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首页> 外文期刊>Journal of comparative effectiveness research >A stakeholder-informed randomized, controlled comparative effectiveness study of an order prescribing intervention to improve colony stimulating factor use for cancer patients receiving myelosuppressive chemotherapy: the TrACER study
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A stakeholder-informed randomized, controlled comparative effectiveness study of an order prescribing intervention to improve colony stimulating factor use for cancer patients receiving myelosuppressive chemotherapy: the TrACER study

机译:一个利益相关者信息的随机,受控的对比有效性研究,以改善接受髓抑制化疗的癌症患者的殖民刺激因子用途:探测器研究

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摘要

Colony stimulating factors (CSF) are widely prescribed to avoid febrile neutropenia (FN) among cancer patients receiving chemotherapy, but studies show their use is often not consistent with practice guidelines. In addition, there is limited high quality evidence assessing benefits and harms of primary prophylactic-CSF (PP-CSF) in the setting of chemotherapy that poses an intermediate risk of FN. To address these issues, with funding from the Patient Centered Outcomes Research Institute (PCORI) and the National Cancer Institute's Community Oncology Research Program, SWOG is sponsoring a prospective, cluster randomized controlled pragmatic trial of an automated order entry protocol for PP-CSF among patients with breast, lung and colorectal cancer receiving myelosuppressive chemotherapy, with a nested randomized controlled trial of PP-CSF for patients receiving intermediate risk chemotherapy. Primary outcomes include adherence to practice guidelines, overall rates of FN and rates of FN among persons receiving intermediate risk chemotherapy. The study, the first pragmatic trial in the National Cancer Institute's cancer cooperative clinical trials network, will provide critical evidence to inform physician and patient decision-making around PP-CSF use and practice policies regarding automated orders in cancer components.
机译:殖民地刺激因子(CSF)被广泛规定,以避免接受化疗的癌症患者的发热中性粒细胞病(FN),但研究表明他们的使用通常与实践指南不一致。此外,在造成Fn的中间风险的化疗中,存在有限的高质量证据评估原丙烯 - CSF(PP-CSF)的益处和危害。为了解决这些问题,通过患者中心成果研究所(PCORI)和国家癌症研究所的社区肿瘤学研究计划的资金,正在赞助患者中PP-CSF的自动阶数入境协议的前瞻性,集群随机对照务实试验随着乳腺癌,肺癌和结肠直肠癌接受髓抑制化疗,具有嵌套随机对照试验的PP-CSF,用于接受中间风险化疗的患者。主要成果包括遵守实践指导方针,接受中间风险化疗的人群的总体FN和FN率的总体税率。该研究,第一次务实审判在国家癌症学院的癌症合作临床试验网络中,将提供关键证据,以通知医生和患者决策,围绕PP-CSF使用以及癌症组分自动订单的实践政策。

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