Development and pilot implementation of a remote monitoring system for acute toxicity using electronic patient-reported outcomes for patients undergoing radiation therapy for breast cancer Journal Article


Authors: Lapen, K.; Sabol, C.; Tin, A. L.; Lynch, K.; Kassa, A.; Mabli, X.; Ford, J.; Cha, E.; Bernstein, M. B.; Braunstein, L. Z.; Cahlon, O.; Daly, B. M.; Sandler, K.; McCloskey, S. A.; Vickers, A. J.; Khan, A. J.; Gillespie, E. F.
Article Title: Development and pilot implementation of a remote monitoring system for acute toxicity using electronic patient-reported outcomes for patients undergoing radiation therapy for breast cancer
Abstract: Purpose: We aimed to develop and study the implementation of a remote system for toxicity assessment and management of acute side effects of breast radiation using electronic patient-reported outcomes (ePROs). Methods and Materials: A response-adapted Patient-Reported Outcomes Common Terminology Criteria for Adverse Events–based assessment for breast radiation toxicity was administered weekly during and for 8 weeks after radiation from June 2019 to July 2020. The care team received alerts when “severe” symptoms were reported by patients, who were then contacted. Treatment, clinic, and sociodemographic characteristics were abstracted from patient records. A subsample of patients and care team members was qualitatively interviewed at follow-up. Results: Overall, 5787 assessments were sent to 678 patients, of whom 489 (72%) completed 2607 assessments (45%). Moderate or greater toxicity was reported by 419 responders (86%; 95% CI, 82%-89%). Clinician alerts for severe toxicity were generated for 264 assessments among 139 unique patients, of which 83% occurred posttreatment. The proportion of surveys that prompted an alert was significantly higher after treatment (219 [13%]) than during treatment (45 [5%]) (P < .001). Survey completion rates in the posttreatment period were higher among patients undergoing partial breast irradiation than postmastectomy radiation (incidence rate ratio, 0.70; 95% CI, 0.60-0.81) (P < .001) despite these patients experiencing less severe toxicity. Interviews (15) found that patients had a positive experience with ePROs, although many thought the primary purpose was for research rather than symptom management. Conclusions: With the majority of toxicity occurring after breast radiation has ended, remote symptom monitoring with ePROs appears to fill a gap in clinical practice, particularly for patients undergoing shorter courses of radiation. It is important to properly onboard patients and explain that the purpose of ePROs is to aid clinical care. Further research is needed to determine whether the costs associated with ePROs can be offset by reducing routine clinic visits and whether this approach is acceptable and appropriate. © 2021 Elsevier Inc.
Keywords: side effect; breast cancer; radiotherapy; radiation effects; clinical research; patient-reported outcomes; toxicity; acute toxicity; surveys; post treatment; methods and materials; pilot implementation; toxicity assessment; remote monitoring system; remote systems
Journal Title: International Journal of Radiation Oncology, Biology, Physics
Volume: 111
Issue: 4
ISSN: 0360-3016
Publisher: Elsevier Inc.  
Date Published: 2021-11-15
Start Page: 979
End Page: 991
Language: English
PMCID: PMC8530913
DOI: 10.1016/j.ijrobp.2021.07.1692
PROVIDER: scopus
PUBMED: 34314814
DOI/URL:
Notes: Article
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MSK Authors
  1. Oren Cahlon
    158 Cahlon
  2. Andrew J Vickers
    882 Vickers
  3. Amy Lam Ling Tin
    114 Tin
  4. Robert M Daly
    78 Daly
  5. Christopher Sabol
    14 Sabol
  6. Atif Jalees Khan
    153 Khan
  7. Erin Faye Gillespie
    149 Gillespie
  8. Kathleen A Lynch
    71 Lynch
  9. Kaitlyn Ann Lapen
    38 Lapen
  10. Elaine Cha
    9 Cha
  11. Alyse Marie Kassa
    4 Kassa
  12. Xiaolin Mabli
    2 Mabli
  13. John Ford
    2 Ford