2017
DOI: 10.1200/jop.2016.018390
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Implementing a Method for Evaluating Patient-Reported Outcomes Associated With Oral Oncolytic Therapy

Abstract: PROs can be evaluated through the use of a standardized tool, such as the ESAS-r, in oncology patients receiving oral oncolytic therapy. Implementing such a tool in both community and academic practices is feasible and may facilitate improvements in the quality of care.

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Cited by 17 publications
(21 citation statements)
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References 11 publications
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“…In another recent publication, the esas-r was also successfully used to evaluate symptom burden in patients prescribed oral cancer therapy 14 .…”
Section: Discussionmentioning
confidence: 99%
“…In another recent publication, the esas-r was also successfully used to evaluate symptom burden in patients prescribed oral cancer therapy 14 .…”
Section: Discussionmentioning
confidence: 99%
“… 28 Oral oncolytics are associated with a wide array of adverse effects, and data indicate that patients who receive these treatments frequently experience moderate-to-severe symptoms. 29 To mitigate these and other adverse effects, it is imperative that providers diligently monitor patients who receive oral oncolytic therapy. For example, in a recent clinical trial, 766 patients were randomly assigned to use either a Web-based tool that enabled them to report adverse effects or standard-of-care reporting methods.…”
Section: Monitoring and Follow-upmentioning
confidence: 99%
“… 30 Use of patient-reported outcomes (PROs) in patients who receive oral oncolytic therapy is in the early phases of development, but one can assume that the benefits would be similar to those for patients who receive intravenous chemotherapy. 29 , 31 …”
Section: Monitoring and Follow-upmentioning
confidence: 99%
“…However, it cannot be used to monitor all treatment toxicities because only 10 symptoms are assessed; the ESAS does not include digestive symptoms (eg, vomiting, diarrhea), cutaneous symptoms, fluid retention (eg, edema), or sepsis. However, its routine use was associated with a 6% increase in 1-year overall survival in a retrospective matched cohort study of 128,893 patients [ 20 - 22 ].…”
Section: Effectiveness Criteriamentioning
confidence: 99%