Neoplasms Clinical Trial
Official title:
Evaluation of the Cost and Effectiveness in the First-line Treatment of Advanced Renal Cell Cancer With Sunitinib Compared to Interferon-alfa in Finland.
Patient receiving sunitinib according the clinician's independent decision as first-line
treatment of advanced renal cell carcinoma (RCC) will be asked for informed consent.
Treatment with sunitinib will start and end solely on the treating clinicians and the
patients independent discretion. Consenting patients will prospectively answer standardized
quality of life questionnaires (15D, EQ-5D) during the treatment. Data on health care
resource utilisation will be collected prospectively (outpatient visits, hospital stays,
concomitant drugs, investigations, sick-leaves, travels). In addition, after treatment
failure anti-cancer drugs, hospital stays and date of death will be recorded.
The health economic data during sunitinib treatment and the length of the sunitinib
treatment will be compared with the corresponding previously published data collected
retrospectively from patients with the same condition treated with IFN-alfa. Stepwise
regression analysis will be used to explore whether patient and tumor characteristics
explain potential variation in treatment duration and costs that is not explained by the
treatment.
Health-related quality of life (HRQoL) data will be presented as descriptive data and
compared to age-standardized general population.
At least four major Finnish oncology centers have consented to participate in this study.
The inclusion time will be approximately 24 months, and the study time approximately 48
months. Eighty patients will be included.
n/a
Observational Model: Cohort, Time Perspective: Prospective
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