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Comparative effectiveness and cost of adding rituximab to first-line chemotherapy for elderly patients diagnosed with diffuse large B-cell lymphoma

机译:一线化疗中加用利妥昔单抗对诊断为弥漫性大B细胞淋巴瘤的老年患者的比较效果和成本

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BACKGROUND: Clinical trials indicate that rituximab improves the survival of patients with diffuse large B-cell lymphoma (DLBCL). Economic models using multiple data sources, including clinical trials for survival outcomes, have projected cost offsets/savings and favorable cost-effectiveness associated with rituximab. In this study, the authors evaluated survival and cost impacts of adding rituximab to first-line chemotherapy for DLBCL using a single database that reflects routine clinical practice among elderly patients in the United States. METHODS: By using Surveillance, Epidemiology, and End Results (SEER) data linked to Medicare, the authors identified 5484 elderly patients who were diagnosed with DLBCL between January 1999 and December 2005 who had claims through December 2007. Included patients began chemotherapy with or without rituximab within 180 days of diagnosis. Multivariate analyses were conducted to estimate the impact of rituximab on mortality and costs to Medicare. The cost per life-year gained of rituximab was calculated using cost and survival estimates from the multivariate analyses. RESULTS: The mean patient age was 76 years, 43% of patients had stage III or IV disease, and 64% received rituximab. In a Cox regression model, rituximab resulted in lower 4-year all-cause mortality (hazard ratio [HR], 0.68; 95% confidence interval [CI], 0.61-0.74) and cancer mortality, and the incremental cumulative survival was 0.37 years. In least-squares regression, rituximab resulted in higher 4-year total costs ($23,097; 95% CI, $19,129-$27,298), immunochemotherapy costs ($12,069; 95% CI, $10,687-$13,634), other cancer costs ($7655; 95% CI, $5067-$10,489), and noncancer costs ($3461; 95% CI, $1319-$5650). The cost per life-year gained was $62,424. CONCLUSIONS: In routine clinical practice, rituximab was associated with survival benefits comparable to those observed in clinical trials. However, these benefits did not translate into the previously reported cost savings.
机译:背景:临床试验表明,利妥昔单抗可改善弥漫性大B细胞淋巴瘤(DLBCL)患者的生存率。使用多种数据源的经济模型,包括用于生存结果的临床试验,已经预测了与利妥昔单抗相关的成本补偿/节省和有利的成本效益。在这项研究中,作者使用一个数据库反映了美国老年患者的常规临床实践,评估了将利妥昔单抗添加到DLBCL一线化疗的生存率和成本影响。方法:通过使用与Medicare关联的监测,流行病学和最终结果(SEER)数据,作者确定了5484名在1999年1月至2005年12月之间被诊断出患有DLBCL的老年患者,这些患者在2007年12月之前一直主张化疗。诊断后180天内使用利妥昔单抗。进行了多变量分析,以评估利妥昔单抗对死亡率和医疗保险费用的影响。利妥昔单抗每生命年获得的成本是根据多元分析的成本和生存率估算得出的。结果:平均患者年龄为76岁,43%的患者患有III或IV期疾病,64%的患者接受了利妥昔单抗治疗。在Cox回归模型中,利妥昔单抗可降低4年全因死亡率(危险比[HR],0.68; 95%置信区间[CI],0.61-0.74)和癌症死亡率,累积累积生存期为0.37年。在最小二乘回归中,利妥昔单抗导致较高的4年总成本(23,097美元; 95%CI,19,129- $ 27,298),免疫化学疗法成本(12,069; 95%CI,10,687- $ 13,634),其他癌症成本(7655美元; 95%CI) ,$ 5067- $ 10,489)和非癌费用($ 3461; 95%CI,$ 1319- $ 5650)。每生命年增加的成本为62,424美元。结论:在常规临床实践中,利妥昔单抗在生存获益方面与在临床试验中观察到的相当。但是,这些好处并没有转化为先前报告的成本节省。

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