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首页> 外文期刊>Gynecologic Oncology: An International Journal >Addressing clinical trials: can the multidisciplinary Tumor Board improve participation? A study from an academic women's cancer program.
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Addressing clinical trials: can the multidisciplinary Tumor Board improve participation? A study from an academic women's cancer program.

机译:开展临床试验:多学科肿瘤委员会能否改善参与度?一项学术性女性癌症计划的研究。

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OBJECTIVE: The Tumor Board (TB) allows for an interdisciplinary approach to cancer treatment designed to encourage evidence-based treatment. However, its role in facilitating clinical trial participation has not been reported. We aimed to determine whether a prospective TB is an effective strategy for trial recruitment and to identify steps within the TB process that facilitate discussion of trial eligibility and optimize accrual. METHODS: We conducted a retrospective cross-sectional analysis of women presented to Gynecologic Oncology TB between March and December 2008. Patient demographics, TB recommendations, and post-TB patient discussions were abstracted. These were compared to data derived from the Department of Oncology Research to determine research team awareness of eligible patients and confirm trial enrollment(s). Data analysis was completed with Chi-square test; risk ratios and confidence intervals were calculated as summary measures. RESULTS: We reviewed 1213 case presentations involving 916 women. Overall, 358 TB recommendations (30%) identified eligible patients, of which enrollment consisted of 87 (24%) trials (6% therapeutic trials and 18% non-therapeutic trials). Compared to other types of TB recommendations, those involving trials were discussed less frequently at post-TB patient visits (79% vs. 44%). Documentation of trial discussion at the post-TB visit was more likely to result in trial participation, versus solely relying on the research staff to communicate enrollment eligibility with the treating team (RR 2.5, p=0.006). CONCLUSIONS: Patients identified by the TB were 2.5-times as likely to enroll in a clinical trial, but trials were mentioned only 44% of the time. Interventions that facilitate trial discussions during post-TB meetings are needed to improve trial participation.
机译:目的:肿瘤委员会(TB)允许采用跨学科的癌症治疗方法,以鼓励循证治疗。但是,尚未报道其在促进临床试验参与中的作用。我们旨在确定预期的结核病是否是有效的试验招募策略,并确定结核病过程中可促进讨论试验资格并优化应计成本的步骤。方法:我们对2008年3月至12月间送给妇科肿瘤结核病的妇女进行了回顾性横断面分析。摘要了患者的人口统计学资料,结核病的建议和结核病后的讨论。将这些数据与从肿瘤学研究部获得的数据进行比较,以确定研究小组对合格患者的认识并确认试验入组。数据分析通过卡方检验完成;计算风险比和置信区间作为汇总指标。结果:我们审查了1213例病例报告,涉及916名妇女。总体而言,有358 TB推荐(30%)的患者为合格患者,其中包括87(24%)个试验(6%的治疗性试验和18%的非治疗性试验)。与其他类型的结核病推荐相比,在结核病患者就诊时,涉及试验的讨论较少(79%比44%)。与仅依靠研究人员与治疗团队沟通入组资格相比,结核病访视后的试验讨论记录更有可能导致试验参与(RR 2.5,p = 0.006)。结论:结核病患者入选临床试验的可能性为2.5倍,但只有44%的病例被提及。需要进行干预,以促进结核病后会议期间的讨论,以提高试验的参与度。

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