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Final Results of the IELSG-19 Randomized Trial of Mucosa-Associated Lymphoid Tissue Lymphoma: Improved Event-Free and Progression-Free Survival With Rituximab Plus Chlorambucil Versus Either Chlorambucil or Rituximab Monotherapy.

Zucca, E; Conconi, A; Martinelli, G; Bouabdallah, R; Tucci, A; Vitolo, U; Martelli, M; Pettengell, R; Salles, G; Sebban, C; et al. Zucca, E; Conconi, A; Martinelli, G; Bouabdallah, R; Tucci, A; Vitolo, U; Martelli, M; Pettengell, R; Salles, G; Sebban, C; Guillermo, AL; Pinotti, G; Devizzi, L; Morschhauser, F; Tilly, H; Torri, V; Hohaus, S; Ferreri, AJM; Zachée, P; Bosly, A; Haioun, C; Stelitano, C; Bellei, M; Ponzoni, M; Moreau, A; Jack, A; Campo, E; Mazzucchelli, L; Cavalli, F; Johnson, P; Thieblemont, C (2017) Final Results of the IELSG-19 Randomized Trial of Mucosa-Associated Lymphoid Tissue Lymphoma: Improved Event-Free and Progression-Free Survival With Rituximab Plus Chlorambucil Versus Either Chlorambucil or Rituximab Monotherapy. J Clin Oncol, 35 (17). pp. 1905-1912. ISSN 1527-7755 https://doi.org/10.1200/JCO.2016.70.6994
SGUL Authors: Pettengell, Ruth

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Abstract

Purpose There is no consensus on the optimal systemic treatment of patients with extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue. The IELSG-19 phase III study, to our knowledge, was the first such study to address the question of first-line treatment in a randomized trial. Patients and Methods Eligible patients were initially randomly assigned (1:1 ratio) to receive either chlorambucil monotherapy (6 mg/m2/d orally on weeks 1 to 6, 9 to 10, 13 to 14, 17 to 18, and 21 to 22) or a combination of chlorambucil (same schedule as above) and rituximab (375 mg/m2 intravenously on day 1 of weeks 1, 2, 3, 4, 9, 13, 17, and 21). After the planned enrollment of 252 patients, the protocol was amended to continue with a three-arm design (1:1:6 ratio), with a new arm that included rituximab alone (same schedule as the combination arm) and with a final sample size of 454 patients. The main end point was event-free survival (EFS). Analysis of chlorambucil versus the combination arm was performed and reported separately before any analysis of the third arm. Results At a median follow-up of 7.4 years, addition of rituximab to chlorambucil led to significantly better EFS (hazard ratio, 0.54; 95% CI, 0.38 to 0.77). EFS at 5 years was 51% (95% CI, 42 to 60) with chlorambucil alone, 50% (95% CI, 42 to 59) with rituximab alone, and 68% (95% CI, 60 to 76) with the combination ( P = .0009). Progression-free survival was also significantly better with the combination ( P = .0119). Five-year overall survival was approximately 90% in each arm. All treatments were well tolerated. No unexpected toxicities were recorded. Conclusion Rituximab in combination with chlorambucil demonstrated superior efficacy in mucosa-associated lymphoid tissue lymphoma; however, improvements in EFS and progression-free survival did not translate into longer overall survival.

Item Type: Article
Additional Information: © 2017 by American Society of Clinical Oncology Errata available at http://doi.org/10.1200/JCO.2017.74.4441
Keywords: Adult, Aged, Aged, 80 and over, Antineoplastic Combined Chemotherapy Protocols, Chlorambucil, Disease-Free Survival, Endpoint Determination, Female, Humans, Kaplan-Meier Estimate, Lymphoma, B-Cell, Marginal Zone, Male, Middle Aged, Rituximab, Treatment Outcome, Humans, Chlorambucil, Antineoplastic Combined Chemotherapy Protocols, Disease-Free Survival, Treatment Outcome, Endpoint Determination, Adult, Aged, Aged, 80 and over, Middle Aged, Female, Male, Lymphoma, B-Cell, Marginal Zone, Kaplan-Meier Estimate, Rituximab, 1112 Oncology And Carcinogenesis, Oncology & Carcinogenesis
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title: J Clin Oncol
ISSN: 1527-7755
Language: eng
Dates:
DateEvent
10 June 2017Published
29 March 2017Published Online
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
ICP OCS-01356-03-2003Oncosuissehttp://dx.doi.org/10.13039/501100004201
PubMed ID: 28355112
Web of Science ID: WOS:000403155200008
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/110370
Publisher's version: https://doi.org/10.1200/JCO.2016.70.6994

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