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开发一种成像缓解策略,以招募接受 tanezumab 神经生长因子抑制剂 (NGF-ab) 治疗的患者,重点是评估合格性。

Development of an imaging mitigation strategy for patient enrolment in the tanezumab nerve growth factor inhibitor (NGF-ab) program with a focus on eligibility assessment.

机构信息

Quantitative Imaging Center (QIC), Department of Radiology, Boston University School of Medicine, Boston, MA; Department of Radiology, University of Erlangen-Nuremberg, Erlangen, Germany.

Alacrita, Cambridge, MA.

出版信息

Semin Arthritis Rheum. 2017 Dec;47(3):323-330. doi: 10.1016/j.semarthrit.2017.05.008. Epub 2017 May 20.

Abstract

OBJECTIVE

Nerve growth factor antibodies (NGF-ab) have shown promising analgesic efficacy. Aim was to describe reader training efforts and present reliability data focusing on radiographic eligibility in the tanezumab program.

METHODS

A multi-step process was used for reader calibration and reliability testing. First, a reference standard set of cases was created and diagnostic performance was evaluated. A second exercise focused on agreement of ordinal assessment (Kellgren-Lawrence grading) of radiographic osteoarthritis. Subsequently, 11 readers were trained and read a test set of 100 cases focused on eligibility assessments. Additional reliability testing and calibration of five core readers assessing eligibility of 30 cases was performed 3 and 6 months after study start.

RESULTS

Sensitivity for the reference standard readings ranged from 0.50 to 0.90 and specificity from 0.40 to 0.83. Overall agreement for Kellgren-Lawrence grading ranged from 71.4% to 82.9%. For the 11 reader exercise, in 76% of cases at least 8 of 11 readers agreed on eligibility status. For the reliability testing 3 months after study start, in 80.0% of cases at least 4 of 5 readers agreed on eligibility with a κ = 0.43 (95% CI: 0.32-0.54). For the reliability testing after 6 months, in 83.3% of cases at least 4 of 5 readers agreed on eligibility with a κ = 0.52 (95% CI: 0.41-0.63).

CONCLUSIONS

After intense efforts spent in the development of an imaging program for an NGF-ab clinical program, the achieved reliability for eligibility assessment is substantial but not perfect. Ongoing efforts of calibration prior to including additional readers to the program and during study conduct between current readers will be needed to ensure agreement on potential adverse events and radiographic disease severity.

摘要

目的

神经生长因子抗体(NGF-ab)已显示出有希望的镇痛疗效。目的是描述在 tanezumab 项目中,针对放射学合格性的读者培训工作和呈现可靠性数据。

方法

使用多步骤的过程进行读者校准和可靠性测试。首先,创建一个参考标准集的病例,并评估诊断性能。第二项练习侧重于对放射性骨关节炎的等级评估(Kellgren-Lawrence 分级)的一致性。随后,对 11 名读者进行培训,并对 100 例病例的测试集进行阅读,重点是合格性评估。在研究开始后 3 个月和 6 个月,对 30 例病例的 5 名核心读者的额外可靠性测试和资格评估进行了校准。

结果

参考标准阅读的敏感性范围为 0.50 至 0.90,特异性范围为 0.40 至 0.83。Kellgren-Lawrence 分级的总体一致性范围为 71.4%至 82.9%。对于 11 名读者的练习,在 76%的病例中,至少有 8 名读者同意合格状态。在研究开始后 3 个月的可靠性测试中,在 80.0%的病例中,至少有 4 名读者对资格评估达成一致,κ 值为 0.43(95%CI:0.32-0.54)。在研究开始后 6 个月的可靠性测试中,在 83.3%的病例中,至少有 4 名读者对资格评估达成一致,κ 值为 0.52(95%CI:0.41-0.63)。

结论

在为 NGF-ab 临床项目开发成像计划方面付出了巨大努力之后,对于合格性评估的实现可靠性是可观的,但并不完美。在将额外的读者纳入该计划之前,以及在当前读者之间进行研究期间,需要进行持续的校准工作,以确保在潜在的不良事件和放射学疾病严重程度方面达成一致。

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