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)

被引：12
|
作者：
Pappot, Helle [1 ]
Baeksted, Christina [1 ,2 ]
Knoop, Ann [1 ]
Mitchell, Sandra A. [3 ]
Nissen, Aase [2 ]
Johansen, Christoffer [4 ]
机构：
[1] Rigshosp, Finsen Ctr, Dept Oncol, Copenhagen, Denmark
[2] Danish Canc Soc, Documentat & Qual, Copenhagen, Denmark
[3] NCI, Outcomes Res Branch, Div Canc Control & Populat Sci, Rockville, MD USA
[4] Danish Canc Soc Res Ctr, Unit Survivorship, Copenhagen, Denmark
来源：
BREAST JOURNAL | 2019年 / 25卷 / 02期
关键词：
adjuvant chemotherapy; breast cancer; patient reported outcome; PRO-CTCAE; toxicity; FOLLOW-UP;
D O I：
10.1111/tbj.13204
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
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.
引用
收藏
页码：269 / 272
页数：4
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