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

机译:FDA针对PRO的行业指南:制药公司的观点

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摘要

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.
机译:人们普遍认识到患者关于其健康状况的重要性。患者报告的结果是一个广义术语,涵盖患者报告的各种不同健康数据,例如症状,功能状态,生活质量和与健康相关的生活质量。在多年的研究中已经开发出与健康相关的生活质量的测量方法,并且存在许多经过验证的问卷。但是,很少有人尝试使仪器特性的评估标准化,也没有建议对与健康相关的生活质量结果进行解释,特别是有关导致治疗方法改变的临床意义的建议。此外,在临床试验中健康相关生活质量评估的真正价值尚未完全确定。 2006年2月发布的FDA指南代表了在药物开发中更结构化和更频繁地使用患者报告结果的重要一步。在本文中,我们旨在报告有关此指南的一些注意事项。我们的评论特别关注使用的工具的特性,最小重要差异及其计算方法。此外,正如制药公司所看到的,我们展示了在药物开发中使用患者报告结果的优势和机会。患者报告的结果可以提供更多数据,以使药物比同类药理学的药物更具竞争力,并且充分证明对患者健康状况和日常生活的积极影响可能会导致更高的价格和/或将其纳入报销清单。在下一个试验中广泛应用FDA指南可能会导致更广泛的主观测量文化,并导致更多考虑患者对其护理的意见。此外,开处方的医生和付款人可以从主观信息中受益,以更好地定义药物的价值。

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