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Capturing Patient Voice to Improve Outcomes That Matter to Patients with Desmoid Tumor

机译:捕捉患者声音以改善对硬纤维瘤患者重要的结果

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摘要

Desmoid tumors (DT) are rare, intermediate-grade sarcomas characterized by locally aggressive growths that commonly occur intra-abdominally, in the abdominal wall, or in the extremities. Desmoid tumors are 2-3–fold more common in females than males, with most patients aged 80% at 20 years. However, patient morbidity and DT symptom burden can be high. DT significantly reduce patient quality of life, imposing substantial physical, emotional, and social burdens. Pain, fatigue, and insomnia are common symptoms; disfigurement, mobility restrictions, and, rarely, the need for amputation may also result. Despite its limited impact on survival, patients with DT may have anxiety and depression levels commensurate with those associated with malignant sarcomas. Thus, DT impose an array of significant, long-term morbidities on a young patient population. In order to evaluate the impact of these morbidities, patient-reported outcome (PRO) tools are used, which assess outcomes of importance to patients that extend beyond traditional oncology endpoints. General or oncology-related PROs can be used; although currently, the only DT-specific, validated PRO measure is the GOunder/Desmoid Tumor Research Foundation DEsmoid Symptom/Impact Scale (GODDESS©), consisting of an 11-item DT Symptom Scale (DTSS) and a 17-item DT Impact Scale (DTIS). DTSS and DTIS were secondary endpoints in DeFi, a randomized phase 3 trial of nirogacestat; blinded, pooled data from DeFi were used to validate GODDESS reliability and responsiveness as a PRO measure in DT. Another DT-specific PRO measure, the Desmoid-Type Fibromatosis Quality of Life (DTF-QoL) questionnaire, has been developed but not validated. As novel DT therapies continue to be developed, incorporating DT-specific PRO measures into clinical trials will be key to capturing patient voice, improving outcomes of importance to this unique patient population, and assisting patients and providers in selecting optimal treatment.
机译:硬纤维瘤 (DT) 是罕见的中级别肉瘤,其特征是局部侵袭性生长,通常发生在腹腔内、腹壁或四肢。女性硬纤维瘤的发病率是男性的 2-3 倍,大多数患者诊断时年龄为 80%。然而,患者的发病率和 DT 症状负担可能很高。DT 显着降低患者的生活质量,带来巨大的身体、情感和社会负担。疼痛、疲劳和失眠是常见症状;还可能导致毁容、行动受限以及极少数情况下需要截肢。尽管 DT 对生存率的影响有限,但 DT 患者的焦虑和抑郁水平可能与恶性肉瘤相关患者相当。因此,DT 对年轻患者群体造成了一系列重大的长期发病率。为了评估这些发病率的影响,使用了患者报告结果 (PRO) 工具,这些工具评估了超出传统肿瘤学终点的患者重要结果。可以使用一般或肿瘤相关 PRO;尽管目前唯一特定于 DT 的、经过验证的 PRO 措施是 GOunder/硬纤维瘤研究基金会 DEsmoid 症状/影响量表 (GODDESS),©由 11 项 DT 症状量表 (DTSS) 和 17 项 DT 影响量表 (DTIS) 组成。DTSS 和 DTIS 是 DeFi 的次要终点,DeFi 是一项 nirogacestat 的随机 3 期试验;来自 DeFi 的盲法、汇集数据用于验证 GODDESS 的可靠性和响应性,作为 DT 中的 PRO 度量。另一种 DT 特异性 PRO 措施,即硬纤维瘤病生活质量 (DTF-QoL) 问卷,已经开发但尚未验证。随着新型 DT 疗法的不断开发,将 DT 特异性 PRO 措施纳入临床试验将是捕捉患者声音、改善对这一独特患者群体具有重要意义的结果以及协助患者和提供者选择最佳治疗方法的关键。

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