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Effect of Contract Research Organization Bureaucracy in Clinical Trial Management: A Model From Lung Cancer.

Authors :
Gobbini E
Pilotto S
Pasello G
Polo V
Di Maio M
Arizio F
Galetta D
Petrillo P
Chiari R
Matocci R
Di Costanzo A
Di Stefano TS
Aglietta M
Cagnazzo C
Sperduti I
Bria E
Novello S
Source :
Clinical lung cancer [Clin Lung Cancer] 2018 Mar; Vol. 19 (2), pp. 191-198. Date of Electronic Publication: 2017 Oct 28.
Publication Year :
2018

Abstract

Introduction: Contract research organization (CRO) support is largely included in clinical trial management, although its effect in terms of time savings and benefit has not yet been quantified. We performed a retrospective multicenter analysis of lung cancer trials to explore differences in term of trial activation timelines and accrual for studies with and without CRO involvement.<br />Materials and Methods: Results regarding study timelines from feasibility data to first patient enrollment were collected from 7 Italian thoracic oncology departments. The final accruals (screened/enrolled patients) are reported. We considered CRO/sponsor-administered and CRO-free trials according to who was responsible for the management of the crucial setup phases.<br />Results: Of 113 trials, 62 (54.9%) were CRO-administered, 34 (30.1%) were sponsor-administered, and 17 (15.0%) were CRO-free. The median time from feasibility invitation to documentation obtainment was 151 days in the CRO-administered trials versus 128 in the sponsor-administered and 120 in the CRO-free trials. The time from document submission to contract signature was 142 days in the CRO-administered versus 128 in the sponsor-administered and 132 in the CRO-free trials. The time from global accrual opening to first patient enrollment was 247 days for the CRO-administered versus 194 in the sponsor-administered and 151 in the CRO-free trials. No significant differences were observed in terms of the median overall timeline: 21 months in the CRO-administered, 15 in the sponsor-administered, and 18 months in the CRO-free studies (P = .29).<br />Conclusion: Although no statistically significant differences were identified, the results of our analysis support the idea that bureaucratic procedures might require more time in CRO-administered trials than in sponsor-administered and CRO-free studies. This bureaucratic delay could negatively affect Italian patients' screening and enrollment compared with other countries.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1938-0690
Volume :
19
Issue :
2
Database :
MEDLINE
Journal :
Clinical lung cancer
Publication Type :
Academic Journal
Accession number :
29153968
Full Text :
https://doi.org/10.1016/j.cllc.2017.10.012