Literature DB >> 20869232

Choosing patient-reported outcome measures for cancer clinical research--practical principles and an algorithm to assist non-specialist researchers.

T Luckett1, M T King.   

Abstract

AIM: The purpose of this article is to give practical advice to researchers wishing to choose measures of quality of life and other patient-reported outcomes (PROs) for cancer clinical research.
METHOD: Readers are guided through the process of selecting a patient-reported outcome measure (PROM) by means of six principles, illustrated with examples.
RESULTS: PROM selection should always be undertaken with consideration of specific objectives, samples, treatments and available resources. Guiding principles include: (1) always consider PROMs early in the design process within the context of other methodological decisions; (2) choose a primary PROM that is as proximal to the cancer and/or its treatment as will add to knowledge and inform practice; (3) identify candidate PROMs primarily on the grounds of scaling and content; (4) appraise the reliability, validity and 'track records' of candidate PROMs in studies similar to that planned; (5) look ahead to practical concerns; and (6) take a minimalist approach to ad hoc items.
CONCLUSION: The principles and algorithms presented in this article will assist cancer clinical researchers who lack specialist expertise in patient-reported outcome measurement to make appropriate choices when selecting PROMs for their next study. Crown
Copyright © 2010. Published by Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20869232     DOI: 10.1016/j.ejca.2010.08.002

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  17 in total

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2.  Evaluating patients for psychosocial distress and supportive care needs based on health-related quality of life in primary brain tumors: a prospective multicenter analysis of patients with gliomas in an outpatient setting.

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Journal:  J Neurooncol       Date:  2016-09-16       Impact factor: 4.130

Review 3.  Patient-reported outcome measures in inflammatory bowel disease.

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Journal:  Can J Gastroenterol Hepatol       Date:  2014-11

4.  COVID-19 Emergency and the Need to Speed Up the Adoption of Electronic Patient-Reported Outcomes in Cancer Clinical Practice.

Authors:  Laura Marandino; Andrea Necchi; Massimo Aglietta; Massimo Di Maio
Journal:  JCO Oncol Pract       Date:  2020-05-01

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6.  The sixth international RASopathies symposium: Precision medicine-From promise to practice.

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Journal:  Am J Med Genet A       Date:  2019-12-11       Impact factor: 2.802

Review 7.  Patient-reported outcomes in neurofibromatosis and schwannomatosis clinical trials.

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Journal:  Support Care Cancer       Date:  2019-04-16       Impact factor: 3.603

9.  Quality of Life in Vulnerable Older Patients with Metastatic Colorectal Cancer Receiving Palliative Chemotherapy-The Randomized NORDIC9-Study.

Authors:  Gabor Liposits; Henrik Rode Eshøj; Sören Möller; Stine Brændegaard Winther; Halla Skuladottir; Jesper Ryg; Eva Hofsli; Carl-Henrik Shah; Laurids Østergaard Poulsen; Åke Berglund; Camilla Qvortrup; Pia Österlund; Bengt Glimelius; Halfdan Sorbye; Per Pfeiffer
Journal:  Cancers (Basel)       Date:  2021-05-26       Impact factor: 6.639

10.  Measuring the Effect of Cutaneous Neurofibromas on Quality of Life in Neurofibromatosis Type 1.

Authors:  Sheilagh Maguiness; Yemima Berman; Nathan Rubin; Melissa Dodds; Scott R Plotkin; Claire Wong; Christopher Moertel
Journal:  Neurology       Date:  2021-07-06       Impact factor: 11.800

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