The Feasibility, Acceptability, and Effectiveness of Electronic Patient-Reported Outcome Symptom Monitoring for Immune Checkpoint Inhibitor Toxicities: A Systematic Review

被引:12
|
作者
Lai-Kwon, Julia [1 ,2 ]
Cohen, Jordan E. [3 ]
Lisy, Karolina [2 ,4 ,5 ]
Rutherford, Claudia [6 ,7 ]
Girgis, Afaf [8 ]
Basch, Ethan [9 ]
Jefford, Michael [1 ,2 ,4 ,5 ]
机构
[1] Peter MacCallum Canc Ctr, Dept Med Oncol, Melbourne, Vic, Australia
[2] Peter MacCallum Canc Ctr, Dept Hlth Serv Res, Melbourne, Vic, Australia
[3] South Western Sydney Local Hlth Dist, Liverpool Hosp, Sydney, NSW, Australia
[4] Peter MacCallum Canc Ctr, Australian Canc Survivorship Ctr, Melbourne, Vic, Australia
[5] Univ Melbourne, Sir Peter MacCallum, Dept Oncol, Melbourne, Vic, Australia
[6] Univ Sydney, Sch Psychol, Sydney Qual Life Off, Fac Sci, Sydney, NSW, Australia
[7] Univ Sydney, Susan Wakil Sch Nursing & Midwifery, Fac Med & Hlth, Canc Care Res Unit CCRU, Sydney, NSW, Australia
[8] Univ New South Wales, Univ New South Wales Med & Hlth, South West Sydney Clin Campuses, Sydney, NSW, Australia
[9] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC USA
来源
关键词
CELL LUNG-CANCER; PHASE-III; BREAST-CANCER; CARE; IMMUNOTHERAPY; PEMBROLIZUMAB; CHEMOTHERAPY; MANAGEMENT; DOCETAXEL; TRIALS;
D O I
10.1200/CCI.22.00185
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Increasing use of immune checkpoint inhibitors (ICIs) in routine cancer care will increase the incidence of immune-related adverse events (irAEs). Systems are needed to support remote monitoring for irAEs. Electronic patient-reported outcome (ePRO) symptom monitoring systems can help monitor and manage symptoms and side effects. We assessed the content and features of ePRO symptom monitoring systems for irAEs, and their feasibility, acceptability, and impact on patient outcomes and health care utilization. METHODS A systematic literature search was conducted in May 2022 on MEDLINE, Embase, PsycINFO, and Cochrane Central Register of Controlled Trials. Quantitative and qualitative data relevant to the review questions were extracted and synthesized in tables. RESULTS Seven papers describing five ePRO systems were included. All systems collected PROs between clinic visits. Two of five used validated symptom questionnaires, 3/5 provided prompts to complete questionnaires, 4/5 provided reminders to self-report, and 3/5 provided clinician alerts for severe/worsening side effects. Four of five provided coverage of >= 26/30 irAEs in the ASCO irAE guideline. Feasibility and acceptability were demonstrated with consent rates of 54%-100%, 17%-27% of questionnaires generating alerts, and adherence rates of 74%-75%. One paper showed a reduction in grade 3-4 irAEs, treatment discontinuation, clinic visit duration, and emergency department presentations, while another showed no difference in these outcomes or the rate of steroid use. CONCLUSION There is preliminary evidence of the feasibility and acceptability of ePRO symptom monitoring for irAEs. However, further studies are needed to confirm the impact on ICI-specific outcomes, such as the frequency of grade 3-4 irAEs and duration of immunosuppression. Suggestions for the content and features of future ePRO systems for irAEs are provided.
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页数:24
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