Patient Self-Reports of Symptoms and Clinician Ratings as Predictors of Overall Cancer Survival

Chantal Quinten(European Organisation for Research and Treatment of Cancer), John Maringwa(European Organisation for Research and Treatment of Cancer), Carolyn Gotay(University of British Columbia), Francesca Martinelli(University of British Columbia), Corneel Coens(European Organisation for Research and Treatment of Cancer), Bryce B. Reeve(European Organisation for Research and Treatment of Cancer), Hans‐Henning Flechtner(European Organisation for Research and Treatment of Cancer), Eva Greimel(Medical University of Graz), Madeleine King(The University of Sydney), David Osoba(European Organisation for Research and Treatment of Cancer), Charles S. Cleeland(European Organisation for Research and Treatment of Cancer), Jolie Ringash(University of Toronto), J. Schmucker-Von Koch(University of Regensburg), Martin J. B. Taphoorn(Vrije Universiteit Amsterdam), Joachim Weis(University of Freiburg), Andrew Bottomley(European Organisation for Research and Treatment of Cancer)
JNCI Journal of the National Cancer Institute
December 7, 2011
Cited by 225Open Access
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Abstract

BACKGROUND: The National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) reporting system is widely used by clinicians to measure patient symptoms in clinical trials. The European Organization for Research and Treatment of Cancer's Quality of Life core questionnaire (EORTC QLQ-C30) enables cancer patients to rate their symptoms related to their quality of life. We examined the extent to which patient and clinician symptom scoring and their agreement could contribute to the estimation of overall survival among cancer patients. METHODS: We analyzed baseline data regarding six cancer symptoms (pain, fatigue, vomiting, nausea, diarrhea, and constipation) from a total of 2279 cancer patients from 14 closed EORTC randomized controlled trials. In each trial that was selected for retrospective pooled analysis, both clinician and patient symptom scoring were reported simultaneously at study entry. We assessed the extent of agreement between clinician vs patient symptom scoring using the Spearman and kappa correlation statistics. After adjusting for age, sex, performance status, cancer severity, and cancer site, we used Harrell concordance index (C-index) to compare the potential for clinician-reported and/or patient-reported symptom scores to improve the accuracy of Cox models to predict overall survival. All P values are from two-sided tests. RESULTS: Patient-reported scores for some symptoms, particularly fatigue, did differ from clinician-reported scores. For each of the six symptoms that we assessed at baseline, both clinician and patient scorings contributed independently and positively to the predictive accuracy of survival prognostication. Cox models of overall survival that considered both patient and clinician scores gained more predictive accuracy than models that considered clinician scores alone for each of four symptoms: fatigue (C-index = .67 with both patient and clinician data vs C-index = .63 with clinician data only; P <.001), vomiting (C-index = .64 vs .62; P = .01), nausea (C-index = .65 vs .62; P < .001), and constipation (C-index = .62 vs .61; P = .01). CONCLUSION: Patients provide a subjective measure of symptom severity that complements clinician scoring in predicting overall survival.


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