Development of a conceptual framework for an electronic patient-reported outcome (ePRO) system measuring symptoms and impacts of CAR T-cell therapies in patients with haematological malignancies

患者报告的结果 医学 结果(博弈论) 重症监护医学 生活质量(医疗保健) 护理部 数学 数理经济学
作者
Foram Khatsuria,Christel McMullan,Olalekan Lee Aiyegbusi,Karen Shaw,Roshina Iqbal,Francesca Kinsella,Keith Wilson,Lester Pyatt,Marlene Lewis,Sophie M R Wheldon,David Burns,Ronjon Chakraverty,Melanie Calvert,Sarah Hughes
出处
期刊:Lancet Oncology [Elsevier BV]
卷期号:25 (10): e476-e488 被引量:3
标识
DOI:10.1016/s1470-2045(24)00256-0
摘要

Chimeric antigen receptor (CAR) T-cell therapy is associated with potentially severe toxicities that create a substantial burden for patients. Patient-reported outcomes (PROs) offer valuable insights into symptoms, functioning, and other complex constructs of interest. In this Review, we aimed to identify symptom and impact concepts important to patients receiving CAR T-cell therapy, construct a conceptual framework for an electronic patient-reported outcome (ePRO) system, and identify timepoints to capture PRO data for CAR T-cell therapies. We searched MEDLINE (OVID) and Web of Science (Clarivate) for articles in English published from Aug 30, 2017, to March 2, 2023. No restrictions on study design were applied. 178 symptoms or constructs were extracted from 44 articles reporting PRO collection in adults with haematological malignancies receiving CAR T-cell therapy. Six health-care professionals and 11 patients and caregiver partners verified construct relevance to clinical management and lived experience, respectively. 109 constructs were sorted according to the four domains of conceptual framework: symptom burden, impact of disease and treatment, tolerability, and health-related quality of life. The identification of concepts beyond symptom burden underscores the importance of PRO measurement for long-term monitoring, to align outcomes with patient concerns. The framework will facilitate PRO measure selection for systematic gathering of PROs from individuals with haematological malignancies receiving CAR T-cell therapies.

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