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Treatment of older patients with mantle-cell lymphoma

Authors :
Kluin-Nelemans, J.C. (Hanneke)
Hoster, E. (Eva)
Hermine, O. (Olivier)
Walewski, J. (Jan)
Trneny, M. (Marek)
Geisler, C.H. (Christian)
Stilgenbauer, S. (S.)
Thieblemont, C. (C.)
Vehling-Kaiser, U. (U.)
Doorduijn, J.K. (Jeanette)
Coiffier, B. (Bertrand)
Forstpointner, R. (R.)
Tilly, H. (Herve)
Kanz, L. (Lothar)
Feugier, P. (Pierre)
Szymczyk, M. (M.)
Hallek, M. (M.)
Kremers, S. (Stef)
Lepeu, G. (G.)
Sanhes, L. (L.)
Zijlstra, J. (Jose)
Bouabdallah, R. (Reda)
Lugtenburg, P.J. (Pieternella)
Macro, M.
Pfreundschuh, M. (Michael)
Procházka, V. (V.)
Di Raimondo, F. (F.)
Ribrag, V. (Vincent)
Uppenkamp, M. (M.)
André, J.-L. (Jean-Luc)
Klapper, W. (Wolfram)
Hiddemann, W. (Wolfgang)
Unterhalt, M. (Michael)
Dreyling, M. (Martin)
Kluin-Nelemans, J.C. (Hanneke)
Hoster, E. (Eva)
Hermine, O. (Olivier)
Walewski, J. (Jan)
Trneny, M. (Marek)
Geisler, C.H. (Christian)
Stilgenbauer, S. (S.)
Thieblemont, C. (C.)
Vehling-Kaiser, U. (U.)
Doorduijn, J.K. (Jeanette)
Coiffier, B. (Bertrand)
Forstpointner, R. (R.)
Tilly, H. (Herve)
Kanz, L. (Lothar)
Feugier, P. (Pierre)
Szymczyk, M. (M.)
Hallek, M. (M.)
Kremers, S. (Stef)
Lepeu, G. (G.)
Sanhes, L. (L.)
Zijlstra, J. (Jose)
Bouabdallah, R. (Reda)
Lugtenburg, P.J. (Pieternella)
Macro, M.
Pfreundschuh, M. (Michael)
Procházka, V. (V.)
Di Raimondo, F. (F.)
Ribrag, V. (Vincent)
Uppenkamp, M. (M.)
André, J.-L. (Jean-Luc)
Klapper, W. (Wolfram)
Hiddemann, W. (Wolfgang)
Unterhalt, M. (Michael)
Dreyling, M. (Martin)
Publication Year :
2012

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

Details

Database :
OAIster
Notes :
New England Journal of Medicine vol. 367 no. 6, pp. 520-531, English
Publication Type :
Electronic Resource
Accession number :
edsoai.ocn929970801
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1056.NEJMoa1200920