2018
DOI: 10.1007/s00066-018-1395-y
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Patient- versus physician-reported outcomes in prostate cancer patients receiving hypofractionated radiotherapy within a randomized controlled trial

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Cited by 42 publications
(37 citation statements)
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“…Studies varied on the tool of HRQOL assessment and the factors affecting it. Rammant et al 10 demonstrated that there was high under-reporting with the physician -reported outcomes as compared to patient-reported outcomes. All the HRQOL tools used in the studies assessed patient's self-reported outcomes, making their data reliable but partially subjective.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Studies varied on the tool of HRQOL assessment and the factors affecting it. Rammant et al 10 demonstrated that there was high under-reporting with the physician -reported outcomes as compared to patient-reported outcomes. All the HRQOL tools used in the studies assessed patient's self-reported outcomes, making their data reliable but partially subjective.…”
Section: Discussionmentioning
confidence: 99%
“…8,9 Many studies have focused on the assessment of HRQOL with much focus on the effects of treatment on HRQOL. [10][11][12][13] Radical prostatectomy (RP) and radiotherapy (RT) are the most common therapy options for prostate cancer patients, conventionally used to manage the localized disease. 14 Although patients with advanced disease receiving Androgen Deprivation Therapy (ADT) have been found to have the poorest HRQOL scores, 11 and worse symptom burden when combined with radiotherapy or radical prostatectomy, 15 there is still no consensus on the optimal treatment regimen and knowledge of its long-term effects is limited.…”
Section: Introductionmentioning
confidence: 99%
“…There are limitations to comparing our toxicity data with published studies because of its retrospective nature and differences in scoring systems, methods and timings of analyses, frequency of follow up and dose fractionation schedules of LDR-EBRT and HDR-HDR-EBRT [8]. We have also only reported grade 3 toxicities and have not collected patient reported outcomes, which more accurately measure adverse events [35]. A comparison of our results with previously published studies is shown in Table 3.…”
Section: Discussionmentioning
confidence: 96%
“…Third, although we found no significant difference with respect to the incidence of late grade 3 GU and GI toxicities (with 5‐year TFS estimates >95% for both groups), the low event rates suggest that our analyses still may have been underpowered to detect clinically important differences. We posit that our low event rates may have been because of limited follow‐up (maximum, 5 years) and the clinician‐reported nature of our outcomes, which may be more susceptible to underreporting relative to patient‐reported outcomes . Finally, our study does not include patients who were initially planned for PBT but were re‐planned for IMRT after failing to meet rectal dose constraints.…”
Section: Discussionmentioning
confidence: 99%
“…We posit that our low event rates may have been because of limited follow-up (maximum, 5 years) and the clinician-reported nature of our outcomes, which may be more susceptible to underreporting relative to patient-reported outcomes. [60][61][62] Finally, our study does not include patients who were initially planned for PBT but were re-planned for IMRT after failing to meet rectal dose constraints.…”
Section: Limitationsmentioning
confidence: 99%