Department of Radiation Oncology (MAASTRO), GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, The Netherlands.
Department of Radiation Oncology (MAASTRO), GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, The Netherlands.
Radiother Oncol. 2018 Jan;126(1):163-169. doi: 10.1016/j.radonc.2017.08.004. Epub 2017 Aug 24.
To investigate whether breast cancer patients' visits to an outpatient clinic for late outcome (OCLO) can be replaced by patient reported outcome measures (PROMs), by comparing late toxicity scored at the OCLO with PROMs.
All breast cancer patients treated in our institute with adjuvant radiotherapy 10-11years ago were invited to visit the OCLO, and for filling out PROM-questionnaires. Concordance rate between PROMs and OCLO-reported outcome and the percentage of patients with ≥2 degrees difference in toxicity level between patient and clinician was assessed.
686 of 1029 patients were still alive. 249 patients visited the OCLO, and 341 patients returned a questionnaire. At a group level, patients reported higher toxicity rates than clinicians. The mean concordance for individual patients was 58% between patient and clinician reported outcome. In 2.8%, the clinician reported ≥2 degrees higher toxicity than the patients did, whereas in 6.8% patients reported ≥2 degrees higher toxicity.
PROMs do not underestimate late side-effects at a group level. In spite of the low concordance rate, PROMS can be used to identify patients who experience a heavy burden of side-effects, requiring specific attention. Therefore, patients can be spared a visit to the OCLO.
通过比较门诊就诊时的迟发性毒性评分与患者报告的结局测量(PROMs),探讨乳腺癌患者是否可以用 PROMs 替代门诊就诊评估迟发性结局。
邀请我院 10-11 年前接受辅助放疗的所有乳腺癌患者到门诊就诊,同时填写 PROM 问卷。评估 PROMs 与门诊就诊报告的结局之间的一致性,以及患者和临床医生之间毒性水平差异≥2 度的患者比例。
1029 例患者中有 686 例仍存活。249 例患者就诊于门诊,341 例患者返回问卷。从群体水平来看,患者报告的毒性发生率高于临床医生。个别患者的平均一致性为 58%,即患者报告的结局和临床医生报告的结局一致。在 2.8%的情况下,临床医生报告的毒性比患者报告的高 2 度,而在 6.8%的情况下,患者报告的毒性比临床医生报告的高 2 度。
PROMs 在群体水平上不会低估迟发性副作用。尽管一致性率较低,但 PROMS 可用于识别经历严重副作用负担的患者,需要特别关注。因此,可以免去患者门诊就诊。