Implementing Electronic Patient-Reported Outcomes for Patients With New Oral Chemotherapy Prescriptions at an Academic Site and a Community Site

Author:

Doolin Jim W.1ORCID,Berry Jonathan L.1,Forbath Natalia S.2,Tocci Noah X.2,Dechen Tenzin2,Li Stephanie2ORCID,Hartwell Rebekah A.3ORCID,Espiritu Jennifer K.4,Roberts Daniel A.4ORCID,Zerillo Jessica A.1ORCID,Shea Meghan1

Affiliation:

1. Division of Hematology-Oncology, Beth Israel Deaconess Medical Center, Boston, MA

2. Center for Healthcare Deliver Science, Beth Israel Deaconess Medical Center, Boston, MA

3. Clovis Oncology, Boulder, CO

4. Dana-Farber Cancer Institute, Boston, MA

Abstract

PURPOSE Oral chemotherapy challenges providers' abilities to safely monitor patients' symptoms, adherence, and financial toxicity. COVID-19 has increased the urgency of caring for patients remotely. Collection of electronic patient-reported outcomes (ePROs) has demonstrated efficacy for patients on intravenous chemotherapy, but limited data support their use in oral chemotherapy. We undertook a pilot project to assess the feasibility of implementing an ePRO system for patients starting oral chemotherapy at our cancer center, which includes both an academic site and a community site. METHODS Patients initiating oral chemotherapy were asked to participate. A five-question tool was built in REDCap. Concerning responses triggered outreach within one business day. The primary outcome was time to first symptom assessment. For comparison, we used a historical cohort of patients who had been prescribed oral chemotherapies by providers in the same disease groups at the cancer center. RESULTS Twenty-five of 62 (40%) patients completed ePRO assessments. Fifty historical charts were reviewed. Time to first symptom assessment was 7 days (IQR, 4-14 days) in the historical group compared with 3 days (IQR, 2-4 days) in the ePRO group. Time to clinical action was 14 days (7-35 days) in the historical group compared with 8 days (4-19 days) in the ePRO group. No statistically significant differences were detected in 30-day emergency department visit or hospitalization (12% for both groups) or 90-day emergency department visit or hospitalization rates (historical 28% and ePRO 20%). CONCLUSION An ePRO tool monitoring patient concerns about adherence, cost, and toxicities for patients with new oral chemotherapy regimens is feasible and improves time to symptom assessment. Further investigation is needed to improve patient engagement with ePROs and evaluate the long-term impacts for patients on oral chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

General Medicine

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