Volume 5, Issue 5 pp. 465-473
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Patient accrual and interim statistical analysis in long-term randomized clinical trials: The French chronic lymphocytic leukemia CLL 80 protocol as a case study

Claude Chastang

Claude Chastang

Département de Biostatistique et d'Informatique Médicale, CHU Lariboisière Saint-Louis, 91 Boulevard de l'Hǒpital, 75634 Paris Cédex 13, France

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Philippe Travade

Philippe Travade

Département d'Hématologie, Groupe hospitalier Pitié-Salpětrière, 47 Boulevard de l'Hǒpital, 75651 Paris Cèdex 13, France

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Jacques Benichou

Jacques Benichou

Département de Biostatistique et d'Informatique Médicale, CHU Lariboisière Saint-Louis, 91 Boulevard de l'Hǒpital, 75634 Paris Cédex 13, France

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Guillaume Dighiero

Guillaume Dighiero

Département d'Hématologie, Groupe hospitalier Pitié-Salpětrière, 47 Boulevard de l'Hǒpital, 75651 Paris Cédex 13, France

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Jacques-Louis Binet

Jacques-Louis Binet

Département d'Hématologie, Groupe hospitalier Pitié-Salpětrière, 47 Boulevard de l'Hǒpital, 75651 Paris Cédex 13, France

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First published: September/October 1986
Citations: 2

Abstract

The CLL 80 clinical trial of treatment for chronic lymphocytic leukemia was designed using a three-stage prognostic classification. Within each stage patients received one of two treatments allocated by randomization, two adjacent stages having a common treatment. The fixed-sample design required 850 patients entered over a period of 8.5 years.

Active patient recruitment led to 741 patients being randomized in four years. The first interim analysis, carried out at this point, showed a treatment difference in one stage which was statistically significant (p = 0.001) and justified an early termination of the protocol. This paper discusses practical aspects of patient accrual and interim analysis in this study.

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