Johnson F Reed, Ozdemir Semra, Mansfield Carol, Hass Steven, Miller David W, Siegel Corey A, Sands Bruce E
Research Triangle Institute/RTI International, Research Triangle Park, North Carolina, USA.
Gastroenterology. 2007 Sep;133(3):769-79. doi: 10.1053/j.gastro.2007.04.075. Epub 2007 May 3.
BACKGROUND & AIMS: Regulatory assessments of drug risks do not routinely consider patient preferences, despite evidence that some patients are willing to accept increased side-effect risk in exchange for therapeutic benefits. The aim of this study is to estimate the willingness of Crohn's disease (CD) patients to accept life-threatening adverse event risks in exchange for CD symptom relief.
Patients with CD completed choice-format conjoint trade-off tasks involving hypothetical treatments with varying efficacy and risk levels. The treatment features included daily symptoms and activity limitations, serious complications (fistulas, abscesses, bowel obstructions), time between flare-ups, oral steroid use and risk of 3 serious adverse events (SAEs) known to be associated with CD treatment (progressive multifocal leukoencephalopathy (PML), serious infections, and lymphoma). The mean maximum acceptable annual risk (MAR) for each of the SAEs was calculated for various levels of clinical benefit.
Daily symptom severity was the most important factor in treatment preferences. Higher MAR was observed for trade-off tasks involving higher levels of clinical benefit. The MAR was similar across the 3 SAEs. For improvements from severe daily symptoms to remission and from moderate daily symptoms to remission, the MARs ranged from 0.69% to 0.81% and from 0.39% to 0.55%, respectively.
Patients with CD have well-defined preferences among treatment attributes and are willing to accept tradeoffs among attributes. The patients indicated they are willing to accept elevated SAE risks in exchange for clinical efficacy. The perspective of the patients on the benefit versus risk balance can assist in making treatment and regulatory decisions.
尽管有证据表明一些患者愿意接受增加的副作用风险以换取治疗益处,但药物风险的监管评估通常不会考虑患者偏好。本研究的目的是评估克罗恩病(CD)患者为缓解CD症状而接受危及生命的不良事件风险的意愿。
CD患者完成了选择格式的联合权衡任务,涉及具有不同疗效和风险水平的假设治疗。治疗特征包括每日症状和活动受限、严重并发症(瘘管、脓肿、肠梗阻)、发作间隔时间、口服类固醇使用以及已知与CD治疗相关的3种严重不良事件(SAE)的风险(进行性多灶性白质脑病(PML)、严重感染和淋巴瘤)。针对不同水平的临床益处,计算每种SAE的平均最大可接受年度风险(MAR)。
每日症状严重程度是治疗偏好中最重要的因素。在涉及更高临床益处水平的权衡任务中,观察到更高的MAR。3种SAE的MAR相似。从严重每日症状改善到缓解以及从中度每日症状改善到缓解,MAR分别为0.69%至0.81%和0.39%至0.55%。
CD患者在治疗属性方面有明确的偏好,并且愿意在属性之间进行权衡。患者表示他们愿意接受更高的SAE风险以换取临床疗效。患者对益处与风险平衡的看法有助于做出治疗和监管决策。