Multi-Stakeholder Qualitative Interviews to Inform Measurement of Patient Reported Outcomes After CAR-T

被引:15
作者
Akinola, Idayat M. [1 ]
Cusatis, Rachel [1 ]
Pasquini, Marcelo C. [1 ]
Shaw, Bronwen E. [1 ]
Bollu, Vamsi [2 ]
Dalal, Anand [2 ]
Tesfaye, Mimi [2 ]
Flynn, Kathryn E. [1 ,3 ]
机构
[1] Med Coll Wisconsin, Milwaukee, WI USA
[2] Novartis Pharmaceut, E Hanover, NJ USA
[3] CIBMTR, Med Coll Wisconsin, Patient Reported Outcomes, Milwaukee Campus,9200 Wisconsin Ave,Suite C5500, Milwaukee, WI 53226 USA
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2023年 / 29卷 / 04期
基金
美国国家卫生研究院;
关键词
Chimeric antigen receptor T cell; therapy; Qualitative; Patient experience; Patient-reported outcomes;
D O I
10.1016/j.jtct.2023.01.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Toxicities after chimeric antigen receptor T cell (CAR-T) therapy are well known, yet the patient experience during and after CAR-T therapy has not been well described outside of the trial setting. We explored the patient experience after CAR-T therapy to inform the patient-reported outcomes (PRO) measurement approach for the Center for International Blood andMarrowTransplant Research (CIBMTR). We recruited (1) adult patients diagnosed with a hematologic malignancy 14 days to 6 months after receiving a commercial CAR T cell product who had agreed to be contacted by the CIBMTR, (2) caregivers of those patients, and (3) clinical experts in CAR-T therapy. Telephone interviews were conducted following a semistructured guide that included open-ended questions about symptoms and functioning. We conducted a systematic content analysis of each transcript using prespecified codes representing common domains of health, as well as open coding for emergent themes. Forty patients at 29 centers, 15 of their caregivers, and 15 experts from 9 centers participated, representing diversity with respect to age, sex, race/ethnicity, and years in practice (experts). Patients, caregivers, and experts shared largely consistent impressions of the patient experience after CAR-T therapy. Commonly described themes included anxiety, cognitive dysfunction, depression, fatigue, pain, impaired physical function, gastrointestinal symptoms, sexual dysfunction, sleep difficulties, need for support, financial impact, hospitalization, communication with healthcare providers, and the COVID-19 pandemic. Limitations in patients' ability to participate in social roles and activities was the most prevalent theme, found in nearly all interviews. In the setting of CAR-T therapy, a multidimensional approach to PRO measurement is needed that includes physical, mental, and social health, as well as the financial impact of this novel treatment. High-quality existing PRO tools are available to measure these concepts. Results will inform the CIBMTR measurement of PROs after CAR-T therapy and may be applicable to other CAR-T studies that aim to represent patient experiences. (c) 2023 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:254.e1 / 254.e9
页数:9
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