Cargando…
The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial
BACKGROUND: Patient-reported outcomes (PROs) are getting widely implemented, but little is known of the impact of applying PROs in specific cancer diagnoses. We report the results of a randomized controlled trial (RCT) of the active use of PROs in patients with locally advanced or metastatic bladder...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562329/ https://www.ncbi.nlm.nih.gov/pubmed/37812306 http://dx.doi.org/10.1186/s41687-023-00640-5 |
_version_ | 1785118102571188224 |
---|---|
author | Taarnhøj, Gry Assam Johansen, Christoffer Carus, Andreas Dahlrot, Rikke Hedegaard Dohn, Line Hammer Hjøllund, Niels Henrik Knudsen, Mark Bech Tolver, Anders Lindberg, Henriette Pappot, Helle |
author_facet | Taarnhøj, Gry Assam Johansen, Christoffer Carus, Andreas Dahlrot, Rikke Hedegaard Dohn, Line Hammer Hjøllund, Niels Henrik Knudsen, Mark Bech Tolver, Anders Lindberg, Henriette Pappot, Helle |
author_sort | Taarnhøj, Gry Assam |
collection | PubMed |
description | BACKGROUND: Patient-reported outcomes (PROs) are getting widely implemented, but little is known of the impact of applying PROs in specific cancer diagnoses. We report the results of a randomized controlled trial (RCT) of the active use of PROs in patients with locally advanced or metastatic bladder cancer (BC) undergoing medical oncological treatment (MOT) with focus on determining the clinical effects of using PROs during chemo- or immunotherapy compared to standard of care. METHODS: We recruited patients from four departments of oncology from 2019 to 2021. Inclusion criteria were locally advanced or metastatic BC, initiating chemo- or immunotherapy. Patients were randomized 1:1 between answering selected PRO-CTCAE questions electronically once weekly with a built-in alert-algorithm instructing patients of how to handle reported symptoms as a supplement to standard of care for handling of side effects (intervention arm (IA)) vs standard procedure for handling of side effects (control arm (CA)). No real-time alerts were sent to the clinic when PROs exceeded threshold values. Clinicians were prompted to view the completed PROs in the IA at each clinical visit. The co-primary clinical endpoints were hospital admissions and treatment completion rate. Secondary endpoints were overall survival (OS), quality of life (EORTC’s QLQ-C30 and QLQ-BLM30) and dose reductions. RESULTS: 228 patients with BC were included, 76% were male. 141 (62%) of the patients had metastatic disease. 51% of patients in the IA completed treatment vs. 56% of patients in the CA, OR 0.83 (95% CI 0.47–1.44, p = 0.51). 41% of patients in the IA experienced hospitalization vs. 32% in the CA, OR 1.48 (95% CI 0.83–2.65, p = 0.17). OS was comparable between the two arms (IA: median 22.3mo (95% CI 17.0-NR) vs. CA: median 23.1mo (95% CI 17.7-NR). Patient and clinician compliance was high throughout the study period (80% vs 94%). CONCLUSIONS: This RCT did not show an effect of PRO on completion of treatment, hospitalizations or OS for BC patients during MOT despite a high level of patient and clinician compliance. The lack of real-time response to alerts remains the greatest limitation to this study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41687-023-00640-5. |
format | Online Article Text |
id | pubmed-10562329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-105623292023-10-11 The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial Taarnhøj, Gry Assam Johansen, Christoffer Carus, Andreas Dahlrot, Rikke Hedegaard Dohn, Line Hammer Hjøllund, Niels Henrik Knudsen, Mark Bech Tolver, Anders Lindberg, Henriette Pappot, Helle J Patient Rep Outcomes Research BACKGROUND: Patient-reported outcomes (PROs) are getting widely implemented, but little is known of the impact of applying PROs in specific cancer diagnoses. We report the results of a randomized controlled trial (RCT) of the active use of PROs in patients with locally advanced or metastatic bladder cancer (BC) undergoing medical oncological treatment (MOT) with focus on determining the clinical effects of using PROs during chemo- or immunotherapy compared to standard of care. METHODS: We recruited patients from four departments of oncology from 2019 to 2021. Inclusion criteria were locally advanced or metastatic BC, initiating chemo- or immunotherapy. Patients were randomized 1:1 between answering selected PRO-CTCAE questions electronically once weekly with a built-in alert-algorithm instructing patients of how to handle reported symptoms as a supplement to standard of care for handling of side effects (intervention arm (IA)) vs standard procedure for handling of side effects (control arm (CA)). No real-time alerts were sent to the clinic when PROs exceeded threshold values. Clinicians were prompted to view the completed PROs in the IA at each clinical visit. The co-primary clinical endpoints were hospital admissions and treatment completion rate. Secondary endpoints were overall survival (OS), quality of life (EORTC’s QLQ-C30 and QLQ-BLM30) and dose reductions. RESULTS: 228 patients with BC were included, 76% were male. 141 (62%) of the patients had metastatic disease. 51% of patients in the IA completed treatment vs. 56% of patients in the CA, OR 0.83 (95% CI 0.47–1.44, p = 0.51). 41% of patients in the IA experienced hospitalization vs. 32% in the CA, OR 1.48 (95% CI 0.83–2.65, p = 0.17). OS was comparable between the two arms (IA: median 22.3mo (95% CI 17.0-NR) vs. CA: median 23.1mo (95% CI 17.7-NR). Patient and clinician compliance was high throughout the study period (80% vs 94%). CONCLUSIONS: This RCT did not show an effect of PRO on completion of treatment, hospitalizations or OS for BC patients during MOT despite a high level of patient and clinician compliance. The lack of real-time response to alerts remains the greatest limitation to this study. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s41687-023-00640-5. Springer International Publishing 2023-10-09 /pmc/articles/PMC10562329/ /pubmed/37812306 http://dx.doi.org/10.1186/s41687-023-00640-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Taarnhøj, Gry Assam Johansen, Christoffer Carus, Andreas Dahlrot, Rikke Hedegaard Dohn, Line Hammer Hjøllund, Niels Henrik Knudsen, Mark Bech Tolver, Anders Lindberg, Henriette Pappot, Helle The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title | The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title_full | The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title_fullStr | The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title_full_unstemmed | The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title_short | The iBLAD study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
title_sort | iblad study: patient-reported outcomes in bladder cancer during oncological treatment: a multicenter national randomized controlled trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562329/ https://www.ncbi.nlm.nih.gov/pubmed/37812306 http://dx.doi.org/10.1186/s41687-023-00640-5 |
work_keys_str_mv | AT taarnhøjgryassam theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT johansenchristoffer theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT carusandreas theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT dahlrotrikkehedegaard theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT dohnlinehammer theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT hjøllundnielshenrik theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT knudsenmarkbech theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT tolveranders theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT lindberghenriette theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT pappothelle theibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT taarnhøjgryassam ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT johansenchristoffer ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT carusandreas ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT dahlrotrikkehedegaard ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT dohnlinehammer ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT hjøllundnielshenrik ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT knudsenmarkbech ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT tolveranders ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT lindberghenriette ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial AT pappothelle ibladstudypatientreportedoutcomesinbladdercancerduringoncologicaltreatmentamulticenternationalrandomizedcontrolledtrial |