Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials

Research output: Contribution to journalJournal articleResearchpeer-review

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Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials. / Gamper, Eva M; Musoro, Jammbe Z; Coens, Corneel; Stelmes, Jean-Jacques; Falato, Claudette; Groenvold, Mogens; Velikova, Galina; Cocks, Kim; Flechtner, Hans-Henning; King, Madeleine T; Bottomley, Andrew; EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups.

In: BMC Cancer, Vol. 21, No. 1, 1083, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Gamper, EM, Musoro, JZ, Coens, C, Stelmes, J-J, Falato, C, Groenvold, M, Velikova, G, Cocks, K, Flechtner, H-H, King, MT, Bottomley, A & EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups 2021, 'Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials', BMC Cancer, vol. 21, no. 1, 1083. https://doi.org/10.1186/s12885-021-08609-7

APA

Gamper, E. M., Musoro, J. Z., Coens, C., Stelmes, J-J., Falato, C., Groenvold, M., Velikova, G., Cocks, K., Flechtner, H-H., King, M. T., Bottomley, A., & EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups (2021). Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials. BMC Cancer, 21(1), [1083]. https://doi.org/10.1186/s12885-021-08609-7

Vancouver

Gamper EM, Musoro JZ, Coens C, Stelmes J-J, Falato C, Groenvold M et al. Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials. BMC Cancer. 2021;21(1). 1083. https://doi.org/10.1186/s12885-021-08609-7

Author

Gamper, Eva M ; Musoro, Jammbe Z ; Coens, Corneel ; Stelmes, Jean-Jacques ; Falato, Claudette ; Groenvold, Mogens ; Velikova, Galina ; Cocks, Kim ; Flechtner, Hans-Henning ; King, Madeleine T ; Bottomley, Andrew ; EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups. / Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials. In: BMC Cancer. 2021 ; Vol. 21, No. 1.

Bibtex

@article{0370a53d73b44d9ba0469ee45ba4c780,
title = "Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials",
abstract = "BACKGROUND: The aim of the study was to estimate the minimally important difference (MID) for interpreting group-level change over time, both within a group and between groups, for the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) scores in patients with prostate cancer.METHODS: We used data from two published EORTC trials. Clinical anchors were selected by strength of correlations with QLQ-C30 scales. In addition, clinicians' input was obtained with regard to plausibility of the selected anchors. The mean change method was applied for interpreting change over time within a group of patients and linear regression models were fitted to estimate MIDs for between-group differences in change over time. Distribution-based estimates were also evaluated.RESULTS: Two clinical anchors were eligible for MID estimation; performance status and the CTCAE diarrhoea domain. MIDs were developed for 7 scales (physical functioning, role functioning, social functioning, pain, fatigue, global quality of life, diarrhoea) and varied by scale and direction (improvement vs deterioration). Within-group MIDs ranged from 4 to 14 points for improvement and - 13 to - 5 points for deterioration and MIDs for between-group differences in change scores ranged from 3 to 13 for improvement and - 10 to - 5 for deterioration.CONCLUSIONS: Our findings aid the meaningful interpretation of changes on a set of EORTC QLQ-C30 scale scores over time, both within and between groups, and for performing more accurate sample size calculations for clinical trials in prostate cancer.",
author = "Gamper, {Eva M} and Musoro, {Jammbe Z} and Corneel Coens and Jean-Jacques Stelmes and Claudette Falato and Mogens Groenvold and Galina Velikova and Kim Cocks and Hans-Henning Flechtner and King, {Madeleine T} and Andrew Bottomley and {EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups}",
note = "{\textcopyright} 2021. The Author(s).",
year = "2021",
doi = "10.1186/s12885-021-08609-7",
language = "English",
volume = "21",
journal = "B M C Cancer",
issn = "1471-2407",
publisher = "BioMed Central Ltd.",
number = "1",

}

RIS

TY - JOUR

T1 - Minimally important differences for the EORTC QLQ-C30 in prostate cancer clinical trials

AU - Gamper, Eva M

AU - Musoro, Jammbe Z

AU - Coens, Corneel

AU - Stelmes, Jean-Jacques

AU - Falato, Claudette

AU - Groenvold, Mogens

AU - Velikova, Galina

AU - Cocks, Kim

AU - Flechtner, Hans-Henning

AU - King, Madeleine T

AU - Bottomley, Andrew

AU - EORTC Genito-Urinary Tract Cancer Group and Quality of Life Groups

N1 - © 2021. The Author(s).

PY - 2021

Y1 - 2021

N2 - BACKGROUND: The aim of the study was to estimate the minimally important difference (MID) for interpreting group-level change over time, both within a group and between groups, for the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) scores in patients with prostate cancer.METHODS: We used data from two published EORTC trials. Clinical anchors were selected by strength of correlations with QLQ-C30 scales. In addition, clinicians' input was obtained with regard to plausibility of the selected anchors. The mean change method was applied for interpreting change over time within a group of patients and linear regression models were fitted to estimate MIDs for between-group differences in change over time. Distribution-based estimates were also evaluated.RESULTS: Two clinical anchors were eligible for MID estimation; performance status and the CTCAE diarrhoea domain. MIDs were developed for 7 scales (physical functioning, role functioning, social functioning, pain, fatigue, global quality of life, diarrhoea) and varied by scale and direction (improvement vs deterioration). Within-group MIDs ranged from 4 to 14 points for improvement and - 13 to - 5 points for deterioration and MIDs for between-group differences in change scores ranged from 3 to 13 for improvement and - 10 to - 5 for deterioration.CONCLUSIONS: Our findings aid the meaningful interpretation of changes on a set of EORTC QLQ-C30 scale scores over time, both within and between groups, and for performing more accurate sample size calculations for clinical trials in prostate cancer.

AB - BACKGROUND: The aim of the study was to estimate the minimally important difference (MID) for interpreting group-level change over time, both within a group and between groups, for the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) scores in patients with prostate cancer.METHODS: We used data from two published EORTC trials. Clinical anchors were selected by strength of correlations with QLQ-C30 scales. In addition, clinicians' input was obtained with regard to plausibility of the selected anchors. The mean change method was applied for interpreting change over time within a group of patients and linear regression models were fitted to estimate MIDs for between-group differences in change over time. Distribution-based estimates were also evaluated.RESULTS: Two clinical anchors were eligible for MID estimation; performance status and the CTCAE diarrhoea domain. MIDs were developed for 7 scales (physical functioning, role functioning, social functioning, pain, fatigue, global quality of life, diarrhoea) and varied by scale and direction (improvement vs deterioration). Within-group MIDs ranged from 4 to 14 points for improvement and - 13 to - 5 points for deterioration and MIDs for between-group differences in change scores ranged from 3 to 13 for improvement and - 10 to - 5 for deterioration.CONCLUSIONS: Our findings aid the meaningful interpretation of changes on a set of EORTC QLQ-C30 scale scores over time, both within and between groups, and for performing more accurate sample size calculations for clinical trials in prostate cancer.

U2 - 10.1186/s12885-021-08609-7

DO - 10.1186/s12885-021-08609-7

M3 - Journal article

C2 - 34620124

VL - 21

JO - B M C Cancer

JF - B M C Cancer

SN - 1471-2407

IS - 1

M1 - 1083

ER -

ID: 282097061