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A population-based approach to compare patient-reported outcomes of long-term Hodgkin's lymphoma survivors according to trial participation: a joint study from the Patient-Reported Outcomes Following Initial Treatment and Long-term Evaluation of Survivorship registry and European Organisation for Research and Treatment of Cancer
- Source :
- European Journal of Cancer Prevention, 26(September). Lippincott Williams and Wilkins, European journal of cancer prevention, 26 Joining forces for better cancer registration in Europe, S223-S228. Lippincott Williams and Wilkins
- Publication Year :
- 2017
-
Abstract
- Survival discrepancy between patients treated in a clinical trial and routine practice is well recognized. No study has assessed the health-related quality of life (HRQL) of long-term Hodgkin's lymphoma survivors (HLS) according to trial participation. We applied a population-based approach to examine the differences in HRQL, healthcare utilization, and satisfaction with healthcare among long-term HLS who had participated in a trial (tHLS) and those treated in routine care (rHLS). All HLS diagnosed during the period 1989-1998 and living in southern Netherlands were selected from the Netherlands Cancer Registry in 2004 to participate in the Patient Reported Outcomes Following Initial treatment and Long-term Evaluation of Survivorship registry study. Data linkage with the European Organisation for Research and Treatment of Cancer was performed in November 2014 to identify trial participation. The 65 tHLS and 67 rHLS had comparable demographic and clinical characteristics. Unadjusted and adjusted models indicated no association between trial participation and HRQL. There was no evidence of differences in healthcare satisfaction. Trial participation was associated with 48% more visits to specialists in the past year (adjusted 95% confidence interval: 10-99). No association of trial participation with cancer-related contacts was observed. tHLS and rHLS had comparable long-term HRQL. Although trial participation was associated with more specialist visits, there was no evidence of an association with healthcare satisfaction and the number of cancer-related visits. Identification of trial participation in population-based cancer registry through data linkage with clinical trials enables a population-based approach to examine patient-reported outcomes differences between tHLS and rHLS.
- Subjects :
- Adult
Male
Cancer Research
medicine.medical_specialty
Biomedical Research
Time Factors
Adolescent
Epidemiology
Population
03 medical and health sciences
Young Adult
0302 clinical medicine
Quality of life
Survivorship curve
Health care
medicine
Humans
030212 general & internal medicine
Patient Reported Outcome Measures
Registries
Survivors
Young adult
Patient participation
education
Aged
Netherlands
education.field_of_study
Clinical Trials as Topic
business.industry
Public Health, Environmental and Occupational Health
Middle Aged
Hodgkin Disease
Cancer registry
Clinical trial
Europe
Treatment Outcome
Oncology
030220 oncology & carcinogenesis
Population Surveillance
Physical therapy
Female
Patient Participation
business
Subjects
Details
- ISSN :
- 14735709 and 09598278
- Database :
- OpenAIRE
- Journal :
- European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)
- Accession number :
- edsair.doi.dedup.....133d2cf37d7bae67a031d14fc8b82b93