首页> 美国卫生研究院文献>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:一项利益相关者告知的随机对照比较有效性研究该研究为改善骨髓抑制性化疗的癌症患者开具干预措施以改善集落刺激因子的使用开出了序号:TrACER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:广泛采用了菌落刺激因子(CSF)来避免接受化疗的癌症患者出现发热性中性粒细胞减少症(FN),但研究表明,其使用通常与实践指南不一致。此外,在评估初次预防性CSF(PP-CSF)在发生FN的中度风险的化学疗法中的利弊方面,目前尚缺乏高质量的证据。为了解决这些问题,SWOG获得了以患者为中心的结果研究所(PCORI)和美国国家癌症研究所的社区肿瘤学研究计划的资助,赞助了一项针对患者中PP-CSF自动化订单输入方案的前瞻性,整群随机对照的实用试验。接受骨髓抑制性化疗的乳腺癌,肺癌和大肠癌患者,以及接受中度风险化疗的PP-CSF巢式随机对照试验。主要结果包括遵守操作指南,总的FN率和接受中度风险化疗的人中的FN率。这项研究是美国国家癌症研究所癌症合作临床试验网络中的第一项实用试验,将提供重要证据,为医师和患者有关PP-CSF使用和有关癌症成分自动订购的实施政策的决策提供依据。

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