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Blood, 15 September 2008, Vol. 112, No. 6, pp. 2248-2260.
Prepublished online as a Blood First Edition Paper on July 8, 2008; DOI 10.1182/blood-2008-03-145128.


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CLINICAL TRIALS AND OBSERVATIONS

A prospective clinicopathologic study of dose-modified CODOX-M/IVAC in patients with sporadic Burkitt lymphoma defined using cytogenetic and immunophenotypic criteria (MRC/NCRI LY10 trial)

Graham M. Mead1, Sharon L. Barrans2, Wendi Qian3, Jan Walewski4, John A. Radford5, Max Wolf6, Simon M. Clawson3, Sally P. Stenning3, Claire L. Yule3, Andrew S. Jack2, on behalf of the UK National Cancer Research Institute Lymphoma Clinical Studies Group and the Australasian Leukaemia and Lymphoma Group

1 Southampton University Hospitals Trust, Southampton, United Kingdom; 2 Haematological Malignancy Diagnostic Service, Leeds General Infirmary, Leeds, United Kingdom; 3 MRC Clinical Trials Unit, London, United Kingdom; 4 MSCM Cancer Center, Warsaw, Poland; 5 Christie Hospital, Manchester, United Kingdom; and 6 Peter MacCallum Cancer Centre, Melbourne, Australia

This prospective study aimed to develop reproducible diagnostic criteria for sporadic Burkitt lymphoma (BL), applicable to routine practice, and to evaluate the efficacy of dose-modified (dm) CODOX-M/IVAC in patients diagnosed using these criteria. The study was open to patients with an aggressive B-cell lymphoma with an MKI67 fraction approaching 100%. Immunophenotype and fluorescent in situ hybridization (FISH) were used to separate BL from other aggressive B-cell lymphomas. BL was characterized by the presence of a cMYC rearrangement as a sole cytogenetic abnormality occurring in patients with a germinal center phenotype with absence of BCL-2 expression and abnormal TP53 expression. A total of 128 patients were eligible for the study, of whom 58 were considered to have BL and 70 to have diffuse large B-cell lymphoma (DLBCL). There were 110 clinically fit patients who received dmCODOX-M (methotrexate, dose 3 g/m2) with or without IVAC according to risk group. The 2-year progression-free survival was 64% (95% confidence interval [CI] 51%-77%) for BL, 55% (95% CI 42%-66%) for DLBCL, 85% (95% CI 73%-97%) for low risk, and 49% (95% CI 38%-60%) for high-risk patients. The observed differences in outcome and other clinical features validate the proposed diagnostic criteria. Compared with the previous trial LY06 with full-dose methotrexate (6.7 g/m2), there was a reduction in toxicity with comparable outcomes. This study was registered at www.clinicaltrials.gov as NCT00040690 [ClinicalTrials.gov] .


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E. Tholouli, S. Watt, G. S. Lucas, J. Burthem, J. A. L. Yin, J. Cavet, H. Greenfield, and J. B. Houghton
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A. S. Jack, S. L. Barrans, W. Qian, S. P. Stenning, and G. M. Mead
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