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Publication | Open Access

Health-related quality of life and cancer clinical trials

221

Citations

101

References

2011

Year

TLDR

Patient‑reported outcomes, especially health‑related quality of life (HRQoL), have evolved over the past four decades and are now routinely measured in tens of thousands of cancer patients using validated questionnaires. This review surveys recent HRQoL data to guide clinicians and underscores the need for a clear method to determine the clinical meaningfulness of score changes. The authors analyze a curated selection of HRQoL studies published over the last decade, targeting healthcare professionals. HRQoL assessments in trials reveal treatment impacts, improve methodological rigor, predict survival better than performance status, and are poised to become a standard endpoint.

Abstract

The measurement of patient-reported outcomes, including health-related quality of life, is a new initiative which has emerged and grown over the past four decades. Following the development of reliable and valid self-report questionnaires, health-related quality of life has been assessed in tens of thousands of patients and a wide variety of cancers. This review is based on a selection of data published in the last decade and is intended primarily for healthcare professionals. The assessments in clinical trials have been particularly useful for elucidating the effects of various cancers and their treatments on patients' lives and have provided additional information that enhances the usual clinical endpoints used for determining the benefits and toxicity of treatment. With growing experience the quality of the health-related quality of studies has improved and, in general, recent studies are more likely to be methodologically robust than those that were performed in earlier decades. Health-related quality of life has become a more accurate predictor of survival than some other clinical parameters, such as performance status. The overall outlook for the routine assessment of patient-reported outcomes in clinical trials is assured and, eventually, it is likely to become a standard part of clinical practice. However, there is still a need for a clear method for determining the clinical meaningfulness of changes in scores. The answer will probably come from the greater use of patient-reported outcomes and the consequent growth of experience that is necessary to make such judgements.

References

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