Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Helle Pappot; Christina Bæksted; Ann Knoop; Sandra A. Mitchell; Aase Nissen; Christoffer Johansen

doi:10.1111/tbj.13204

Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE)

Helle Pappot^*, Christina Bæksted, Ann Knoop, Sandra A. Mitchell, Aase Nissen, Christoffer Johansen

^*Corresponding author af dette arbejde

Institut for Klinisk Medicin

5 Citationer (Scopus)

Abstract

The Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE) was developed by the National Cancer Institute to capture patient self-reports of symptomatic toxicities during cancer treatment. The aim of this short communication is to describe the design of a national study, which examine the effect of using patients’ electronic PRO-CTCAE reporting with real-time feedback to clinicians on treatment events for breast cancer patients receiving adjuvant chemotherapy. The study's end-points are defined as dose reduction, hospitalization, and febrile neutropenia. This is the first report on the impact of PRO-CTCAE in a national breast cancer population during chemotherapy treatment.

Originalsprog	Engelsk
Tidsskrift	Breast Journal
Vol/bind	25
Udgave nummer	2
Sider (fra-til)	269-272
Antal sider	4
ISSN	1075-122X
DOI	https://doi.org/10.1111/tbj.13204
Status	Udgivet - 2019

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10.1111/tbj.13204

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Citationsformater

Pappot, H., Bæksted, C., Knoop, A., Mitchell, S. A., Nissen, A., & Johansen, C. (2019). Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE). Breast Journal, 25(2), 269-272. https://doi.org/10.1111/tbj.13204

Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE). / Pappot, Helle; Bæksted, Christina; Knoop, Ann et al.

I: Breast Journal, Bind 25, Nr. 2, 2019, s. 269-272.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

Pappot, H, Bæksted, C, Knoop, A, Mitchell, SA, Nissen, A & Johansen, C 2019, 'Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE)', Breast Journal, bind 25, nr. 2, s. 269-272. https://doi.org/10.1111/tbj.13204

Pappot H, Bæksted C, Knoop A, Mitchell SA, Nissen A, Johansen C. Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE). Breast Journal. 2019;25(2):269-272. doi: 10.1111/tbj.13204

Pappot, Helle ; Bæksted, Christina ; Knoop, Ann et al. / Routine surveillance for symptomatic toxicities with real-time clinician reporting in Danish breast cancer patients—Organization and design of the first national, cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE). I: Breast Journal. 2019 ; Bind 25, Nr. 2. s. 269-272.

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