Treatment of Older Patients with Mantle-Cell Lymphoma

Hanneke C. Kluin‐Nelemans(University Medical Center Groningen), Eva Hoster(University of Namur), Olivier Hermine(University of Namur), Jan Walewski(University of Namur), Marek Trněný(University of Namur), Carsten Geisler(University of Namur), Stephan Stilgenbauer(University of Namur), Catherine Thiéblemont(University of Namur), Ursula Vehling‐Kaiser(University of Namur), Jeanette K. Doorduijn(University of Namur), Bertrand Coiffier(University of Namur), Roswitha Forstpointner(University of Namur), Hervé Tilly(University of Namur), Lothar Kanz(University of Namur), Pierre Feugier(University of Namur), Michał Szymczyk(University of Namur), Michael Hallek(University of Namur), Stephan Kremers(University of Namur), G. Lepeu(University of Namur), Laurence Sanhès(University of Namur), Josée M. Zijlstra(University of Namur), Réda Bouabdallah(University of Namur), Pieternella J. Lugtenburg(University of Namur), Margaret Macro(University of Namur), Michael Pfreundschuh(University of Namur), Vít Procházka(University of Namur), Francesco Di Raimondo(University of Namur), Vincent Ribrag(University of Namur), M. Uppenkamp(University of Namur), Marc André(University of Namur), W. Klapper(University of Namur), W. Hiddemann(University of Namur), Michael Unterhalt(University of Namur), Martin Dreyling(University of Namur)
New England Journal of Medicine
August 8, 2012
Cited by 517Open Access
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Abstract

BACKGROUND: The long-term prognosis for older patients with mantle-cell lymphoma is poor. Chemoimmunotherapy results in low rates of complete remission, and most patients have a relapse. We investigated whether a fludarabine-containing induction regimen improved the complete-remission rate and whether maintenance therapy with rituximab prolonged remission. METHODS: We randomly assigned patients 60 years of age or older with mantle-cell lymphoma, stage II to IV, who were not eligible for high-dose therapy to six cycles of rituximab, fludarabine, and cyclophosphamide (R-FC) every 28 days or to eight cycles of rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) every 21 days. Patients who had a response underwent a second randomization to maintenance therapy with rituximab or interferon alfa, each given until progression. RESULTS: Of the 560 patients enrolled, 532 were included in the intention-to-treat analysis for response, and 485 in the primary analysis for response. The median age was 70 years. Although complete-remission rates were similar with R-FC and R-CHOP (40% and 34%, respectively; P=0.10), progressive disease was more frequent with R-FC (14%, vs. 5% with R-CHOP). Overall survival was significantly shorter with R-FC than with R-CHOP (4-year survival rate, 47% vs. 62%; P=0.005), and more patients in the R-FC group died during the first remission (10% vs. 4%). Hematologic toxic effects occurred more frequently in the R-FC group than in the R-CHOP group, but the frequency of grade 3 or 4 infections was balanced (17% and 14%, respectively). In 274 of the 316 patients who were randomly assigned to maintenance therapy, rituximab reduced the risk of progression or death by 45% (in remission after 4 years, 58%, vs. 29% with interferon alfa; hazard ratio for progression or death, 0.55; 95% confidence interval, 0.36 to 0.87; P=0.01). Among patients who had a response to R-CHOP, maintenance therapy with rituximab significantly improved overall survival (4-year survival rate, 87%, vs. 63% with interferon alfa; P=0.005). CONCLUSIONS: R-CHOP induction followed by maintenance therapy with rituximab is effective for older patients with mantle-cell lymphoma. (Funded by the European Commission and others; ClinicalTrials.gov number, NCT00209209.).


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