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美国食品药品监督管理局关于患者报告结局的行业指南:一家制药公司的观点。

The FDA guidance for industry on PROs: the point of view of a pharmaceutical company.

作者信息

Arpinelli Fabio, Bamfi Francesco

机构信息

Health Technology Assessment, Medical Department, GSK S.p.A. Verona, Italy.

出版信息

Health Qual Life Outcomes. 2006 Oct 31;4:85. doi: 10.1186/1477-7525-4-85.

Abstract

The importance of the patients point of view on their health status is widely recognised. Patient-reported outcomes is a broad term encompassing a large variety of different health data reported by patients, as symptoms, functional status, Quality of Life and Health-Related Quality of Life. Measurements of Health-Related Quality of Life have been developed during many years of researches, and a lot of validated questionnaires exist. However, few attempts have been made to standardise the evaluation of instruments characteristics, no recommendations are made about interpretation on Health-Related Quality of Life results, especially regarding the clinical significance of a change leading a therapeutic approach. Moreover, the true value of Health-Related Quality of Life evaluations in clinical trials has not yet been completely defined. An important step towards a more structured and frequent use of Patient-Reported Outcomes in drug development is represented by the FDA Guidance, issued on February 2006. In our paper we aim to report some considerations on this Guidance. Our comments focus especially on the characteristics of instruments to use, the Minimal Important Difference, and the methods to calculate it. Furthermore, we present the advantages and opportunities of using the Patient-Reported Outcomes in drug development, as seen by a pharmaceutical company. The Patient-Reported Outcomes can provide additional data to make a drug more competitive than others of the same pharmacological class, and a well demonstrated positive impact on the patient' health status and daily life might allow a higher price and/or the inclusion in a reimbursement list. Applying extensively the FDA Guidance in the next trials could lead to a wider culture of subjective measurement, and to a greater consideration for the patient's opinions on his/her care. Moreover, prescribing doctors and payers could benefit from subjective information to better define the value of drugs.

摘要

患者对自身健康状况的观点的重要性已得到广泛认可。患者报告结局是一个宽泛的术语,涵盖患者报告的大量不同健康数据,如症状、功能状态、生活质量和健康相关生活质量。健康相关生活质量的测量在多年研究中得以发展,存在许多经过验证的问卷。然而,在标准化评估工具特性方面所做的尝试很少,对于健康相关生活质量结果的解释,尤其是关于导致治疗方法改变的变化的临床意义,没有给出相关建议。此外,健康相关生活质量评估在临床试验中的真正价值尚未完全明确。2006年2月发布的美国食品药品监督管理局(FDA)指南代表了在药物研发中朝着更结构化、更频繁地使用患者报告结局迈出的重要一步。在我们的论文中,我们旨在报告对该指南的一些思考。我们的评论尤其关注所使用工具的特性、最小重要差异以及计算它的方法。此外,我们从一家制药公司的角度阐述了在药物研发中使用患者报告结局的优势和机遇。患者报告结局可以提供额外数据,使一种药物比同一药理类别的其他药物更具竞争力,并且对患者健康状况和日常生活有充分证明的积极影响可能允许更高的价格和/或被列入报销清单。在下一次试验中广泛应用FDA指南可能会形成更广泛的主观测量文化,并更重视患者对其治疗的意见。此外,开处方的医生和付款人可以从主观信息中受益,以便更好地界定药物的价值。

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