Details

Autor(en) / Beteiligte

• Itzstein, Mitchell S.
• Railey, Elda
• Smith, Mary L.
• White, Carol B.
• Sledge, George W.
• Howell, John R.
• Lawton, Wendy
• Marinucci, Donna M.
• Unni, Nisha
• Gerber, David E.

Titel

Patient familiarity with, understanding of, and preferences for clinical trial endpoints and terminology

Ist Teil von

• Cancer, 2020-04, Vol.126 (8), p.1605-1613

Ort / Verlag

United States: Wiley Subscription Services, Inc

Erscheinungsjahr

2020

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Background Although there is increased attention to designing and explaining clinical trials in ways that are clinically meaningful for patients, there is limited information on patient preferences, understanding, and perceptions of this content. Methods Maximum difference scaling (MaxDiff) methodology was used to develop a survey for assessing patients' understanding of 19 clinical terms and perceived importance of 9 endpoint surrogate phrases used in clinical trials and consent forms. The survey was administered electronically to individuals with metastatic breast cancer affiliated with the Metastatic Breast Cancer Alliance. Analyses were performed using Bayesian P values with statistical software. Results Among 503 respondents, 77% had a college degree, 70% were diagnosed with metastatic disease ≥2 years before survey completion, and 77% had received ≥2 lines of systemic therapy. Less than 35% of respondents reported understanding “fairly well” the terms symptomatic progression, duration of disease control, time to treatment cessation, and endpoints. Income level and time since onset of metastatic disease correlated with comprehension. Patients who had received ≥6 lines of therapy perceived that time until serious side effects (P < .001) and time on therapy (P < .001) were more important compared with those who had received only 1 line of therapy. Positively phrased parameters were associated with increased perceived importance. Conclusions Even among educated, heavily pretreated patients, many commonly used clinical research terms are poorly understood. Comprehension and the perceived importance of trial endpoints vary over the course of disease. These observations may inform the design, discussion, and reporting of clinical trials. Regulatory and professional organizations increasingly recognize that patients should play an important role in the design of cancer clinical trials. Findings from this study indicate several endpoints that patients perceive as most important and that the importance of endpoints may change over the disease course, which should be considered in the design of clinical trials.