, inpatient, and emergency department utilization vs the TI cohort. All-cause costs were numerically higher in the TD and TR cohorts vs the TI cohort ($14,655 and $14,249 vs $8,191). Incremental increases in HCRU and costs were also observed with increasing anemia severity. All-cause medical and pharmacy costs for no, mild, moderate, and severe anemia cohorts were $4,689, $7,268, $10,439, and $13,590, respectively.

CONCLUSIONS

This retrospective analysis of the US Medicare FFS database descriptively evaluated patients by transfusion status and anemia severity and showed that costs and HCRU were numerically lower for patients with transfusion independence compared with those with transfusion dependence. Similar trends were seen when comparing patients based on anemia status, with numerically lower HCRU and cost observed with decreasing anemia severity.

摘要

背景

骨髓纤维化(MF)是一种罕见但侵袭性的骨髓增生性肿瘤,通常影响老年患者,发病平均年龄大于 60 岁。至少三分之一的原发性 MF 患者在诊断时贫血,几乎所有患者随着时间的推移都会贫血;大约一半的患者在诊断后一年内需要输血。贫血和输血依赖是总体生存的主要负预后因素,与 MF 患者的生活质量下降和医疗保健相关的经济负担增加有关。

目的

描述美国医疗保险费用分担制(FFS)人群中诊断为 MF 的患者根据输血状态和贫血严重程度的基线特征、医疗保健资源利用(HCRU)和成本。

方法

这项回顾性队列研究纳入了 2012 年 1 月 1 日至 2020 年 12 月 31 日期间出现在 100%医疗保险 FFS 数据库中的诊断为 MF 的患者。患者分为血红蛋白水平队列(无、轻度、中度和重度贫血)和输血状态队列(输血独立 [TI]、输血需求 [TR]或输血依赖 [TD])。在各队列中,在基线时评估人口统计学和疾病特征;在随访期间,按患者每月报告所有原因的 HCRU 和医疗及药物费用。所有结果均进行描述性总结。

结果

输血状态队列(N=1749)包括 TI(n=980)、TR(n=559)和 TD(n=210)患者;贫血严重程度队列(N=365)包括无贫血(n=100)、轻度贫血(n=128)、中度贫血(n=99)和重度贫血(n=38)患者。平均而言,TR 和 TD 患者或中重度贫血患者的德约-查尔森合并症指数评分高于 TI 患者或轻度或无贫血患者。TR 和 TD 队列报告的所有原因门诊、住院和急诊就诊次数均多于 TI 队列。与 TI 队列相比,所有原因的成本在 TD 和 TR 队列中均较高($14655 和 $14249 比 $8191)。随着贫血严重程度的增加,HCRU 和成本也呈递增趋势。无、轻度、中度和重度贫血患者的所有原因医疗和药物费用分别为$4689、$7268、$10439 和$13590。

结论

这项对美国医疗保险 FFS 数据库的回顾性分析描述性地评估了根据输血状态和贫血严重程度的患者,结果显示,与输血依赖的患者相比,输血独立的患者的成本和 HCRU 较低。基于贫血状态进行比较时,也出现了类似的趋势,随着贫血严重程度的降低,HCRU 和成本也呈下降趋势。