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首页> 外文期刊>Journal of Clinical Oncology >Effects of the US Food and Drug Administration Boxed Warning of Erythropoietin-Stimulating Agents on Utilization and Adverse Outcome
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Effects of the US Food and Drug Administration Boxed Warning of Erythropoietin-Stimulating Agents on Utilization and Adverse Outcome

机译:促红细胞生成素刺激剂对利用和不利结果的影响

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PurposeIn March 2007, a US Food and Drug Administration boxed warning was issued for erythropoietin-stimulating agents (ESAs) regarding serious adverse events, such as venous thromboembolism (VTE). We evaluated the US Food and Drug Administration's boxed warning of ESAs used to treat chemotherapy-induced anemia because evidence on the effectiveness of boxed warnings remains inconclusive.Patients and MethodsUsing 2004 to 2009 SEER-Medicare data, we exploited a natural experiment to examine the effects of ESA boxed warnings on utilization and risk of VTE. The intervention group included Medicare fee-for-services patients diagnosed with colorectal, breast, or lung cancers targeted by this warning and undergoing chemotherapy; the control group included patients with myelodysplastic syndromes not targeted by this warning. The period from January 2004 to September 2006 was used as the prewarning period; the period from April 2007 to September 2009 was used as the postwarning period. The two binary dependent variables included ESA use and hospitalized VTE. Linear probability models with a difference-in-differences specification were used for estimation.ResultsOur sample consisted of 45,319 unique patients between 2004 and 2009. The trends in ESA use remained similar between the intervention and control groups before the warning, but started declining sharply in the intervention group only after the warning. The trends in hospitalized VTE were relatively stable. Regressions showed that the ESA boxed warning was associated with a 20.2-percentage-point reduction (P < .001) in the likelihood of ESAs being used to treat cancers targeted by the warning, but not significantly associated with the likelihood of hospitalized VTE.ConclusionOur study showed that the warning was effective in reducing ESA utilization. Future studies should examine other regulatory drug safety actions, such as the Risk Evaluation and Mitigation Strategy initiative, whose effectiveness remains unknown.
机译:目的于2007年3月,美国食品和药物管理局盒装警告是针对促红细胞生成素刺激剂(ESAs)的严重不良事件(如静脉血栓栓塞(VTE))发出的。我们评估了美国食品和药物管理局用于治疗化疗诱导的贫血的欧洲兽察的盒装警告,因为盒装警告有效的证据仍然是不确定的.Patiant和MetableSusing 2004年至2009年Seer-Medicare数据,我们利用了一种自然的实验来检查效果ESA盒装警告对利用与vte风险。干预组包括被诊断出患有该警告和接受化疗的结肠直肠,乳腺癌或肺癌的医疗保险费患者;该对照组包括未受此警告的髓型增强症的患者。 2004年1月至2006年9月的期限被用作预警期;从2007年4月到2009年9月的期间被用作出正后期。两个二进制依赖变量包括ESA使用和住院VTE。具有差异差异差异规范的线性概率模型用于估计。审计样本组成为2004年至2009年间的45,319名独特的患者。在警告前的干预和对照组之间的ESA使用趋势仍然相似,但在警告之前仍然相似,但在警告前仍然相似,但在警告前仍然相似,但开始急剧下降干预组只在警告后。住院VTE的趋势相对稳定。回归表明,ESA盒装警告与ESAS用于治疗警告时的癌症的可能性,但与住院VTE的可能性没有显着相关的ESA盒装警告与eSAS的可能性有关.Conclusionour研究表明,警告可有效降低ESA利用率。未来的研究应检查其他监管药物安全行动,例如风险评估和缓解战略倡议,其有效性仍然不明。

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