PLoS ONE (Jan 2013)

Description of the protocols for randomized controlled trials on cancer drugs conducted in Spain (1999-2003).

  • Xavier Bonfill,
  • Mónica Ballesteros,
  • Ignasi Gich,
  • María Antonia Serrano,
  • Fernando García López,
  • Gerard Urrútia

DOI
https://doi.org/10.1371/journal.pone.0079684
Journal volume & issue
Vol. 8, no. 11
p. e79684

Abstract

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ObjectiveTo describe the characteristics of randomized controlled clinical trials (RCT) on cancer drugs conducted in Spain between 1999 and 2003 based on their protocols.MethodsWe conducted an observational retrospective cohort study to identify the protocols of RCTs on cancer drugs authorized by the Agencia Española del Medicamento y Productos Sanitarios (AEMPS) (Spanish Agency for Medicines and Medical Devices) during 1999-2003. A descriptive analysis was completed and the association between variables based on the study setting and sponsorship were assessed.ResultsWe identified a total of 303 protocols, which included 176,835 potentially eligible patients. Three-quarter of the studies were internationally-based, 61.7% were phase III, and 76.2% were sponsored by pharmaceutical companies. The most frequently assessed outcomes were response rate (24.7%), overall survival (20.7%), and progression-free survival (14.5%). Of all protocols, 10.6% intended to include more than 1000 patients (mean: 2442, SD: 2724). Compared with their national counterparts, internationally-based studies were significantly larger (pConclusionRCTs on cancer drugs conducted in Spain between 1999 and 2003 were more likely to be promoted by pharmaceutical companies rather than by non-profit national groups. The former were more often part of international studies, which generally had better methodological quality than national ones. There are some worldwide on-going initiatives that aim to increase the transparency and quality of future research.