Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, Maryland, USA.
Center for Devices and Radiological Health, US Food and Drug Administration, Silver Spring, Maryland, USA.
Clin Genitourin Cancer. 2024 Aug;22(4):102113. doi: 10.1016/j.clgc.2024.102113. Epub 2024 May 7.
Food and Drug Administration must make decisions about emerging high intensity focused ultrasound (HIFU) devices that may lack relevant clinical oncologic data but present with known side effects. This study aims to capture patients' perspective by quantifying their preferences regarding the available benefit and important side effects associated with HIFU for localized prostate cancer.
Preferences for HIFU outcomes were examined using a discrete choice experiment survey. Participants were asked to choose a preferred treatment option in 9 choice questions. Each included a pair of hypothetical treatment profiles that have similar attributes/outcomes with varying levels. Outcomes included prostate biopsy outcome and treatment-related risks of erectile dysfunction (ED) and urinary incontinence (UI). We calculated the maximum risk of side effect patients were willing to tolerate in exchange for increased benefit. Preferences were further explored via clinical and demographic data.
About 223 subjects with a mean age of 64.8 years completed the survey. Respondents were willing to accept a 1.51%-point increase in new ED risk for a 1%-point increase in favorable biopsy outcome. They were also willing to accept a 0.93%-point increase in new UI risk for a 1%-point increase in biopsy outcome. Subjects who perceived their cancer to be more aggressive had higher risk tolerance for UI. Younger men were willing to tolerate less ED risk than older men. Respondents with greater than college level of education had a lower risk tolerance for ED or UI.
Results may inform development and regulatory evaluation for future HIFU ablation devices by providing supplemental information from the patient perspective.
食品和药物管理局必须对新兴的高强度聚焦超声(HIFU)设备做出决策,这些设备可能缺乏相关的临床肿瘤学数据,但具有已知的副作用。本研究旨在通过量化患者对 HIFU 治疗局限性前列腺癌的可用益处和重要副作用的偏好,从患者角度捕捉信息。
采用离散选择实验调查研究 HIFU 结果的偏好。参与者被要求在 9 个选择题中选择一个首选的治疗方案。每个问题都包括一对假设的治疗方案,这些方案具有相似的属性/结果,但水平不同。结果包括前列腺活检结果以及与治疗相关的勃起功能障碍(ED)和尿失禁(UI)风险。我们计算了患者愿意忍受的最大副作用风险,以换取增加的益处。通过临床和人口统计学数据进一步探讨了偏好。
约 223 名平均年龄为 64.8 岁的受试者完成了调查。受访者愿意接受新 ED 风险增加 1.51%,以换取活检结果改善 1%。他们也愿意接受新 UI 风险增加 0.93%,以换取活检结果改善 1%。认为自己癌症更具侵袭性的患者对 UI 的风险容忍度更高。年轻男性比老年男性更愿意忍受较少的 ED 风险。受教育程度高于大学的受访者对 ED 或 UI 的风险容忍度较低。
这些结果可能会为未来的 HIFU 消融设备的开发和监管评估提供信息,从患者角度提供补充信息。