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Annals of Oncology Advance Access originally published online on January 27, 2007
Annals of Oncology 2007 18(4):775-781; doi:10.1093/annonc/mdl494
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© 2007 European Society for Medical Oncology

quality of life and supportive care

Has the quality of health-related quality of life reporting in cancer clinical trials improved over time? Towards bridging the gap with clinical decision making

F Efficace1,*, D Osoba2, C Gotay3, M Sprangers4, C Coens1 and A Bottomley1

1 European Organisation for Research and Treatment of Cancer (EORTC) Data Center, Quality of Life Unit, Brussels, Belgium
2 QOL Consultant, West Vancouver, British Columbia, Canada
3 Cancer Research Center of Hawaii, University of Hawaii, Honolulu, HI, USA
4 Academic Medical Center, Department of Medical Psychology, University of Amsterdam, Amsterdam, The Netherlands

* Correspondence to: Dr F. Efficace, Mediterranean Institute of Hematology (IME), GIMEMA Data Center, Via Benevento, 6, 00161 Rome, Italy. Phone: +39 06 441 639850; Fax: +39 06 440 2516. E-mail: f.efficace{at}fondazioneime.org

Background: Previous work highlighted a number of methodological constraints when reporting health-related quality of life (HRQOL) outcomes from randomized controlled trials (RCTs). Given this, the objective of this study was to investigate whether the quality of such HRQOL reports has improved over time.

Materials and methods: On the basis of a predefined set of criteria, 159 RCTs with a HRQOL end point, published between 1990 and 2004 were identified and analyzed. Each study was evaluated by a number of issues (e.g. sample size and industry sponsorship) and by the ‘minimum standard checklist for evaluating HRQOL outcomes in cancer clinical trials’.

Results: The quality of HRQOL reports, as measured by the overall checklist score, was independently related to more recently published studies (P < 0.0001). This relationship was independent of industry funded, HRQOL end point (primary versus secondary), cancer disease site, size of the study and HRQOL difference between treatment arms. While only 39.3% of studies published between 1990 and 2000 (89/159 RCTs) were identified as being probably robust, thus likely to support clinical decision making, this percentage was 64.3% for studies published after 2000 (70/159 RCTs).

Conclusion: Since we found a significant learning curve in HRQOL trial reporting since 1990, it can be expected that HRQOL data will increasingly impact on clinical decision making and treatment policies in the near future.

Key words: Cancer, clinical decision-making, clinical trial, quality of life

Received for publication September 18, 2006. Revision received November 20, 2006. Accepted for publication December 7, 2006.


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